Studies on the nucleophilic addition to 3,5-disubstituted pyridinium salts
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (31) , 6445-6454
- https://doi.org/10.1016/s0040-4020(01)88234-x
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- 19-hydroxytubotaiwine : total synthesis. Assignment of absolute configuration to a natural isomerTetrahedron Letters, 1991
- Total syntheses of tubotaiwine and 19,20-dihydro-20-epi-akuammicineThe Journal of Organic Chemistry, 1991
- Total synthesis of the Strychnos alkaloid tubotaiwineJournal of the Chemical Society, Chemical Communications, 1991
- General method for the synthesis of bridged indole alkaloids. Nucleophilic addition of indoleacetic ester enolates to N-alkylpyridinium saltsThe Journal of Organic Chemistry, 1990
- Addition of Stabilized Carbon Nucleophiles to N-Alkylpyridinium Salts. Applications to Alkaloids SynthesisHETEROCYCLES, 1988
- An enantioselective access to the (−)-tubotaiwine skeletonTetrahedron Letters, 1987
- An enantioselective entry into the strychnos alkaloid skeletonTetrahedron Letters, 1987
- Indole Alkaloid SynthesisHETEROCYCLES, 1984
- A uniform numbering system for indole alkaloidsCellular and Molecular Life Sciences, 1965
- Monomers and Polymers. V. Vinylpyridines and Vinylquinolines1,2Journal of the American Chemical Society, 1948