Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Methods of synthesis of glycosyl fluorides.

Literature DB >> 10968673

Methods of synthesis of glycosyl fluorides.

Abstract

In recent years glycosyl fluorides have been utilized as versatile sugar donors in the synthesis of natural products and carbohydrates. This paper provides an update on the advances made in the preparation of glycosyl fluorides during the last decade (1988-1998).

Entities: Chemical

Mesh：

Substances：

Year: 2000 PMID： 10968673 DOI： 10.1016/s0008-6215(99)00324-9

Source DB: PubMed Journal: Carbohydr Res ISSN： 0008-6215 Impact factor: 2.104

Keyword Cloud
Cited

7 in total

1. 4-Deoxy-4-fluoro-β-D-glucopyranose.

Authors: Wenhui Zhang; Allen G Oliver; Anthony S Serianni
Journal: Acta Crystallogr C Date: 2010-09-04 Impact factor: 1.172

2. Co-crystals of 3-deoxy-3-fluoro-α-D-glucopyranose and 3-deoxy-3-fluoro-β-D-glucopyranose.

Authors: Wenhui Zhang; Allen G Oliver; Anthony S Serianni
Journal: Acta Crystallogr C Date: 2010-10-21 Impact factor: 1.172

3. Glycosyl Exchange of Unactivated Glycosidic Bonds: Suppressing or Embracing Side Reactivity in Catalytic Glycosylations.

Authors: Joshua L Martin; Girish C Sati; Tanmay Malakar; Jessica Hatt; Paul M Zimmerman; John Montgomery
Journal: J Org Chem Date: 2022-04-12 Impact factor: 4.198

Methods of synthesis of glycosyl fluorides.

1. 4-Deoxy-4-fluoro-β-D-glucopyranose.

2. Co-crystals of 3-deoxy-3-fluoro-α-D-glucopyranose and 3-deoxy-3-fluoro-β-D-glucopyranose.

3. Glycosyl Exchange of Unactivated Glycosidic Bonds: Suppressing or Embracing Side Reactivity in Catalytic Glycosylations.

Review 4. Chemical O-Glycosylations: An Overview.

5. Electrospray ionization mass spectrometric analysis of highly reactive glycosyl halides.

6. Synthesis of Glycosyl Fluorides by Photochemical Fluorination with Sulfur(VI) Hexafluoride.

7. Diastereoselective synthesis of new O-alkylated and C-branched inositols and their corresponding fluoro analogues.