Cu-Catalysed synthesis of benzo[f]indole-2,4,9(3H)-triones by the reaction of 2-amino-1,4-napthoquinones with α-bromocarboxylates-Reference-Cited by-同舟云学术

Cu-Catalysed synthesis of benzo[f]indole-2,4,9(3H)-triones by the reaction of 2-amino-1,4-napthoquinones with α-bromocarboxylates

Published:2020 Issue:34 Volume:18 Page:6724-6731
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yang Fazhou¹²³⁴,Liu Ziyan¹²³⁴,Liu Hao¹²³⁴,Shangguan Yu¹²³⁴,Deng Hao¹²³⁴,Huang Jiaxing¹²³⁴,Xiao Yumei¹²³⁴,Guo Hongchao¹²³⁴⁵^ORCID,Zhang Cheng¹²³⁴^ORCID

Affiliation:

1. Department of Applied Chemistry

2. China Agricultural University

3. Beijing 100193

4. China

5. College of Public Health

Abstract

Cu-Catalysed oxidant-free cascade ester amidation/radical cyclization of 2-amino-1,4-napthoquinones with α-bromocarboxylates to afford benzo[f]indole-2,4,9(3H)-triones.

Funder

China Agricultural University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00291G

Reference51 articles.

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5. Structure–Activity Relationship Study of Vitamin K Derivatives Yields Highly Potent Neuroprotective Agents

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