SYNTHESIS OF 1-CHLOROACETYL-1-DEHYDROXY-2,3,5-TRI-O-BENZOYL-BETA-D-RIBOFURANOSE - A POTENTIALLY VERSATILE INTERMEDIATE FOR THE SYNTHESIS OF C-NUCLEOSIDES

被引：6

作者：

HAN, HK

LEE, JC

KANG, YH

KIM, JH

CHI, DY

机构：

[1] KOREA INST SCI & TECHNOL,MED CHEM LAB,POB 131,SEOUL,SOUTH KOREA

[2] HAN YANG UNIV,ANSAN,SOUTH KOREA

来源：

SYNTHETIC COMMUNICATIONS | 1992年 / 22卷 / 19期

关键词：

D O I：

10.1080/00397919208021547

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

New key carbohydrate intermediate, 1-chloroacetyl-1-dehydroxy-2,3,5-tri-O-benzoyl-beta-D-ribofuranose (1a), has been synthesized. The application of this key intermediate would be very wide. We have very conveniently synthesized several C-nucleosides including monocyclic and 5,5-membered bicyclic compounds from this intermediate.

引用

页码：2815 / 2822

页数：8

共 7 条

[1] C-HETEROARYLATION OF SUGARS BY INDOLYLBROMOMAGNESIUM SALTS - SYNTHESIS OF 3-(ALDITOL-1-YL)INDOLES AND THEIR CYCLIZATION TO INDOLE C-NUCLEOSIDE ANALOGS [J].