A stereoselective synthesis of trisubstituted alkenes. Part 2. The nickel-catalysed coupling of Grignard reagents with 6-alkyl-3,4-dihydro-2H-pyrans and acyclic enol ethers-Reference-Cited by-同舟云学术

A stereoselective synthesis of trisubstituted alkenes. Part 2. The nickel-catalysed coupling of Grignard reagents with 6-alkyl-3,4-dihydro-2H-pyrans and acyclic enol ethers

Published:1992 Issue:24 Volume: Page:3431-3438
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Ashworth Philip A.,Dixon Nicholas J.,Kocieński Philip J.,Wadman Sjoerd N.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920003431

Reference19 articles.

1. A stereoselective synthesis of trisubstituted alkenes. Part 1. Nickel-catalysed coupling of Grignard reagents with 5-alkyl-2,3-dihydrofurans

2. Transformation of carbon-oxygen into carbon-carbon bonds mediated by low-valent nickel species

3. Thermodynamics of Vinyl Ethers. IX. The Relative Stabilities of 4-Methylene-1,3-dioxane and 4-Methyl-1,3-dioxene-(4).

4. Thermodynamics of Vinyl Ethers. XII. The Relative Stabilities of 2-Alkylidenetetrahydrofurans and 5-Alkyl-2,3-dihydrofurans.

5. Wittig and horner-wittig coupling reactions of 2-substituted cyclic ethers and their application to spiroketal synthesis

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