Glycosylation reaction via a mild and efficient one-pot reaction using doped natural phosphate with iodine as catalyst

Nucleosides, Nucleotides and Nucleic Acids

Volumn 26, Issue 8-9, 2007, Pages 1095-1098

  Lazrek, H B ^a   Ouzebla, D ^a   Baddi, L ^a   Vasseur, J J ^b  

^a FACULTÉ DES SCIENCES SEMLALIA   (Morocco)

^b UNIVERSITÉ DE MONTPELLIER   (France)

Author keywords

Catalyst; D ribonucleoside; Iodine; Natural phosphate

Indexed keywords

ADENINE; CYTOSINE; IODINE; NUCLEIC ACID BASE; PHOSPHATE; RIBONUCLEOSIDE; THYMINE; URACIL;

ARTICLE; CATALYST; CHEMICAL REACTION; DOPING; GLYCOSYLATION; ONE POT SYNTHESIS; SILYLATION; SYNTHESIS;

ANTINEOPLASTIC AGENTS; ANTIVIRAL AGENTS; CATALYSIS; GLYCOSYLATION; IODINE; METHODS; ORGANOSILICON COMPOUNDS; PHOSPHATES; RIBONUCLEOSIDES;

EID: 36849007399     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770701519106     Document Type: Article

References (6)

1. Mizuno, Y. The Organic Chemistry of Nucleic Acids Kodansha Ltd., Tokyo, 1986, pp. 41-72.
2. Hadd, M.J.; Gervay, J. Glycosyl iodides are highly efficient donors under neutral conditions. Carbohydr. Res. 1999, 320, 61-69.
3. Karimi, B.; Golshani, B. Mild and highly efficient method for the silylation of alcohols using hexamethyldisilazane catalyzed by iodine under nearly neutral reaction conditions. J. Org. Chem. 2000, 65(21), 7228-7230.
4. -1.
5. Zahouily, M.; Mezdar, A.; El maksoudi, A.; Mounir, B.; Rayadh, A.; Sebti, S.; Lazrek, H.B. Comparison of different Lewis acids supported on natural phosphate as new catalysts for chemoselective dithioacetalization of carbonyl compounds under solvent-free conditions ARKIVOC 2006 (ii) 42-51, and references cited therein.
6. Lazrek, H.B.; Ouzebla, D.; Rochdi, A.; Redwane, N.; Vasseur, J.J A one pot synthesis of Dribonucleosides using Natural phosphate doped with KI in HMDS. Lett. Orga. Chem. 2006, 3(4), 313-314, and references cited therein.