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- W1914311384 endingPage "5246" @default.
- W1914311384 startingPage "5229" @default.
- W1914311384 abstract "Abstract Biocatalytically derived enantiopure α‐substituted β‐hydroxy esters serve as excellent chirons for the synthesis of a diverse set of structures such as oxetanes, a carbohydrate mimic, an ϵ‐lactone, and carbocyclic and aromatic cyclitols. The starting materials can be easily accessed in enantiopure form from α‐substituted β‐keto esters by biocatalytic reduction with Klebsiella pneumoniae (NBRC 3319). Ring‐closing metathesis (RCM) is one of the key transformations used to create the carbocyclic/heterocyclic frameworks reported in this article. The synthesized cyclitols were screened for their inhibitory effect on α‐ and β‐glucosidases." @default.
- W1914311384 created "2016-06-24" @default.
- W1914311384 creator A5023022419 @default.
- W1914311384 creator A5036354675 @default.
- W1914311384 creator A5049530069 @default.
- W1914311384 creator A5071094708 @default.
- W1914311384 date "2014-07-15" @default.
- W1914311384 modified "2023-10-17" @default.
- W1914311384 title "Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ϵ-Lactone, and Cyclitols from Biocatalytically Derived β-Hydroxy Esters as Chiral Precursors" @default.
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