SYNTHETIC STUDIES ON CELL-SURFACE GLYCANS .101. A REGIOSELECTIVE AND STEREOSELECTIVE SYNTHESIS OF 4-O-SULFATED CHONDROITIN DISACCHARIDES AND TETRASACCHARIDES BASED ON THE STRATEGY DESIGNED FOR THE ELONGATION OF THE REPEATING UNIT

被引：16

作者：

TAMURA, J

NEUMANN, KW

OGAWA, T

机构：

[1] RIKEN,INST PHYS & CHEM RES,WAKO,SAITAMA 35101,JAPAN

[2] UNIV TOKYO,DEPT CELLULAR BIOCHEM,BUNKYO KU,TOKYO 113,JAPAN

来源：

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 1995年 / 5卷 / 13期

关键词：

D O I：

10.1016/0960-894X(95)00222-F

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

4-O-Sulfated chondroitin di- and tetrasaccharide [beta-D-GalNAc(4-SO3)(1-->4)beta-D-GlcA and beta-D-GaINAc(4-SO3)(1-->4)beta-D-GlcA(1-->3)beta-D-GalNAc(4-SO3)(1-->4)beta-D-GlcA] were regio- and stereoselectively synthesized based on the synthetic route suitably designed for the elongation of the repeating unit.

引用

页码：1351 / 1354

页数：4

共 15 条

[11] A CONVENIENT AND HIGHLY CHEMOSELECTIVE METHOD FOR THE REDUCTIVE ACETYLATION OF AZIDES [J].