Synthetic study on carbocyclic analogs of cyclic ADP-ribose, a novel second messenger: An efficient synthesis of cyclic IDP-carbocyclic-ribose
Author(s) -
Makoto Fukuoka,
Satoshi Shuto,
Noriaki Minakawa,
Yoshihito Ueno,
Akira Matsuda
Publication year - 1999
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/42.1.11
Subject(s) - ribose , chemistry , stereochemistry , pyridine , cyclic adp ribose , derivative (finance) , amine gas treating , medicinal chemistry , organic chemistry , stem cell , cd34 , genetics , cd38 , economics , financial economics , biology , enzyme
An efficient synthesis of cyclic IDP-carbocyclic-ribose, as a stable mimic for cyclic ADP-ribose, was achieved. 8-Bromo-N1-carbocyclic-ribosylinosine derivative 10, prepared from N1-(2,4-dinitrophenyl)inosine derivative 5 and an optically active carbocyclic amine 6, was converted to 8-bromo-N1-carbocyclic-ribosylinosine bisphosphate derivative 15. Treatment of 15 with I2 in the presence of molecular sieves in pyridine gave the desired cyclic product 16 quantitatively, which was deprotected and reductively debrominated to give the target cyclic IDP-carbocyclic-ribose (3).
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