Enantioselective Photocyclization of Amides to -Lactam Derivatives in Inclusion Crystals with an Optically Active Host (CROSBI ID 90150)
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Podaci o odgovornosti
Toda, Fumio ; Miyamoto, Hisakazu ; Inoue, Mitsuhiro ; Yasaka, Shunpei ; Matijašić, Ivanka
engleski
Enantioselective Photocyclization of Amides to -Lactam Derivatives in Inclusion Crystals with an Optically Active Host
Irradiation of inclusion crystals of 2-(N-acyl-N-alkylamino)cyclohex-2-enones and N,N-dimethylphenylglyoxylamide with chiral host molecules gave the opticaly active N-alkyl-1-azaspiro[3,5]-nonane-2,5-diones and 3-hydroxy-1-methyl-3-phenylazetidin-2-one, respectively. The crystal structure of the 1:1 inclusion complex of N,N-dimethylphenylglyoxylamide with (-)-trans-1,4-bis[3-(o-chlorophenyl)-3-hydroxy-3-phenylprop-1-ynyl]-2,3,5,6-tetrachloro-2,5-cyclohexadiene-1,4-diol was analyzed by X-ray diffraction.
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