2,4-Dinitrobenzenesulfonamide-Directed SN2-Type Displacement Reaction Enables Synthesis of β-d-Glycosaminosides-Reference-Cited by-同舟云学术

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2,4-Dinitrobenzenesulfonamide-Directed SN2-Type Displacement Reaction Enables Synthesis of β-d-Glycosaminosides

Published:2019-03-22 Issue:7 Volume:21 Page:2402-2407
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Xianyang¹²,Wang Peng¹²,Li Dongwei¹²,Li Ming¹²^ORCID

Affiliation:

1. School of Medicine and Pharmacy, Ocean University of China, Key Laboratory of Marine Medicine, Chinese Ministry of Education, Qingdao 266003 China

2. Laboratory for Marine Drugs and Bioproducts, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237 China

Funder

National Natural Science Foundation of China

Shandong Province

Natural Science Foundation of Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00688

Reference42 articles.

1. Selective Glycosylations: Synthetic Methods and Catalysts

2. The Experimental Evidence in Support of Glycosylation Mechanisms at the SN1–SN2 Interface

3. Synthesis of .beta.-D-mannopyranosides and .beta.-L-rhamnopyranosides by glycosidation at C-1

4. Selective demesylation of 2-O-(methylsulfonyl)-d-mannopyranoside derivatives with sodium amalgam and 2-propanol

5. Direct Synthesis of the β-l-Rhamnopyranosides

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