143789-19-9Relevant academic research and scientific papers
Regio- and enantio-selective photoreactions of cyclohex-2-enone, coumarin and acrylanilide as inclusion complexes with optically active host compounds
Tanaka,Toda,Ueda,Fukiwara
, p. 43 - 47 (1994)
Regio- and enantio-selective photodimerization reactions of cyclohex-2-enone (4) and coumarin (7), and enantioselective photocyclization of acrylanilides (12, 16, 18, and 20) in inclusion crystal with optically active host compounds (1, 2, and 3) are reported. X-ray structure studies of the inclusion crystal are also reported.
Control of the Stereochemistry in the Photocyclisation of Acrylanilides to 3,4-Dihydroquinolin-2(1H)-ones. Delicate Dependence on the Host Compound
Tanaka, Koichi,Kakinoki, Osamu,Toda, Fumio
, p. 1053 - 1054 (1992)
The stereochemistry of the photocyclisation of acrylanilides to 3,4-dihydroquinolin-2(1H)-ones is controlled almost completely by irradiation in a crystalline inclusion compound with an optically active host compound derived from tartaric acid; the config
Enantioselective photocyclization of acrylanilides and N-Ethyl-N-methylbenzoylformamide in inclusion crystals with (R,R)-(-)-[trans]-2,3-bis(α-hydroxydiphenylmethyl)-1,4-dioxaspiro-[4.4]nonan e and -[4.5]decane. Mechanistic study based on x-ray crystal st
Ohba, Shigeru,Hosomi, Hiroyuki,Tanaka, Koichi,Miyamoto, Hisakazu,Toda, Fumio
, p. 2075 - 2085 (2007/10/03)
X-Ray structure analyses of the inclusion complexes indicated that the high stereo- and enantioselectivities in photocyclization of cyclohex-1-enecarboic acid methyl-phenyl-amide (3), N-methyl, N-{(E)-methylmethacryloyl}anilide (5), N-methyl, N-(methacryl
