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Synthetic studies of carbocyclic analogs of cyclic ADP-ribose. Formation of a cyclic dimer, a 36-membered-ring product, in the condensation reaction of an 8-bromo-N1-[5-(phenylthiophosphoryl)carbocyclic-ribosyl]inosine 5′-phosphate derivative mediated by AgNO3

✍ Scribed by Satoshi Shuto; Michiyo Shirato; Yuji Sumita; Yoshihito Ueno; Akira Matsuda

Book ID
108387027
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
266 KB
Volume
39
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

Nucleosides and Nucleotides. 173. Synthe
Nucleosides and Nucleotides. 173. Synthesis of Cyclic IDP-carbocyclic-ribose, a Stable Mimic of Cyclic ADP-ribose. Significant Facilitation of the Intramolecular Condensation Reaction of N -1-(Carbocyclic-ribosyl)inosine 5‘,6‘‘-Diphosphate Derivatives by an 8-Bromo-Substitution at the Hypoxanthine Moiety
✍ Shuto, Satoshi; Shirato, Michiyo; Sumita, Yuji; Ueno, Yoshihito; Matsuda, Akira 📂 Article 📅 1998 🏛 American Chemical Society 🌐 English ⚖ 138 KB