Electrophilic aromatic substitution. Part 30. The effects of the p-bicyclo[2.2.2]octan-1-yl, adamantan-1-yl, exo- and endo-norbornan-2-yl, and neopentyl substituents in detritiation. Steric acceleration of hyperconjugation-Reference-Cited by-同舟云学术

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Electrophilic aromatic substitution. Part 30. The effects of the p-bicyclo[2.2.2]octan-1-yl, adamantan-1-yl, exo- and endo-norbornan-2-yl, and neopentyl substituents in detritiation. Steric acceleration of hyperconjugation

Published:1982 Issue:2 Volume: Page:181
ISSN:0300-9580
Container-title:Journal of the Chemical Society, Perkin Transactions 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Archer William J.,Hossaini Morteza A.,Taylor Roger

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1982/P2/P29820000181

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. One-pot aromatic bromination-rearrangement catalyzed by GaCl3;Arkivoc;2003-05-29

2. Intramolecular Charge-Transfer Polymers between Dithiafulvene and Pyridinium Units: Conjugative Effect through Saturated Polymethylene Chains;Bulletin of the Chemical Society of Japan;2002-12

3. Is hyperconjugation responsible for the “gauche effect” in 1-fluoropropane and other 2-substituted-1-fluoroethanes? †;J. Chem. Soc., Perkin Trans. 2;1999

4. Expanded Tetrahedral Molecules from 1,3,5,7-Tetraphenyladamantane;Macromolecules;1994-11

5. A survey of Hammett substituent constants and resonance and field parameters;Chemical Reviews;1991-03-01

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