Density Functional Theory Study of a Lewis Acid Catalyzed Diels−Alder Reaction. The Butadiene + Acrolein Paradigm-Reference-Cited by-同舟云学术

Density Functional Theory Study of a Lewis Acid Catalyzed Diels−Alder Reaction. The Butadiene + Acrolein Paradigm

Published:1998-02-25 Issue:10 Volume:120 Page:2415-2420
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

García J. I.¹,Martínez-Merino V.¹,Mayoral J. A.¹,Salvatella L.¹

Affiliation:

1. Contribution from the Departamento de Química Orgánica, Instituto de Ciencia de Materiales de Aragón, Facultad de Ciencias, C.S.I.C.-Universidad de Zaragoza, E-50009 Zaragoza, Spain, and Departamento de Química Aplicada, Universidad Pública de Navarra, E-31006 Pamplona, Spain

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9722279

Reference28 articles.

1. Transition structures of the Lewis acid-catalyzed Diels-Alder reaction of butadiene with acrolein. The origins of selectivity

2. Fine Tuning [4 + 2] and [2 + 4] Diels-Alder Reactions Catalyzed by Lewis Acids

3. Influence of Alkyl Substituent on the Asynchronous Transition Structure of Boron-Catalyzed Diels-Alder Cycloaddition of .alpha.,.beta.-Unsaturated Aldehydes with 1,1-Dimethyl-1,3-butadiene Derivatives

4. The role of hard Lewis acids in the tunning of the exo/endo stereoselectivity in Diels-Alder reactions: ab initio calculations

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