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Glycal

About: Glycal is a research topic. Over the lifetime, 897 publications have been published within this topic receiving 17422 citations.


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Journal ArticleDOI
TL;DR: This review places special emphasis on two aspects of exo-glycals including general methods of preparation and synthetic applications for making biologically important molecules, namely C-glycosides, enzyme inhibitors and bioactive natural products.
Abstract: It is well known that carbohydrates play an indispensable role in a variety of essential biological activities, such as cell-cell adhesion, bacteria and virus infections, and tumor metastasis. Among an increasing number of sugars and sugar mimetics that have been designed and synthesized for the purpose of drug discovery, C-glycosides are considered to be one of the best choices on account of their stability and resemblance as they differ from normal glycosides only in glycosidic linkages. exo-Glycals are unsaturated sugars that have a double bond attached to the anomeric center outside the sugar ring. These carbohydrate molecules are useful for the synthesis of C-glycosides and compounds containing quaternary carbons, provided that the olefin can be properly reduced or functionalized. This review places special emphasis on two aspects of exo-glycals including general methods of preparation and synthetic applications for making biologically important molecules. The first half discusses the methods of addition/elimination and Ramburg-Backlund rearrangement that offer many beneficial features including a wide range of double bond substitutions, limited reaction steps, easy operation and good overall yields. The rest of the article demonstrates a number of synthetic studies using exoglycals as the starting materials. The target molecules can be categorized into three groups, namely C-glycosides, enzyme inhibitors and bioactive natural products.

39 citations

Journal ArticleDOI
TL;DR: In this article, a short and efficient synthesis of UDP-exo-galactofuranosyl-glycal was presented, which displayed an interesting time-dependent inactivation of UDP -galactopyranose mutase, an essential enzyme of the mycobacterial cell wall biosynthesis.

39 citations

Journal ArticleDOI
TL;DR: In this paper, a facile aza-Claisen rearrangement was used to obtain 2-C-Methylene-N-glycosyl amides from 2-(hydroxymethyl) glycals.

39 citations

Journal ArticleDOI
TL;DR: A highly stereoselective rapid C-glycosylation reaction has been developed between glycal and unactivated alkynes in the presence of coppertriflate and ascorbic acid at low catalyst loading and at room temperature.

39 citations

Journal ArticleDOI
TL;DR: The DCC mediated coupling reaction of 3,4,6-tri-O -benzyl-1,2-dideoxy-d -arabino-hex-1-enitol gave esters 7a-d in good yield as mentioned in this paper.

39 citations

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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202312
202211
202111
202011
20197
201819