.beta.-Substituted organolithium compounds. Reaction with alkyl halides, dimethyl disulfide, and imines
作者:Jose Barluenga、Francisco J. Fananas、Jorge Villamana、Miguel Yus
DOI:10.1021/jo00347a037
日期:1982.4
BARLUENGA, J.;FANANAS, F. J.;VILLAMANA, J.;YUS, M., J. ORG. CHEM., 1982, 47, N 8, 1560-1564
作者:BARLUENGA, J.、FANANAS, F. J.、VILLAMANA, J.、YUS, M.
DOI:——
日期:——
BRUNET, E.;CARRENO, M. C.;GALLEGO, M. T.;RUANO, J. L. G.;ALCUDIA, F., J. CHEM. SOC. PERKIN TRANS., 1983, N 7, 937-942
作者:BRUNET, E.、CARRENO, M. C.、GALLEGO, M. T.、RUANO, J. L. G.、ALCUDIA, F.
DOI:——
日期:——
Stereochemistry of sulphur organic compounds. Part 11. A conformational study of some 2-thio-derivatives of N-phenyl-1-phenylethylamine
作者:Ernesto Brunet、M. Carmen Carreño、M. Teresa Gallego、José L. García Ruano、Felipe Alcudia
DOI:10.1039/p29830000937
日期:——
The syntheses and a conformational study of N-phenyl-2-Y-1-phenylethylamine [Y = SCH3, SOCH3(two diastereoisomers), SO2CH3, and +S(CH3)2] are reported. Conformational preferences have been established from changes in the vicinal coupling constants induced by protonation at the amine nitrogen. This determines the electrostatic character of the interactions between the two heteroatoms functions. In addition