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- W2018997237 abstract "The title compound, C41H32Cl4N4O2S, was synthesized by the intermolecular [3 + 2] cycloaddition of azomethine ylide, derived from isatin and sarcosine by a decarboxylative route, and 5-(4-chloro)phenyl-10-(4-chloro)benzylidene-2-(2,4-dichloro)benzylidene-2,3,6,7,8,9-hexahydro-5H,10H-cyclohepteno[1,2-d]thiazolo[3,2-a]pyrimidin-3-one. In the molecule, the two spiro junctions link a planar 2-oxindole ring, a pyrrolidine ring in an envelope conformation and a 10-(arylmethylene)hexahydrocyclohepteno[1,2-d]thiazolo[3,2-a]pyrimidin-3-one ring. The packing of the molecules in the crystal structure is mainly due to N—H⋯O hydrogen bonds." @default.
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- W2018997237 date "2005-04-23" @default.
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- W2018997237 title "10′′-(4-Chlorobenzylidene)-5′′-(4-chlorophenyl)-4′-(2,4-dichlorophenyl)-1′-methyl-2,3,2′′,3′′,7′′,8′′,9′′,10′′-octahydro-1<i>H</i>,5′′<i>H</i>,6′′<i>H</i>-indole-3-spiro-2′-pyrrolidine-3′-spiro-2′′-cyclohepteno[1,2-<i>d</i>]thiazolo[3,2-<i>a</i>]pyrimidine-2,3′′-dione" @default.
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- W2018997237 doi "https://doi.org/10.1107/s1600536805011621" @default.
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