A Bispericyclic Transition Structure Allows for Efficient Relief of Antiaromaticity Enhancing Reactivity and Endo Stereoselectivity in the Dimerization of the Fleeting Cyclopentadienone-Reference-Cited by-同舟云学术

A Bispericyclic Transition Structure Allows for Efficient Relief of Antiaromaticity Enhancing Reactivity and Endo Stereoselectivity in the Dimerization of the Fleeting Cyclopentadienone

Published:2003-06-24 Issue:15 Volume:68 Page:6035-6038
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Quadrelli Paolo¹,Romano Silvano¹,Toma Lucio¹,Caramella Pierluigi¹

Affiliation:

1. Dipartimento di Chimica Organica, Università degli Studi di Pavia, Viale Taramelli 10, 27100 Pavia, Italy, and Istituto Nazionale Fisica della Materia, Dipartimento di Fisica “A. Volta”, Università degli Studi di Pavia, Via Bassi 6, 27100 Pavia, Italy caramell@chifis.unipv.it

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034401j

Reference49 articles.

1. Orbital Symmetries and Orientational Effects in a Sigmatropic Reaction

2. Tetrahedron report number 149

3. Do Secondary Orbital Interactions Really Exist?

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