Versatility of glycals in synthetic organic chemistry: coupling reactions, diversity oriented synthesis and natural product synthesis-Reference-Cited by-同舟云学术

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Versatility of glycals in synthetic organic chemistry: coupling reactions, diversity oriented synthesis and natural product synthesis

Published:2019 Issue:17 Volume:17 Page:4153-4182
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Kinfe Henok H.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. Center of Synthesis and Catalysis

3. University of Johannesburg

4. Auckland Park 2006

5. South Africa

Abstract

Versatility of glycals in the stereoselective synthesis of natural products.

Funder

University of Johannesburg

National Research Foundation

Department of Science and Technology, Republic of South Africa

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00343F

Reference105 articles.

1. Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules

2. Diversity-oriented synthesis: producing chemical tools for dissecting biology

3. 4,6-Di-O-acetyl-aldehydo-2,3-dideoxy-D-erythro-trans-hex-2-enose. Probable reason for the 'al' in Emil Fischer's triacetyl glucal

4. Substitution-with-Allylic-Rearrangement Reactions of Glycal Derivatives

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