Electrostatic repulsion by the charged tail of a radical controls the stereochemistry of coupling with anthracenide. Reversibility of benzylic fragmentation 1,2-Reference-Cited by-同舟云学术

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Electrostatic repulsion by the charged tail of a radical controls the stereochemistry of coupling with anthracenide. Reversibility of benzylic fragmentation 1,2

Published:1997 Issue:11 Volume: Page:2135-2140
ISSN:0300-9580
Container-title:Journal of the Chemical Society, Perkin Transactions 2
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Mall Thomas,Stamm Helmut

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1997/P2/A705248K

Cited by 6 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. The Lewis acid-catalyzed [3+1+1] cycloaddition of azomethine ylides with isocyanides;Tetrahedron;2014-09

2. Generation and ring opening of aziridine N-carbonyl radicals;Chemical Communications;2005

3. Benzylic Fragmentation (BFR), an Aromatic Analogue of E1cB Including a Homolytic Variant, as either Nucleofugal or Homolytic Path to Aryl Stabilized Carbanions or Ketyls, respectively;Journal für praktische Chemie;2000-06

4. Nucleophilic ring opening of aziridines;J PRAK CHEM-CHEM ZTG;1999

5. Two-Step 1,2-Shifts by β-Cleavage of Carbenium Ions and Recombination in Friedel−Crafts Reactions of 2-tert-Butyl-1-tosylaziridines1;The Journal of Organic Chemistry;1998-10-01

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