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Desymmetrization of Achiral Heterobicyclic Alkenes through Catalytic Asymmetric Hydrophosphination.
Sadeer, Abdul; Ong, Yew Jin; Kojima, Tadayuki; Foo, Ce Qing; Li, Yongxin; Pullarkat, Sumod A; Leung, Pak-Hing.
Afiliação
  • Sadeer A; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Ong YJ; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Kojima T; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Foo CQ; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Li Y; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Pullarkat SA; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
  • Leung PH; School of Physical and Mathematical Sciences: Division of Chemistry & Biological Chemistry, Nanyang Technological University, 21 Nanyang Link, Singapore, 637371, Singapore.
Chem Asian J ; 13(19): 2829-2833, 2018 Oct 04.
Article em En | MEDLINE | ID: mdl-30022614
Asymmetric addition of diarylphosphines to oxa- and azabicyclic alkenes proceeded in the presence of a chiral phosphapalladacycle catalyst and a mild acid at room temperature to give exclusively the enantioenriched addition products in excellent yields and good selectivities. Three new chiral carbon centers were generated stereoselectively by the catalytic hydrophosphination reaction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura