Tandem carbophilic addition-N-acyliminium ion cyclization for the synthesis of functionalized pyrrolo[2,1-a]isoquinolones: Key intermediates for the preparation of Erythrina-type alkaloids
- 21 October 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (43) , 7841-7844
- https://doi.org/10.1016/0040-4039(96)01745-5
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- On the cyclization of acyliminium salts derived from pyroglutamic acidTetrahedron Letters, 1996
- Stereoselective Total Synthesis of Natural (+)-Streptazolin via a Palladium-Catalyzed Enyne Bicyclization ApproachJournal of the American Chemical Society, 1996
- Conformationally Restricted Peptide Mimetics: The Incorporation of 6,5-Bicyclic Lactam Ring Skeletons into PeptidesThe Journal of Organic Chemistry, 1995
- Asymmetric Synthesis of Both Enantiomers of Pyrrolidinoisoquinoline Derivatives from L-Malic Acid and L-Tartaric AcidThe Journal of Organic Chemistry, 1995
- Convergent stereocontrolled construction of 5-7-6 tricyclic aza analogues of phorbol and aconite alkaloidsTetrahedron Letters, 1995
- Mannich Biscyclizations. Total Synthesis of (-)-AjmalicineJournal of the American Chemical Society, 1995
- New Routes to Acyliminium Ion Precursors and a Synthesis of the Nuevamine SkeletonSynlett, 1995
- Use of theN-Formyliminium Ion Cyclization for the Synthesis of 3-Aryl-1,2,3,4-tetrahydroisoquinolinesSynthesis, 1992
- Intramolecular reactions of N-acyliminium intermediatesTetrahedron, 1985
- Recent developments in alkaloid synthesisRecueil des Travaux Chimiques des Pays-Bas, 1981