269715-87-9Relevant articles and documents
Stereoselective synthesis of a tricyclic guanidinium model of cylindrospermopsin
McAlpine, Indrawan J.,Armstrong, Robert W.
, p. 1849 - 1853 (2007/10/03)
An 11-step enantioselective synthesis of the A-ring of cylindrospermopsin is described using an intramolecular conjugate addition as the key step to forming the piperidine ring. Further elaboration generates a tricyclic guanidine via a sequential double displacement strategy as a model for the cylindrospermopsin guanidinium core. (C) 2000 Elsevier Science Ltd.