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  Highly stereoselective synthesis of tetrasubstituted alkenes via [2,3]-wittig rearrangement

Mulzer, J., & List, B. (1994). Highly stereoselective synthesis of tetrasubstituted alkenes via [2,3]-wittig rearrangement. Tetrahedron Letters, 35(48), 9021-9024. doi:10.1016/0040-4039(94)88416-1.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-A510-C Version Permalink: https://hdl.handle.net/21.11116/0000-0008-38AF-5
Genre: Journal Article

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 Creators:
Mulzer, Johann1, Author
List, Benjamin1, Author           
Affiliations:
1Institut für Organische Chemie der Freien Universität Berlin, Takustraβe 3, D-14195 Berlin, FRG, ou_persistent22              

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Free keywords: [2;3]-Wittig rearrangement; Claisen rearrangement; Horner-Wadsworth-Emmons reaction; tetrasubstituted alkenes
 Abstract: Tetrasubstituted alkenes were prepared stereoselectively by using the Wittig-Still rearrangement. Eight examples are given.
A highly stereoselective synthesis of tetrasubstituted alkenes via the sequence Horner-Wadsworth-Emmons-, Grignard- and [2,3]-Wittig reaction is described, eight examples are given.

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Language(s): eng - English
 Dates: 1994-11-28
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/0040-4039(94)88416-1
 Degree: -

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Title: Tetrahedron Letters
  Abbreviation : Tetrahedron Lett.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 35 (48) Sequence Number: - Start / End Page: 9021 - 9024 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772