Transition Structures of [2,3]-Wittig Rearrangement of 2-Oxa-5-methylhexene-1-carboxylic Acid
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/26/1/26_1_81/_pdf
Reference25 articles.
1. Stereochemistry of [2,3]Sigmatropic Rearrangements
2. Enantioselective synthesis of macrocyclic propargylic alcohols by [2,3] Wittig ring contraction. Synthesis of (+)-aristolactone and cembranoid precursors
3. Synthesis of 6-hydroxycembrane precursors by conformationally controlled diastereoselective [2,3] wittig ring contraction
4. Enantioselective [2,3] wittig ring contraction induced by chiral bases. The total synthesis and absolute configuration of (+)-aristolactone
5. [2,3]-Wittig rearrangement of a 13-membered diallylic ether. Six-step synthesis of costunolide
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1. [2,3]-Wittig Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. Substituent-Control of Two Modes of Intramolecular Reactions of Allyloxy-Silyllithiums and Propargyloxy-Silyllithiums;Bulletin of the Chemical Society of Japan;2005-08
3. One or More CH and/or CC Bond(s) Formed by Rearrangement;Comprehensive Organic Functional Group Transformations II;2005
4. The Ester Dienolate [2,3]-WittigRearrangement - Development, Opportunities, andLimitations;Synlett;2003
5. [2,3]-Wittig rearrangement of γ-allyloxy-β-ketoesters. A new access to tetronic acids;Tetrahedron Letters;2001-07
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