920756-48-5Relevant academic research and scientific papers
Direct asymmetric α-sulfamidation of α-branched aldehydes: A novel approach to enamine catalysis
Vogt, Henning,Baumann, Thomas,Nieger, Martin,Braese, Stefan
, p. 5315 - 5338 (2007/10/03)
Proline-catalysed reactions between α-branched aldehydes and sulfonyl azides provide scalemic configurationally stabilised α-sulfamidated products with ee values of up to 86%. The reactions can also be carried out in a one-pot fashion, with catalyst, alde
Sulfamidation of 2-arylaldehydes and ketones with chloramine-T
Baumann, Thomas,Bachle, Michael,Brase, Stefan
, p. 3797 - 3800 (2007/10/03)
A series of aliphatic and aromatic carbonyl compounds has been transformed into the corresponding sulfamidated products by means of amine-catalyzed nitrene transfer of chloramine-T. Depending on the residues R, either α-sulfamidation in the case of aromat
