Understanding the reactivity and selectivity of Diels–Alder reactions involving furans-Reference-Cited by-同舟云学术

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

Published:2023 Issue:38 Volume:21 Page:7767-7775
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Alves Tiago Vinicius¹^ORCID,Fernández Israel²^ORCID

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

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01343J

Reference61 articles.

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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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