An intramolecular conjugate addition of γ-trichloroacetimidoyloxy-α,β-unsaturated esters: a very concise route to daunosamine, acosamine, ristosamine and 3-epi-daunosamine precursors-Reference-Cited by-同舟云学术

An intramolecular conjugate addition of γ-trichloroacetimidoyloxy-α,β-unsaturated esters: a very concise route to daunosamine, acosamine, ristosamine and 3-epi-daunosamine precursors

Published:2006-12 Issue:49 Volume:47 Page:8777-8780
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Matsushima Yoshitaka,Kino Jun

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. The role of carbohydrates in biologically active natural products

2. Interaction of Calicheamicin with Duplex DNA: Role of the Oligosaccharide Domain and Identification of Multiple Binding Modes

3. Biosynthesis of deoxyaminosugars in antibiotic-producing bacteria

4. Mutational Analysis and Reconstituted Expression of the Biosynthetic Genes Involved in the Formation of 3-Amino-5-hydroxybenzoic Acid, the Starter Unit of Rifamycin Biosynthesis in Amycolatopsis mediterraneiS699

5. A new simple route to deoxyamino sugars from non-sugar material: synthesis of d-tolyposamine and 4-epi-d-tolyposamine and formal synthesis of d-vicenisamine

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