Tandem Michael–Wittig–Horner Reaction: Application to the Synthesis of Bisabolanes
Author:
Affiliation:
1. a Laboratoire de Chimie Organique , Photochimie et Synthèse , Université Claude Bernard Lyon I , Villeurbanne Cedex, France
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/SCC-120015768
Reference34 articles.
1. Tandem Michael−Wittig−Horner Reaction: One-Pot Synthesis of δ-Substituted α,β-Unsaturated Carboxylic Acid Derivatives − Application to a Concise Synthesis of (Z)- and (E)-Ochtoden-1-al
2. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
3. Ho , T.L. 1992. Enantioselective Synthesis: Natural Products from Chiral Terpenes 43–52. New York: Wiley.
4. Total synthesis of (+)-cheimonophyllon E, a bisabolane sesquiterpenoid
5. Stereoselective Synthesis of Exocyclic Alkenes by Cu-Catalyzed Allylmagnesiation, Pd-Catalyzed Alkylation, and Ru-Catalyzed Ring-Closing Metathesis: Highly Stereoselective Synthesis of (Z)- and (E)-γ-Bisabolenes
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