Dehydroxylated C-3 Alkylation of Indole Accompanied by 1,2-Sulfur Migration
Author:
Affiliation:
1. State Key Laboratory of Natural Medicines, Department of Organic Chemistry, China Pharmaceutical University, No. 24 Tongjiaxiang Road, Nanjing 210009, P.R. China
Funder
China Pharmaceutical University
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c00573
Reference31 articles.
1. Recent Advances in the Electrochemical Synthesis and Functionalization of Indole Derivatives
2. Harnessing the Chemistry of the Indole Heterocycle to Drive Discoveries in Biology and Medicine
3. Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds
4. Synthesis of C3-Alkylated Indoles on DNA via Indolyl Alcohol Formation Followed by Metal-Free Transfer Hydrogenation
5. Electrochemical Dearomative 2,3-Difunctionalization of Indoles
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1. Ca(II)-Catalyzed Cascade Reaction of Tryptamines with Propargylic Alcohols: Temperature-Driven Ring Opening and Closing via the Allene Migration Pathway for the Synthesis of Pyrrolo[1,2-a]indoles;Organic Letters;2024-02-02
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