2-O-N-Benzylcarbamoyl as a Protecting Group To Promote β-Selective Glycosylation and Its Applications in the Stereoselective Synthesis of Oligosaccharides-Reference-Cited by-同舟云学术

2-O-N-Benzylcarbamoyl as a Protecting Group To Promote β-Selective Glycosylation and Its Applications in the Stereoselective Synthesis of Oligosaccharides

Published:2018-03-07 Issue:7 Volume:83 Page:3688-3701
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lu Yin-Jen¹,Lai Yen-Hsun¹,Lin You-Yu¹,Wang Yi-Chi¹,Liang Pi-Hui¹^ORCID

Affiliation:

1. School of Pharmacy, College of Medicine, National Taiwan University, Taipei 100, Taiwan

Funder

Ministry of Science and Technology, Taiwan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00047

Reference64 articles.

1. Selective Glycosylations: Synthetic Methods and Catalysts

2. Neighboring-Group Participation in Sugars

3. An efficient approach to stereoselective glycosylation of ceramide derivatives: Use of pivaloyl group as a stereocontrolling auxiliary

4. Oligosaccharide Synthesis with Glycosyl Phosphate and Dithiophosphate Triesters as Glycosylating Agents

5. Exploring the Mechanism of Neighboring Group Assisted Glycosylation Reactions

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