𝔖 Bobbio Scriptorium
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Hypoxanthine nucleoside counterparts of the antibiotic, cordycepin

✍ Scribed by Vasu Nair; Arthur G. Lyons

Book ID
108372369
Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
809 KB
Volume
46
Category
Article
ISSN
0040-4020

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πŸ“œ SIMILAR VOLUMES

Simultaneous production of isomeric di-
Simultaneous production of isomeric di- and mono-glucopyranosyl hypoxanthines (synthesis in nucleoside antibiotics, IV)
✍ Takeshi Hashizume; Hajime Yamazaki πŸ“‚ Article πŸ“… 1967 πŸ› Elsevier Science 🌐 French βš– 314 KB

In the course of the investigations on the synthesis of nucleoside anl;ibiotics, we have closely examined the reaction products of bromomercuri derivative of hyporanthine with acetobromoglucose, and found that two isomeric diglucosylhypoxanthines are produced simultaneously in considerable yields be

Molecular orbital studies on nucleoside
Molecular orbital studies on nucleoside antibiotics. IV. conformation of 3'-deoxyadenosine (cordycepin) and 3'-amino-3'-deoxyadenosine
✍ Anil Saran; Lalit N. Patnaik πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 English βš– 479 KB

## Abstract PCILO computations have been carried out on the conformation of 3'‐deoxyadenosine (cordycepin) and 3'‐amino‐3'‐deoxyadenosine. These nucleoside antibiotics results as a consequence of modification in the sugar part of adenosine. Both C(2')‐endo and C(3')‐endo sugar puckerings have been