ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
COLUMN CHROMATOGRAPHY;
DRUG SYNTHESIS;
INFRARED SPECTROSCOPY;
ISOMER;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
X RAY DIFFRACTION;
Matsuda T., Yoshikawa T., Suzuki M., Asano S., Somboonthum P., Takuma K., Nakano Y., Morita T., Nakasu Y., Kim H.S., Egawa M., Tobe A., Baba A. Jpn. J. Pharmacol. 69:1995;366.
Epoxides 2 and 3 were prepared, respectively, from N-benzyl-3-pyrrolidinone and N-benzyl-4-piperidone according to the method described
Epoxides 2 and 3 were prepared, respectively, from N-benzyl-3-pyrrolidinone and N-benzyl-4-piperidone according to the method described by Popp F.D., Watts R.F. J. Heterocycl. Chem. 15:1978;675.
Soukri, M.; Lazar, S.; Leger, J. M.; Jarry, C.; Akssira, M.; Guillaumet, G. IXèmes Conférences Européennes du Groupement des Pharmacochimistes de l'ARC Atlantique, Tours, 11-12 septembre 2000.
Hammarberg E., Nordvall G., Leideborg R., Nylof N., Hanson S., Johansson L., Thorberg S.O., Tolf B.R., Svantesson G.T., Mohell N., Ahlgren C., Westlind-Danielsson A., Csoregh I., Johansson R. J. Med. Chem. 43:2000;2850.
University Chemical Lab; Lensfield Road Cambridge, CB2 1EW, UK
Supplementary X-ray Crystallographic data: Cambridge Crystallographic Data Centre, University Chemical Lab; Lensfield Road Cambridge, CB2 1EW, UK, e-mail: http://www.deposit@chemcrys.cam.ac.uk.