dc.creatorCampos Fernández, Cristian Saúl
dc.creatorPineda Cedeño, Leslie William
dc.creatorCabezas Pizarro, Jorge A.
dc.date.accessioned2020-08-06T18:50:29Z
dc.date.available2020-08-06T18:50:29Z
dc.date.created2020-08-06T18:50:29Z
dc.date.issued2019
dc.identifierhttp://scripts.iucr.org/cgi-bin/paper?S2414314619015852
dc.identifier2414-3146
dc.identifierhttps://hdl.handle.net/10669/81414
dc.identifier10.1107/S2414314619015852
dc.description.abstractThe title compound, C9H7NO2, was prepared by alkynylation of 4-iodo­nitro­benzene with 1,3-dili­thio­propyne in the presence of 1 equivalent of CuI and catalytic amounts of Pd(PPh3)2Cl2. The complete mol­ecule is generated by crystallographic twofold symmetry with the C—N and C—C[triple bond]C—C units lying on the rotation axis. No directional inter­actions beyond normal van der Waals contacts could be identified in the packing.
dc.languageen_US
dc.sourceIUCrData. vol.4(11), pp.1-3
dc.subjectAlquino
dc.subjectEstructura de rayos X
dc.subjectPropargilación
dc.subject1,3-dilitiopropino
dc.subjectCrystal structure
dc.subjectAlkynes
dc.subject1,3-dilithiopropyne
dc.subjectPropargylation.
dc.title1-Nitro-4-(1-propyn-1-yl)benzene
dc.typeartículo científico


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