Stereoselective synthesis of E,Z-1,3-dienes via tandem nucleophile addition to a dienylphosphonium salt followed by wittig reaction-Reference-Cited by-同舟云学术

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Stereoselective synthesis of E,Z-1,3-dienes via tandem nucleophile addition to a dienylphosphonium salt followed by wittig reaction

Published:1992-01 Issue:5 Volume:33 Page:577-580
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

White James D.,Jensen Mark S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Total synthesis of (+)-latrunculin A

2. The Wittig reaction: comments on the mechanism and application as a tool in the synthesis of conjugated dienes

3. -1-butadienyltriphenylphosphonium bromide: A reagent for the 1,3-cyclohexadienylation of carbonyl groups.

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1. Formation of Dienes and Polyenes;Comprehensive Organic Transformations;2018-02-28

2. ChemInform Abstract: Stereoselective Synthesis of E,Z-1,3-Dienes via Tandem Nucleophile Addition to a Dienylphosphonium Salt Followed by Wittig Reaction.;ChemInform;2010-08-21

3. Synthesis of Conjugated Dienes and Polyenes;PATAI'S Chemistry of Functional Groups;2009-12-15

4. Natural Product Synthesis Using Multicomponent Reaction Strategies;Chemical Reviews;2009-05-29

5. Preparation of Difunctional Compounds;Compendium of Organic Synthetic Methods;2006-11-22

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