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Highly diastereoselective and enantioselective formal [4 + 3] cycloaddition of donor-acceptor cyclobutanes with nitrones.
Hu, Jiang-Lin; Wang, Lijia; Xu, Hao; Xie, Zuowei; Tang, Yong.
Afiliación
  • Hu JL; †The State Key Laboratory of Organometallic Chemistry and Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
  • Wang L; †The State Key Laboratory of Organometallic Chemistry and Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
  • Xu H; †The State Key Laboratory of Organometallic Chemistry and Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
  • Xie Z; §Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China.
  • Tang Y; †The State Key Laboratory of Organometallic Chemistry and Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Org Lett ; 17(11): 2680-3, 2015 Jun 05.
Article en En | MEDLINE | ID: mdl-25974724
ABSTRACT
The first highly diastereoselective and enantioselective catalytic formal [4 + 3] cycloaddition of 1,1-cyclobutane diester with nitrone has been developed. Sterically hindered chiral SaBOX/Cu(II) complex promotes the reaction efficiently with a broad substrate scope, producing a range of multifunctionalized optically active 1,2-oxazepanes with excellent stereocontrol (up to >99/1 dr and 97% ee).
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oxazepinas / Ciclobutanos / Óxidos de Nitrógeno Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2015 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oxazepinas / Ciclobutanos / Óxidos de Nitrógeno Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2015 Tipo del documento: Article