A short diastereoselective synthesis of 1-aminoindolo-[2,3-a]quinolizidines via an N-acyliminium ion cyclisation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
2. A new diastereoselective synthesis of (±) cis 1-aminoindoloquinolizidine
3. Ducrot, P.; Rabhi, C.; Thal, C. Tetrahedron, submitted for publication.
4. General methods of synthesis of indole alkaloids. VI. Syntheses of dl-corynantheidine and a camptothecin model
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3. Concise Construction of Sarain A Core According to a Biosynthetic Proposal: Cyclization through an Intramolecular Mannich-type Reaction Involving an Endocyclic N-Acyliminium ion;Chemistry - A European Journal;2011-08-02
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