A synthesis of 5′-amino-3′,5′-dideoxyuridine

被引:0
作者
Bender, DM [1 ]
Hennings, DD [1 ]
Williams, RM [1 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
来源
SYNTHESIS-STUTTGART | 2000年 / 03期
关键词
3; 5; '-dideoxy-5; '-aminouridine; mureidomycin; nucleoside; deoxygenation; azidation;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of 3',5'-dideoxy-5'-aminouridine starting from uridine is described.
引用
收藏
页码:399 / 402
页数:4
相关论文
共 28 条
[1]   NEW METHOD FOR DEOXYGENATION OF SECONDARY ALCOHOLS [J].
BARTON, DHR ;
MCCOMBIE, SW .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1975, (16) :1574-1585
[2]   Slow binding inhibition of phospho-N-acetylmuramyl-pentapeptide-translocase (Escherichia coli) by mureidomycin A [J].
Brandish, PE ;
Burnham, MK ;
Lonsdale, JT ;
Southgate, R ;
Inukai, M ;
Bugg, TDH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7609-7614
[3]   NAPSAMYCINS, NEW PSEUDOMONAS ACTIVE ANTIBIOTICS OF THE MUREIDOMYCIN FAMILY FROM STREPTOMYCES SP HIL Y-82,11372 [J].
CHATTERJEE, S ;
NADKARNI, SR ;
VIJAYAKUMAR, EKS ;
PATEL, MV ;
GANGULI, BN ;
FEHLHABER, HW ;
VERTESY, L .
JOURNAL OF ANTIBIOTICS, 1994, 47 (05) :595-598
[4]   Effects of modifications in the pentose moiety and conformational changes on the binding of nucleoside ligands to uridine phosphorylase from Toxoplasma gondii [J].
elKouni, MH ;
Naguib, FNM ;
Panzica, RP ;
Otter, BA ;
Chu, SH ;
Gosselin, G ;
Chu, CK ;
Schinazi, RF ;
Shealy, YF ;
Goudgaon, N ;
Ozerov, AA ;
Ueda, T ;
Iltzsch, MH .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (12) :1687-1700
[5]   NUCLEOSIDES .1. 5'-AMINO-5'-DEOXYURIDINE AND 5'-AMINO-5'-DEOXYTHYMIDINE [J].
HORWITZ, JP ;
TOMSON, AJ ;
URBANSKI, JA ;
CHUA, J .
JOURNAL OF ORGANIC CHEMISTRY, 1962, 27 (09) :3045-3048
[6]   SELECTIVE-INHIBITION OF THE BACTERIAL TRANSLOCASE REACTION IN PEPTIDOGLYCAN SYNTHESIS BY MUREIDOMYCINS [J].
INUKAI, M ;
ISONO, F ;
TAKATSUKI, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (05) :980-983
[7]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .1. TAXONOMY, FERMENTATION, ISOLATION AND PHYSICOCHEMICAL PROPERTIES [J].
INUKAI, M ;
ISONO, F ;
TAKAHASHI, S ;
ENOKITA, R ;
SAKAIDA, Y ;
HANEISHI, T .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :662-666
[8]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .3. BIOLOGICAL PROPERTIES [J].
ISONO, F ;
KATAYAMA, T ;
INUKAI, M ;
HANEISHI, T .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :674-679
[9]   MUREIDOMYCINS-A-D, NOVEL PEPTIDYLNUCLEOSIDE ANTIBIOTICS WITH SPHEROPLAST FORMING ACTIVITY .2. STRUCTURAL ELUCIDATION [J].
ISONO, F ;
INUKAI, M ;
TAKAHASHI, S ;
HANEISHI, T ;
KINOSHITA, T ;
KUWANO, H .
JOURNAL OF ANTIBIOTICS, 1989, 42 (05) :667-673
[10]   MUREIDOMYCIN-A, A NEW INHIBITOR OF BACTERIAL PEPTIDOGLYCAN SYNTHESIS [J].
ISONO, F ;
INUKAI, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (02) :234-236