Late-Stage Photoredox C–H Amidation of N-Unprotected Indole Derivatives: Access to N-(Indol-2-yl)amides-Reference-Cited by-同舟云学术

Late-Stage Photoredox C–H Amidation of N-Unprotected Indole Derivatives: Access to N-(Indol-2-yl)amides

Published:2021-03-22 Issue:7 Volume:23 Page:2710-2714
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Weng Yue¹,Ding Bo²,Liu Yunqing²,Song Chunlan²,Chan Lo-Ying³,Chiang Chien-Wei³^ORCID

Affiliation:

1. Ministry-of-Education Key Laboratory for the Synthesis and Application of Organic Functional Molecule & School of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, P. R. China

2. College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei 430072, P. R. China

3. Department of Chemistry, Soochow University, No. 70, Linhsi Road, Shihlin District, Taipei 111002, Taiwan

Funder

Soochow University

Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00609

Reference34 articles.

1. Indole as an intercellular signal in microbial communities

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit (July 1997 to December 1998)

3. Indole Alkaloids and Quassinoids from the Stems of Brucea mollis

4. Regioselective direct arylation of indoles on the benzenoid moiety

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