Samarium(II) Triflate as a New Reagent for the Grignard-Type Carbonyl Addition Reaction
Author:
Affiliation:
1. Department of Applied Chemistry, Chuo University, Kasuga, Bunkyo-ku, Tokyo 112, Japan, and Research Laboratory of Resources Utilization, Tokyo Institute of Technology, Nagatsuda, Midori-ku, Yokohama 226, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo960260s
Reference41 articles.
1. Reviews: (a) Molander, G. A.Chem. Rev.1992,92, 29Comprehensive OrganicSynthesis; Trost B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 1, pp 251−282.Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; Wiley: Chichester, 1995; pp 4428−4432. (b) Imamoto, T.Lanthanides in Organic Synthesis; Academic Press: London, 1994.
2. Reactions of acyl anions generated from acid chlorides and diiodosamarium
3. Samarium diiodide in tetrahydropyran : Preparation and some reactions in organic chemistry
4. Samarium dibromide an efficient reagent for the Pinacol coupling reactions
5. Preparation and Reactions of New Low-Valent Samarium Reagents.
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