De Novo highly stereocontrolled synthesis of 2,6-dideoxy-C-3-branched carbohydrates by use of 2,6-anhydro-2-thio sugar: l-cladinose and its C-3 epimer-Reference-Cited by-同舟云学术

De Novo highly stereocontrolled synthesis of 2,6-dideoxy-C-3-branched carbohydrates by use of 2,6-anhydro-2-thio sugar: l-cladinose and its C-3 epimer

Published:1991-08 Issue:33 Volume:32 Page:4139-4142
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Toshima Kazunobu,Yoshida Takehito,Mukaiyama Satsuki,Tatsuta Kuniaki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. The use of 2,6-anhydro-2-thio sugar for a highly stereocontrolled glycosylation: A novel strategy for synthesis of 2,6-dideoxy-α-glycosides

2. The use of 2,6-anhydro-2-thio glycopyranosyl fluoride for a highly α-stereoselective glycosylation

3. Erythromycin. I. Properties and Degradation Studies1

4. The synthesis of L-()-mycarose and L-()-cladinose

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1. 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one;Encyclopedia of Reagents for Organic Synthesis;2009-03-15

2. Synthesis of l-Cladinose Using Enantioselective Desymmetrization;Synlett;2008-09-10

3. 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

4. Highly Diastereoselective Conjugate Addition of Carbon Nucleophiles to a Chiral Oxygenated α,β-Unsaturated δ-Lactone. A Straightforward Synthesis of Functionalized Branched-Chain l-Sugars;The Journal of Organic Chemistry;1996-01-01

5. Application of Highly Stereocontrolled Glycosidations Employing 2,6-Anhydro-2-thio Sugars to the Syntheses of Erythromycin A and Olivomycin A Trisaccharide;Journal of the American Chemical Society;1995-04