Alkylation of 3,4-dihydro-β-carboline
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 14,p. 991-992
- https://doi.org/10.1039/c39900000991
Abstract
Alkylation of 3,4-dihydro-β-carboline has been accomplished with organo-copper and -lithium reagents by activation of BF3·OEt2 or trimethylsilyl trifluoromethanesulphonate.Keywords
This publication has 11 references indexed in Scilit:
- Total Synthesis of (-)-Eudistomin FHETEROCYCLES, 1990
- Total synthesis of (-)-eudistomin L and (-)-debromoeudistomin LJournal of the American Chemical Society, 1989
- A synthesis of so-called fumitremorgin CTetrahedron, 1989
- Chiral and achiral formamidines in synthesis. The first asymmetric route to (-)-yohimbine and an efficient total synthesis of (.+-.)-yohimbineJournal of the American Chemical Society, 1988
- Total synthesis of (+)-fumitremorgin B, its epimeric isomers, and demethoxy derivativesTetrahedron, 1988
- Synthetic Studies on NaulafineHETEROCYCLES, 1988
- Synthesis of naucléfine, angustidine, angustine, and (±)-13b, 14-dihydroangustineJournal of the Chemical Society, Chemical Communications, 1988
- Reactions of allylstannanes with in situ generated immonium salts in protic solvent: a facile aminomethano destannylation processThe Journal of Organic Chemistry, 1987
- Total synthesis of fumitremorgin BTetrahedron Letters, 1986
- Activated imines as carbon electrophiles: applications in alkaloid synthesisJournal of the Chemical Society, Chemical Communications, 1986