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Addressing the configuration stability of lithiated secondary benzylic carbamates for the development of a noncryogenic stereospecific boronate rearrangement.
Fandrick, Keith R; Patel, Nitinchandra D; Mulder, Jason A; Gao, Joe; Konrad, Michael; Archer, Elizabeth; Buono, Frederic G; Duran, Adil; Schmid, Rolf; Daeubler, Juergen; Fandrick, Daniel R; Ma, Shengli; Grinberg, Nelu; Lee, Heewon; Busacca, Carl A; Song, Jinhua J; Yee, Nathan K; Senanayake, Chris H.
Afiliação
  • Fandrick KR; Department of Chemical Development, Boehringer-Ingelheim Pharmaceuticals Inc. , 900 Ridgebury Road, P.O. Box 368, Ridgefield, Connecticut 06877-0368, United States.
Org Lett ; 16(17): 4360-3, 2014 Sep 05.
Article em En | MEDLINE | ID: mdl-25153850
A practical noncryogenic process for the Aggarwal stereospecific boronate rearrangement with chiral secondary benzylic carbamates has been developed. The use of LDA instead of sec-BuLi combined with an in situ trapping of the unstable lithiated carbamate was critical to success. Furthermore, this new process increased the substrate scope to include the versatile aryl iodide and bromide substrates. The methodology was applied to a diverse array of substrates and was demonstrated on multikilogram scale.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Benzil / Ácidos Borônicos / Carbamatos Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Benzil / Ácidos Borônicos / Carbamatos Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos