scholarly journals N-[1,4,4-Trimethyltricyclo[6.3.1.03,9]dodec-8(12)-en-2-yl]acetamide

IUCrData ◽  
2017 ◽  
Vol 2 (6) ◽  
Author(s):  
Noureddine Mazoir ◽  
Ahmed Benharref ◽  
Jean-Claude Daran ◽  
Abdelouahd Oukhrib ◽  
Mustapha Ait Elhad ◽  
...  

The title compound, C17H27NO, crystallizes with three independent molecules in the asymmetric unit with almost identical conformations. Each molecule is built up from a seven-membered ring to which a bridged six-membered ring is fused. In each of the three molecules, the seven-membered rings have a twist-chair conformation, while the cyclohexenyl rings display perfect boat conformations. In the crystal, N—H...O hydrogen bonds link the molecules into zigzag chains running along theb-axis direction.

IUCrData ◽  
2017 ◽  
Vol 2 (2) ◽  
Author(s):  
Mustapha Ait Elhad ◽  
Ahmed Benharref ◽  
Lahcen El Ammari ◽  
Mohamed Saadi ◽  
Abdelouahd Oukhrib ◽  
...  

The title compound, C16H23Cl2NO, crystallizes in the monoclinic space groupP21with two independent molecules (AandB) in the asymmetric unit. They have essentially the same conformation. Each molecule is built up from fused six- and seven-membered rings and an additional three-membered ring. The six-membered ring has an envelope conformation, with the C atom belonging to the three-membered ring forming the flap, while the seven-membered ring displays a boat conformation. In the crystal, molecules are linked into chains propagating along thea-axis direction by N—H...O hydrogen bonds.


IUCrData ◽  
2017 ◽  
Vol 2 (7) ◽  
Author(s):  
Amed Benharref ◽  
Mustapha Ait Elhad ◽  
Noureddine Mazoir ◽  
Jean-Claude Daran ◽  
Abdelouahd Oukhrib ◽  
...  

The title compound, C17H29NO3, was synthesized in two steps from β-himachalene (2,6,6,9-tetramethylbicyclo[5.4.01,7]undeca-1,8-diene), which was isolated from an oil of the Atlas cedar (Cedrus Atlantica). The asymmetric unit contains two independent molecules (A and B): B features an intramolecular O—H...O hydrogen bond whereas A forms an intermolecular O—H...O link to B. Each molecule is built up from a seven-membered ring to which a bridged six-membered ring is fused: the cycloheptane rings have twist-chair conformations, while the bridged cyclohexane rings display near-perfect boat conformations. In the crystal, the molecules are linked by N—H...O and O—H...O hydrogen bonds forming helical chains propagating along the b-axis direction. Some weak C—H...O interactions are also observed.


2015 ◽  
Vol 71 (10) ◽  
pp. o778-o779
Author(s):  
Mehmet Akkurt ◽  
Jerry P. Jasinski ◽  
Shaaban K. Mohamed ◽  
Omran A. Omran ◽  
Mustafa R. Albayati

The asymmetric unit of the title compound, C54H64O12S4, consists of one half of the molecule, which is located on an inversion centre. The heterocyclic six-membered ring adopts a distorted envelope conformation with the spiro C atom as the flap. In the crystal, molecules are linked by weak C—H...O hydrogen bonds with anR22(14) motif, forming a chain along theb-axis direction.


2014 ◽  
Vol 70 (5) ◽  
pp. o526-o526 ◽  
Author(s):  
Mohamed Zaki ◽  
Ahmed Benharref ◽  
Jean-Claude Daran ◽  
Moha Berraho

The title compound, C16H24Br2O, was synthesized from the reaction of β-himachalene (3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzocycloheptene), which was isolated from Atlas cedar (Cedrus atlantica). The asymmetric unit contains two independent molecules with similar conformations. Each molecule is built up from two fused seven-membered rings and an additional three-membered ring. In both molecules, one of the seven-membered rings has a chair conformation, whereas the other displays a screw-boat conformation.


2007 ◽  
Vol 63 (11) ◽  
pp. o4439-o4439
Author(s):  
Hao Shi

The title compound, C22H26O8, prepared from the natural diterpenoid Macrocalyxin J, is built up from five fused rings. Cyclohenane ring A adopts a chair conformation, ring B exists in a screw-boat conformation and ring C adopts a boat conformation; the two five membered rings adopt envelope conformations. Two unique molecules are present in the asymmetric unit; both independent molecules have the same absolute configuration, the absolute configuration being deduced from the chirality of Macrocalyxin A, which was isolated from the same plant (i.e. Rabdosia macrocalyx) as Macrocalyxin J. The crystal structure displays intermolecular O—H...O hydrogen bonds.


2014 ◽  
Vol 70 (3) ◽  
pp. o301-o302 ◽  
Author(s):  
Adriano Bof de Oliveira ◽  
Bárbara Regina Santos Feitosa ◽  
Christian Näther ◽  
Inke Jess

There are two independent molecules in the asymmetric unit of the title compound, C12H15N3S, both of which display disorder of several C atoms in the N-bound ring (occupancy ratios of 0.75:0.25 in the first independent molecule and 0.50:0.50 in the second) with the methyl H atoms also being disordered in the first molecule (occupancy ratio of 0.70:0.30). The planes of the benzene ring and the N—N—C—N fragment make dihedral angles of 12.92 (14)° in the first independent molecule and 7.60 (13)° in the second. In the crystal, molecules are linked by weak N—H...S hydrogen bonds into chains along thea-axis direction. The crystal packing ressembles a herringbone arrangement.


2012 ◽  
Vol 68 (6) ◽  
pp. o1735-o1735
Author(s):  
S. Sundaramoorthy ◽  
N. Sivakumar ◽  
M. Bakthadoss ◽  
D. Velmurugan

The asymmetric unit of the title compound, C19H20N2O3, contains two independent molecules in both of which the pyrrolidine ring adopts an envelope conformation, but with a C atom as the flap in one molecule and the N atom in the other. The pyran ring adopts a half-chair conformation in both molecules. In the crystal, molecules are linked via C—H...O hydrogen bonds and C—H...π interactions.


IUCrData ◽  
2019 ◽  
Vol 4 (8) ◽  
Author(s):  
Mulveer Singh ◽  
Sumati Anthal ◽  
Sandeep S. Sankpal ◽  
Madhukar B. Deshmukh ◽  
Rajni Kant

The asymmetric unit of the title compound, C8H15N3S, contains two independent molecules. In both molecules, the seven-membered cycloheptane ring adopts a chair conformation. An intramolecular N—H...N hydrogen bond is observed in both molecules, forming S(5) graph-set motifs. In the crystal, the two independent molecules are connected through N—H...S hydrogen bonds, forming dimers which are in turn further connected by N—H...S hydrogen bonds into chains along [010].


Author(s):  
Rachid Outouch ◽  
Saadia Oubaassine ◽  
Mustapha Ait Ali ◽  
Larbi El Firdoussi ◽  
Anke Spannenberg

The asymmetric unit of the title compound, C14H25NO3, contains two independent molecules with similar geometry. The morpholine and cyclohexane rings of both molecules adopt a chair conformation. Intramolecular O—H...N hydrogen bonds are observed. In the crystal, molecules are linked by O—H...O hydrogen bonds into chains parallel to the [101] direction. The chains are further connected through C—H...O hydrogen bonds forming undulating layers parallel to the (-101) plane. The absolute configuration was assigned by reference to an unchanging chiral centre in the synthetic procedure.


2014 ◽  
Vol 70 (6) ◽  
pp. o662-o662
Author(s):  
Juan Feng ◽  
Jian-Long Zhang ◽  
Rong-Rong Zhang ◽  
Li-Jun Ruan ◽  
Ren-Wang Jiang

The title compound, C24H30O7, is a diterpenoid isolated from the seeds ofCaesalpinia minax. It consists of two cyclohexane rings (AandB), one unsaturated six-membered ring (C) and one furan ring (D). The stereochemistry of the ring junctures isA/B transandB/C trans. RingsAandBhave normal chair conformations whileCadopts a twisted half-chair conformation due to fusion to the furan ring which is planar [r.m.s. deviation = 0.0009 (2) Å]. In the crystal, hydroxyl O—H...Ocarbonylhydrogen bonds link the molecules into a chain structure extending along thea-axis direction.


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