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Cited by 233

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

In-Plane Aromaticity in 1,3-Dipolar Cycloadditions. Solvent Effects, Selectivity, and Nucleus-Independent Chemical Shifts

Cossío, Fernando P., Morao, Iñaki, Jiao, Haijun, Schleyer, Paul von Ragué·1999·Journal of the American Chemical Society

Abstract

The aromaticity and the regiochemistry of several 1,3-dipolar cycloadditions have been studied computationally. It is found that all the transition structures associated with concerted supra-supra processes are in-plane aromatic, and this aromaticity is compatible with a ring current circulating along the molecular plane. Solvent effects enhance the activation barrier of the reaction and diminish its synchronicity, with little impact on aromaticity. According to our calculations, aromaticity is important but does not determine the regiochemistry of the reaction. Other phenomena such as electrostatic interactions and solvent effects can modify the regiochemical and the stereochemical outcome.

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Metadata

Authors
Cossío, F. P., Morao, I., Jiao, H., & Schleyer, P. V. R.
Venue
Journal of the American Chemical Society
Published
1999-07-01
Volume
121
Issue
28
Pages
6737-6746
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2087037012
Cited by
233
References
1
FWCI
9.83
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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