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ChemInform Abstract: Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ε‐Lactone, and Cyclitols from Biocatalytically Derived β‐Hydroxy Esters as Chiral Precursors. Issue 9 (March 2015)
Record Type:
Journal Article
Title:
ChemInform Abstract: Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ε‐Lactone, and Cyclitols from Biocatalytically Derived β‐Hydroxy Esters as Chiral Precursors. Issue 9 (March 2015)
Main Title:
ChemInform Abstract: Stereoselective Synthesis of Enantiopure Oxetanes, a Carbohydrate Mimic, an ε‐Lactone, and Cyclitols from Biocatalytically Derived β‐Hydroxy Esters as Chiral Precursors.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Enantiopure α‐substituted β‐hydroxy esters, which are obtained by biocatalytic reduction with Klebsiella pneumoniae, serve as chirons for preparation of oxetanes (II), carbohydrate mimic (V), ε‐lactone (VII) and cyclitols (X), (XI), and (XV).</p> </abstract>