Understanding the reactivity and selectivity of Diels–Alder reactions involving furans

Author:

Alves Tiago Vinicius1ORCID,Fernández Israel2ORCID

Affiliation:

1. Departamento de Físico-Química, Instituto de Química – Universidade Federal da Bahia, Salvador, 40170-115, Bahia, Brazil

2. Departmento de Química Orgánica and Centro de Innovación en Química Avanzada (ORFEO-CINQA), Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria, 28040 Madrid, Spain

Abstract

The origins of the reactivity and endo/exo selectivity of the Diels–Alder cycloaddition reactions involving furan and substituted furans as dienes have been computationally explored.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Ministerio de Ciencia e Innovación

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference61 articles.

1. Synthesen in der hydroaromatischen Reihe

2. F.Fringuelli and A.Taticchi , The Diels–Alder Reaction: Selected Practical Methods , Wiley , Hoboken , 2002

3. S.Sankararaman , Pericyclic Reactions – A Textbook: Reactions, Applications and Theory , Wiley , Weinheim , 2005

4. Evolution of the Diels–Alder Reaction Mechanism since the 1930s: Woodward, Houk with Woodward, and the Influence of Computational Chemistry on Understanding Cycloadditions

5. P. T.Anastas and J. C.Warner , Green Chemistry: Theory and Practice , Oxford University Press , Oxford, New York , 1998

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