Garcı́a Martı́nez, AntonioTeso Vilar, EnriqueMoreno Jiménez, FlorencioÁlvarez Garcı́a, Ana Mª2023-06-202023-06-202004-01-260957-416610.1016/j.tetasy.2003.10.023https://hdl.handle.net/20.500.14352/52835A short and convenient procedure for the stereoselective synthesis of novel optically active 2-hydroxy-1-norbornanesulfonamides starting from commercially available natural camphor and fenchone is reported. The synthetic route involves a nucleophilic substitution at the sulfenyl sulfur atom of 2-methylene-1-norbornylthiotriflates followed by oxidation of the intermediate sulfenamides and highly diastereoselective reduction of the carbonyl group of the parent 2-oxo-1-norbornanesulfonamides.engjournal articlehttps://doi.org/10.1016/j.tetasy.2003.10.023restricted access542.966.091547.1stereoselective synthesis2-hydroxy-1-norbornanesulfonamidesQuímica orgánica (Química)2306 Química Orgánica