Lithium aluminum hydride reduction of 1-aryl-3-halopropenes, 1-aryl-3-halobutenes, and (9-anthryl)arylmethyl halides. Nucleophilic substitution vs. single electron transfer-Reference-Cited by-同舟云学术

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Lithium aluminum hydride reduction of 1-aryl-3-halopropenes, 1-aryl-3-halobutenes, and (9-anthryl)arylmethyl halides. Nucleophilic substitution vs. single electron transfer

Published:1985-05 Issue:11 Volume:50 Page:1797-1802
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hirabe Tomoatsu,Takagi Masato,Muraoka Kiyoshige,Nojima Masatomo,Kusabayashi Shigekazu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00211a002

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Electron Transfer Initiated Reactions: Bond Formation and Bond Dissociation;Chemical Reviews;2008-07-01

2. Nucleophilic dearomatizing (DNAr) reactions of aromatic C,H-Systems. A mature paradigm in organic synthesis;CHEM REV;2007

3. Nucleophilic Dearomatizing (DNAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis;Chemical Reviews;2007-05-01

4. Drastic effects of dioxygen on the selectivity of reduction by LiAlH4. Milder conditions made possible by strictly anaerobic conditions;Tetrahedron Letters;1995-09

5. Mechanistic investigation of the reaction between .alpha.-sulfonyl carbanions and polyhalogenmethanes. Electron transfer versus polar pathways;Journal of the American Chemical Society;1992-05

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