A versatile approach to the synthesis of mannosamine glycosides-Reference-Cited by-同舟云学术

A versatile approach to the synthesis of mannosamine glycosides

Published:2020 Issue:34 Volume:18 Page:6682-6695
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Alex Catherine¹²³⁴⁵,Visansirikul Satsawat¹²³⁴⁵,Demchenko Alexei V.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry

2. University of Missouri – St. Louis

3. One University Boulevard

4. St. Louis

5. USA

Abstract

The 3-O-picoloyl protected glycosyl donor provides high β-manno stereoselectivity, whereas 3-O-benzoylated donor leads to complete α-manno stereoselectivity.

Funder

Division of Chemistry

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01640C

Reference64 articles.

1. Stereoselective Glycosylation Reactions with Chiral Auxiliaries

2. Stereoselective Glycosylations Using (R)- or (S)-(Ethoxycarbonyl)benzyl Chiral Auxiliaries at C-2 of Glycopyranosyl Donors

3. Stereoselective glycosylation using oxathiane glycosyl donors

4. Neighbouring group participation vs. addition to oxacarbenium ions: studies on the synthesis of mycobacterial oligosaccharides

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