A possible nucleophilic ipso-aromatic substitution with a benzyl anion as the leaving group-Reference-Cited by-同舟云学术

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A possible nucleophilic ipso-aromatic substitution with a benzyl anion as the leaving group

Published:1981-03 Issue:5 Volume:103 Page:1213-1214
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Collins Clair J.,Hombach Hans Peter,Maxwell Brian E.,Benjamin Ben M.,McKamey Donna

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00395a037

Cited by 14 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. Extremely Efficient Cross-Coupling of Benzylic Halides with Aryltitanium Tris(isopropoxide) Catalyzed by Low Loadings of a Simple Palladium(II) Acetate/Tris(p-tolyl)phosphine System;Advanced Synthesis & Catalysis;2010-07-07

2. The Birch reduction–dialkylation reaction. Scope and limitations;Tetrahedron Letters;2006-02

3. Aziridines. Part 60. Electron transfer from radical anions to N-alkanoylaziridines. Exocyclic cleavage of an aziridino ketyl;Journal of the Chemical Society, Perkin Transactions 1;1993

4. The Birch Reduction of Aromatic Compounds;Organic Reactions;1992-06-12

5. Competition between Birch reduction and bond cleavage in 1,2-bis(4-methyl-1-naphthyl)ethane;The Journal of Organic Chemistry;1989-07

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