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Chem Asian J ; 12(12): 1309-1313, 2017 Jun 19.
Article in English | MEDLINE | ID: mdl-28474489

ABSTRACT

An asymmetric route to (-)-α-lycorane and (-)-zephyranthine, and a formal total synthesis of (+)-clivonine were achieved. A pivotal intermediate, which serves as a potent precursor for the divergent syntheses of these natural products, was accessed by a diastereoselective Pd-catalyzed cinnamylation of an N-tert-butanesulfinyl imine.


Subject(s)
Alkaloids/chemical synthesis , Amaryllidaceae Alkaloids/chemical synthesis , Phenanthridines/chemical synthesis , Alkaloids/chemistry , Amaryllidaceae Alkaloids/chemistry , Crystallography, X-Ray , Models, Molecular , Molecular Structure , Phenanthridines/chemistry , Stereoisomerism
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