Z-Selective intramolecular Horner–Wadsworth–Emmons reaction for the synthesis of macrocyclic alkenes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
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5. Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
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1. Direct Intramolecular Coupling of Primary/Secondary Alcohols with Secondary Alcohols for Macrocyclic Alkenylation Using Ni‐Zeolite Catalyst Under Continuous‐Flow Conditions;Advanced Synthesis & Catalysis;2024-01-31
2. 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
3. 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;Bulletin of the Chemical Society of Japan;2022-06-15
4. Stereoselective Synthesis of Trisubstituted (Z)-Alkenes from Ketones via the Julia–Kocienski Olefination Using 1-Methyl- and 1-tert-Butyl-1H-tetrazol-5-yl Alkyl Sulfones;Organic Letters;2020-08-21
5. Modular total syntheses of thymifodioic/incanic acids;Arabian Journal of Chemistry;2019-12
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