scholarly journals (1S,3R,8R,11S)-2,2,11-Tribromo-10-bromomethyl-3,7,7-trimethyltricyclo[6.4.0.01,3]dodec-9-ene

IUCrData ◽  
2016 ◽  
Vol 1 (5) ◽  
Author(s):  
Abdoullah Bimoussa ◽  
Aziz Auhmani ◽  
My Youssef Ait Itto ◽  
Jean-Claude Daran ◽  
Abdelwahed Auhmani
Keyword(s):  
Hydrogen Bonds ◽  
Essential Oil ◽  
Absolute Configuration ◽  
Title Compound ◽  
Resonant Scattering ◽  
Cedrus Atlantica ◽  
Compound C ◽  
The Absolute

The title compound, C16H22Br4, was synthesized in two steps from β-himachalene, which was isolated from essential oil of the Atlas cedar (cedrus atlantica). It is built up from three fused rings, a seven-membered heptane ring, a six-membered cyclohexyl ring bearing both a bromine and a bromomethyl substituent, and a three-membered propane ring bearing two Br atoms. In the crystal, molecules are linked by C—H...Br hydrogen bonds, forming chains propagating along [001]. The absolute configuration was deduced from the chemical pathway and confirmed by resonant scattering [Flack parameter = 0.012 (10)].

(3R,4R)-(–)-3-Hydroxymethyl-4-phenyl-2-o-toluoyl-1,2,3,4-tetrahydroisoquinoline

2006 ◽  
Vol 62 (5) ◽  
pp. o1774-o1776 ◽  
Author(s):  
Andrzej Gzella ◽  
Maria Chrzanowska ◽  
Agnieszka Dreas ◽  
Michał S. Kaczmarek ◽  
Zenon Woźniak
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Phenyl Ring ◽  
Heterocyclic Ring ◽  
Hydroxymethyl Group ◽  
Envelope Conformation ◽  
Compound C ◽  
The Absolute

The absolute configuration of the title compound, C24H23NO2, has been confirmed as 3R,4R. The hydroxymethyl group and phenyl ring at the asymmetric C atoms exhibit α and β orientations, respectively, and the non-planar heterocyclic ring of the tetrahydroisoquinoline system adopts an envelope conformation. The crystal structure is stabilized through hydrogen bonds.

(4S,1′R)-Diethyl 6-methyl-2-[(1′-phenylethylimino)methyl]-4-(2-thienyl)-1,4-dihydropyridine-3,5-dicarboxylate

2006 ◽  
Vol 62 (7) ◽  
pp. o2759-o2761
Author(s):  
Viktor Vrábel ◽  
Pavol Skubák ◽  
Štefan Marchalín ◽  
Vratislav Langer ◽  
Barbora Baumlová
Keyword(s):  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Thiophene Ring ◽  
Boat Conformation ◽  
Compound C ◽  
The Absolute

The absolute configuration of the title compound, C25H28N2O4S, has been determined. The molecules are interconnected by weak C—H...O hydrogen bonds. The 1,4-dihydropyridine (1,4-DHP) ring adopts the usual shallow boat conformation. The thiophene ring is nearly planar.

scholarly journals 1,6-Diacetyl-2-isopropyl-4,7-dimethylnaphthalene

IUCrData ◽  
2016 ◽  
Vol 1 (4) ◽  
Author(s):  
Ahmed Benharref ◽  
Abdelouhed Oukhrib ◽  
Mustapha Ait Elhad ◽  
Lahcen El Ammari ◽  
Mohamed Saadi ◽  
...  
Keyword(s):  
Hydrogen Bonds ◽  
Essential Oil ◽  
Title Compound ◽  
Cedrus Atlantica ◽  
Compound C

The title compound, C19H22O2, was synthesized in three steps from a mixture of α-, β- and γ-himachalene, which was isolated from an essential oil of the Atlas cedar (Cedrus atlantica). In the crystal, molecules are linked by C—H...O hydrogen bonds into chains running parallel to thebaxis.

scholarly journals N-(2-Acetamido-2-deoxy-β-D-glucopyranosyl)-N-(3-azidopropyl)-O-methylhydroxylamine

2016 ◽  
Vol 72 (3) ◽  
pp. 340-342 ◽  
Author(s):  
Stefan Munneke ◽  
Bridget L. Stocker ◽  
Mattie S. M. Timmer ◽  
Graeme J. Gainsford
Keyword(s):  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Crystal Plate ◽  
Starting Material ◽  
Screw Axis ◽  
Compound C ◽  
The Absolute ◽  
Thin Crystal ◽  
Adequate Data

The structure of the title compound, C12H23N5O6, solved using adequate data from a thin crystal plate, confirmed that this useful glycoconjugate was obtained in the ring-closed β-pyranose configuration with4C1conformation. The molecules are bound by O—H...O(OH) hydrogen bonds, notably in a zigzagC(2) chain along the shortb(screw) axis, supplemented with anR22(12)O—H...O(carbonyl) link along theaaxis and otherC(2) links. The absolute configuration was not unambiguously determined but was known from the synthetic chemistry, which used natural 2-acetamido-2-deoxy-D-glucose as the starting material.

(3aS,5aR,6R,8aR)-3a-Hydroxy-5a-methyl-6-[(1R,2E,4R)-1,4,5-trimethyl-2-hexen-1-yl]-3a,4,5,5a,6,7,8,8a-octahydro-2H-cyclopenta[e]benzofuran-2-one

2007 ◽  
Vol 63 (11) ◽  
pp. o4196-o4196
Author(s):  
Wen-liang Wang ◽  
Hong-wen Tao ◽  
Wei Sun ◽  
Qian-Qun Gu ◽  
Wei-Ming Zhu
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Optical Rotation ◽  
Side Chain ◽  
Compound C ◽  
Extended Chain ◽  
Halotolerant Fungus ◽  
The Absolute

The title compound, C21H32O3, also known as dimethylincisterol A3, was isolated from halotolerant fungus THW-18. It is composed of three fused rings and a side chain. In the crystal structure, the molecules interact with each other via O—H...O hydrogen bonds, resulting in an extended chain along the b axis. The absolute configuration was assigned from the measured optical rotation and reference to the literature.

(1R,4S,8R,12S,13S,14R,16S,19R)-14-Hydroxy-7,7-dimethyl-17-methylene-2,9,18-trioxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadec-19-yl acetate

2007 ◽  
Vol 63 (11) ◽  
pp. o4439-o4439
Author(s):  
Hao Shi
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Chair Conformation ◽  
Boat Conformation ◽  
Asymmetric Unit ◽  
Compound C ◽  
Independent Molecules ◽  
The Absolute

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.

scholarly journals 5α-Hydroxyeudesm-4(15),11(13)-dien-8β,12-olide

2012 ◽  
Vol 68 (4) ◽  
pp. o1208-o1208 ◽  
Author(s):  
Xue Gao ◽  
Gang Chen
Keyword(s):  
Hydrogen Bonds ◽  
Sesquiterpene Lactone ◽  
Absolute Configuration ◽  
Title Compound ◽  
Aerial Parts ◽  
Compound C ◽  
Ring Junction ◽  
Twist Conformation ◽  
Cyclopentane Ring ◽  
The Absolute

The title compound, C15H20O3, a sesquiterpene lactone, was isolated from the aerial parts ofCarpesium minusHemsl. (Compositae). The molecule is composed of three rings, with the two cyclohexane rings in chair conformations and the cyclopentane ring adopting a twist conformation. TheA/Bring junction istrans-fused. The absolute configuration shown has been arbitrarily assigned. In the crystal, molecules are linked into [100] chains by O—H...O hydrogen bonds.

scholarly journals Crystal structure of (1S,2R,4S)-1-[(morpholin-4-yl)methyl]-4-(prop-1-en-2-yl)cyclohexane-1,2-diol

2015 ◽  
Vol 71 (1) ◽  
pp. 79-81 ◽  
Author(s):  
Rachid Outouch ◽  
Saadia Oubaassine ◽  
Mustapha Ait Ali ◽  
Larbi El Firdoussi ◽  
Anke Spannenberg
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Chair Conformation ◽  
Asymmetric Unit ◽  
Compound C ◽  
Synthetic Procedure ◽  
Independent Molecules ◽  
The Absolute

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.

(+)-N-[(R)-1-(2-Hydroxy-5-methylphenyl)propyl]-N-[(R)-2-methyl-1-phenylpropyl]ammonium chloride

2006 ◽  
Vol 62 (7) ◽  
pp. o2622-o2624 ◽  
Author(s):  
Xiao-Feng Yang ◽  
Da-Qi Wang ◽  
Guang-You Zhang ◽  
Takuji Hirose
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Hydrogen Bonds ◽  
Ammonium Chloride ◽  
Absolute Configuration ◽  
Title Compound ◽  
Condensation Reaction ◽  
Compound C ◽  
The Absolute ◽  
Phenol Ring

The title compound, C20H28NO+·Cl−, was synthesized by a condensation reaction. The absolute configuration of the new stereogenic centre (the C atom between the N atom and the phenol ring) was determined as R. The crystal structure is stabilized through N—H...Cl and O—H...Cl hydrogen bonds and intramolecular N—H...O hydrogen bonding.

(1′S,2′S,5′R)-3-(2-Bromopropionyl)-2′-isopropyl-5′-methylspiro[2H-1,3-benzoxazine-2,1′-cyclohexan]-4(3H)-one

2006 ◽  
Vol 62 (7) ◽  
pp. o3011-o3012 ◽  
Author(s):  
Qing Yuan ◽  
Ming Lei
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonds ◽  
Absolute Configuration ◽  
Title Compound ◽  
Anomalous Scattering ◽  
Compound C ◽  
Scattering Effects ◽  
The Absolute

The absolute configuration of the title compound, C20H26BrNO3, was determined from both the synthetic precursor and anomalous scattering effects. In the crystal structure, non-classical C—H...O hydrogen bonds link the molecules into a sheet parallel to the b axis.

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