RT Journal Article
T1 A short and convenient procedure for the stereoselective synthesis of 2-hydroxy-1-norbornanesulfonamides
A1 Garcı́a Martı́nez, Antonio
A1 Teso Vilar, Enrique
A1 Moreno Jiménez, Florencio
A1 Álvarez Garcı́a, Ana Mª
AB A 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.
PB Elsevier Ltd.
SN 0957-4166
YR 2004
FD 2004-01-26
LK https://hdl.handle.net/20.500.14352/52835
UL https://hdl.handle.net/20.500.14352/52835
LA eng
NO Ministerio de Ciencia e Innovación (MICINN)
NO Universidad Nacional de Educación a Distancia (UNED)
DS Docta Complutense
RD 7 abr 2025