Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies-Reference-Cited by-同舟云学术

Synthesis of carbohydrate building blocks via regioselective uniform protection/deprotection strategies

Published:2019 Issue:20 Volume:17 Page:4934-4950
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Tinghua¹²³⁴⁵,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

Scope 1: sugar is uniformly protected leaving only one (or two) free hydroxyl group; scope 2: uniformly protected sugar is deprotected to liberate only one (or two) hydroxyl group.

Funder

National Institute of General Medical Sciences

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/2019/OB/C9OB00573K

Reference179 articles.

1. S. Oscarson , Protective group strategies , in The organic chemistry of sugars , ed. D. E. Levi and P. Fugedi , CRC, Taylor & Francis , Boca Raton - London - New York , 2006 , pp. 53–88

2. P. G. M. Wuts and T. W.Greene , Greene's Protective Groups in Organic Synthesis , Wiley-Interscience , 4th edn, 2007

3. A. G. Volbeda , G. A.van der Marel and J. D. C.Codée , Protecting Group Strategies in Carbohydrate Chemistry , in Protecting Groups – Strategies and Applications in Carbohydrate Chemistry , ed. S. Vidal , Wiley-VCH , Weinheim , 2019 , pp. 1–28

4. Orthogonal protecting group strategies in carbohydrate chemistry

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