53009-06-6Relevant articles and documents
Synthesis and stereochemistry of 8,13-diaza-2,3-dimethoxygona-1,3,5(10),9(11)-tetraen-12-one and D-homo derivatives
Goendoes, Gyoergy,Gera, Lajos,Toth, Gabor,Kalman, Alajos,Bridson, John
, p. 375 - 382 (1998)
From the condensation reaction of O-methylbutyrolactim (2), O-methylvalerolactim (3), O-methylcaprolactim (4) and O-methyl-4-t-butylcaprolactim (5) with ethyl 6,7-dimethoxy-α-acetate (1), 8,13-diaza-2,3-dimethoxygona-1,3,5(10),9(11)-tetraen-12-one (6) D-homo-derivatives (7-9), and medium sized ring cyclic diamides (10,11) were obtained.The stereoselective reduction of compounds 6-9 by Adam's platinum catalyst afforded 8,13-diaza-2,3-dimethoxygona-1,3,5(10)-trien-12-one (12) and its D-homo derivatives (13-15).The structures of thecompounds obtained were established by NMR and X-ray crystallographic analyses. - Keywords: 8,13-diazasteroids; stereochemistry; X-ray structure analysis