SYNTHESE ET ETUDE CONFORMATIONELLE PAR R.M.N.-13C DE β-NUCLEOSIDES PYRIMIDIQUES CONTENANT UNE OU DEUX SOUSUNITES HEXOPYRANOSYLES: APPLICATION A LA CONFORMATION DE L'ANTHELMYCINE
Several new peracetylated pyrimidine N-1 nucleosides containing one two β-D-hexopyranosyl residues have been synthesized and their physical characteristics are reported.The conformation of these nucleosides has been investigated by highresolution 13C-n.m.r. analysis after deblocking.It was poddible to distinguish between the syn and anti rotamers of 3-β-D-glucopyranosyluracyl, and to establish the favored anti conformation in solution of the nucleoside disaccharide, antibiotic anthelmycin.
Vuilhorgne, Marc,Ennifar, Sofiane,Das, Bhupesh C.
p. 19 - 30
(2007/10/02)
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