Regio- and Stereoselectivity of Captodative Olefins in 1,3-Dipolar Cycloadditions. A DFT/HSAB Theory Rationale for the Observed Regiochemistry of Nitrones-Reference-Cited by-同舟云学术

Regio- and Stereoselectivity of Captodative Olefins in 1,3-Dipolar Cycloadditions. A DFT/HSAB Theory Rationale for the Observed Regiochemistry of Nitrones

Published:2001-01-27 Issue:4 Volume:66 Page:1252-1263
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Herrera Rafael¹,Nagarajan Arumugam¹,Morales Miguel A.¹,Méndez Francisco¹,Jiménez-Vázquez Hugo A.¹,Zepeda L. Gerardo¹,Tamariz Joaquín¹

Affiliation:

1. Departamento de Química Orgánica, Escuela Nacional de Ciencias Biológicas, IPN, Prol. Carpio y Plan de Ayala, 11340 México, D.F., and Departamento de Química, División de Ciencias Básicas e Ingeniería, Universidad Autónoma Metropolitana-Iztapalapa, A.P. 55-534, 09340 México, D.F., México

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001393n

Reference113 articles.

1. (b) Carruthers, W.Cycloaddition Reactions in OrganicSynthesis; Pergamon Press: Oxford, 1990; pp 269−331.

2. (c) Torssell, K. B. G.Nitrile Oxides, Nitrones, and Nitronates in Organic Synthesis; VCH: New York, 1988.

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

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