Search results for "Lasubin II"

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ChemInform Abstract: Stereoselective Synthesis of Quinolizidine Alkaloids: (-)-Lasubin II.

2008

Initially, lasubin II was synthesized diastereoselectively in racemic form [3]. Asymmetric syntheses of lasubin II were achieved based on stereoselective transformations of enantiomerically pure substrates [4] or, for example, via a diastereoselective aza-Diels-Alder reaction using a resolved chiral arylaldehyde tricarbonylchromium complex [5]. Recently, an enantioselectively catalyzed aza-Diels-Alder reaction [6] and a [2+2+2] cycloaddition reaction [7] were successfully used for the synthesis of enantiomerically pure lasubin II.

chemistry.chemical_compoundLasubin IIQuinolizidinechemistryStereochemistryOrganic chemistryStereoselectivityGeneral MedicineCycloadditionCatalysisChemInform
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Stereoselective Synthesis of Quinolizidine Alkaloids: (–)-Lasubin II

2008

Initially, lasubin II was synthesized diastereoselectively in racemic form [3]. Asymmetric syntheses of lasubin II were achieved based on stereoselective transformations of enantiomerically pure substrates [4] or, for example, via a diastereoselective aza-Diels-Alder reaction using a resolved chiral arylaldehyde tricarbonylchromium complex [5]. Recently, an enantioselectively catalyzed aza-Diels-Alder reaction [6] and a [2+2+2] cycloaddition reaction [7] were successfully used for the synthesis of enantiomerically pure lasubin II.

chemistry.chemical_compoundLasubin IIQuinolizidinechemistryStereochemistryStereoselectivityGeneral ChemistryCycloadditionCatalysisZeitschrift für Naturforschung B
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