Transformation of D-erythrose to some pseudoaldopentofuranoses. Syntheses of (1S,2R,3S,4S)-, (1R,2R,3S,4S)-, and (1R,2S,3S,4S)-2,3,4-trihydroxy-1-(hydroxymethyl)cyclopentanes and (1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)-1-cyclopentanamine
- 1 April 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (7) , 1427-1432
- https://doi.org/10.1021/jo00242a016
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- A novel and stereospecific synthesis of (.+-.)- and (-)-aristeromycinThe Journal of Organic Chemistry, 1986
- Synthesis of carbocyclic C-nucleoside analogues from 8,9,10-trinorborn-5-en-2-olJournal of the Chemical Society, Perkin Transactions 1, 1985
- Carbocyclic Arabinofuranosyladenine (Cyclaradine): Efficacy Against Genital Herpes in Guinea PigsScience, 1983
- Enantioselective synthesis of the carbocyclic nucleosides (-)-aristeromycin and (-)-neplanocin A by a chemicoenzymatic approachJournal of the American Chemical Society, 1983
- Carbocyclic analog of 3-deazaadenosine: a novel antiviral agent using S-adenosylhomocysteine hydrolase as a pharmacological targetJournal of Medicinal Chemistry, 1982
- Carbocyclic analogs of 5-fluorouracil nucleosidesJournal of Medicinal Chemistry, 1981
- Studies on neplanocin A,new antitumor antibiotic. II. Structure determination.The Journal of Antibiotics, 1981
- Synthesis of carbocyclic aminonucleosidesThe Journal of Organic Chemistry, 1978
- Synthesis of cyclohexyl carbocyclic puromycin and its inhibition of protein synthesisJournal of Medicinal Chemistry, 1977
- Carbocyclic arabinosyladenine, an adenosine deaminase resistant antiviral agentJournal of Medicinal Chemistry, 1977