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Mechanochemically Induced Dehydrogenation Coupling and [3+2] Cycloaddition of Indolizines with Allenes Using Piezoelectric Materials.
Huang, Mingzhou; Deng, Lichan; Lao, Tianfeng; Zhang, Ziwu; Su, Zhengquan; Yu, Yue; Cao, Hua.
Afiliación
  • Huang M; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Centre, Guangdong Pharmaceutical University, Zhongshan 528458, China.
  • Deng L; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Centre, Guangdong Pharmaceutical University, Zhongshan 528458, China.
  • Lao T; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Centre, Guangdong Pharmaceutical University, Zhongshan 528458, China.
  • Zhang Z; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Centre, Guangdong Pharmaceutical University, Zhongshan 528458, China.
  • Su Z; Guangdong Engineering Research Centre of Natural Products and New Drugs, Guangdong Provincial University Engineering Technology Research Centre of Natural Products and Drugs, Guangdong Pharmaceutical University, Guangzhou 510006, China.
  • Yu Y; School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Centre, Guangdong Pharmaceutical University, Zhongshan 528458, China.
  • Cao H; Guangdong Pharmaceutical University-University of Hong Kong Joint Biomedical Innovation Platform, Zhongshan 528437, China.
J Org Chem ; 87(5): 3265-3275, 2022 Mar 04.
Article en En | MEDLINE | ID: mdl-35080180
ABSTRACT
A wide range of indolizines with allenes proceeded smoothly under mechanochemically induced conditions via a [3+2] annulation process, affording various substituted pyrrolo[2,1,5-cd]indolizines in good yields. The reaction efficiency was greatly improved by using piezoelectric material as the charge transfer catalyst. The photophysical properties of the resulting pyrrolo[2,1,5-cd]indolizine were characterized.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article País de afiliación: China