Iminium organocascade catalysis

The same group also developed the first organocascade reaction combining dienamine- and iminium-mediated catalysis to produce adducts containing y,p-stereocenters [22]. A y-amino-p-hydroxyalcohol was obtained from 2-heptenal... 

The first example of dual organocascade catalysis involving iminium/enamine activation was published in 2005 (Scheme 35.15) [6]. In this report, a, 3-unsaturated... 

Organocascade Catalysis Combinations of Enamine and Iminium Catalysis [55]... 

Woodward probably conducted the most outstanding work on iminium catalysis before its rebirth in 2000. In this work. Woodward applied proUne catalysis in a triple organocascade reaction consisting of a deracemization (via aretro-Michael, Michael addition) and an intramolecular aldol reaction that determine the stereochemical outcome of the reaction (Scheme 1.5), leading to the synthesis of erythromycin [13]. 

S. Roy, K. Chen, Org. Lett. 2012,14, 2496-2499. Three-component organocascade kinetic resolution of racemic nitroal-lylic acetates via sequential iminium/enatnine asymmetric catalysis. 

The enamine (/dienamine)-iminium cycle-specific cascade catalysis is an important constituent of amine-catalyzed cascade reactions [10]. This strategy has been explored extensively and also applied to natural product synthesis. One such example is the total synthesis of dihydrocorynantheol, which was first isolated from the bark of Aspidosperma marcgravianum in 1967 [29]. This indole alkaloid is a member of the corynantheine and was found to exhibit antiparasitic, antiviral, or analgetic activities, which have attracted considerable attention from the synthetic community. Among those reported total syntheses, Itoh et al. developed a Mannich-Michael cascade reaction catalyzed by L-proline 52 for the total synthesis of ent-dihydrocorynantheol 54 (Scheme 3.8) [30], The cascade reaction of 3-ethyl-3-buten-2-one 51 with dihydro-P-carboline 50 catalyzed by 30mol% of (S)-proline afforded the tetracyclic core structure 53 in 85% yield. Excellent stereoselectivity was achieved in this cascade reaction (99% enantiomeric excess and almost complete diastereomeric control). Therefore, this organocascade reaction could lead expeditiously to construction of the core structure, which enabled the authors to accomplish the total synthesis of enl-dihydrocorynantheol 54 in just five steps. 

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