The fischer indolization of 2-azabicyclo[3.3.1]nonan-7-ones. A new entry to the dasycarpidan ring system
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (17) , 2449-2452
- https://doi.org/10.1016/s0040-4039(00)97386-6
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Synthesis and absolute configuration of the Aristotelia alkaloid peduncularineJournal of the American Chemical Society, 1989
- Synthesis of 2-(4-Piperidylmethyl)indoles. Intermediates for the Synthesis of Strychnos AlkaloidsHETEROCYCLES, 1988
- Functionalized 2-azabicyclo[3.3.1]nonanes. 6. Studies directed to the synthesis of pentacyclic Strychnos indole alkaloidsThe Journal of Organic Chemistry, 1987
- 2-Cyano-.DELTA.3-piperidines. V. Towards the synthesis of corynanthe-type indole alkaloids. Computer-assisted study of the conformations of an "inside" indoloquinolizidine seriesThe Journal of Organic Chemistry, 1982
- Direction of cyclization in the Fischer indole synthesis. Mechanistic considerationsThe Journal of Organic Chemistry, 1978
- Synthetic studies in the strychnos-type alkaloid fieldPublished by Walter de Gruyter GmbH ,1975
- The conversion of oxindoles to the aspidosperma skeleton the synthesis of d1-N(a)-acetyl-desethylaspidospermidineTetrahedron Letters, 1972
- Synthesen in der Reihe der Indole und Indolalkaloide, VII1) Synthese eines undecacyclischen Di‐indolin‐diäthers vom Typ dimerer Calebassencurare‐AlkaloideEuropean Journal of Organic Chemistry, 1968
- The Total Synthesis of dl-Aspidospermine and of dl-QuebrachamineJournal of the American Chemical Society, 1963
- Chemische Korrelation von Condylocarpin mit AkuammicinHelvetica Chimica Acta, 1963