In the quinoline fused-ring system of the title compound, C(9)H(9)NO, the pyridine ring is planar to within 0.011 (3) Å, while the partially saturated cyclo-hexene ring adopts a sofa conformation with an asymmetry parameter ΔC(s)(C6) = 1.5 (4)°. There are no classical hydrogen bonds in the crystal structure. Mol-ecules form mol-ecular layers parallel to (100) with a distance between the layers ...

This work presents the results of studying behavior catalytic systems formed on basis trichlorotris-(tetrahydrofuranate)chromium(III) in presence sulfur-containing tridentate SOS-type ligands and activated by various organoaluminum compounds. In formation systems, following compounds were used: - bis-(2-methylthioethyl) ether, bis-(2-ethylthioethyl) ether bis-(2-phenylthioethyl) triethylaluminu...

P eter H. M ühlenbrock, G erhard Fink* M ax-Planck-Institut für Kohlenforschung, Kaiser-W ilhelm-Platz 1, D-45470 Mülheim an der Ruhr Herrn Professor Dr. Dr. h. c. mult. Günther Wilke zum 70. Geburtstag gewidmet Z. N aturforsch. 50b, 423-429 (1995); eingegangen am 7. O k tober 1994 M etallocenes, E thene/a-O lefin Copolym erization, R ate Enhancem ent Effect, Influence of the Tem perature E the...

ExposureofheptanesolutionsofMo(NAr)(CHCMe2Ph)(Me2Pyr)(OAr) (1a;Ar=2,6-diisopropylphenyl), Mo(NAr)(CHCMe3)(Me2Pyr)[OCMe(CF3)2] (1b), and Mo(NAr)(CHCMe2Ph)(Me2Pyr)(OSiPh3) (1c) to one atmosphere of ethylene for 12 h yields the ethylene complexes, Mo(NAr)(CH2CH2)(Me2Pyr)(OAr) (2a), Mo(NAr)(CH2CH2)(Me2Pyr)[OCMe(CF3)2] (2b), and Mo(NAr)(CH2CH2)(Me2Pyr)(OSiPh3) (2c). Addition of 1 equiv of triphenyls...

In the title mol-ecule, C(16)H(14)N(2)O(2), the fused cyclo-hexene and pyran rings adopt an envelope and a flattened boat conformation, respectively. In the crystal, N-H⋯N and N-H⋯O hydrogen bonds link the mol-ecules into corrugated sheets parallel to the bc plane.

The title compound, C(21)H(25)ClO, was semi-synthesized from isocostic acid, isolated from the aerial part of Inula Viscosa- (L) Aiton [or Dittrichia Viscosa- (L) Greuter]. The cyclo-hexene ring has a half-chair conformation, whereas the cyclo-hexane ring displays a chair conformation.

The title compound, C(10)H(11)Cl(5)O, is a chiral mol-ecule with two stereogenic centres. However, it crystallizes as a racemate. One of enanti-omers reveals the relative configuration (2S*,5R*). The cyclo-hexene ring adopts a half-chair conformation.

A simple Pd/SiO2 catalyst which was modified with the ionic liquid [BMPL][DCA] gave an excellent yield of 88% towards cis-2-hexene in the stereoselective hydrogenation of 2-hexyne. The catalyst outperforms, even at full conversion, the commonly used lead-poisoned, toxic Lindlar catalyst and supported colloidal-based Pd as well.

In the mol-ecule of pinnatane A, C(30)H(48)O(3), isolated from the bark of Walsura pinnata Hassk, the four cyclo-hexane rings adopt chair conformations; the carboxyl and hydr-oxy substituents occupy axial positions. The cyclo-hexene ring is envelope-shaped. Adjacent mol-ecules are linked by O-H⋯O hydrogen bonds into a chain running along the c axis.

In the title mol-ecule, C(25)H(30)O(4), the two cyclo-hexene rings adopt envelope conformations. The two hy-droxy groups are involved in the formation of intra-molecular O-H⋯O hydrogen bonds. In the crystal structure, weak inter-molecular C-H⋯O hydrogen bonds link mol-ecules related by translation along the axis a into chains.