Development of the biocatalytic resolution of 2-azabicyclo[2.2.1]hept-5-en-3-one as an entry to single-enantiomer carbocyclic nucleosides-Reference-Cited by-同舟云学术

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:1993-06 Issue:6 Volume:4 Page:1117-1128
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Taylor Stephen JC,McCague Raymond,Wisdom Richard,Lee Carol,Dickson Karen,Ruecroft Graham,O'Brien Fergal,Littlechild Jennifer,Bevan Jennifer,Roberts Stanley M,Evans Christopher T

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference13 articles.

1. Carbocyclic nucleosides

2. Definition of subclasses of adenosine receptors associated with adenylate cyclase: interaction of adenosine analogs with inhibitory A1 receptors and stimulatory A2 receptors

3. Synthesis of carbocyclic aminonucleosides

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