Reactions of PhSCH2Li and NCCH2Li with Benzaldehyde and Benzophenone: When Does the Mechanism Change from ET to Polar?-Reference-Cited by-同舟云学术

Reactions of PhSCH2Li and NCCH2Li with Benzaldehyde and Benzophenone: When Does the Mechanism Change from ET to Polar?

Published:2001-02-23 Issue:6 Volume:66 Page:2131-2135
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yamataka Hiroshi¹,Sasaki Daizo¹,Kuwatani Yoshiyuki¹,Mishima Masaaki¹,Shimizu Makoto¹,Tsuno Yuho¹

Affiliation:

1. Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka 567-0047, Institute for Fundamental Research of Organic Chemistry, Kyushu University, Higashi-ku, Fukuoka, 812-8581, and Department of Chemistry, Faculty of Science, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010003%2B

Reference31 articles.

1. Carbon-13 kinetic isotope effects in the reactions of Grignard reagents with benzophenone

2. Organometallic reaction mechanisms. 17. Nature of alkyl transfer in reactions of Grignard reagents with ketones. Evidence for radical intermediates in the formation of 1,2-addition product involving tertiary and primary Grignard reagents

3. Electron Transfer from Alkylmagnesium Compounds to Organic Substrates.

4. New methodology in determining evidence for single electron transfer in the reaction of Grignard reagents with ketones

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