Selective synthesis of 3-deoxy-5-hydroxy-1-amino-carbasugars as potential α-glucosidase inhibitors

Author:

Jiang Chunfeng12345,Liu Quan675,Liu Jiaming12345,Liu Kaixuan12345,Tian Liangliang12345,Duan Mingfei12345,Wang Ying12345,Shen Zhufang675ORCID,Xu Youjun12345ORCID

Affiliation:

1. School of Pharmaceutical Engineering

2. and Key Laboratory of Structure-Based Drug Design & Discovery (Ministry of Education)

3. Shenyang Pharmaceutical University

4. Shenyang 110016

5. P. R. China

6. Chinese Academy of Medical Sciences and Peking Union Medical College

7. Beijing 100050

Abstract

A selective synthesis of 13 and 15, which could be converted to carbasugars as α-glucosidase inhibitors, was developed.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

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