Glycosylation with N-Troc-protected glycosyl donors

被引:110
作者
Ellervik, U [1 ]
Magnusson, G [1 ]
机构
[1] LUND UNIV,LUND INST TECHNOL,CTR CHEM,S-22100 LUND,SWEDEN
关键词
N-Troc-protected glycosyl donors; glycosylation;
D O I
10.1016/0008-6215(95)00318-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N-Troc-protected (Troc = 2,2,2-trichloroethoxycarbonyl) glucosamine and galactosamine glycosyl donors (1-O-acetyl sugar, bromo sugar, and thioglycoside) were compared with the corresponding N-Phth-protected derivatives in glycosylations of 2-(trimethylsilyl)ethanol, 2-bromoethanol, methyl 3-mercaptopropionate, N-Fmoc-protected serine, and 2-(trimethylsilyl)ethyl 6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside. The N-Troc-protected donors gave pure beta-glycosides in somewhat higher yields than the N-Phth-protected counterparts. The N-Troc protecting group can be removed by reduction with zinc, which allows selective N-deprotection in oligosaccharides containing both N-Troc and N-Phth groups.
引用
收藏
页码:251 / 260
页数:10
相关论文
共 24 条
[1]   NUCLEOTIDES .45. DERIVATIVES OF BETA-2-AMINO-2-DEOXY-D-GLUCOSE (BETA-D-GLUCOSAMINE) 1-PHOSPHATE [J].
BALUJA, G ;
CHASE, BH ;
KENNER, GW ;
TODD, A .
JOURNAL OF THE CHEMICAL SOCIETY, 1960, (NOV) :4678-4681
[2]   Syntheses with glucosamine. [J].
Bergmann, M ;
Zervas, L .
BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1931, 64 :975-980
[3]   THE USE OF N-ALKOXYCARBONYL DERIVATIVES OF 2-AMINO-2-DEOXY-D-GLUCOSE AS DONORS IN GLYCOSYLATION REACTIONS [J].
BOULLANGER, P ;
JOUINEAU, M ;
BOUAMMALI, B ;
LAFONT, D ;
DESCOTES, G .
CARBOHYDRATE RESEARCH, 1990, 202 :151-164
[4]   DIRECT INCORPORATION OF A 6-ALPHA(7-ALPHA)-FORMAMIDO GROUP INTO PENICILLIN AND CEPHALOSPORIN SULFIDES AND SULFOXIDES [J].
BRANCH, CL ;
PEARSON, MJ ;
SMALE, TC .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (10) :2865-2873
[5]   USE OF SULFENYL HALIDES IN CARBOHYDRATE REACTIONS .1. ALKYL SULFENYL TRIFLATE AS ACTIVATOR IN THE THIOGLYCOSIDE-MEDIATED FORMATION OF BETA-GLYCOSIDIC LINKAGES DURING OLIGOSACCHARIDE SYNTHESIS [J].
DASGUPTA, F ;
GAREGG, PJ .
CARBOHYDRATE RESEARCH, 1988, 177 :C13-C17
[6]   NOVEL STEREOSELECTIVE GLYCOSIDATION BY THE COMBINED USE OF TRITYL HALIDE AND LEWIS ACID [J].
HIGASHI, K ;
NAKAYAMA, K ;
SOGA, T ;
SHIOYA, E ;
UOTO, K ;
KUSAMA, T .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1990, 38 (12) :3280-3282
[7]  
HIGASHI K, 1992, CHEM PHARM BULL, V40, P1042
[8]  
HIGASHI K, 1991, CHEM PHARM BULL, V39, P590
[9]   TOTAL SYNTHESIS OF ESCHERICHIA-COLI LIPID-A, THE ENDOTOXICALLY ACTIVE PRINCIPLE OF CELL-SURFACE LIPOPOLYSACCHARIDE [J].
IMOTO, M ;
YOSHIMURA, H ;
SHIMAMOTO, T ;
SAKAGUCHI, N ;
KUSUMOTO, S ;
SHIBA, T .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1987, 60 (06) :2205-2214
[10]   2-(TRIMETHYLSILYL)ETHYL GLYCOSIDES .3. SYNTHESIS, ANOMERIC DEBLOCKING, AND TRANSFORMATION INTO 1,2-TRANS 1-O-ACYL SUGARS [J].
JANSSON, K ;
AHLFORS, S ;
FREJD, T ;
KIHLBERG, J ;
MAGNUSSON, G ;
DAHMEN, J ;
NOORI, G ;
STENVALL, K .
JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (24) :5629-5647