On a sulfurated grignard reagent equivalent to that of 2-chloromethyl-1,3-butadiene. New syntheses of ipsenol (2-methyl-6-methylene-7-octen-4-OL) and of (E)-β-farnesene ((E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene)-Reference-Cited by-同舟云学术

On a sulfurated grignard reagent equivalent to that of 2-chloromethyl-1,3-butadiene. New syntheses of ipsenol (2-methyl-6-methylene-7-octen-4-OL) and of (E)-β-farnesene ((E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene)

Published:1979-09 Issue:1 Volume:177 Page:67-74
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Cazes Bernard,Guittet Eric,Julia Sylvestre,Ruel Odile

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference32 articles.

1. Synthesis of the principal components of the sex attractant from male Ips confusus frass: 2-methyl-6-methylene-7-octen-4-ol, 2-methyl-6-methylene-2,7-octadien-4-ol, and (+)-cis-verbenol

2. Generation of allyllithium reagents by lithium-tetrahydrofuran reduction of allylic mesitoates. New procedure for selective allylic cross coupling and allylcarbinol synthesis

3. Metalation of limonene. Novel method for the synthesis of bisabolane sesquiterpenes

4. A simple procedure for preparing allyllithium and methallyllithium, and it application to coupling with organic halides

5. Synthesis of compounds containing the isoprene unit. A new stereospecific synthesis of the geranyl and farnesyl skeleton.

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