TY - JOUR
T1 - Preparation and Properties of 1,1′-Disubstituted Trichotomine Derivatives with a Twisted C=C Bond
AU - Irikawa, Hajime
AU - Kanke, Satoru
AU - Mito, Kousuke
AU - Kobayashi, Yasuhiro
AU - Akasaka, Tomoko
AU - Atsumi, Tadashi
AU - Arimoto, Hirokazu
AU - Okumura, Yasuaki
PY - 1996/6
Y1 - 1996/6
N2 - Green trichotomine derivatives bearing alkyl groups on C1 and C1′ were prepared. In their absorption spectra, the λmax shifted to longer wavelengths as the 1,1′-substituents became bulkier, and the bathochromism indicated twisting of the central C2=C2′ double bond. A 1,1′-dimethyltrichotomine derivative underwent autooxidation to give orange-red 1,11b-dihydroxylated and 1,11b-seco-dicarbonyl compounds, in which twisting of the central C2=C2′ double bond might be relieved by the decreasing steric interactions between the substituents on C1 and the C3′ carbonyl groups.
AB - Green trichotomine derivatives bearing alkyl groups on C1 and C1′ were prepared. In their absorption spectra, the λmax shifted to longer wavelengths as the 1,1′-substituents became bulkier, and the bathochromism indicated twisting of the central C2=C2′ double bond. A 1,1′-dimethyltrichotomine derivative underwent autooxidation to give orange-red 1,11b-dihydroxylated and 1,11b-seco-dicarbonyl compounds, in which twisting of the central C2=C2′ double bond might be relieved by the decreasing steric interactions between the substituents on C1 and the C3′ carbonyl groups.
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U2 - 10.1246/bcsj.69.1673
DO - 10.1246/bcsj.69.1673
M3 - Article
AN - SCOPUS:2742601326
SN - 0009-2673
VL - 69
SP - 1673
EP - 1677
JO - Bulletin of the Chemical Society of Japan
JF - Bulletin of the Chemical Society of Japan
IS - 6
ER -