4.7 Review

Neoglycorandomization and chemoenzymatic glycorandomization: Two complementary tools for natural product diversification

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 68, Issue 11, Pages 1696-1711

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/np0502084

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Funding

  1. NCI NIH HHS [CA84374] Funding Source: Medline
  2. NIAID NIH HHS [AI56652, AI52218] Funding Source: Medline
  3. NIGMS NIH HHS [GM70637] Funding Source: Medline

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In an effort to explore the contribution of the sugar constituents of pharmaceutically relevant glycosylated natural products, chemists have developed glycosylation methods that are amenable to the generation of libraries of analogues with a broad array of glycosidic attachments. Recently, two complementary glycorandomization strategies have been described, namely, neoglycorandomization, a chemical approach based on a one-step sugar ligation reaction that does not require any prior sugar protection or activation, and chemoenzymatic glycorandomization, a biocatalytic approach that relies on the substrate promiscuity of enzymes to activate and attach sugars to natural products. Since both methods require reducing sugars, this review first highlights recent advances in monosaccharide generation and then follows with an overview of recent progress in the development of neoglycorandomization and chemoenzymatic glycorandomization.

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