An efficient and stereoselective synthesis of enantiopure 1,2,7-trihydroxylated pyrrolizidines
- 13 August 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (33) , 6083-6086
- https://doi.org/10.1016/s0040-4039(99)01265-4
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Enantioselective Total Syntheses of (+)-Castanospermine, (+)-6-Epicastanospermine, (+)-Australine, and (+)-3-EpiaustralineJournal of the American Chemical Society, 1999
- Synthesis of (1R,2R,3R,7R,7aR)-Hexahydro-3-(Hydroxymethyl)-1H-pyrrolizine-1,2,7-triol: 7-EpiaustralineJournal of the American Chemical Society, 1998
- Pyrrolizidine alkaloidsNatural Product Reports, 1998
- Pyrrolizidine alkaloidsNatural Product Reports, 1997
- RECENT ADVANCES IN THE STEREOSELECTIVE SYNTHESIS OF HYDROXYLATED PYRROLIZIDINES. A REVIEWOrganic Preparations and Procedures International, 1996
- Pyrrolizidine alkaloidsNatural Product Reports, 1996
- Casuarine: A very highly oxygenated pyrrolizidine alkaloidTetrahedron Letters, 1994
- Recent Progress in Asysmmetric Synthesis of PyrrolizidinesHETEROCYCLES, 1990
- Australine, a Novel Pyrrolizidine Alkaloid Glucosidase Inhibitor from Castanospermum australeJournal of Natural Products, 1988
- Isolation from and x-ray crystal structure of alexine, (1r,2r,3r,7s,8s)-3-hydroxymethyl-1,2,7-trihydroxypyrrolizidine [(2r,3r,4r,5s,6s)-2-hydroxymethyl-1-azabicyclo[3.3.0]octan-3,4,6-triol], a unique pyrrolizidine alkaloidTetrahedron Letters, 1988