Dehydrative Glycosylation Enabled by a Comproportionation Reaction of 2‐Aryl‐1,3‐dithiane 1‐Oxide †-Reference-Cited by-同舟云学术

Dehydrative Glycosylation Enabled by a Comproportionation Reaction of 2‐Aryl‐1,3‐dithiane 1‐Oxide †

Published:2019-11-22 Issue:1 Volume:38 Page:43-49
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Cai Lei¹,Zeng Jing¹,Li Ting¹,Xiao Ying¹,Ma Xiang¹,Xiao Xiong¹,Zhang Qin¹,Meng Lingkui¹,Wan Qian¹²

Affiliation:

1. Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of PharmacyHuazhong University of Science and Technology, 13 Hangkong Road Wuhan Hubei 430030 China

2. Institute of Brain Research, Huazhong University of Science and Technology, 13 Hangkong Road Wuhan Hubei 430030 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.201900419

Reference98 articles.

1. Methods for 2-Deoxyglycoside Synthesis

2. “One-Pot” Protection, Glycosylation, and Protection–Glycosylation Strategies of Carbohydrates

3. Catalytic Glycosylations in Oligosaccharide Synthesis

4. Acid–Base Catalysis in Glycosidations: A Nature Derived Alternative to the Generally Employed Methodology

5. Gold(I)-Catalyzed Glycosylation with Glycosyl o-Alkynylbenzoates as Donors

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