Synthesis of All Regioisomers of 2-Arylazaindole-3-acetic Acid Derivatives

  • Kim, Taewook; 
  • Park, Ju Hyeon; 
  • Jeong, Cheol; 
  • Park, Eunjoon; 
  • Kim, Jong Mu; 
  • ... Cheon, Cheol-Hong; 
  • 외 2명
Citations

WEB OF SCIENCE

2
Citations

SCOPUS

2

초록

A novel protocol was developed for synthesizing 2-aryl-substituted azaindole-3-acetic acid derivatives from 2-aminoazacinnamic acid derivatives and aryl aldehydes through an imino-Stetter reaction. Condensation of 2-aminoazacinnamic acid derivatives with aldehydes forms the corresponding aldimines, which are then treated with cyanide to yield the desired 2-aryl-substituted azaindole-3-acetic acid derivatives. Notably, this protocol could be employed for the synthesis of all regioisomers of azaindole-3-acetic acid derivatives by using the appropriate azacinnamic acid derivatives.

키워드

azaindoles; regioisomers; azacinnamic acid derivatives; imino-Stetter reaction; cyanide; 7-AZAINDOLES
제목
Synthesis of All Regioisomers of 2-Arylazaindole-3-acetic Acid Derivatives
저자
Kim, Taewook; Park, Ju Hyeon; Jeong, Cheol; Park, Eunjoon; Kim, Jong Mu; Kim, You-Jin; Heo, Jung-Nyoung; Cheon, Cheol-Hong
DOI
10.1055/a-2206-5900
발행일
2024-01-02
유형
Article
저널명
Synthesis
권
56
호
05
페이지
860 ~ 870