Enantiospecific syntheses of indolizidines 167B and 209D
- 7 May 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (19) , 3119-3122
- https://doi.org/10.1016/s0040-4039(00)93394-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- An enantiospecific synthesis of β-amino acidsTetrahedron Letters, 1993
- Enantioselective synthesis of (5R,9R)-5-propyl-octahydroindolizine [(−)-gephyrotoxin 167B]Tetrahedron: Asymmetry, 1992
- The piclavines, antimicrobial indolizidines from the tunicateTetrahedron Letters, 1992
- Short, enantiogenic syntheses of (-)-indolizidine 167B and (+)-monomorineJournal of the American Chemical Society, 1991
- Stereoselective synthesis of (.+-.)-indolizidines 167B, 205A, and 207A. Enantioselective synthesis of (-)-indolizidine 209BThe Journal of Organic Chemistry, 1991
- Carbon-Carbon Bond Forming Reactions of α-Aminonitriles Under Dissolving Metal Conditions: Synthesis of Gephyrotoxin-167BSynlett, 1991
- Enantioselective total syntheses of indolizidine alkaloids 167B and 209DThe Journal of Organic Chemistry, 1990
- Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidinesTetrahedron, 1986
- Amino acids and peptides. LXXIX. α-Pyrrolo analogues of α-amino acidsCollection of Czechoslovak Chemical Communications, 1968
- Catalytic hydrogenolysis as an alternative to the wolff-kishner or clemmensen reduction methods for azabicyclic ketonesTetrahedron Letters, 1967