Two isomeric butadiene–N-(acetoxy­phenyl)maleimide Diels–Alder adducts: supramolecular structure directed by C—H⋯X (X = O and π) hydrogen bonds and perpendicular dipole carbonyl–carbonyl inter­actions

Trujillo-Ferrara, J.G.; Santillán-Baca, R.L.; Farfán-García, N.; Padilla-Martínez, I.I.; García-Báez, E.V.

doi:10.1107/S0108270106002186

Acta Crystallographica Section C
Acta Crystallographica
Section C STRUCTURAL CHEMISTRY

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Figure 4
The supramolecular structure of the title para Diels–Alder adduct, (II)

, viewed along the b axis. [Symmetry codes: (iii) x, y + 1, z; (iv) x, −y + $[{3\over 2}]$ , z + $[{1\over 2}]$ ; (v) x, −y + $[{3\over 2}]$ , z − $[{1\over 2}]$ ; (vi) x, −y + $[{5\over 2}]$ , z − $[{1\over 2}]$ .]

STRUCTURAL
CHEMISTRY

ISSN: 2053-2296

Volume 62| Part 3| February 2006| Pages o125-o128

doi:10.1107/S0108270106002186

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