Concerted vs Stepwise Mechanism in 1,3-Dipolar Cycloaddition of Nitrone to Ethene, Cyclobutadiene, and Benzocyclobutadiene. A Computational Study
Author:
Affiliation:
1. Dipartimento di Chimica Organica, Università di Pavia, V.le Taramelli 10, 27100 Pavia, Italy, and Dipartimento di Chimica, Università di Modena, Via Campi 183, 41100 Modena, Italy
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo000569i
Reference70 articles.
1. Tufariello, J. J.Nitrones in 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; John Wiley and Sons: New York, 1984; Vol. 2, p 1.
2. Steric effects vs secondary orbital interactions in nitrone cycloadditions
3. How important are secondary orbital interactions in favoring the endo mode in 1,3-dipolar cycloadditions of nitrones?
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