Diastereoselective synthesis of dimethyl cyclopropane-1,1-dicarboxylates from a γ-alkoxy-alkylidene malonate and sulfur and phosphorus ylides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Novel synthesis of vinyl cyclopropane carboxylic acids: Application to the synthesis of (d,l)- and (d)-cis-chrysanthemic acid
2. Synthesis of functionalized cyclopropanes by MIRC reactions of aziridinyl-methylenemalonates
3. Stereoselective conjugate addition of organolithium and organocopper reagents to δ-oxygenated α,β-unsaturated carbonyl systems derived from glyceraldehyde acetonide
4. Control of asymmetry through conjugate addition reactions
5. Diastereoselectivity of the conjugate addition of organocopper reagents to .gamma.-alkoxy .alpha.,.beta.-unsaturated carbonyl derivatives. Importance of the reagent type and the double-bond geometry
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