flustramine-a has been researched along with pyrrolidine* in 1 studies
1 other study(ies) available for flustramine-a and pyrrolidine
Article | Year |
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Enantioselective total synthesis of (-)-flustramines A, B and (-)-flustramides A, B via domino olefination/isomerization/Claisen rearrangement sequence.
The concise total synthesis of marine alkaloids, (-)-flustramines A and B, and (-)-flustramides A and B has been achieved through the domino olefination/isomerization/Claisen rearrangement (OIC) for highly enantioselective construction of the asymmetric quaternary carbon center and the chemoselective reduction-cyclization (RC) for pyrrolidine formation as key steps. Topics: Alkaloids; Alkenes; Cyclization; Indole Alkaloids; Isomerism; Models, Chemical; Oxidation-Reduction; Pyrrolidines; Stereoisomerism | 2006 |