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Cited by 191

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Hyperconjugative π-Aromaticity: How To Make Cyclopentadiene Aromatic

Nyulászi, László, Schleyer, Paul von Ragué·1999·Journal of the American Chemical Society

Abstract

Cyclopentadienes, when 5,5-disubstituted with electropositive groups, have considerably enhanced cyclic conjugation in comparison with the parent molecule, C 5 H 6 . According to various aromaticity indices, 5,5-distannylcyclopentadiene is nearly as aromatic as furan. Previous observations on the reactivity were interpreted in the light of the observed aromatic stabilization.

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Metadata

Authors
Nyulászi, L., & Schleyer, P. V. R.
Venue
Journal of the American Chemical Society
Published
1999-07-01
Volume
121
Issue
29
Pages
6872-6875
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1991514129
Cited by
191
References
1
FWCI
5.22
Type
journal article
Language
en
Open access
closed

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