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Yield (engineering)

Papers (5)

Synthesis and Biological Evaluation of Substituted Fused Dipyranoquinolinones

Evangelia-Eirini N. Vlachou, Eleni Pontiki, Dimitra J. Hadjipavlou-Litina & Konstantinos E. Litinas · Organics · 2023

New methyl-substituted, and diphenyl-substituted fused dipyranoquinolinones are prepared in excellent yields via the triple bond activation and 6-endo-dig cyclization of propargyloxycoumarin derivatives by gold nanoparticles supported on TiO2 in chlorobenzene under microwave irra...

Open access Research Article 10.3390/org4030027

Thia-Michael Reaction under Heterogeneous Catalysis

Giovanna Bosica, Roderick Abdilla & Alessio Petrellini · Organics · 2023

Thia-Michael reactions between aliphatic and aromatic thiols and various Michael acceptors were performed under environmentally-friendly solvent-free conditions using Amberlyst® A21 as a recyclable heterogeneous catalyst to efficiently obtain the corresponding adducts in high yie...

Open access Research Article 10.3390/org4010007

Synthesis and Wittig Rearrangement of 3- and 4-Benzyloxyphenylphosphonamidates

R. Alan Aitken & Ryan A. Inwood · Organics · 2023

A series of seven O-ethyl-N-butylphenylphosphonamidates with benzyl ether substituents at the para or meta position have been prepared and fully characterised. Upon treatment with n-butyllithium in THF at RT, these undergo Wittig rearrangement in six cases to give the novel phosp...

Open access Research Article 10.3390/org4010005

Micellar Suzuki Cross-Coupling between Thiophene and Aniline in Water and under Air

Dawod Yousif, Silvia Tombolato, Elmehdi Ould Maina, Riccardo Po, Paolo Biagini, Antonio Papagni & Luca Vaghi · Organics · 2021

The Suzuki–Miyaura cross-coupling reaction plays a fundamental role in modern synthetic organic chemistry, both in academia and industry. For this reason, scientists continue to search for new, more effective, cheaper and environmentally friendly procedures. Recently, micellar sy...

Open access Research Article 10.3390/org2040025

Esterifications with 2-(Trimethylsilyl)ethyl 2,2,2-Trichloroacetimidate

Wenhong Lin, Shea Meyer, Shawn Dormann & John Chisholm · Organics · 2021

2-(Trimethylsilyl)ethyl 2,2,2-trichloroacetimidate is readily synthesized from 2-trimethylsilylethanol in high yield. This imidate is an effective reagent for the formation of 2-trimethylsilylethyl esters without the need for an exogenous promoter or catalyst, as the carboxylic a...

Open access Research Article 10.3390/org2010002