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Inter- and Intramolecular Differentiation of Enantiotopic Dioxane Acetals Through Oxazaborolidinone-Mediated Enantioselective Ring-Cleavage Reaction: Kinetic Resolution of Racemic 1,3-Alkanediols and Asymmetric Desymmetrization of meso-1,3-Polyols.

✍ Scribed by Toshiro Harada; Takayuki Egusa; Yasuto Igarashi; Motoharu Kinugasa; Akira Oku

Publisher: John Wiley and Sons
Year: 2003
Weight: 297 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200311022

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📜 SIMILAR VOLUMES

ChemInform Abstract: Kinetic Resolution

ChemInform Abstract: Kinetic Resolution of Cyclic Acetals Derived from 1,3-Alkanediols via Oxazaborolidine-Mediated Enantioselective Ring-Cleavage Reaction.

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ChemInform Abstract: Chiral Oxazaborolid

ChemInform Abstract: Chiral Oxazaborolidinone-Mediated Enantioselective Ring-Cleavage Reaction of a Mixture of Diastereomeric 1,3-Dioxolane Acetals: Application to Asymmetric Desymmetrization of meso-1,2-Diols.

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: Enantioselective Ri

ChemInform Abstract: Enantioselective Ring Cleavage of Dioxane Acetals Mediated by a Chiral Lewis Acid: Application to Asymmetric Desymmetrization of meso-1,3-Diols.

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