79082-19-2Relevant academic research and scientific papers
ON THE CRYSTAL STRUCTURE OF THE DIELS-ALDER ADDUCT OF THE HYDROGENATED LACTAMS OBTAINED BY REDUCTIVE PHOTOCYCLIZATION OF N-CYCLOHEX-1-ENYLBENZAMIDE
Naito, Takeaki,Ninomiya, Ichiya,Doi, Mitsunobu,Inoue, Masatoshi
, p. 1215 - 1217 (2007/10/02)
The stereostructure of the Diels-Alder adduct (5) of the hydrogenated lactam (3) with maleic anhydride was unequivocally esthablished by X-ray analysis, thus confirmed the stereochemical course of reductive photocyclization of the enamide (1).
Photocyclisation of Enamides. Part 23. Reductive Photocyclisation of Enamides
Naito, Takeaki,Tada, Yukiko,Nishiguchi, Yoshino,Ninomiya, Ichiya
, p. 487 - 492 (2007/10/02)
Irradiation of the enamides (1), (9), and (13) in the presence of sodium borohydride led to reductive photocyclisation to afford two types of hydrogenated lactams, the lactams with a conjugated diene moiety (4a-c), (5), (10a and b), and (11) and the lacta
REDUCTIVE PYOTOCYCLIZATION OF ENAMIDES
Naito,Takeaki,Tada, Yukiko,Nishiguchi, Yoshino,Ninomiya, Ichiya
, p. 1137 - 1140 (2007/10/02)
Irradiation of thr enamines (1a and b) and (7a and b), prepared from N-cyclohexylidenebenzylamine and 3,4-dihydro-1-methylisoquinoline, in the presence of a hydride agent led to the reductive photocyclization to afford the hydrogenated lactams (3a and b),
