Stereoselective catalytic double osmylation of 1,2-dihydropyridines leading to amino-arabinose and to amino-altrose derivatives and to potential glycosidase inhibitors.-Reference-Cited by-同舟云学术

Stereoselective catalytic double osmylation of 1,2-dihydropyridines leading to amino-arabinose and to amino-altrose derivatives and to potential glycosidase inhibitors.

Published:1994-01 Issue:4 Volume:50 Page:1135-1152
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tschamber Théophile,Backenstrass Frédérique,Neuburger Marcus,Zehnder Margareta,Strieth Jacques

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Stereospecific double glycolisation of 1,2-dihydropyridines with OsO4. Synthesis of (±) aminoarabinose- and of (±) aminoaltrose derivatives [1].

2. Catalytic osmylation of conjugated dienes: a one-pot stereoselective synthesis of polyols

3. Osmium tetraoxide cis hydroxylation of unsaturated substrates

4. Catalytic One-Pot Osmylation of Cyclohexadienes: Stereochemical and conformational studies of the resulting polyols

5. Inhibition of HIV replication by amino-sugar derivatives

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