An asymmetric synthesis of indole alkaloids
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (28), 3291-3294
- https://doi.org/10.1016/s0040-4039(00)98280-7
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The N-9, C-1 dianion of tetrahydro-β-carbolines. Regioselective alkylation leading to indole alkaloid systemsTetrahedron Letters, 1984
- A convenient synthesis of 1-azabicycloalkanes and their lactamsTetrahedron Letters, 1984
- Hochenantioselektive Alkylierung von Tetrahydroisochinolinen mit einem Valinolderivat als Hilfsreagens: asymmetrische Synthese von (S)‐IsochinolinalkaloidenAngewandte Chemie, 1984
- .alpha.-Amino carbanions via formamidines. Alkylation of pyrrolidines, piperidines, and related heterocyclesJournal of the American Chemical Society, 1984
- Enantioselective alkylation ofα-amino carbanionsTetrahedron, 1984
- Asymmetric alkylation of α-amino carbanions. An enantioselective synthesis of (S)-1-alkyl-1,2,3,4-tetrahydroisoquinolinesJournal of the American Chemical Society, 1983
- A novel entry into indole alkaloidsThe Journal of Organic Chemistry, 1982
- Dipole stabilized α-amino carbanions. II. Alkylation of tetrahydroisoquinolines in the 1-position.Tetrahedron Letters, 1981
- Amino acids and peptides. XIII. A new approach to the biogenetictype, asymmetric synthesis of indole and isoquinoline alkaloids by 1,3-transfer of asymmetry.CHEMICAL & PHARMACEUTICAL BULLETIN, 1974
- Isolation of Tetrahydroharman from Petalostyles labicheoidesNature, 1951