Xinshan Ye

Xinshan Ye


Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
20 October 2010 in Molecules
Verified
Journal Article
Open access
PDF file
JGJian Guo
Jian Guo
XYXinshan Ye
Xinshan Ye
Saccharides are polyhydroxy compounds, and their synthesis requires complex protecting group manipulations. Protecting groups are usually used to temporarily mask a functional group which may interfere with a certain reaction, but protecting groups in carbohydrate chemistry do more than protecting groups usually do. Particularly, protecting groups can participate in reactions directly or indirectly, thus affecting the stereochemical outcomes, which is important for synthesis of oligosaccharides. Herein we present an overview of recent advances in protecting groups influencing stereoselectivity in glycosylation reactions, including participating protecting groups, and conformation-constraining protecting groups in general.

16 March 2017 in Nature Communications
Verified
Journal Article
Open access
PDF file
YWYong Wu
Yong Wu
DXDe-Cai Xiong
De-Cai Xiong
SCSi-Cong Chen
Si-Cong Chen
YWYong-Shi Wang
Yong-Shi Wang
XYXinshan Ye
Xinshan Ye
Carbohydrates are diverse bio-macromolecules with highly complex structures that are involved in numerous biological processes. Well-defined carbohydrates obtained by chemical synthesis are essential to the understanding of their functions. However, synthesis of carbohydrates is greatly hampered by its insufficient efficiency. So far, assembly of long carbohydrate chains remains one of the most challenging tasks for synthetic chemists. Here we describe a highly efficient assembly of a 92-mer polysaccharide by the preactivation-based one-pot glycosylation protocol. Several linear and branched oligosaccharide/polysaccharide fragments ranging from 5-mer to 31-mer in length have been rapidly constructed in one-pot manner, which enables the first total synthesis of a biologically important mycobacterial arabinogalactan through a highly convergent [31+31+30] coupling reaction. Our results show that the preactivation-based one-pot glycosylation protocol may provide access to the construction of long and complicated carbohydrate chains.

22 May 2007 in Organic & Biomolecular Chemistry
Verified
Journal Article
Closed access
PDF file
YWYuhang Wang
Yuhang Wang
XYXinshan Ye
Xinshan Ye
Liangren ZhangLiangren Zhang
Liangren Zhang
Saccharide synthesis is a formidable task for synthetic chemists. Although in recent years many advances have been made in this area, development of more convenient and efficient strategies for oligosaccharide synthesis is still in great demand. This review focuses on one of these new strategies—the one-pot sequential glycosylation approach as a potent tool for oligosaccharide assembly.

31 May 2016 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
LSLifeng Sun
Lifeng Sun
XWXiaowei Wu
Xiaowei Wu
DXDe-Cai Xiong
De-Cai Xiong
XYXinshan Ye
Xinshan Ye

29 September 2022 in Nature Synthesis
Verified
Journal Article
Closed access
PDF file
WYWenlong Yao
Wenlong Yao
DXDe-Cai Xiong
De-Cai Xiong
YYYun Yang
Yun Yang
CGChunmei Geng
Chunmei Geng
ZCZisen Cong
Zisen Cong
XYXinshan Ye
Xinshan Ye

7 January 2011 in ACS Chemical Biology
Verified
Journal Article
Closed access
FYFan Yang
Fan Yang
XZXiu-Jing Zheng
Xiu-Jing Zheng
CHChang-Xin Huo
Chang-Xin Huo
YWYue Wang
Yue Wang
YZYe Zhang
Ye Zhang
XYXinshan Ye
Xinshan Ye