Highly stereoselective and general synthesis of (z)-3-methyl-2-alken-1-ols via palladium-catalyzed cross coupling of (z)-3-iodo-2-buten-1-ol with organozincs and other organometals-Reference-Cited by-同舟云学术

Highly stereoselective and general synthesis of (z)-3-methyl-2-alken-1-ols via palladium-catalyzed cross coupling of (z)-3-iodo-2-buten-1-ol with organozincs and other organometals

Published:1993-02 Issue:9 Volume:34 Page:1437-1440
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Negishi Ei-ichi,Ay Mehmet,Gulevich Yuri V.,Noda Yumiki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Stereospecific synthesis of trisubstituted and tetrasubstituted olefins. Conjugate addition of dialkylcopper-lithium reagents to .alpha.,.beta.-acetylenic esters

2. Synthetic studies on insect hormones. VIII. Stereospecific synthesis of trisubstituted olefins from organocopper reagents and acetylenes

3. Specific hydromagnesiation of prop-2-ynylic alcohols. A simple and specific route to terpenoids

4. New stereospecific synthesis of trisubstituted olefins. Stereospecific synthesis of farnesol

5. (E)-3-(Trimethylsilyl)-2-propen-1-ol. An improved preparation

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