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One-Pot Regiospecific Synthesis of Indolizines: A Solvent-Free, Metal-Free, Three-Component Reaction of 2-(Pyridin-2-yl)acetates, Ynals, and Alcohols or Thiols.
Yang, Daji; Yu, Yue; Wu, Yuanheng; Feng, Huiyi; Li, Xuechen; Cao, Hua.
Afiliação
  • Yang D; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center , Guangdong Pharmaceutical University , Zhongshan 528458 , China.
  • Yu Y; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center , Guangdong Pharmaceutical University , Zhongshan 528458 , China.
  • Wu Y; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center , Guangdong Pharmaceutical University , Zhongshan 528458 , China.
  • Feng H; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center , Guangdong Pharmaceutical University , Zhongshan 528458 , China.
  • Li X; Department of Chemistry, State Key Lab of Synthetic Chemistry , The University of Hong Kong , Pokfulam, Hong Kong SAR , China.
  • Cao H; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center , Guangdong Pharmaceutical University , Zhongshan 528458 , China.
Org Lett ; 20(8): 2477-2480, 2018 04 20.
Article em En | MEDLINE | ID: mdl-29613809
A novel approach for the synthesis of indolizines from 2-(pyridin-2-yl)acetates, ynals, and alcohols or thiols has been developed. This MCR (multicomponent reaction) that proceeds under the solvent- and metal-free conditions has provided a straightforward path to construct indolizines. Furthermore, this reaction demonstrates other attractive features such as widely available starting materials, mild conditions, good functional group tolerance, and high efficiency.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article