Stereoselective Preparation of E Vinyl Zirconium Derivatives from E or Z Enol Ethers-Reference-Cited by-同舟云学术

Stereoselective Preparation of E Vinyl Zirconium Derivatives from E or Z Enol Ethers

Published:2000-09-28 Issue:21 Volume:65 Page:7218-7220
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liard Annie¹,Marek Ilan¹

Affiliation:

1. Department of Chemistry and Institute of Catalysis Science and Technology, Technion-Israel Institute of Technology, Technion City, 32000 Haifa, Israel chilanm@tx.technion.ac.il

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo005561n

Reference32 articles.

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2. Negishi, E.I. InComprehensiveOrganicSynthesis; Paquette, L. A., Ed.; Pergamon Press: Oxford, 1991; Vol. 5, p 1163.

3. Zirconocene-promoted stereoselective bicyclization of 1,6- and 1,7-dienes to produce trans-zirconabicyclo[3.3.0]octanes and cis-zirconabicyclo[4.3.0]nonanes

4. Regio- and stereoselective carbon-carbon bond formation through transition metal catalysis. The influence of catalyst chirality on selective ethylmagnesiation of chiral, nonracemic alcohols and ethers

5. Zirconium-catalyzed ethylmagnesiation of hydroxylated terminal alkenes; a catalytic and diastereoselective carbon-carbon bond-forming reaction

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