The first stereospecific synthesis of (+)-(1r,2s,4r)-4-amino-2-hydroxy-1-cyclopentanemethanol and (+)-carbocyclic thymidine.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (50) , 6381-6384
- https://doi.org/10.1016/s0040-4039(01)91379-6
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Chemoenzymatic approach to carbocyclic analogues of ribonucleosides and nicotinamide ribose.Tetrahedron Letters, 1987
- Resolution of racemic carbocyclic analogs of purine nucleosides through the action of adenosine deaminase. Antiviral activity of the carbocyclic 2'-deoxyguanosine enantiomersJournal of Medicinal Chemistry, 1987
- A novel approach to carbocyclic analogues of nucleosidesTetrahedron Letters, 1986
- The design of chemotherapeutic agentsAccounts of Chemical Research, 1986
- Carbocyclic analogs of 5-halocytosine nucleosidesJournal of Medicinal Chemistry, 1986
- A novel and stereospecific synthesis of (.+-.)- and (-)-aristeromycinThe Journal of Organic Chemistry, 1986
- Synthesis and antiviral activity of the carbocyclic analogs of 5-ethyl-2'-deoxyuridine and of 5-ethynyl-2'-deoxyuridineJournal of Medicinal Chemistry, 1986
- An improved method of synthesis of neplanocin and related cyclopentenyl-containing nucleosidesTetrahedron Letters, 1985
- Resolution of aristeromycin enantiomersJournal of Medicinal Chemistry, 1985
- Enantioselective synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)-neplanocin A by a chemicoenzymatic approachJournal of the American Chemical Society, 1983