A Study of the Reactivity of (Aza‐)Quinone Methides in Selective C6‐Alkylations of Indoles-Reference-Cited by-同舟云学术

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A Study of the Reactivity of (Aza‐)Quinone Methides in Selective C6‐Alkylations of Indoles

Published:2020-09-02 Issue:20 Volume:12 Page:5053-5057
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Yan Jiyao¹²^ORCID,Zhang Zhihan¹^ORCID,Chen Min¹²,Lin Zhenyang¹^ORCID,Sun Jianwei¹²^ORCID

Affiliation:

1. Department of Chemistry The Hong Kong University of Science and Technology (HKUST) Clear Water Bay Kowloon Hong Kong SAR P. R. China

2. HKUST-Shenzhen Research Institute No. 9 Yuexing 1st Rd South Area Hi-tech Park Nanshan Shenzhen 518057 P. R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.202000850

Reference71 articles.

1.

2. R. J. Sundberg inIndoles Academic Press London 1996;

3. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

4. A review on recent developments of indole-containing antiviral agents

5. Marine Indole Alkaloids

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3. Structure‐Guided Mutagenesis Reveals the Catalytic Residue that Controls the Regiospecificity of C6‐Indole Prenyltransferases;ChemCatChem;2023-05-16

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5. Solvent-Mediated Tunable Regiodivergent C6- and N1-Alkylations of 2,3-Disubstituted Indoles with p-Quinone Methides;The Journal of Organic Chemistry;2023-02-13

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