Silyl modification of biologically active compounds. 5. Hydrolytic stability and biological activity of trialkylsilyl derivatives of some heterocyclic bases

被引:0
作者
Lukevics, E [1 ]
Segal, I [1 ]
Birgele, I [1 ]
Zablotskaya, A [1 ]
机构
[1] Latvian Organ Synth Inst, LV-1006 Riga, Latvia
来源
KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII | 1998年 / 09期
关键词
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
引用
收藏
页码:1253 / 1258
页数:6
相关论文
共 16 条
[1]   TRIALKYLSILYL MOIETIES AS POTENTIAL PHARMACOKINETIC MODIFYING GROUPS FOR AMINOALCOHOLS [J].
BECKETT, AH ;
TAYLOR, DC ;
GORROD, JW .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1975, 27 (08) :588-593
[2]   3'-SPIRO NUCLEOSIDES, A NEW CLASS OF SPECIFIC HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INHIBITORS - SYNTHESIS AND ANTIVIRAL ACTIVITY OF [2',5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-XYLO AND RIBOFURANOSE]-3'-SPIRO-5''-[4''-AMINO-1'',2''-OXATHIOLE 2'',2''-DIOXIDE] (TSAO) PYRIMIDINE NUCLEOSIDES [J].
CAMARASA, MJ ;
PEREZPEREZ, MJ ;
SANFELIX, A ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (15) :2721-2727
[3]  
FAST DI, 1992, J LEUKOCYTE BIOL, P255
[4]  
Freshney R., 1994, CULTURE ANIMAL CELLS, P296
[5]  
GRZYBOWSKA J, 1983, SCI PHARM, V51, P301
[6]   NEW CATALYSTS AND PROCEDURES FOR THE DIMETHOXYTRITYLATION AND SELECTIVE SILYLATION OF RIBONUCLEOSIDES [J].
HAKIMELAHI, GH ;
PROBA, ZA ;
OGILVIE, KK .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1982, 60 (09) :1106-1113
[7]  
LEVIER RR, 1978, BIOCH SILICON RELATE, P479
[8]  
LEVIER RR, 1978, BIOCH SILICON RELATE, P485
[9]  
Lukevics E, 1997, KHIM GETEROTSIKL+, P270
[10]   Synthesis and neurotropic activity of novel quinoline derivatives [J].
Lukevics, E ;
Segal, I ;
Zablotskaya, A ;
Germane, S .
MOLECULES, 1997, 2 (12) :180-185