Access to polyhydroxylated cycloheptane derivatives through stereoselective nitrile oxide intramolecular cycloaddition. Synthesis of an analogue of calystegine B2
- 18 February 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (8) , 1059-1062
- https://doi.org/10.1016/s0040-4039(00)91860-4
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Diastereoselectivity in the intramolecular nitrone, oxime, and nitrile oxide cycloaddition reactions. Synthesis of amino inositol derivatives as α-glucosidase inhibitorsTetrahedron, 1991
- Enantiospecific total synthesis of (−)-allosamizoline, and aminocyclitol moiety of the insect chitinase inhibitor allosamidinTetrahedron Letters, 1991
- Enantiospecific Total Synthesis of a β-Glucosidase Inhibitor, CyclophellitolTetrahedron Letters, 1990
- Structure of the Calystegines: New alkaloids of the nortropane family.Tetrahedron Letters, 1990
- Synthetic studies on the 1-hydroxy nortropane system: An approach to Calystegines.Tetrahedron Letters, 1990
- Zinc Azide Mediated Mitsunobu Substitution. An Expedient Method for the One-Pot Azidation of AlcoholsSynthesis, 1990
- A plasmid of Rhizobium meliloti 41 encodes catabolism of two compounds from root exudate of Calystegium sepiumJournal of Bacteriology, 1988
- Structure and synthesis of physoperuvine: x-ray crystal and molecular structures of the n-benzoyl derivatives of (±)-3- and (+)-4-methylaminocycloheptanoneTetrahedron, 1984
- Carbocyclische Verbindungen aus Monosacchariden. I. Umsetzungen in der glucosereiheHelvetica Chimica Acta, 1979