Pregled bibliografske jedinice broj: 295980
Synthesis and Enzymic Hydrolysis of Acylated Adenosine Derivatives
Synthesis and Enzymic Hydrolysis of Acylated Adenosine Derivatives // Journal of carbohydrate chemistry, 25 (2006), 713-723 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 295980 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and Enzymic Hydrolysis of Acylated Adenosine Derivatives
Autori
Car, Željka ; Petrović, Vesna ; Tomić, Srđanka
Izvornik
Journal of carbohydrate chemistry (0732-8303) 25
(2006);
713-723
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Acylated adenosine; Hydrolases; Enzymic hydrolysis
Sažetak
Various derivatives of adenosine were prepared by acylation of adenosine (6-amino-9-(betha- D-ribofuranosyl)purine (1) with different molar equivalents of acetic anhydride and/or pivaloyl chloride in pyridine. Compounds 6-acetylamino-9-[(2, 3, 5-tri-O-acetyl)-betha-Dribofuranosyl] purine (3), 6-amino-9-[(2, 3, 5-tri-O-acetyl)-betha-D-ribofuranosyl]purine (4), and 6-pivaloylamino-9-[(2, 3, 5-tri-O-pivaloyl)-betha-D-ribofuranosyl]purine (5) were subsequently submitted to hydrolysis catalyzed by a number of hydrolytic enzymes. Regioselective enzymic deacetylation at the primary hydroxyl group of 3 and 4 with butyrylcholinesterase (BChE) produced 6-acetylamino-9-[(2, 3-di-O-acetyl)-betha-D-ribofuranosyl] purine (9) and 6-amino-9-[(2, 3-di-O-acetyl-betha-D-ribofuranosyl]purine (10), respectively. All structures were established by 1H and 13C NMR spectroscopies.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus