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J Am Chem Soc ; 124(40): 11870-1, 2002 Oct 09.
Article in English | MEDLINE | ID: mdl-12358529

ABSTRACT

A "(+)-sparteine-like" chiral diamine, readily synthesized in three steps from (-)-cytisine, has been evaluated in four different asymmetric transformations; in each case, selectivity in an enantiocomplementary fashion to (-)-sparteine was observed.


Subject(s)
Diamines/chemistry , Sparteine/chemistry , Alkaloids/chemistry , Alkaloids/isolation & purification , Azocines , Diamines/chemical synthesis , Molecular Mimicry , Pyridones/chemical synthesis , Pyridones/chemistry , Quinolizines , Sparteine/analogs & derivatives , Stereoisomerism
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