Mechanism of the Reaction of Tri-n-butylstannyl Anion with n-Butyl Bromide and Iodide As Studied by the 119Sn CIDNP Technique-Reference-Cited by-同舟云学术

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Mechanism of the Reaction of Tri-n-butylstannyl Anion with n-Butyl Bromide and Iodide As Studied by the 119Sn CIDNP Technique

Published:1999-07-10 Issue:16 Volume:18 Page:2941-2943
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Wakasa Masanobu¹,Kugita Tsuyoshi²

Affiliation:

1. Molecular Photochemistry Laboratory, The Institute of Physical and Chemical Research (RIKEN), Wako, Saitama 351-0198, Japan

2. Department of Environmental & Material Science, Teikyo University of Science and Technology, Uenohara, Yamanashi 409-0193, Japan

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om990094p

Reference26 articles.

1. Single-electron transfer, a major reaction pathway in organic chemistry. An answer to recent criticisms

2. Solvent and counterion effects on the stereochemistry and the competition between electron-transfer and SN2 mechanisms in the reactions of (trimethylstannyl)alkalis with bromides

3. A critical evaluation of studies employing alkenyl halide "mechanistic probes" as indicators of single-electron-transfer processes

4. Electron-transfer, halogen-metal exchange, and direct processes in formal nucleophilic substitutions on alkyl halides by trimethyltinsodium

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1. Catenated Compounds – Group 14 (Ge, Sn, Pb);Comprehensive Inorganic Chemistry II;2013

2. Low-Coordinate Cobalt Fluoride Complexes: Synthesis, Reactions, and Production from C–F Activation Reactions;Organometallics;2012-01-19

3. Chemically induced dynamic nuclear polarization in the dehalogenation of gem-dihalocyclopropanes under the action of i-Bu2AlH in the presence of Zr(acac)4;Kinetics and Catalysis;2007-09

4. Tin Organometallics;Comprehensive Organometallic Chemistry III;2007

5. Synthesis of Hexabutylditin from Tributyltin Hydride and bis(Tributyltin)oxide;Synthetic Communications;2004-12-31

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