Literature DB >> 12509896

2-Deoxy-2-iodo-beta-glucopyranosyl fluorides: mild and highly stereoselective glycosyl donors for the synthesis of 2-deoxy-beta-glycosides from beta-hydroxy ketones.

Nicolas Blanchard1, William R Roush.   

Abstract

2-Deoxy-2-iodo-beta-glucopyranosyl fluoride 14 is a highly stereoselective glucopyranosyl donor that may be activated under mild conditions. Application of this new glycosyl donor to the glycosidation reactions of a variety of acceptors including beta-hydroxy ketones affords beta-glycosides with high efficiency and stereoselectivity. [reaction--see text]

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Year:  2003        PMID: 12509896     DOI: 10.1021/ol027257h

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  Total synthesis of (-)-spinosyn A.

Authors:  Dustin J Mergott; Scott A Frank; William R Roush
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-01       Impact factor: 11.205

Review 2.  Methods for 2-Deoxyglycoside Synthesis.

Authors:  Clay S Bennett; M Carmen Galan
Journal:  Chem Rev       Date:  2018-06-28       Impact factor: 60.622

3.  Stereoselective synthesis of 2-deoxy-beta-glycosides using anomeric O-alkylation/arylation.

Authors:  William J Morris; Matthew D Shair
Journal:  Org Lett       Date:  2009-01-01       Impact factor: 6.005

4.  Scope and limitations of 2-deoxy- and 2,6-dideoxyglycosyl bromides as donors for the synthesis of β-2-deoxy- and β-2,6-dideoxyglycosides.

Authors:  Miho Kaneko; Seth B Herzon
Journal:  Org Lett       Date:  2014-05-01       Impact factor: 6.005

5.  Scope and Limitations of 3-Iodo-Kdo Fluoride-Based Glycosylation Chemistry using N-Acetyl Glucosamine Acceptors.

Authors:  Barbara Pokorny; Paul Kosma
Journal:  ChemistryOpen       Date:  2015-07-29       Impact factor: 2.911

  5 in total

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