Reactions of organomagnesium and organolithium compounds with diethyl (2,3-epoxybutylidene)malonate. A simple synthesis of cyclopropane carboxylates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Reactions of sulfur-containing carbanions with ethyl 4-bromocrotonate. A facile synthesis of cyclopropanecarboxylates
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3. Reaction of methyl 4-bromocrotonate with lithium ester enolates: direct SN2 displacement vs. Michael-initiated ring closure
4. a highly stereoselective synthesis of carbocyclic compounds by the michael induced intramolecular alkylation a stereocontrol of extracyclic chiral centers
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1. Unveiling the beauty of cyclopropane formation: a comprehensive survey of enantioselective Michael initiated ring closure (MIRC) reactions;Organic Chemistry Frontiers;2024
2. Methods for the synthesis of donor-acceptor cyclopropanes;Russian Chemical Reviews;2018-03-01
3. Conjugate Addition to α,β-Unsaturated Nitriles, Carboxylic Acids, and Derivatives;Comprehensive Organic Transformations;2018-02-28
4. Regio- and Stereocontrol in the Michael-Initiated Ring-Closure Reactions of γ,δ-Epoxy-α,β-unsaturated Esters, Ketones, Sulfones, and Amides;The Journal of Organic Chemistry;2013-12-03
5. ChemInform Abstract: Reactions of Organomagnesium and Organolithium Compounds with Diethyl ( 2,3-Epoxybutylidene)malonate. A Simple Synthesis of Cyclopropane Carboxylates.;ChemInform;2010-08-22
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