TY - JOUR
T1 - Nucleosides. CXLIII. Synthesis of 5’-Deoxy-5’-substituted-2,2’-anhydro-l-(β-D-arabinofuranosyl)uracils. A New 2,5’- to 2,2’-Anhydro-nucleoside Transformation. Studies Directed toward the Synthesis of 2‘-Deoxy-2’-substituted arabino Nucleosides. (4)1)
AU - Pankiewicz, Krzysztofai W.
AU - Watanabe, Kyoichi A.
PY - 1987
Y1 - 1987
N2 - Treatment of 2,5’-anhydro-3’-O-acetyl-2’-O-triflyluridine with a nucleophile such as NaOAc, NaN3, LiCl or LiBr, did not afford the 2’-substituted 2,5’-anhydro-arabinosyluracil, but gave 2,2’-anhydro-l-(5-substituted-β-D-arabinofuranosyl)uracil instead.
AB - Treatment of 2,5’-anhydro-3’-O-acetyl-2’-O-triflyluridine with a nucleophile such as NaOAc, NaN3, LiCl or LiBr, did not afford the 2’-substituted 2,5’-anhydro-arabinosyluracil, but gave 2,2’-anhydro-l-(5-substituted-β-D-arabinofuranosyl)uracil instead.
KW - 2‘-anhydroabinosyluracil new transformation
KW - 2’-anhydrouracilnucleoside 2
KW - 5‘-anhydro-3‘-O-acetyl-2‘
KW - 5’-anhydrouracilnucleoside 2
KW - O-triflyluridine 5‘-substituted-2
KW - nucleoside anhydronucleoside 2
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U2 - 10.1248/cpb.35.4494
DO - 10.1248/cpb.35.4494
M3 - Article
C2 - 3442883
AN - SCOPUS:0042922008
SN - 0009-2363
VL - 35
SP - 4494
EP - 4497
JO - Chemical and Pharmaceutical Bulletin
JF - Chemical and Pharmaceutical Bulletin
IS - 11
ER -