Highly E-Selective Solvent-Free Horner-Wadsworth-Emmons Reaction for the Synthesis of α-Methyl-α,β-Unsaturated Esters Using Either LiOH·H2O or Ba(OH)2·8H2O
Author:
Affiliation:
1. Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20220052
Reference39 articles.
1. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
2. Recent Progress in the Horner-Wadsworth-Emmons Reaction
3. Recent topics of the natural product synthesis by Horner–Wadsworth–Emmons reaction
4. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
5. Practical synthesis of Z-unsaturated esters by using a new Horner-Emmons reagent, ethyl diphenylphosphonoacetate
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1. In water, Green and Efficient Multicomponent Synthesis of 4H-Pyran Derivatives catalyzed by LiOH·H 2 O under Ultrasound Irradiation;2024-08-01
2. An enhanced stereoselective synthesis of α,β-unsaturated esters through the Horner–Wadsworth–Emmons reaction in deep eutectic solvents;Organic & Biomolecular Chemistry;2024
3. Practical Synthesis of Terminal Vinyl Fluorides;The Journal of Organic Chemistry;2023-07-13
4. One-Pot O2-Oxidation and the Horner–Wadsworth–Emmons Reaction of Primary Alcohols for the Synthesis of (Z)-α,β-Unsaturated Esters;The Journal of Organic Chemistry;2022-07-13
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