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Metal-Free One-Pot Synthesis of 3-Phosphinoylbenzofurans via Phospha-Michael Addition/Cyclization of H-Phosphine Oxides and in Situ Generated ortho-Quinone Methides.
Du, Ji-Yuan; Ma, Yan-Hua; Yuan, Rui-Qing; Xin, Nana; Nie, Shao-Zhen; Ma, Chun-Lin; Li, Chen-Zhong; Zhao, Chang-Qiu.
Afiliação
  • Du JY; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Ma YH; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Yuan RQ; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Xin N; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Nie SZ; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Ma CL; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Li CZ; College of Chemistry and Chemical Engineering, Liaocheng University , Liaocheng, Shandong 252059, China.
  • Zhao CQ; Florida International University, Biomedical Engineering Department EC2671 , 10555 West Flagler Street, Miami, Florida 33174, United States.
Org Lett ; 20(2): 477-480, 2018 01 19.
Article em En | MEDLINE | ID: mdl-29313691
ABSTRACT
A novel metal-free one-pot protocol for the effective and efficient synthesis of 3-phosphinoylbenzofurans via a phospha-Michael addition/cyclization of H-phosphine oxides and in situ generated ortho-quinone methides is described. Based on the expeditious construction of C(sp2)-P bonds, asymmetric synthesis of optically pure 3-phosphinoylbenzofurans containing chiral P-stereogenic center has also been probed by using chiral RP-(-)-menthyl phenylphosphine oxide.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China