Your browser doesn't support javascript.
loading
Enantioselective one-pot synthesis of 4H-chromene derivatives catalyzed by a chiral Ni(ii) complex.
Yu, Xuan; Lan, Wenjie; Li, Jiaqi; Bai, Hui; Qin, Zhaohai; Fu, Bin.
Afiliación
  • Yu X; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
  • Lan W; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
  • Li J; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
  • Bai H; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
  • Qin Z; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
  • Fu B; Department of Applied Chemistry, China Agricultural University West Yuanmingyuan Rd. 2 Beijing 100193 People's Repubic of China fubinchem@cau.edu.cn +86-10-62730243 +86-10-62730243.
RSC Adv ; 10(72): 44437-44441, 2020 Dec 09.
Article en En | MEDLINE | ID: mdl-35517147
ABSTRACT
A Ni(ii)-bis(oxazoline) complex and p-TSOH are used to form enantioenriched 4H-chromenes from ortho-quinone methides (o-QMs) and dicarbonyls, providing the desired products in up to 95% ee. The method is compatible with various ß-ketoester substrates, and the products obtained could be converted into biologically active 4H-chromene derivatives.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2020 Tipo del documento: Article