RESUMEN
Two complementary strategies for the synthesis of febrifugine are detailed based on previously developed chemoenzymatic approaches to the 3-hydroxypiperidine skeleton. The introduction of the quinazolone-containing side chain in both strategies was based on an N-acyliminium ion-mediated coupling reaction.
Asunto(s)
Piperidinas/síntesis química , Quinazolinas/síntesis química , Catálisis , Piperidinas/química , Quinazolinas/química , Estereoisomerismo , Especificidad por SustratoRESUMEN
The stereoselective total synthesis of the novel quinolizidine alkaloid (+)-epiquinamide is presented, starting from the amino acid l-allysine ethylene acetal. Key steps in the synthesis involved a highly diastereoselective N-acyliminium ion allylation and a ring-closing metathesis reaction to provide the bicyclic skeleton. [reaction: see text]
Asunto(s)
Alcaloides/síntesis química , Quinolizinas/síntesis química , Alcaloides/química , Ciclización , Conformación Molecular , Estructura Molecular , Quinolizinas/química , EstereoisomerismoRESUMEN
A stereoselective synthesis of (+)-epiquinamide is presented in combination with determination of the absolute configuration of the natural product. Key steps in the sequence involved chemoenzymatic formation of an enantiomerically pure cyanohydrin, reductive cyclization to the corresponding cyclic N,N-acetal, and subsequent conversion into a suitable N-acyliminium ion precursor to enable construction of the second ring.
Asunto(s)
Acetales/química , Cationes/química , Iminas/química , Quinolizinas/síntesis química , Animales , Anuros , Productos Biológicos/síntesis química , Productos Biológicos/química , Quinolizinas/química , Estereoisomerismo , Especificidad por SustratoRESUMEN
The nitrile hydrolyzing properties of the bacterium strain Rhodococcus erythropolis NCIMB 11540 have been investigated. Using whole cells of the microorganism, a wide variety of aromatic and aliphatic cyanide-containing substrates was successfully hydrolyzed to the corresponding amide or acid. In the case of dicyanides, selective monohydrolysis took place, which was further explored in the desymmetrization of malononitriles resulting in the corresponding cyano amides in enantiomeric excesses of up to 98%.