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Asymmetric Synthesis of Tertiary and Secondary Cyclopropyl Boronates via Cyclopropanation of Enantioenriched Alkenyl Boronic Esters.
Gutiérrez-Bonet, Álvaro; Popov, Stasik; Emmert, Marion H; Hughes, Jonathan M E; Nolting, Andrew F; Ruccolo, Serge; Wang, Yunyi.
Afiliación
  • Gutiérrez-Bonet Á; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, West Point, Pennsylvania 19486, United States.
  • Popov S; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, Rahway, New Jersey 07065, United States.
  • Emmert MH; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, Rahway, New Jersey 07065, United States.
  • Hughes JME; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, Rahway, New Jersey 07065, United States.
  • Nolting AF; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, West Point, Pennsylvania 19486, United States.
  • Ruccolo S; Process Research & Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, Rahway, New Jersey 07065, United States.
  • Wang Y; Analytical Research and Development, Merck Research Laboratories (MRL), Merck & Company, Incorporated, West Point, Pennsylvania 19486, United States.
Org Lett ; 24(19): 3455-3460, 2022 05 20.
Article en En | MEDLINE | ID: mdl-35544734
ABSTRACT
The cyclopropanation of alkenyl boronates and subsequent derivatization of the boronate handle are a convenient strategy to quickly build molecular complexity and access diverse compounds with a high sp3 fraction. Herein, we describe the asymmetric cyclopropanation of enantioenriched hydrobenzoin-derived alkenyl boronic esters toward the synthesis of tertiary and secondary cyclopropyl boronates.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Boro / Ésteres Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Boro / Ésteres Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos