Copper-catalyzed ambient-temperature decarboxylative annulation of isatins with amidine hydrochlorides: a facile access to 2-(1,3,5-triazin-2-yl)aniline derivatives-Reference-Cited by-同舟云学术

Copper-catalyzed ambient-temperature decarboxylative annulation of isatins with amidine hydrochlorides: a facile access to 2-(1,3,5-triazin-2-yl)aniline derivatives

Published:2018 Issue:23 Volume:16 Page:4223-4226
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jia Feng-Cheng¹²³⁴,Xu Cheng⁵⁶⁷⁸⁹,Wang Yu-Wei¹²³⁴,Chen Zhi-Peng¹²³⁴,Chen Yun-Feng¹²³⁴,Wu An-Xin⁵⁶⁷⁸⁹^ORCID

Affiliation:

1. School of Chemistry and Environmental Engineering

2. Wuhan Institute of Technology

3. Wuhan 430073

4. China

5. Key Laboratory of Pesticide & Chemical Biology

6. Ministry of Education

7. College of Chemistry

8. Central China Normal University

9. Wuhan 430079

Abstract

A copper-catalyzed domino protocol for the synthesis of 2-(1,3,5-triazin-2-yl)anilines has been developed from isatins and amidine hydrochlorides at ambient temperature.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB00904J

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3. In Vitro Cytotoxic Activities of 2-Alkyl-4,6-diheteroalkyl-1,3,5-triazines: New Molecules in Anticancer Research