109007-62-7Relevant academic research and scientific papers
Chiral N-acyloxazolidines: Synthesis, structure, and mechanistic insights
Avalos, Martin,Babiano, Reyes,Cintas, Pedro,Jimenez, Jose L.,Light, Mark E.,Palacios, Juan C.,Perez, Esther M. S.
, p. 661 - 672 (2008/09/17)
(Chemical Equation Presented) A series of chiral imines derived from 1-amino-1-deoxyalditols such as D-glucamine, a rather unexplored raw material from the chiral pool, have been serendipitiously transformed into a novel family of N-acetyl-1,3-oxazolidines by means of an unexpected acetylation. The structure of these substances is supported by spectroscopic and crystallographic data. The acetylates also trigger a complex dynamic transformation, in which an initially configured trans oxazolidine converts into a more stable cis-configured derivative. Both isomers can also exist as rotational conformers (E,Z) as a consequence of the restricted rotation around the N-acetyl bond. The barriers to rotation have been determined by variable-temperature experiments. Overall, this transformation most likely involves the intermediacy of a chiral iminium ion, which has been documented in the synthesis of nitrogen heterocycles, thus explaining the experimental facts.
ELECTRO-ORGANIC REACTIONS. PART 33. REDUCTION OF SUGAR OXIMES
Ryan, Gary,Utley, H. P.,Jones, Haydn F.
, p. 3699 - 3702 (2007/10/02)
Monosaccharide oximes reduce irreversibly at ca.-1.73V vs Ag/AgI in the presence of a proton donor; preparative scale constrant current electro-reduction, in aqueous solution, gives efficient conversion into the corresponding glycamines which are isolated as Schiff base or acetate derivatives.
