martinelline has been researched along with coerulescine* in 1 studies
1 other study(ies) available for martinelline and coerulescine
Article | Year |
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Synthesis of highly functionalized pyrrolidines as tunable templates for the direct access to (±)-coerulescine and the tricyclic core of martinellines.
An aza-Michael induced ring closure (aza-MIRC) tandem reaction of benzyl (2-bromoethyl)carbamate with various Michael acceptors is described. The N-Cbz-β-gem-disubstituted pyrrolidines thus obtained were proved to be versatile intermediates for the rapid access to both martinelline and spirooxindole backbones. An application of this strategy towards an expedient 4 step total synthesis of (±)-coerulescine is also presented. Topics: Aniline Compounds; Molecular Structure; Pyrroles; Pyrrolidines; Quinolines; Stereoisomerism | 2013 |