par  Colau, Brigitte  ;Hootele, Claude
;Hootele, Claude  ;Tourwe, Dirk
;Tourwe, Dirk 
Référence Tetrahedron, 40, 11, page (2171-2175)
Publication Publié, 1984
           ;Hootele, Claude
;Hootele, Claude  ;Tourwe, Dirk
;Tourwe, Dirk 
Référence Tetrahedron, 40, 11, page (2171-2175)
Publication Publié, 1984
                                                                                                       
			Article révisé par les pairs
                                                  
        | Résumé : | The preferred solution conformation of 9 Sedum alkaloids and derivatives (sedinine, dihydrosedinine. 8-episedinine, diacetylsedinine, sedinone, 2-episedinone, sedacrine, 2-episedacrine and sedacryptine) was established by high resolution 1H and13C NMR spectroscopy. These compounds may be divided into three classes based on the existence or the absence of an intramolecular hydrogen bond between the nitrogen atom and the hydroxyl group at C8 or at C10. In all of them (except sedacryptine) the N-CH3 group was found to be axially oriented. © 1984. | 



