Efficient syntheses of alpha- and beta-C-nucleosides and the origin of anomeric selectivity-Reference-Cited by-同舟云学术

Efficient syntheses of alpha- and beta-C-nucleosides and the origin of anomeric selectivity

Published:2018 Issue:12 Volume:5 Page:1992-1999
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Tongchao¹²³⁴⁵,Zhu Zhengdan⁶⁷⁸⁹¹⁰,Ren Huanming⁵⁸⁹¹⁰⁴,Chen Yabin⁵⁸⁹¹⁰⁴,Chen Guohua¹¹¹²¹³⁴,Cheng Maosheng¹²³⁴,Zhao Dongmei¹²³⁴,Shen Jingkang⁵⁸⁹¹⁰⁴,Zhu Weiliang⁶⁷⁸⁹¹⁰,Xiong Bing⁵⁸⁹¹⁰⁴,Chen Yue-Lei⁵⁸⁹¹⁰⁴^ORCID

Affiliation:

1. Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education

2. Shenyang Pharmaceutical University

3. Shenyang 110016

4. P. R. China

5. State Key Laboratory of Drug Research

6. CAS Key Laboratory of Receptor Research

7. Drug Discovery and Design Center

8. Shanghai Institute of Materia Medica

9. Chinese Academy of Sciences

10. Shanghai 201203

11. School of Pharmacy

12. China Pharmaceutical University

13. Nanjing 210009

Abstract

Valuable C-nucleosides are efficiently prepared with excellent anomeric selectivity depending on protecting groups on sugar moiety.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00165K

Reference42 articles.

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4. Nucleophilic Additions to Fused Bicyclic Five-Membered Ring Oxocarbenium Ions: Evidence for Preferential Attack on the Inside Face

5. Stereoselective C-Glycosylation Reactions of Ribose Derivatives: Electronic Effects of Five-Membered Ring Oxocarbenium Ions

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