Stereoselective conversion of (+)cis-2-oxabicyclo[3.3.0]oct-6-en-3-one into methylR-(+)-7-(3-hydroxy-5-oxo-cyclopentenyl)-5-cis-heptenoate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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3. Preparation of an optically active intermediate for the synthesis of prostaglandins
4. A total synthesis of prostaglandin F2α () from 2-oxabicyclo[3.3.0]oct-6-en-3-one
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3. 6′-Carbon-substituted carbocyclic analogs of 2′-deoxyribonucleosides — Synthesis and effect on DNA/RNA duplex stability;Tetrahedron;1996-09
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5. The first stereospecific synthesis of (+)-(1r,2s,4r)-4-amino-2-hydroxy-1-cyclopentanemethanol and (+)-carbocyclic thymidine.;Tetrahedron Letters;1987-01
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