Journal article
A dihydroisoxazole-based route to 2,3,6-trideoxy-3-aminohexose derivatives
Tetrahedron letters, v 30(44), pp 5969-5972
1989
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Acosamine and ristosamine derivatives were prepared via stereoselective reductive cleavage reactions of a benzylidenated dihydroisoxazolyl diol; the diol was prepared from 3-nitro-4,5-dihydroisoxazole via sequential propynylation, Lindlar reduction, and catalytic hydroxylation.
A 3-dihydroisoxazolyl diol was converted to acosamine and ristosamine derivatives by reductive cleavage.
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Details
- Title
- A dihydroisoxazole-based route to 2,3,6-trideoxy-3-aminohexose derivatives
- Creators
- Peter A. Wade - Drexel UniversityJ.Appa Rao - Drexel UniversityJames F. Bereznak - Drexel UniversityC.-K. Yuan - Drexel University
- Publication Details
- Tetrahedron letters, v 30(44), pp 5969-5972
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1989CA78900003
- Scopus ID
- 2-s2.0-0024419905
- Other Identifier
- 991019173809904721
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Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic