On the nature of charge distribution in the 2,4-diphenylbicyclo[3.2.1]oct-6-en-3-one dianion. 13C n.m.r. vs. stability data-Reference-Cited by-同舟云学术

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On the nature of charge distribution in the 2,4-diphenylbicyclo[3.2.1]oct-6-en-3-one dianion. 13C n.m.r. vs. stability data

Published:1987 Issue:22 Volume: Page:1704
ISSN:0022-4936
Container-title:Journal of the Chemical Society, Chemical Communications
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Trimitsis George,Lin Fu-Tyan,Eaton Richard,Jones Samantha,Trimitsis Milton,Lane Scott

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1987/C3/C39870001704

Cited by 5 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. Origins of Stabilization and Evidence for Charge Delocalization in the Bicyclo[3.2.1]octadienyl Anion and Related Species;Australian Journal of Chemistry;2014

2. Cyclopropyl Homoconjugation-Experimental Facts and Interpretations;PATAI'S Chemistry of Functional Groups;2009-12-15

3. Induktiver Effekt, negative Hyperkonjugation und Gegenion sind nicht die Ursache der besonderen Eigenschaften des Bicyclo[3.2.1]octa‐3,6‐dien‐2‐yl‐Anions. — Eine NMR‐Studie mit phenylsubstituierten Modellen;Chemische Berichte;1993-02

4. Gas-phase carbanion chemistry;Accounts of Chemical Research;1992-10-01

5. Homoaromaticity in anions: the effect of electron donor groups;Journal of the Chemical Society, Chemical Communications;1988

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