Paper

Development of the biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one as an entry to single-enantiomer carbocyclic nucleosides

Published Jun 1, 1993 · S. Taylor, R. Mccague, R. Wisdom

Tetrahedron-asymmetry

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Abstract

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Study Snapshot

Biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one enables the production of single-enantiomer carbocyclic nucleosides with natural configuration.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Development of the biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one as an entry to single-enantiomer carbocyclic nucleosides

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