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Enantioselective Enzymatic Reduction of Acrylic Acids.
An, Chihui; Shaw, Megan H; Tharp, Annika; Verma, Deeptak; Li, Hongming; Wang, Heather; Wang, Xiao.
Afiliação
  • An C; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Shaw MH; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Tharp A; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Verma D; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Li H; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Wang H; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
  • Wang X; Department of Process Research & Development, MRL, Merck & Co., Inc., Rahway, New Jersey 07065, United States.
Org Lett ; 22(21): 8320-8325, 2020 11 06.
Article em En | MEDLINE | ID: mdl-33048553
ABSTRACT
An ene-reductase (ERED 36) with broad substrate specificity was identified, and optimization studies led to the development of an enzymatic protocol for the reduction of α,ß-unsaturated acids under mild, aqueous conditions. The substrate scope includes aromatic- and aliphatic-substituted acrylic acids, as well as cyclic α,ß-substituted acrylic acids, yielding chiral α-substituted acids with exquisite levels of enantioselectivity (>99% ee).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases / Acrilatos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases / Acrilatos Idioma: En Ano de publicação: 2020 Tipo de documento: Article