A stereoselective totally synthetic route to methyl .alpha.-peracetylhikosaminide
- 1 March 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (6) , 2193-2204
- https://doi.org/10.1021/ja00188a038
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Stereoselective reactions of alkenylpyranosides: the effect of double bond geometry on conformationJournal of the American Chemical Society, 1988
- On the communication of chirality from furanose and pyranose rings to monosaccharide side chains: anomalous results in the glucose seriesTetrahedron, 1986
- Higher-carbon sugars. Part 2. The synthesis of some decitols via the osmylation of unsaturated precursorsJournal of the Chemical Society, Perkin Transactions 1, 1986
- A stereospecific route to aziridinomitosanes: the synthesis of novel mitomycin congenersJournal of the American Chemical Society, 1985
- Chelation-controlled facially selective cyclocondensation reactions of chiral alkoxy aldehydes: syntheses of a mouse androgen and of a carbon-linked disaccharideJournal of the American Chemical Society, 1985
- A new approach to the synthesis of hexoses: an entry to (.+-.)-fucose and (.+-.)-daunosamineJournal of the American Chemical Society, 1985
- Inhibition of translation in bacterial and eukaryotic systems by the antibiotic anthelmycin (hikizimycin)Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis, 1979
- Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. 54. Structure analysis of the nucleoside disaccharide antibiotic anthelmycin by carbon-13 nuclear magnetic resonance spectroscopy. A structural revision of hikizimycin and its identity with anthelmycinThe Journal of Organic Chemistry, 1977
- Structure de I&Hikizimycine, un Antibiotique NucléosidiqueAgricultural and Biological Chemistry, 1976