Regio- and stereoselective conjugate addition of nitrogen nucleophiles to 2-alkenyl n-methylthiazolium iodides. synthesis of d-3-epi-daunosamine and some lincosamine analogues
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 46 (17) , 6167-6184
- https://doi.org/10.1016/s0040-4020(01)87939-4
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Stereoselective Synthesis of γ‐AminocarboxylatesAngewandte Chemie International Edition in English, 1989
- Organic Synthesis with Sulfur Heterocycles (Thiazoles) as Auxiliaries. The Thiazole Route to Carbohydrates and Biologically Active DerivativesPhosphorus, Sulfur, and Silicon and the Related Elements, 1989
- A Convenient Route to 3′-Amino-3′-deoxythymidineSynthesis, 1989
- A simple, divergent, asymmetric synthesis of all members of the 2,3,6-trideoxy-3-aminohexose familyJournal of the American Chemical Society, 1988
- Syntheses of 2,3,6-trideoxy-3-amino- and 2,3,6-trideoxy-3-nitrohexosesChemical Reviews, 1986
- A new approach to the synthesis of hexoses: an entry to (.+-.)-fucose and (.+-.)-daunosamineJournal of the American Chemical Society, 1985
- Synthesis of enantiomerically pure forms of N-acyl derivatives of C-methyl analogs of the aminodeoxysugar L-acosamine from noncarbohydrate precursorsThe Journal of Organic Chemistry, 1982
- Reactivity of thiazole in electrophilic reactions as determined from solvolysis ratesThe Journal of Organic Chemistry, 1973
- Daunomycin. II. The Structure and Stereochemistry of DaunosamineJournal of the American Chemical Society, 1964
- Daunomycin. I. The Structure of DaunomycinoneJournal of the American Chemical Society, 1964