Mechanism of SN2 Alkylation Reactions of Lithium Organocuprate Clusters with Alkyl Halides and Epoxides. Solvent Effects, BF3 Effects, and Trans-Diaxial Epoxide Opening-Reference-Cited by-同舟云学术

Mechanism of SN2 Alkylation Reactions of Lithium Organocuprate Clusters with Alkyl Halides and Epoxides. Solvent Effects, BF3 Effects, and Trans-Diaxial Epoxide Opening

Published:2000-07-14 Issue:30 Volume:122 Page:7294-7307
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Mori Seiji¹,Nakamura Eiichi¹,Morokuma Keiji¹

Affiliation:

1. Contribution from Department of Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan, and Cherry L. Emerson Center for Scientific Computation and Department of Chemistry, Emory University, Atlanta, Georgia 30322

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0002060

Reference75 articles.

1. Reviews: Klunder, J. M.; Posner, G. H. InComprehensive OrganicSynthesis; Trost, B. M., Fleming, I. Eds. Pergamon Press: Elmsford, NY, 1991; Vol. 3, pp 207−239.

2. Preparation of organocalcium halides in hydrocarbon solvents

3. 6-Methyl-1,6-diazabicyclo[6.2.2]dodecane: an inside, outside six-atom bridged boat piperidine

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