Origin of Catalysis and Selectivity in Lewis Acid-Promoted Diels–Alder Reactions Involving Vinylazaarenes as Dienophiles-Reference-Cited by-同舟云学术

Origin of Catalysis and Selectivity in Lewis Acid-Promoted Diels–Alder Reactions Involving Vinylazaarenes as Dienophiles

Published:2022-07-07 Issue:14 Volume:87 Page:9307-9315
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Portela Susana¹,Fernández Israel¹^ORCID

Affiliation:

1. Departamento de Química Orgánica I and Centro de Innovación en Química Avanzada (ORFEO-CINQA), Facultad de Ciencias Químicas, Universidad Complutense de Madrid, 28040 Madrid, Spain

Funder

Agencia Estatal de Investigación, Ministerio de Ciencia, Innovación y Universidades

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01035

Reference54 articles.

1. The Diels-Alder Reaction in Total Synthesis

2. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

3. Recent applications of intramolecular Diels–Alder reactions to natural product synthesis

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Intermolecular exo-selective Diels–Alder reaction catalysed by dual-functional Brønsted acid: conformational restriction of transition states by hydrogen bonds as the key interaction;RSC Advances;2023

2. Computational molecular refinement to enhance enantioselectivity by reinforcing hydrogen bonding interactions in major reaction pathway;Chemical Science;2023

3. Palladium-catalyzed transfer hydrogenation of terminal alkynes using ethanol as the hydrogen donor;Journal of Chemical Research;2022-11