Design, Synthesis, and Utility of Defined Molecular Scaffolds

References (350)

1. 1 Landsteiner, K. (1962). The Specificity of Serological Reactions, Revised, Dover Publications.
2. 2 King, T.P. (1976). Chemical and Biological Properties of Some Atopic Allergens. Advances in Immunology Volume 23, Elsevier. [DOI]
3. 3 Mayer, 1956, The Significance of Cross-Links in the Formation of Hapten-Carrier Complexes [DOI]
4. 4 Plescia, 1969, The role of the carrier in antibody formation [DOI]
5. 5 Kontiainen, 1975, Immune responses to hapten conjugates in vitro [DOI]
6. 6 King, 1975, Immunochemical studies of dextran coupled ragweed pollen allergen, antigen E [DOI]
7. 7 Carter, 1994, Techniques for conjugation of synthetic peptides to carrier molecules [DOI]
8. 8 Harris, 1999, Keyhole limpet hemocyanin (KLH): A biomedical review [DOI]
9. 9 Bundle, D.R., Paszkiewicz, E., Elsaidi, H.R.H., Mandal, S.S., and Sarkar, S. (2018). A Three Component Synthetic Vaccine Containing a betab-Mannan T-Cell Peptide Epitope and a beta-Glucan Dendritic Cell Ligand. Molecules, 23. [DOI]
10. 10 Molina, N., Martin-Serrano, A., Fernandez, T.D., Tesfaye, A., Najera, F., Torres, M.J., Mayorga, C., Vida, Y., Montanez, M.I., and Perez-Inestrosa, E. (2018). Dendrimeric Antigens for Drug Allergy Diagnosis: A New Approach for Basophil Activation Tests. Molecules, 23. [DOI]
11. 11 Louie, 2010, Multimodality imaging probes: Design and challenges [DOI]
12. 12 Beal, 2012, Molecular scaffolds using multiple orthogonal conjugations: Applications in chemical biology and drug discovery [DOI]
13. 13 Kanfar, 2015, Emerging trends in enzyme inhibition by multivalent nanoconstructs [DOI]
14. 14 Zhao, 2018, Recent developments in multimodality fluorescence imaging probes [DOI]
15. 15 Clave, 2008, A novel heterotrifunctional peptide-based cross-linking reagent for facile access to bioconjugates. Applications to peptide fluorescent labelling and immobilisation [DOI]
16. 16 Batschelet, E. (1979). Introduction to Mathematics for Life Scientists, Springer. [3rd ed.]. [DOI]
17. 17 Jiang, 2015, Polarity-Tunable and Wavelength-Tunable Bacteriochlorins Bearing a Single Carboxylic Acid or NHS Ester. Use in a Protein Bioconjugation Model System [DOI]
18. 18 Bondy, J.A., and Murty, U.S.R. (1976). Graph Theory with Applications, North Holland. [DOI]
19. 19 Galvez, 2008, Some new trends in chemical graph theory [DOI]
20. 20 Amigo, 2009, A review on molecular topology: Applying graph theory to drug discovery and design [DOI]
21. 21 Choi, 2012, Protease-activated drug development [DOI]
22. 22 Ni, 2010, The application of an aryl hydrazine linker prevents beta-elimination side products in the SPPS of C-terminal cysteine peptides [DOI]
23. 23 Price, 2014, Matching chelators to radiometals for radiopharmaceuticals [DOI]
24. 24 Fu, 2018, Small-molecule fluorescent probes and their design [DOI]
25. 25 MacPherson, 2019, A brief overview of metal complexes as nuclear imaging agents [DOI]
26. 26 Chen, 2016, Recent progress in the development of fluorescent, luminescent and colorimetric probes for detection of reactive oxygen and nitrogen species [DOI]
27. 27 Murale, 2017, Photo-affinity labeling (PAL) in chemical proteomics: A handy tool to investigate protein-protein interactions (PPIs) [DOI]
28. 28 Guo, 2018, Advances in redox-responsive drug delivery systems of tumor microenvironment [DOI]
29. 29 Manzano, 2018, Self-immolative chemistry in nanomedicine [DOI]
30. 30 Alouane, 2015, Self-immolative spacers: Kinetic aspects, structure-property relationships, and applications [DOI]
31. 31 Roth, 2016, Dendritic, Oligomeric, and Polymeric Self-Immolative Molecular Amplification [DOI]
32. 32 Dumoulin, 2010, Synthetic pathways to water-soluble phthalocyanines and close analogs [DOI]
33. 33 Pisarek, 2014, Strategies toward the synthesis of amphiphilic porphyrins [DOI]
34. 34 Luciano, M., and Bruckner, C. (2017). Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media. Molecules, 22. [DOI]
35. 35 Ogata, 2019, Activatable Near-Infrared Fluorescence Imaging Using PEGylated Bacteriochlorin-Based Chlorin and BODIPY-Dyads as Probes for Detecting Cancer [DOI]
36. 36 Matsumoto, 2020, Bioconjugatable synthetic chlorins rendered water-soluble with three PEG-12 groups via click chemistry [DOI]
37. 37 Liu, 2020, Aqueous solubilization of hydrophobic tetrapyrrole macrocycles by attachment to an amphiphilic single-chain nanoparticle (SCNP) [DOI]
38. 38 Liu, 2021, Single-Fluorophore Single-Chain Nanoparticle Undergoes Fluorophore-Driven Assembly with Fluorescence Features Retained in Physiological Milieu [DOI]
39. 39 Harris, J.M. (1992). Poly(ethylene glycol) Chemistry: Biotechnical and Biomedical Applications, Plenum Press. [DOI]
40. 40 Zalipsky, 1997, Introduction to Chemistry and Biological Applications of Poly(ethylene glycol) [DOI]
41. 41 Thompson, 2008, Synthesis and applications of heterobifunctional poly(ethylene oxide) oligomers [DOI]
42. 42 Larson, 2012, Polymeric conjugates for drug delivery [DOI]
43. 43 Herzberger, 2016, Polymerization of Ethylene Oxide, Propylene Oxide, and Other Alkylene Oxides: Synthesis, Novel Polymer Architectures, and Bioconjugation [DOI]
44. 44 Kolate, 2014, PEG—A versatile conjugating ligand for drugs and drug delivery systems [DOI]
45. 45 Begum, 1997, Conformational properties of short poly(oxyethylene) chains in water studied by IR spectroscopy [DOI]
46. 46 Lang, 2019, Expanding the “minimalist” small molecule tagging approach to different bioactive compounds [DOI]
47. 47 Zhang, 2012, Design and synthesis of novel photoaffinity probes for study of the target proteins of oleanolic acid [DOI]
48. 48 Sharma, 2019, Targeting Heterogeneous Tumors Using a Multifunctional Molecular Prodrug [DOI]
49. 49 Devalapally, 2007, Beta-galactoside prodrugs of doxorubicin for application in antibody directed enzyme prodrug therapy/prodrug monotherapy [DOI]
50. 50 Jouanno, 2014, Kondrat’eva ligation: Diels-Alder-based irreversible reaction for bioconjugation [DOI]
51. 51 2002, Kappa-squared: From nuisance to new sense
52. 52 Taniguchi, 2017, PhotochemCAD 3: Diverse Modules for Photophysical Calculations with Access to Multiple Spectral Databases [DOI]
53. 53 Qi, 2019, Heuristics from modeling of spectral overlap in forster resonance energy transfer (FRET) [DOI]
54. 54 Lindsey, 2021, The fluorescence quantum yield parameter in Förster resonance energy transfer (FRET)—Meaning, misperception, and molecular design [DOI]
55. 55 Jouanno, 2016, 5-Alkoxyoxazole—A Versatile Building Block in (Bio)organic Synthesis [DOI]
56. 56 Shi, 2011, Transforming a Targeted Porphyrin Theranostic Agent into a PET Imaging Probe for Cancer [DOI]
57. 57 Benov, 2015, Photodynamic therapy: Current status and future directions [DOI]
58. 58 Terra, 2019, Photodynamic therapy in cancer treatment—An update review
59. 59 Ametamey, 2008, Molecular imaging with PET [DOI]
60. 60 Mukai, 2021, Review: PET imaging with macro- and middle-sized molecular probes [DOI]
61. 61 Chen, 2012, Synthesis and Physicochemical Properties of Metallobacteriochlorins [DOI]
62. 62 Yang, 2013, Molecular Electronic Tuning of Photosensitizers to Enhance Photodynamic Therapy: Synthetic Dicyanobacteriochlorins as a Case Study [DOI]
63. 63 Fuwa, 2007, Divergent synthesis of multifunctional molecular probes to elucidate the enzyme specificity of dipeptidic gamma-secretase inhibitors [DOI]
64. 64 Albright, 2005, Matrix metalloproteinase-activated doxorubicin prodrugs inhibit HT1080 xenograft growth better than doxorubicin with less toxicity [DOI]
65. 65 Verwilst, 2017, Reconsidering azobenzene as a component of small-molecule hypoxia-mediated cancer drugs: A theranostic case study [DOI]
66. 66 McKeown, 2014, Defining normoxia, physoxia and hypoxia in tumours-implications for treatment response [DOI]
67. 67 Song, 2018, Polyamine-Targeting Gefitinib Prodrug and its Near-Infrared Fluorescent Theranostic Derivative for Monitoring Drug Delivery and Lung Cancer Therapy [DOI]
68. 68 Yuan, 2014, Targeted theranostic prodrugs based on an aggregation-induced emission (AIE) luminogen for real-time dual-drug tracking [DOI]
69. 69 Qian, 2017, AIE Luminogens for Bioimaging and Theranostics: From Organelles to Animals [DOI]
70. 70 Wang, 2018, Theranostics based on AIEgens [DOI]
71. 71 Moret, 2009, Synthesis and evaluation of new thiodigalactoside-based chemical probes to label galectin-3 [DOI]
72. 72 Weinstain, 2014, In vivo targeting of hydrogen peroxide by activatable cell-penetrating peptides [DOI]
73. 73 Beal, 2012, Click-enabled heterotrifunctional template for sequential bioconjugations [DOI]
74. 74 Akram, 2011, Amino acids: A review article
75. 75 Tang, 2014, “Click” reactions: A versatile toolbox for the synthesis of peptide-conjugates [DOI]
76. 76 Liu, 2010, Multivalent Antimicrobial Peptides as Therapeutics: Design Principles and Structural Diversities [DOI]
77. 77 He, R., Finan, B., Mayer, J.P., and DiMarchi, R.D. (2019). Peptide Conjugates with Small Molecules Designed to Enhance Efficacy and Safety. Molecules, 24. [DOI]
78. 78 Lin, 2019, Activatable cell-biomaterial interfacing with photo-caged peptides [DOI]
79. 79 Poreba, 2020, Protease-activated prodrugs: Strategies, challenges, and future directions [DOI]
80. 80 Kovalova, 2018, Stepwise triple-click functionalization of synthetic peptides [DOI]
81. 81 Jaradat, 2018, Thirteen decades of peptide synthesis: Key developments in solid phase peptide synthesis and amide bond formation utilized in peptide ligation [DOI]
82. 82 Martin, 2020, Greening the synthesis of peptide therapeutics: An industrial perspective [DOI]
83. 83 2012, Recent development in peptide coupling reagents [DOI]
84. 84 Albericio, 2011, Peptide coupling reagents, more than a letter soup [DOI]
85. 85 Montalbetti, 2005, Amide bond formation and peptide coupling [DOI]
86. 86 Alvarez, 2009, Amino acid-protecting groups [DOI]
87. 87 Behrendt, 2016, Advances in Fmoc solid-phase peptide synthesis [DOI]
88. 88 Coin, 2006, Depsipeptide methodology for solid-phase peptide synthesis: Circumventing side reactions and development of an automated technique via depsidipeptide units [DOI]
89. 89 Huang, 2015, Accelerated Fmoc solid-phase synthesis of peptides with aggregation-disrupting backbones [DOI]
90. 90 Albericio, 2016, The road to the synthesis of “difficult peptides” [DOI]
91. 91 2017, Optimized syntheses of Fmoc azido amino acids for the preparation of azidopeptides [DOI]
92. 92 Weis, 2011, Tumor angiogenesis: Molecular pathways and therapeutic targets [DOI]
93. 93 Dou, 2018, Effect of multiple cyclic RGD peptides on tumor accumulation and intratumoral distribution of IRDye 700DX-conjugated polymers [DOI]
94. 94 Renault, 2018, Covalent Modification of Biomolecules through Maleimide-Based Labeling Strategies [DOI]
95. 95 Sun, 2018, Disulfide Bond-Driven Oxidation- and Reduction-Responsive Prodrug Nanoassemblies for Cancer Therapy [DOI]
96. 96 Postma, 2014, Disulfide Formation Strategies in Peptide Synthesis [DOI]
97. 97 Fujiwara, 1994, Racemization-free synthesis of C-terminal cysteine-peptide using 2-chlorotrityl resin [DOI]
98. 98 Lukszo, 1996, 3-(1-Piperidinyl)alanine formation during the preparation of C-terminal cysteine peptides with the Fmoc/t-Bu strategy [DOI]
99. 99 Breman, 2012, Acid-labile Cys-protecting groups for the Fmoc/tBu strategy: Filling the gap [DOI]
100. 100 Stathopoulos, 2013, Side reactions in the SPPS of Cys-containing peptides [DOI]
101. 101 Lelievre, 2016, Native Chemical Ligation Strategy to Overcome Side Reactions during Fmoc-Based Synthesis of C-Terminal Cysteine-Containing Peptides [DOI]
102. 102 Tsuda, 2020, Epimerization-Free Preparation of C-Terminal Cys Peptide Acid by Fmoc SPPS Using Pseudoproline-Type Protecting Group [DOI]
103. 103 Albericio, 2018, Choosing the Right Coupling Reagent for Peptides: A Twenty-Five-Year Journey [DOI]
104. 104 Valeur, 2009, Amide bond formation: Beyond the myth of coupling reagents [DOI]
105. 105 Prasad, 2011, Applications of peptide coupling reagents—An update
106. 106 Tsakos, 2015, Ester coupling reactions--an enduring challenge in the chemical synthesis of bioactive natural products [DOI]
107. 107 Dunetz, 2016, Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals [DOI]
108. 108 Sakakura, 2007, Widely useful DMAP-catalyzed esterification under auxiliary base- and solvent-free conditions [DOI]
109. 109 Renard, 2020, Design of Bimodal Ligands of Neurotensin Receptor 1 for Positron Emission Tomography Imaging and Fluorescence-Guided Surgery of Pancreatic Cancer [DOI]
110. 110 Lelle, 2014, An amino acid-based heterofunctional cross-linking reagent [DOI]
111. 111 Krall, 2014, A bivalent small molecule-drug conjugate directed against carbonic anhydrase IX can elicit complete tumour regression in mice [DOI]
112. 112 Lee, 2010, Light-mediated spatial control via photolabile fluorescently quenched peptide cassettes [DOI]
113. 113 Lock, 2015, Enzyme-Specific Doxorubicin Drug Beacon as Drug-Resistant Theranostic Molecular Probes [DOI]
114. 114 Yan, 2014, A chemical “hub” for absolute quantification of a targeted protein: Orthogonal integration of elemental and molecular mass spectrometry [DOI]
115. 115 Tsukiji, 2009, Quenched ligand-directed tosylate reagents for one-step construction of turn-on fluorescent biosensors [DOI]
116. 116 Huang, 2013, Multifunctional fluorescent probe for sequential detections of glutathione and caspase-3 in vitro and in cells [DOI]
117. 117 Anami, 2017, Enzymatic conjugation using branched linkers for constructing homogeneous antibody-drug conjugates with high potency [DOI]
118. 118 Oriana, 2017, Synthesis of tri-functionalized MMP2 FRET probes using a chemo-selective and late-stage modification of unprotected peptides [DOI]
119. 119 Mishra, 2016, PEGylation in anti-cancer therapy: An overview [DOI]
120. 120 Ewald, 2007, Matrix metalloproteinases and the regulation of tissue remodelling [DOI]
121. 121 Hu, 2007, Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases [DOI]
122. 122 Bode, 2017, Chemical Protein Synthesis with the alpha-Ketoacid-Hydroxylamine Ligation [DOI]
123. 123 Zuo, 2019, One-pot multi-segment condensation strategies for chemical protein synthesis [DOI]
124. 124 Arbour, 2018, Epimerization-free access to C-terminal cysteine peptide acids, carboxamides, secondary amides, and esters via complimentary strategies [DOI]
125. 125 Zuo, 2019, Robust synthesis of C-terminal cysteine-containing peptide acids through a peptide hydrazide-based strategy [DOI]
126. 126 Mariani, 2010, A review on the clinical uses of SPECT/CT [DOI]
127. 127 Israel, 2019, Two decades of SPECT/CT—The coming of age of a technology: An updated review of literature evidence [DOI]
128. 128 Gao, 2019, Improved in Vivo Targeting Capability and Pharmacokinetics of (99m)Tc-Labeled isoDGR by Dimerization and Albumin-Binding for Glioma Imaging [DOI]
129. 129 Chen, 2019, Carboxylesterase-Cleavable Biotinylated Nanoparticle for Tumor-Dual Targeted Imaging [DOI]
130. 130 Li, 2016, A ratiometric theranostic probe for tumor targeting therapy and self-therapeutic monitoring [DOI]
131. 131 Lee, 2011, Construction of a photoactivatable profluorescent enzyme via propinquity labeling [DOI]
132. 132 Hai, 2018, Smart Dual Quenching Strategy Enhances the Detection Sensitivity of Intracellular Furin [DOI]
133. 133 Lai, 2013, Stepwise orthogonal click chemistry toward fabrication of paclitaxel/galactose functionalized fluorescent nanoparticles for HepG2 cell targeting and delivery [DOI]
134. 134 Lai, 2012, Design of multivalent galactosyl carborane as a targeting specific agent for potential application to boron neutron capture therapy [DOI]
135. 135 Lee, 2020, Peptide-based scaffolds for in vivo immobilization and enzyme attachment in therapeutic applications
136. 136 Yao, 2008, Soluble Precipitable Porphyrins for Use in Targeted Molecular Brachytherapy [DOI]
137. 137 Wu, 2012, Synthesis and evaluation of a peptide targeted small molecular Gd-DOTA monoamide conjugate for MR molecular imaging of prostate cancer [DOI]
138. 138 Lee, 2005, Efficient solid-phase synthesis of trifunctional probes and their application to the detection of carbohydrate-binding proteins [DOI]
139. 139 Benito, 2005, Probing secondary carbohydrate-protein interactions with highly dense cyclodextrin-centered heteroglycoclusters: The heterocluster effect [DOI]
140. 140 2013, Multivalency in heterogeneous glycoenvironments: Hetero-glycoclusters, -glycopolymers and -glycoassemblies [DOI]
141. 141 2020, Carbohydrate supramolecular chemistry: Beyond the multivalent effect [DOI]
142. 142 Muller, 2016, Organizing multivalency in carbohydrate recognition [DOI]
143. 143 Goyard, 2019, Heteroglycoclusters With Dual Nanomolar Affinities for the Lectins LecA and LecB From Pseudomonas aeruginosa [DOI]
144. 144 Galan, 2013, Multivalent glyco(cyclo)peptides [DOI]
145. 145 Pifferi, 2017, Cyclopeptide scaffolds in carbohydrate-based synthetic vaccines [DOI]
146. 146 Richard, 2018, Sugar γ-Amino Acids as Building Blocks for the Synthesis of Cyclic Neoglycopeptides [DOI]
147. 147 Thomas, 2015, A multi-ligation strategy for the synthesis of heterofunctionalized glycosylated scaffolds [DOI]
148. 148 Chelius, 2003, Capture of peptides with N-terminal serine and threonine: A sequence-specific chemical method for peptide mixture simplification [DOI]
149. 149 Spears, 2016, Site-selective incorporation and ligation of protein aldehydes [DOI]
150. 150 Melnyk, 2013, alpha-Oxo aldehyde or glyoxylyl group chemistry in peptide bioconjugation [DOI]
151. 151 Mettu, 2020, Synthetic carbohydrate-based vaccines: Challenges and opportunities [DOI]
152. 152 Bringmann, 2007, Synthesis and pharmacological evaluation of fluorescent and photoactivatable analogues of antiplasmodial naphthylisoquinolines [DOI]
153. 153 Liu, 2009, Spectrofluorimetric determination of trace nitrite with a novel fluorescent probe [DOI]
154. 154 Carrigan, 2005, The engineering of membrane-permeable peptides [DOI]
155. 155 Fan, 2020, A (64)Cu-porphyrin-based dual-modal molecular probe with integrin αvβ3 targeting function for tumour imaging [DOI]
156. 156 Ruhl, T., Volke, D., Stembera, K., Hatanaka, Y., Hennig, H., Schumer, F., and Welzel, P. (2002). Isoserine-based biotinylated photoaffinity probes that interact with penicillin-binding protein 1b. Chem. Commun., 1630–1631. [DOI]
157. 157 Dijkgraaf, 2013, Synthesis and application of cNGR-containing imaging agents for detection of angiogenesis [DOI]
158. 158 Seibold, 2014, Bimodal imaging probes for combined PET and OI: Recent developments and future directions for hybrid agent development [DOI]
159. 159 Sun, 2016, Novel Strategy for Preparing Dual-Modality Optical/PET Imaging Probes via Photo-Click Chemistry [DOI]
160. 160 Zhu, 2012, Dynamic PET and Optical Imaging and Compartment Modeling using a Dual-labeled Cyclic RGD Peptide Probe [DOI]
161. 161 Hawala, 2020, An innovative approach for the synthesis of dual modality peptide imaging probes based on the native chemical ligation approach [DOI]
162. 162 Kulkarni, 2018, Rapid and efficient protein synthesis through expansion of the native chemical ligation concept [DOI]
163. 163 Agouridas, 2019, Native Chemical Ligation and Extended Methods: Mechanisms, Catalysis, Scope, and Limitations [DOI]
164. 164 Thapa, 2014, Native chemical ligation: A boon to peptide chemistry [DOI]
165. 165 Debie, 2019, Emerging Fluorescent Molecular Tracers to Guide Intra-Operative Surgical Decision-Making [DOI]
166. 166 Kamada, 2003, A modular cross-linking approach for exploring protein interactions [DOI]
167. 167 Lelle, 2015, Octreotide-Mediated Tumor-Targeted Drug Delivery via a Cleavable Doxorubicin-Peptide Conjugate [DOI]
168. 168 Biniossek, 2009, Development of protein-binding bifunctional linkers for a new generation of dual-acting prodrugs [DOI]
169. 169 Sinisi, R., Morales, A.R.M., Dubikovskaya, E.A., and Singh, R. (2018). Azacyanine Dyes and Use Thereof. (US2018/0079906 A1), U.S. Patent.
170. 170 Nunez, 2018, NanoSIMS for biological applications: Current practices and analyses [DOI]
171. 171 Kabatas, 2019, Boron-Containing Probes for Non-optical High-Resolution Imaging of Biological Samples [DOI]
172. 172 Chang, 2016, A photo-cleavable biotin affinity tag for the facile release of a photo-crosslinked carbohydrate-binding protein [DOI]
173. 173 Kim, 2019, Biomedical applications of copper-free click chemistry: In vitro, in vivo, and ex vivo [DOI]
174. 174 Brodersen, 2011, Synthesis of novel amphiphilic conjugates with a biological recognition function for developing targeted triggered liposomal delivery systems [DOI]
175. 175 Cheng, 2005, Near-infrared fluorescent RGD peptides for optical imaging of integrin αvβ3 expression in living mice [DOI]
176. 176 Ragupathi, 2006, Preparation and evaluation of unimolecular pentavalent and hexavalent antigenic constructs targeting prostate and breast cancer: A synthetic route to anticancer vaccine candidates [DOI]
177. 177 Giacomelli, 2004, [1,3,5]-triazine: A versatile heterocycle in current applications of organic chemistry [DOI]
178. 178 Bretterbauer, 2012, Melamine Derivatives—A Review on Synthesis and Application [DOI]
179. 179 Shinde, 2018, Review on Synthesis and Biological Study of Triazines Derivatives
180. 180 Blotny, 2006, Recent applications of 2,4,6-trichloro-1,3,5-triazine and its derivatives in organic synthesis [DOI]
181. 181 Thurston, 1951, Cyanuric Chloride Derivatives. V. Reaction of Alkoxy-S-Triazines and Aryloxy-Ss-Triazines with Amines [DOI]
182. 182 Yamada, 2012, A novel acid-catalyzed O-benzylating reagent with the smallest unit of imidate structure [DOI]
183. 183 Kunishima, 1999, Synthesis and characterization of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride [DOI]
184. 184 Mibu, 2015, Synthesis and Antiviral Evaluation of Some C(3)-Symmetrical Trialkoxy-Substituted 1,3,5-Triazines and Their Molecular Geometry [DOI]
185. 185 Kunishima, 2012, Study on 1,3,5-triazine chemistry in dehydrocondensation: Gauche effect on the generation of active triazinylammonium species [DOI]
186. 186 Cuthbertson, W.W., and Moffatt, J.S. (1948). 115. Contributions to the chemistry of synthetic antimalarials. Part VI. Some derivatives of 1:3:5-triazine. J. Chem. Soc., 561–564. [DOI]
187. 187 Goi, 1960, Reactivities of Cyanuric Chloride Derivatives. II Displacement Reactions of 2-Chloro-4-substituted-6-anilino-S-triazines with Benzylamine [DOI]
188. 188 Fukushima, Y., Hashida, Y., and Matsui, K. (1972). Substituent Effects in 1,3,5-Triazine Derivatives. Nippon. Kagaku Kaishi, 629–634. [DOI]
189. 189 Hansch, 1991, A Survey of Hammett Substituent Constants and Resonance and Field Parameters [DOI]
190. 190 Fries, 1886, XXXI.—Contributions to a knowledge of cyanuric derivatives [DOI]
191. 191 Diels, 1899, Zur Kenntniss der Cyanurverbindungen [DOI]
192. 192 Steffensen, 2003, Chemoselective building blocks for dendrimers from relative reactivity data [DOI]
193. 193 Simanek, 2010, The 8 year thicket of triazine dendrimers: Strategies, targets and applications
194. 194 Goi, 1960, Reactivities of Cyanuric Chloride Derivatives II Displacement Reactions of 2-Amino-4,6-dichloro-S-triazines with Aromatic Amines [DOI]
195. 195 Moreno, 2008, Identification of Diamine Linkers with Differing Reactivity and their Application in the Synthesis of a Melamine Dendrimers [DOI]
196. 196 Sharma, 2018, Exploring the Orthogonal Chemoselectivity of 2,4,6-Trichloro-1,3,5-Triazine (TCT) as a Trifunctional Linker With Different Nucleophiles: Rules of the Game [DOI]
197. 197 Sharma, 2019, Investigating Triorthogonal Chemoselectivity. Effect of Azide Substitution on the Triazine Core [DOI]
198. 198 Maes, 2020, 1,3,5-Triazine as core for the preparation of dendrons [DOI]
199. 199 Sharma, 2020, Exploiting azido-dichloro-triazine as a linker for regioselective incorporation of peptides through their N, O, S functional groups [DOI]
200. 200 Fujita, 2020, Chromogenic agents built around a multifunctional double-triazine framework for enzymatically triggered cross-linking under physiological conditions [DOI]
201. 201 Bourguet, 2008, Synthesis and conformational studies of pseudopeptides containing an unsymmetrical triazine scaffold [DOI]
202. 202 Amm, 1998, Structural and conformational study of substituted triazines by N-15 NMR and x-ray analysis [DOI]
203. 203 Katritzky, A.R., Ghiviriga, I., Steel, P.J., and Oniciu, D.C. (1996). Restricted rotations in 4,6-bis- and 2,4,6-tris-(N,N-dialkylamino)-s-triazines. J. Chem. Soc. Perk. Trans. 2, 443–447. [DOI]
204. 204 Birkett, 2000, NMR studies of exchange between triazine rotamers [DOI]
205. 205 Birkett, 2002, Molecular modelling studies of side-chain rotation in substituted triazine rings [DOI]
206. 206 Birkett, 2003, Structural investigations of three triazines: Solution-state NMR studies of internal rotation and structural information from solid-state NMR, plus a full structure determination from powder x-ray diffraction in one case [DOI]
207. 207 Kunishima, 2016, Development of acid-catalyzed fluorous benzylating reagents based on a triazinedione core [DOI]
208. 208 Menicagli, 1994, Selective Mono- or Dialkoxylation of 2,4,6-Trichloro-1,3,5-triazine in Solid-Liquid Phase Transfer Conditions [DOI]
209. 209 Fujita, 2015, Study of the Reactivities of Acid-Catalyzed O-Benzylating Reagents Based on Structural Isomers of 1,3,5-Triazine [DOI]
210. 210 Mibu, 2014, Synthesis and Antiviral Activities of Some 2,4,6-Trisubstituted 1,3,5-Triazines [DOI]
211. 211 Fujita, 2018, Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species [DOI]
212. 212 Robb, 1978, Kinetics of Exchange-Reactions of Ethylenediamine with a Series of Cationic Rhodium(I)Complexes
213. 213 Clarke, K., and Rothwell, K. (1960). A Kinetic Study of the Effect of Substituents on the Rate of Formation of Alkylpyridinium Halides in Nitromethane Solution. J. Chem. Soc., 1885–1895. [DOI]
214. 214 Hall, 1957, Steric Effects on the Base Strengths of Cyclic Amines [DOI]
215. 215 Fujii, 1995, Studies on Synthesis of the Antibacterial Agent Nm441. II. Selection of a Suitable Base for Alkylation of 1-Substituted Piperazine with 4-(Bromomethyl)-5-methyl-1,3-dioxol-2-one [DOI]
216. 216 Brown, 1966, Preparation and Reactions of 2,6-Di-t-butylpyridine and Related Hindered Bases. A Case of Steric Hindrance toward the Proton [DOI]
217. 217 Kober, 1962, Reaction of Tertiary Amines with Halo-S-Triazines and Halopyrimidines [DOI]
218. 218 Kolesinska, 2009, The umpolung of substituent effect in nucleophilic aromatic substitution. A new approach to the synthesis of N,N-disubstituted melamines (triazine triskelions) under mild reaction conditions [DOI]
219. 219 Mannion, J.C., Dax, S.L., Colder, F.J., Macintyre, D.E., Mcleod, J., Ozola, V., Suna, E., Shubin, K., Mencel, J.J., and Peng, S.X. (2014). Novel Orally Bioavailable Breathing Control Modulating Compounds, and Methods of Using Same. (Application No WO2014078575A2), International Patent.
220. 220 Fujita, 2020, Enzymatically triggered chromogenic cross-linking agents under physiological conditions [DOI]
221. 221 Brahimi, 2010, A monovalent agonist of TrkA tyrosine kinase receptors can be converted into a bivalent antagonist [DOI]
222. 222 Calvete, 2020, Multifunctionalization of cyanuric chloride for the stepwise synthesis of potential multimodal imaging chemical entities [DOI]
223. 223 Gonzalez, 2017, Synthesis, Characterization, and Activity of a Triazine Bridged Antioxidant Small Molecule [DOI]
224. 224 Lee, 2019, A solid-phase method for synthesis of dimeric and trimeric ligands: Identification of potent bivalent ligands of 14-3-3sigma [DOI]
225. 225 Hutchinson, 2015, Selective Alkylation of C-Rich Bulge Motifs in Nucleic Acids by Quinone Methide Derivatives [DOI]
226. 226 Li, 2014, Triazine-based tool box for developing peptidic PET imaging probes: Syntheses, microfluidic radiolabeling, and structure-activity evaluation [DOI]
227. 227 Zong, 2014, Sequential and parallel dual labeling of nanoparticles using click chemistry [DOI]
228. 228 Nicasio, 2015, Copper-catalysed azide-alkyne cycloadditions (CuAAC): An update [DOI]
229. 229 Meldal, 2020, Recent Fascinating Aspects of the CuAAC Click Reaction [DOI]
230. 230 Fantoni, N.Z., El-Sagheer, A.H., and Brown, T. (2021). A Hitchhiker’s Guide to Click-Chemistry with Nucleic Acids. Chem. Rev. [DOI]
231. 231 Gavrilyuk, 2009, An efficient chemical approach to bispecific antibodies and antibodies of high valency [DOI]
232. 232 Gnjatic, 2010, Toll-like receptor agonists: Are they good adjuvants? [DOI]
233. 233 Kirtland, 2020, Toll-Like Receptor Agonists as Adjuvants for Allergen Immunotherapy [DOI]
234. 234 Tom, 2015, Modulation of Innate Immune Responses via Covalently Linked TLR Agonists [DOI]
235. 235 Kuhri, 2014, A new approach for the photosynthetic antenna-reaction center complex with a model organized around an s-triazine linker [DOI]
236. 236 Wang, 2018, Design and synthesis of tumor-targeting theranostic drug conjugates for SPECT and PET imaging studies [DOI]
237. 237 Vineberg, 2015, Design, synthesis, and biological evaluation of theranostic vitamin-linker-taxoid conjugates [DOI]
238. 238 Vineberg, 2014, Design, synthesis, and biological evaluations of tumor-targeting dual-warhead conjugates for a taxoid-camptothecin combination chemotherapy [DOI]
239. 239 Lee, C., Ji, K., and Simanek, E.E. (2016). Functionalization of a Triazine Dendrimer Presenting Four Maleimides on the Periphery and a DOTA Group at the Core. Molecules, 21. [DOI]
240. 240 Albin, 2019, Linked Toll-Like Receptor Triagonists Stimulate Distinct, Combination-Dependent Innate Immune Responses [DOI]
241. 241 Gilkes, 2020, Tuning Subunit Vaccines with Novel TLR Triagonist Adjuvants to Generate Protective Immune Responses against Coxiella burnetii [DOI]
242. 242 Walsh, 2019, A general approach for the site-selective modification of native proteins, enabling the generation of stable and functional antibody-drug conjugates [DOI]
243. 243 Gao, 2020, [12]aneN3-based multifunctional compounds as fluorescent probes and nucleic acids delivering agents [DOI]
244. 244 Khongorzul, 2020, Antibody-Drug Conjugates: A Comprehensive Review [DOI]
245. 245 Tsuchikama, 2016, Antibody-drug conjugates: Recent advances in conjugation and linker chemistries [DOI]
246. 246 Tiberghien, 2017, An optimised synthesis of SG3376, a non-cleavable antibody-drug conjugate pyrrolobenzodiazepine drug-linker [DOI]
247. 247 Baker, 2012, Molecular multifunctionalization via electronically coupled lactones [DOI]
248. 248 Baker, 2016, Selective and Sequential Aminolysis of Benzotrifuranone: Synergism of Electronic Effects and Ring Strain Gradient [DOI]
249. 249 Li, 2005, Synthesis and self-assembly of functionalized donor-sigma-acceptor molecules [DOI]
250. 250 Li, 2009, Benzotrifuranone: Synthesis, structure, and access to polycyclic heteroaromatics [DOI]
251. 251 Longin, 2019, Synthesis of tris-tertiary amine CycloTriVeratrilene (TACTV) derivatives as water soluble pre-organized three aromatic ring containing molecular scaffolds for the construction of protein mimics [DOI]
252. 252 Longin, 2018, Synthetic antibody protein mimics of infliximab by molecular scaffolding on novel CycloTriVeratrilene (CTV) derivatives [DOI]
253. 253 Fabre, 2018, Tri-Orthogonal Scaffolds for the Solid-Phase Synthesis of Peptides [DOI]
254. 254 Watzke, 2006, A generic building block for C- and N-terminal protein-labeling and protein-immobilization [DOI]
255. 255 Viault, 2013, The first “ready-to-use” benzene-based heterotrifunctional cross-linker for multiple bioconjugation [DOI]
256. 256 Yoshida, 2018, Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions [DOI]
257. 257 Hospital, 2012, Access to functionalised silver(I) and gold(I) N-heterocyclic carbenes by [2 + 3] dipolar cycloadditions [DOI]
258. 258 Yoshida, 2014, Formal C-H-Azidation—Based Shortcut to Diazido Building Blocks for the Versatile Preparation of Photoaffinity Labeling Probes [DOI]
259. 259 Wagner, 1996, Boron-Dipyrromethene Dyes for Incorporation in Synthetic Multi-Pigment Light-Harvesting Arrays [DOI]
260. 260 Azov, 2006, Functionalized Calix[4]resorcinarene Cavitands. Versatile Platforms for the Modular Construction of Extended Molecular Switches [DOI]
261. 261 Yoshida, 2021, Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations [DOI]
262. 262 Ballell, 2006, A new chemical probe for the detection of the cancer-linked galectin-3 [DOI]
263. 263 Rashidian, 2013, Simultaneous dual protein labeling using a triorthogonal reagent [DOI]
264. 264 Rashidian, 2012, Chemoenzymatic reversible immobilization and labeling of proteins without prior purification [DOI]
265. 265 Gaon, 1996, Farnesyl and geranylgeranyl pyrophosphate analogs incorporating benzoylbenzyl ethers: Synthesis and inhibition of yeast protein farnesyltransferase [DOI]
266. 266 Fegan, 2012, Chemically self-assembled antibody nanostructures as potential drug carriers [DOI]
267. 267 Wu, 2014, Bispyrene-fluorescein hybrid based FRET cassette: A convenient platform toward ratiometric time-resolved probe for bioanalytical applications [DOI]
268. 268 Lamos, 2006, Mixed isotope photoaffinity reagents for identification of small-molecule targets by mass spectrometry [DOI]
269. 269 Vall-Sagarra, A., Litau, S., Decristoforo, C., Wangler, B., Schirrmacher, R., Fricker, G., and Wangler, C. (2018). Design, Synthesis, In Vitro, and Initial In Vivo Evaluation of Heterobivalent Peptidic Ligands Targeting Both NPY(Y(1))- and GRP-Receptors–An Improvement for Breast Cancer Imaging?. Pharmaceuticals, 11. [DOI]
270. 270 Yokoi, 2019, Site-selective conversion of azido groups at carbonyl alpha-positions into oxime groups leading triazide to a triple click conjugation scaffold [DOI]
271. 271 Yokoi, 2018, Site-Selective Conversion of Azido Groups at Carbonyl alpha-Positions to Diazo Groups in Diazido and Triazido Compounds [DOI]
272. 272 Daghish, 2002, Tetrafunctional photoaffinity labels based on Nakanish’s m-nitroalkoxy-substituted phenyltrifluoromethyldiazirine [DOI]
273. 273 Sorkin, 2017, Versatile Platform for the Synthesis of Orthogonally Cleavable Heteromultifunctional Cross-Linkers [DOI]
274. 274 Cline, 2011, A molecular umbrella approach to the intracellular delivery of small interfering RNA [DOI]
275. 275 Werkhoven, 2014, Versatile convergent synthesis of a three peptide loop containing protein mimic of whooping cough pertactin by successive Cu(I)-catalyzed azide alkyne cycloaddition on an orthogonal alkyne functionalized TAC-scaffold [DOI]
276. 276 Dai, 2019, Three-Component Protein Modification Using Mercaptobenzaldehyde Derivatives [DOI]
277. 277 Haley, C.A.C., and Maitland, P. (1951). Organic Reactions in Aqueous Solution at Room Temperature. Part 1. The Influence of pH on Condensations Involving the Linking of Carbon to Nitrogen and of Carbon to Carbon. J. Chem. Soc., 3155–3174. [DOI]
278. 278 Medley, 2013, Robinson’s landmark synthesis of tropinone [DOI]
279. 279 Boutureira, 2015, Advances in chemical protein modification [DOI]
280. 280 Shadish, 2020, Site-Selective Protein Modification: From Functionalized Proteins to Functional Biomaterials [DOI]
281. 281 Maruani, 2016, Dual modification of biomolecules [DOI]
282. 282 Tessier, 2019, “Doubly Orthogonal” Labeling of Peptides and Proteins [DOI]
283. 283 Joubert, 2010, Protein chemical modification on endogenous amino acids [DOI]
284. 284 Spicer, 2014, Selective chemical protein modification [DOI]
285. 285 Ramesh, 2016, Highly chemoselective ligation of thiol- and amino-peptides on a bromomaleimide core [DOI]
286. 286 Oliveira, 2019, Azabicyclic vinyl sulfones for residue-specific dual protein labelling [DOI]
287. 287 2010, Vinyl sulfone: A versatile function for simple bioconjugation and immobilization [DOI]
288. 288 Lang, 2012, Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction [DOI]
289. 289 Mushtaq, S., Yun, S.J., and Jeon, J. (2019). Recent Advances in Bioorthogonal Click Chemistry for Efficient Synthesis of Radiotracers and Radiopharmaceuticals. Molecules, 24. [DOI]
290. 290 Koniev, 2015, Developments and recent advancements in the field of endogenous amino acid selective bond forming reactions for bioconjugation [DOI]
291. 291 Gai, 2016, Universal Molecular Scaffold for Facile Construction of Multivalent and Multimodal Imaging Probes [DOI]
292. 292 Hashimoto, 2001, Synthesis of biotinylated bis(D-glucose) derivatives for glucose transporter photoaffinity labelling [DOI]
293. 293 Ji, 2012, Iron transport-mediated drug delivery: Practical syntheses and in vitro antibacterial studies of tris-catecholate siderophore-aminopenicillin conjugates reveals selectively potent antipseudomonal activity [DOI]
294. 294 Knall, 2016, A trifunctional linker suitable for conducting three orthogonal click chemistries in one pot [DOI]
295. 295 Knall, 2013, Inverse electron demand Diels-Alder (iEDDA)-initiated conjugation: A (high) potential click chemistry scheme [DOI]
296. 296 Pagel, 2019, Inverse electron demand Diels-Alder (IEDDA) reactions in peptide chemistry [DOI]
297. 297 Citron, C.A., Wickel, S.M., Schulz, B., Draeger, S., and Dickschat, J.S. (2012). A Diels-Alder/Retro-Diels-Alder Approach for the Enantioselective Synthesis of Microbial Butenolides. Eur. J. Org. Chem., 6636–6646. [DOI]
298. 298 Gramlich, 2010, Reactive Compatibilization of Poly(l-lactide) and Conjugated Soybean Oil [DOI]
299. 299 Ho, 2012, Introducing the Azlactone Functionality into Polymers through Controlled Radical Polymerization: Strategies and Recent Developments [DOI]
300. 300 Carpanez, 2016, Azlactone Reaction Developments [DOI]
301. 301 Yu, X., Herberg, A., and Kuckling, D. (2020). Micellar Organocatalysis Using Smart Polymer Supports: Influence of Thermoresponsive Self-Assembly on Catalytic Activity. Polymers, 12. [DOI]
302. 302 Pantin, 2019, Heteromultifunctional Oxazolones as Versatile Linkers for Click Chemistry Reactions [DOI]
303. 303 Moss, 2006, Solid-phase synthesis and kinetic characterization of fluorogenic enzyme-degradable hydrogel cross-linkers [DOI]
304. 304 Masselin, 2019, Unprecedented Affinity Labeling of Carbohydrate-Binding Proteins with s-Triazinyl Glycosides [DOI]
305. 305 Blencowe, 2011, Self-immolative linkers in polymeric delivery systems [DOI]
306. 306 Gonzaga, 2020, Perspectives About Self-Immolative Drug Delivery Systems [DOI]
307. 307 Jeffrey, 2010, Expanded Utility of the beta-Glucuronide Linker: ADCs That Deliver Phenolic Cytotoxic Agents [DOI]
308. 308 Kumar, 2014, Mitochondrial induced and self-monitored intrinsic apoptosis by antitumor theranostic prodrug: In vivo imaging and precise cancer treatment [DOI]
309. 309 Alsarraf, 2015, A dendritic beta-galactosidase-responsive folate-monomethylauristatin E conjugate [DOI]
310. 310 Legigan, 2012, The first generation of beta-galactosidase-responsive prodrugs designed for the selective treatment of solid tumors in prodrug monotherapy [DOI]
311. 311 Chen, 2018, Highly efficient reduction of nitro compounds: Recyclable Pd/C-catalyzed transfer hydrogenation with ammonium formate or hydrazine hydrate as hydrogen source [DOI]
312. 312 Wiener, 1991, Studies on the Mechanism of Transfer Hydrogenation of Nitroarenes by Formate Salts Catalyzed by Pd/C [DOI]
313. 313 Erez, 2008, The azaquinone-methide elimination: Comparison study of 1,6- and 1,4-eliminations under physiological conditions [DOI]
314. 314 Grinda, 2013, An enzyme-responsive system programmed for the double release of bioactive molecules through an intracellular chemical amplification process [DOI]
315. 315 Kobayashi, 2010, New strategies for fluorescent probe design in medical diagnostic imaging [DOI]
316. 316 Peterson, 2019, Paradigms in Fluorescence Molecular Imaging: Maximizing Measurement of Biological Changes in Disease, Therapeutic Efficacy, and Toxicology/Safety [DOI]
317. 317 Yan, 2016, Molecular imaging of enzyme activity in vivo using activatable probes [DOI]
318. 318 Liu, 2018, Recent progresses in small-molecule enzymatic fluorescent probes for cancer imaging [DOI]
319. 319 Singh, 2019, Small Molecule as Fluorescent Probes for Monitoring Intracellular Enzymatic Transformations [DOI]
320. 320 Baruch, 2004, Enzyme activity—it’s all about image [DOI]
321. 321 Martinon, 2004, Inflammatory caspases: Linking an intracellular innate immune system to autoinflammatory diseases [DOI]
322. 322 Lamkanfi, 2019, Caspases in Cell Death, Inflammation, and Disease [DOI]
323. 323 Hu, 2011, Multicolor, one- and two-photon imaging of enzymatic activities in live cells with fluorescently Quenched Activity-Based Probes (qABPs) [DOI]
324. 324 Zhu, Q., Girish, A., Chattopadhaya, S., and Yao, S.Q. (2004). Developing novel activity-based fluorescent probes that target different classes of proteases. Chem. Commun., 1512–1513. [DOI]
325. 325 Sellars, 2010, Fluorescence quenched quinone methide based activity probes—A cautionary tale [DOI]
326. 326 Gnaim, 2014, Quinone-methide species, a gateway to functional molecular systems: From self-immolative dendrimers to long-wavelength fluorescent dyes [DOI]
327. 327 Gnaim, 2019, Activity-Based Optical Sensing Enabled by Self-Immolative Scaffolds: Monitoring of Release Events by Fluorescence or Chemiluminescence Output [DOI]
328. 328 Chevalier, 2013, Universal dark quencher based on “clicked” spectrally distinct azo dyes [DOI]
329. 329 Huang, 2019, Molecular optical imaging probes for early diagnosis of drug-induced acute kidney injury [DOI]
330. 330 Arja, 2018, Synthesis and Characterization of Novel Fluoro-glycosylated Porphyrins that can be Utilized as Theranostic Agents [DOI]
331. 331 Yang, 2019, Mitochondria-targeting Pt/Mn porphyrins as efficient photosensitizers for magnetic resonance imaging and photodynamic therapy [DOI]
332. 332 Kadish, 2000, Synthesis of meso-Substituted Porphyrins
333. 333 Kadish, 2012, Enumeration of Isomers of Substituted Tetrapyrrole Macrocycles: From Classical Problems in Biology to Modern Combinatorial Libraries
334. 334 Yang, 2020, Metal-Organic Frameworks for Biomedical Applications [DOI]
335. 335 Pliquett, 2018, Design of a multifunctionalizable BODIPY platform for the facile elaboration of a large series of gold(I)-based optical theranostics [DOI]
336. 336 Laine, 2017, Synthesis, structural, spectroscopic, computational and cytotoxic studies of BODIPY dyes [DOI]
337. 337 Gryko, 2001, Studies Related to the Design and Synthesis of a Molecular Octal Counter [DOI]
338. 338 Li, 1999, Template-Directed Synthesis, Excited-State Photodynamics, and Electronic Communication in a Hexameric Wheel of Porphyrins [DOI]
339. 339 Ambroise, 2000, A Self-Assembled Light-Harvesting Array of Seven Porphyrins in a Wheel and Spoke Architecture [DOI]
340. 340 Yu, 2001, Rational Syntheses of Cyclic Hexameric Porphyrin Arrays for Studies of Self-Assembling Light-Harvesting Systems [DOI]
341. 341 Tomizaki, 2003, Synthesis of Cyclic Hexameric Porphyrin Arrays. Anchors for Surface Immobilization and Columnar Self-Assembly [DOI]
342. 342 Lindsey, 2010, Synthetic Routes to meso-Patterned Porphyrins [DOI]
343. 343 Holten, 2002, Probing Electronic Communication in Covalently Linked Multiporphyrin Arrays. A Guide to the Rational Design of Molecular Photonic Devices [DOI]
344. 344 Song, 2006, Mechanisms, Pathways, and Dynamics of Excited-State Energy Flow in Self-Assembled Wheel-and-Spoke Light-Harvesting Architectures [DOI]
345. 345 Song, 2006, Effects of Multiple Pathways on Excited-State Energy Flow in Self-Assembled Wheel-and-Spoke Light-Harvesting Architectures [DOI]
346. 346 Tiede, 2004, Structural Characterization of Modular Supramolecular Architectures in Solution [DOI]
347. 347 Mardis, 2009, Solution-State Conformational Ensemble of a Hexameric Porphyrin Array Characterized Using Molecular Dynamics and X-Ray Scattering [DOI]
348. 348 Geier, 2001, A Survey of Acid Catalysts in Dipyrromethanecarbinol Condensations Leading to meso-Substituted Porphyrins [DOI]
349. 349 Senge, 2011, Stirring the porphyrin alphabet soup–functionalization reactions for porphyrins [DOI]
350. 350 Laha, 2003, A Scalable Synthesis of Meso-Substituted Dipyrromethanes [DOI]

Cited by 75

Showing 39 of 75 known citations — external sources report more than can currently be individually listed.

Related research

• A Novel Catalytic Synthesis of Flavones under Autoclave Conditions and Comparative Study of Anti-cancer Activity — shares topic coverage
• Thermostability and in-vitro Antibacterial Activity of Aqueous Extracts of Tetrapleura tetraptera Pods on Multidrug Resistant Clinical Isolates — shares topic coverage
• Acute Toxicity, Phytochemistry and Anti-diarrheal Effects of Celtis integrifolia Lam. Aqueous Leaf Extract in Wistar Albino Rats — shares topic coverage
• Understanding the Reactivity of Trimethylsilyldiazoalkanes Participating in [3+2] Cycloaddition Reactions towards Diethylfumarate with a Molecular Electron Density Theory Perspective — shares topic coverage
• Understanding the Origin of the Regioselectivity in Non-Polar [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory — shares topic coverage