Stereoselective conjugate addition of organolithium and organocopper reagents to δ-oxygenated α,β-unsaturated carbonyl systems derived from glyceraldehyde acetonide-Reference-Cited by-同舟云学术

Stereoselective conjugate addition of organolithium and organocopper reagents to δ-oxygenated α,β-unsaturated carbonyl systems derived from glyceraldehyde acetonide

Published:1995-11 Issue:47 Volume:51 Page:12843-12858
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Leonard John,Mohialdin Soad,Reed Darrel,Ryan Gary,Swain Philip A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Asymmetric induction in acyclic michael reactions: Addition of organometallic reagents to enones derived from (R)-glyceraldehyde acetonide

2. Stereoselective Conjugate Addition of Organolithium Reagents to Enoates Derived from Glyceraldehyde Acetonide

3. Selective Conjugate Addition of Organolithium Reagents to γ,δ-Unsaturated β-Oxo Esters Derived from Glyceraldehyde Acetonide

4. Tetrahedron report number 195 (R)- and (S)-2,3-0-isopropylideneglyceraldehyde in stereoselective organic synthesis

5. Chirality of plectaniaxanthin

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