Stereospecific synthesis of vinylstannanes using triphenylstannycopper(I) species. preparation of the cis-isomer of the presumed sex attractant of acanthoscelides obtectus.-Reference-Cited by-同舟云学术

Stereospecific synthesis of vinylstannanes using triphenylstannycopper(I) species. preparation of the cis-isomer of the presumed sex attractant of acanthoscelides obtectus.

Published:1982 Issue:27 Volume:23 Page:2797-2798
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Westmijze H.,Ruitenberg K.,Meijer J.,Vermeer P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. Useful new organometallic reagents for the synthesis of allylic alcohols by nucleophilic vinylation

2. A stereoselective synthesis of (+-)-11-hydroxy-trans-8-dodecenoic acid lactone, a naturally occurring macrolide from Cephalosporium recifei

3. Synthesis of antisecretory prostaglandins using vinyl tin precursors

4. Carbometallation (C-Metallation) of Alkynes: Stereospecific Synthesis of Alkenyl Derivatives

5. Reaction of (trimethylstannyl) copper reagents with α, β-acetylenic esters

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