Enantiospecific syntheses of 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine from D-glucuronolactone
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (27) , 3205-3208
- https://doi.org/10.1016/s0040-4039(00)84755-3
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Synthesis of bulgecinine: a new amino acid in bulgecinsTetrahedron Letters, 1985
- Synthesis of 2S-carboxy-3R,4R,5S-trihydroxypiperidine; a naturally occurring inhibitor of β-D-glucuronidaseTetrahedron Letters, 1985
- Isolation and characterization of bulgecins, new bacterial metabolites with bulge-inducing activity.The Journal of Antibiotics, 1985
- Specific inhibition of human β‐D‐glucuronidase and α‐L‐iduronidase by a trihydroxy pipecolic acid of plant originFEBS Letters, 1984
- Structures of bulgecins, bacterial metabolites with bulge-inducing activityTetrahedron, 1984
- A facile synthesis of 1,2,-o-isopropylidene-β-L-idofuranurono-6,3-lactoneTetrahedron Letters, 1980
- Über die darstellung von 5-azido-5-desoxy,-1,2-alkyliden-L-idofuranurono-6,3-laktonTetrahedron Letters, 1978
- 2S-carboxy-4R,5S-dihydroxypiperidine et 2S-carboxy-4S,5S-dihydroxypiperidine a partir de Derris ellipticaPhytochemistry, 1976
- Monosaccharide mit stickstoffhaltigem Ring, XXXI. Synthese und Reaktionen von 5‐Amino‐5‐desoxy‐ L ‐iduronsäureEuropean Journal of Inorganic Chemistry, 1973