RT Journal Article
T1 Synthesis of Enantiopure Allylamines by Reductive Alkylation of Amino Epoxides with Organolithium Reagents
A1 Concellón, José M.
A1 Suárez Álvarez, José Ramón
A1 Solar, Virginia del
AB Transformation of enantiopure (2R,1‘S)-2-(1-aminoalkyl)epoxides into the corresponding allylamines  is described. The opening of the epoxide ring with different organolithium compounds takes place with total selectivity and in high yields.
PB American Chemical Society
SN 1523-7060
YR 2005
FD 2005
LK https://hdl.handle.net/20.500.14352/97151
UL https://hdl.handle.net/20.500.14352/97151
LA eng
NO Concellón, José M., et al. «Synthesis of Enantiopure Allylamines by Reductive Alkylation of Amino Epoxides with Organolithium Reagents». Organic Letters, vol. 8, n.o 2, enero de 2006, pp. 349-51. DOI.org (Crossref), https://doi.org/10.1021/ol0529602.
NO Ministerio de Ciencia y Tecnología (España)
DS Docta Complutense
RD 18 abr 2025