Preparation of a substituted 3-acetamido-3-deoxy-D-ribofuranosyl bromide suitable for the synthesis of puromycin analogs
- 31 May 1975
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 41 (1) , 318-322
- https://doi.org/10.1016/s0008-6215(00)87033-0
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Synthesis of 8-(hydroxyalkyl)adeninesCarbohydrate Research, 1974
- 3-deoxy-2,5-DI-O-p-nitrobenzoyl-α-D-threo-pentofuranosyl bromide, a starting material for the synthesis of nucleosidesCarbohydrate Research, 1974
- Synthesis of a c-nucleoside analog of the antibiotic cordycepinCarbohydrate Research, 1974
- Synthesis of 8β-D-arabinofuranosyladenineCarbohydrate Research, 1974
- Synthesis of cordycepin-C [8-(3′-deoxy-β-D-erythro-pentofuranosyl)adenine]Carbohydrate Research, 1973
- Nucleophilic displacement reactions in carbohydrates : Part XVI1. Syntheses of 3,5-diacetamido-3,5-dideoxy--ribose and 3,5--diacetamido-3,5-dideoxy--xylose derivativesCarbohydrate Research, 1971
- A mild method for the hydrolysis of acetal groups attached to sugars and nucleosidesCarbohydrate Research, 1968
- Puromycin. Synthetic Studies. XIV. Use of the N-Phthalyl Blocking Group for Synthesis of AminonucleosidesJournal of the American Chemical Society, 1955
- Puromycin. Synthetic Studies. IX. Total SynthesisJournal of the American Chemical Society, 1955