The structure was solved by direct methods and refined by full-matrix least squares to a final R = 0.048 for 1519 observed reflections. The molecule as a whole is nearly planar and the methyl groups are both equatorial. A partial pi delocalization is observed.
Stereochemistry of Rings XVI. Indole Derivatives. 1. 2,3-Dimethyl-5-nitroindole / G., Bocelli; Rizzoli, Corrado. - In: ACTA CRYSTALLOGRAPHICA. SECTION C, CRYSTAL STRUCTURE COMMUNICATIONS. - ISSN 0108-2701. - C45:8(1989), pp. 1180-1181. [10.1107/S0108270189000934]
Stereochemistry of Rings XVI. Indole Derivatives. 1. 2,3-Dimethyl-5-nitroindole
RIZZOLI, Corrado
1989-01-01
Abstract
The structure was solved by direct methods and refined by full-matrix least squares to a final R = 0.048 for 1519 observed reflections. The molecule as a whole is nearly planar and the methyl groups are both equatorial. A partial pi delocalization is observed.File in questo prodotto:
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