(E)-6-(2,2,3-Trimethyl-cyclopent-3-enyl)-hex-4-en-3-one

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منابع مشابه

(E)-4-(4-Meth­oxy­phen­yl)but-3-en-2-one

In the title compound, C(11)H(12)O(2), the dihedral angle between the benzene ring and the but-3-en-2-one group is 4.04 (5)°. The crystal packing features chains, parallel to [-101], composed of dimers connected by weak C-H⋯O inter-actions..

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(E)-1-{4-[(E)-3-Chloro­benzyl­idene­amino]­phen­yl}-3-(3-chloro­phen­yl)prop-2-en-1-one

In the title mol-ecule, C(22)H(15)Cl(2)NO, the dihedral angles between the central aromatic ring and the N- and C=O-bonded rings are 43.13 (13) and 0.80 (14)°, respectively. The dihedral angle between the terminal rings is 43.15 (14)°. The major twist occurs about the C(ar)-N bond [C(ar)-C(ar)-N=C = 42.3 (4)°; ar is aromatic].

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(S)-3-[(S,E)-4-(4-Chloro­phen­yl)-1-nitro­but-3-en-2-yl]thian-4-one

The title compound, C(15)H(16)ClNO(3)S, was obtained by the organocatalytic asymmetric Michael addition of thian-4-one to 1-chloro-4-[(1E,3E)-4-nitro-buta-1,3-dien-yl]benzene. The double bond has an E configuration and the thian-4-one six-membered ring adopts a chair conformation. The crystal structure is stabilized by weak inter-molecular C-H⋯O hydrogen bonds.

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(E)-3-(4-Heptyl­oxyphen­yl)-1-phenyl­prop-2-en-1-one

In the title compound, C22H26O2, the aromatic rings are inclined to one another by 8.39 (9)° and the mol-ecule has an E conformation about the C=C bond. In the crystal, mol-ecules stack head-to-tail along the b-axis direction. They are linked by very weak C-H⋯O contacts, forming C(4) chains along [100]. Two chains are linked by a pair of very weak C-H⋯O contacts, enclosing inversion-dimeric R 2...

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(E)-1-(4-Nitro­phen­yl)-3-phenyl­prop-2-en-1-one

In the title compound, C(15)H(11)NO(3), the configuration of the keto group with respect to the olefinic double bond is s-cis. The two benzene rings form a dihedral angle of 5.00 (5)°. The mol-ecules are linked into a two-dimensional network parallel to (04) by C-H⋯O hydrogen bonds.

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ژورنال

عنوان ژورنال: Molbank

سال: 2004

ISSN: 1422-8599

DOI: 10.3390/m388