Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Enantioselective Photocyclization of Amides to -Lactam Derivatives in Inclusion Crystals with an Optically Active Host (CROSBI ID 90150)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Toda, Fumio ; Miyamoto, Hisakazu ; Inoue, Mitsuhiro ; Yasaka, Shunpei ; Matijašić, Ivanka Enantioselective Photocyclization of Amides to -Lactam Derivatives in Inclusion Crystals with an Optically Active Host // Journal of organic chemistry, 65 (2000), 2728-2732-x

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.

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

65

2000.

2728-2732-x

objavljeno

0022-3263

Povezanost rada

Kemija

Indeksiranost