129687-61-2Relevant academic research and scientific papers
Stereoelectronic control of oxazolidine ring-opening: Structural and chemical evidences
Sélambarom, Jimmy,Monge, Sophie,Carré, Francis,Roque, Jean Pierre,Pavia, André A
, p. 9559 - 9566 (2002)
Ring opening of oxazolidines derived from tris(hydroxymethyl)aminomethane, L-serine and L-threonine was investigated. It was shown that n(N)→σ*(C-O) electron delocalization (endo-anomeric effect) occurring in the five-membered ring plays a major role in the cleavage of the intracyclic C-O bond. The present work establishes that when the nitrogen lone pair is conjugated with a carbonyl group (n(N)→π(C=O) delocalization) as happens in N-acyloxazolidines, both hydrolysis and reductive ring-opening become much more difficult as a consequence of a concomitant decrease of oxygen basicity and of an increase of the intracyclic C-O bond strength.
Genotoxicity in oxazolidine derivatives: influence of the nitro group
Vanelle, P,Meo, MP De,Maldonado, J,Nouguier, R,Crozet, MP,et al.
, p. 241 - 250 (2007/10/02)
Tris-(hydroxymethyl)-aminomethane reacts with various aromatic or heterocyclic aldehydes, leading to new mono- or bicyclic oxazolidine derivatives.The importance of molecular surroundings of the nitro group has been evaluated by the genotoxic study of syn
