The synthesis of enantiomerically pure pyrazolo[4,3-C]pyridine carbaribo C-nucleoside

Nucleosides and Nucleotides

Volumn 16, Issue 7-9, 1997, Pages 1427-1429

  Mohar, Barbara ^a   Kobe, Jože ^a  

^a NATIONAL INSTITUTE OF CHEMISTRY   (Slovenia)

Author keywords

[No Author keywords available]

Indexed keywords

3 [2,3 DIHYDROXY 4 (HYDROXYMETHYL)CYCLOPENTAN 1 YL] 1H PYRAZOLO[4,3 C]PYRIDINE 4,6(5H,7H) DIONE; 5 (BETA D RIBOFURANOSYL)TETRAZOLE; NUCLEOSIDE DERIVATIVE; UNCLASSIFIED DRUG;

BASE PAIRING; CHEMICAL REACTION KINETICS; CONFERENCE PAPER; CYCLIZATION; ENANTIOMER; MOLECULAR DYNAMICS; NUCLEOTIDE METABOLISM; SYNTHESIS;

EID: 0030786756     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328319708006198     Document Type: Conference Paper

References (7)

1. Lutz, J.M.; Held, A.H.; Hottinger, M; Hübscher, V.; Benner, A.S. Nucleosides & Nucleotides, 1996, 24, 1308.
2. Sauer, D.R.; Schneller, S.W. ibid, 1989, 8, 1079.
3. (a) Prhavc, M.; Townsend, L.B.; Kobe, J. ibid, 1991, 10, 729.
4. (b) Prhavc, M.; Kobe, J. ibid, 1996, accepted.
5. Mohar, B.; Štimac, A; Kobe, J. ibid, 1993, 12, 793.
6. 4). The concentrated residue is chromatographed on silica gel (eluent petroleum ether/ EtOAc 4:1) to furnish 5 as a light yellow syrup.
7. +).