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Nickel-Hydride-Catalyzed Diastereo- and Enantioselective Hydroalkylation of Cyclopropenes.
Huang, Qingqin; Chen, Ya; Zhou, Xueting; Dai, Lei; Lu, Yixin.
Afiliação
  • Huang Q; Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, Fujian, 350207, China.
  • Chen Y; Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore, Singapore.
  • Zhou X; Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore, Singapore.
  • Dai L; Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, Fujian, 350207, China.
  • Lu Y; Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore, Singapore.
Angew Chem Int Ed Engl ; 61(46): e202210560, 2022 11 14.
Article em En | MEDLINE | ID: mdl-36124410
ABSTRACT
Cyclopropanes are structural motifs that are widely present in natural products and bioactive molecules, and they are also tremendously useful building blocks in synthetic organic chemistry. Asymmetric synthesis of cyclopropane derivatives has been an intensively researched area over the years, but efficient asymmetric preparation of alkylcyclopropane scaffolds remains a challenging topic. Herein, we report a nickel-hydride-catalyzed enantioselective and diastereoselective hydroalkylation of cyclopropenes for facile synthesis of chiral alkylcyclopropane motifs. The reported method is efficient and versatile, taking place under mild reaction conditions, and having broad applicability and excellent functional group tolerance.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Níquel Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Níquel Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China