Cooperative Catalysis-Enabled (4 + 3) Cycloaddition of 2-Indolylmethanols with <i>In Situ-</i>Generated <i>ortho</i>-Naphthoquinone Methides-Reference-Cited by-同舟云学术

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Cooperative Catalysis-Enabled (4 + 3) Cycloaddition of 2-Indolylmethanols with In Situ-Generated ortho-Naphthoquinone Methides

Published:2024-07-03 Issue:14 Volume:89 Page:10197-10211
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lai Bo-Wen¹,Qu Shi-Yu¹,Yin Yu-Xian¹,Li Rui¹,Dong Kuiyong¹^ORCID,Shi Feng¹²³^ORCID

Affiliation:

1. Research Center of Chiral Functional Heterocycles, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou 221116, China

2. School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China

3. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China

Funder

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Project for Excellent Scientific and Technological Innovation Team of Jiangsu Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01080

Reference75 articles.

1. Cyclohepta[b]indoles: A Privileged Structure Motif in Natural Products and Drug Design

2. New syntheses of cycloalka[b]indoles

3. Actinophyllic Acid, a Potent Indole Alkaloid Inhibitor of the Coupled Enzyme Assay Carboxypeptidase U/Hippuricase from the Leaves of Alstonia actinophylla (Apocynaceae)

4. Structure de l'ervitsine alcaloïde α-acylindolique d'un type nouveau.

5. Exotines A and B, Two Heterodimers of Isopentenyl-Substituted Indole and Coumarin Derivatives from Murraya exotica

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