Transamidation reactions of -lactams: a synthesis of ( )-dihydroperiphylline.
Data(s) |
1986
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Resumo |
Ammonolysis of N-(halogenoalkyl)azetidin-2-ones affords medium ring azalactams via transamidation but large or strained rings are not isolated, acyclic ?-amino-amides being produced; two successive transamidative ring expansions from 4-phenylazetidin-2-one give a synthesis of (?)-dihydroperiphylline (I). |
Identificador | |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Crombie , L , Haigh , D & Jones , R C F 1986 , ' Transamidation reactions of -lactams: a synthesis of ( )-dihydroperiphylline. ' Tetrahedron Letters , vol 27 , pp. 5151-5154 . |
Tipo |
article |