Direct Observation of a Stannyl Radical in the Reactions of the Tributylstannyl Anion with Alkyl Halides by a Stopped-Flow Technique
Author:
Affiliation:
1. Molecular Photochemistry Laboratory, The Institute of Physical and Chemical Research (RIKEN), Wako, Saitama 351-01, Japan
2. Department of Material Science, Teikyo University of Science and Technology, Uenohara, Yamanashi 409-01, Japan
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om980022i
Reference13 articles.
1. STUDIES RELATING TO ALKYL TIN COMPOUNDS. I. SOME STANNOETHANES. II. TRIMETHYLBENZYL STANNANE
2. Neumann, W. P.The Organic Chemistry of Tin; Wiley: New York, 1970; p 881.
3. Electron-transfer, halogen-metal exchange, and direct processes in formal nucleophilic substitutions on alkyl halides by trimethyltinsodium
4. Reaction of (CH3)3SnM and Ph3SnM (M = lithium, sodium, potassium) with optically active 2-octyl tosylate, chloride, and bromide
5. Solvent and counterion effects on the stereochemistry and the competition between electron-transfer and SN2 mechanisms in the reactions of (trimethylstannyl)alkalis with bromides
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