Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Isabelle Hladezuk"'
Autor:
Anita R. Maguire, Sebastien Debarge, Veronique Chastagner, Stephen J. Plunkett, Stuart G. Collins, Alan Ford, Isabelle Hladezuk
Publikováno v:
Tetrahedron. 68:1894-1909
Development of rhodium catalysed O–H insertion reactions employing α-diazophosphonates with appropriately protected adenosine, uridine and thymidine derivatives is described. This synthetic methodology leads, following deprotection, to novel phosp
Publikováno v:
Journal of Carbohydrate Chemistry. 17:869-878
Lithium diphenylcuprate treatment of methyl 2,3-anhydro-4,6-O-benzylidene-D-pyranosides in which the anomeric substituent and the three-membered rings are cis oriented furnished the expected trans-diaxial opening products. When the relationship betwe
Publikováno v:
ChemInform. 29
Lithium diphenylcuprate treatment of methyl 2,3-anhydro-4,6-O-benzylidene-D-pyranosides in which the anomeric substituent and the three-membered rings are cis oriented furnished the expected trans-diaxial opening products. When the relationship betwe
Publikováno v:
Carbohydrate research. 337(4)
An improved procedure for the synthesis of N -benzoyl-2′,3′- O -isopropylidene uridine via one-step selective N -benzoylation of 2′,3′- O -isopropylidene uridine has been developed. An efficient synthetic route to N -benzoyl thymidine via ini
Publikováno v:
ChemInform. 32
2-C- and 3-C-[(2′-chloro)pyrid-5′-yl]-hex-5-enopyranosides were synthesized from 4,6-O-benzylidene acetals in three steps. By treatment with mercury or palladium salts, the corresponding cyclohexanones could be obtained. The stereochemistry of th
Publikováno v:
Carbohydrate research. 330(2)
2-C- and 3-C-[(2′-chloro)pyrid-5′-yl]-hex-5-enopyranosides were synthesized from 4,6-O-benzylidene acetals in three steps. By treatment with mercury or palladium salts, the corresponding cyclohexanones could be obtained. The stereochemistry of th