نتایج جستجو برای: acenaphthene 12 dione

تعداد نتایج: 586079  

Journal: :The Journal of the Society of Chemical Industry, Japan 1950

2012
Jianchao Yuan Xiaoli Xie Yufeng Liu Chengping Miao Jing Li

The title compound, C(40)H(32)N(2), has crystallographic twofold rotation symmetry, with two C atoms lying on the axis. The dihedral angle between the two benzene rings of the 4-phenyl-2,6-dimethyl-phenyl group is 35.74 (17)°. The acenaphthene ring makes an angle of 76.93 (11)° with the benzene ring bonded to the N atom and an angle of 41.53 (13)° with the other benzene ring.

Journal: :Proceedings of the Imperial Academy 1939

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2008
Julio C Herrera Graciela Troncone Diana Henríquez Neudo Urdaneta

A chloroform extract from roots of Craniolaria annua provided six new C-11 unsubstituted abietanes, 14-hydroxy-6,12-dione-7,9(11),13-abietatriene (1), 14-hydroxy-12-oxo-7,9(11),13-abietatriene (2), 6,12,14-trihydroxyabieta-5,8,11,13-tetraen-7-one (3), ar-abietatriene-12-ol-6,7-dione-14,16-oxide (4), ar-abietatriene-12,16-diol-14,16-oxide (5) and ar-abietatriene-12-ol-7-one-14,16-oxide (6), and ...

2007
S. Athimoolam V. Anu Radha S. Asath Bahadur R. Ranjith Kumar S. Perumal

In the title compound, C(42)H(33)NO(2), the six-membered cyclo-hexa-none ring adopts a slightly distorted chair conformation and the five-membered pyrrolidine ring is in an envelope conformation. The mol-ecular structure features four intra-molecular C-H⋯O inter-actions and an intra-molecular C-H⋯π inter-action. Furthermore, the crystal packing is stabilized by an inter-molecular C-H⋯O and thre...

Journal: :Dalton transactions 2013
Fergus R Knight Rebecca A M Randall Lucy Wakefield Alexandra M Z Slawin J Derek Woollins

Six related organo–chalconium silver(I) coordination complexes, including two examples of rare organotellurium-silver coordination, have been prepared and structurally characterised by X-ray crystallography. The series of 5-bromo-6-(phenylchalcogeno)acenaphthene ligands L1–L3 [Acenap(Br)(EPh)] (Acenap = acenaphthene-5,6-diyl; E = S, Se, Te) were independently treated with silver(I) salts (AgBF4...

2009
Elsayed M. Afsah Ahmed A. Fadda Samir Bondock Mohamed M. Hammouda

Tetrahydro-1H-benzo[b]azonin-2,7-dione (2a) has been used as a precursor in the synthesis of dibenzo[b,f ][1,5]diazacyclododecene and dibenzo[b,g][1,6]diazacyclododecene ring systems 4 and 5, respectively, via periodate oxidation of the appropriate indolo-benzo[b]azonines 3 and 7. The synthesis of hexahydro-benzo[b][1,4]diazecin-2,7-dione (10) has been achieved by the Schmidt reaction of 2a. Th...

2017
Yoshiyuki Miyazawa Yoshitaka Sekine Takahiro Syuto Masashi Nomura Hidekazu Koike Hiroshi Matsui Yasuhiro Shibata Kazuto Ito Kazuhiro Suzuki

BACKGROUND Adrenal androgens play an important role in the development of castration-resistant prostate cancer therapeutics. The effect of gonadotropin-releasing hormone (GnRH) antagonists on adrenal androgens has not been studied sufficiently. We measured testicular and adrenal androgen levels in patients treated with a GnRH antagonist. METHODS This study included 47 patients with histologic...

2012
Shen-Tang Wang Guang-Bo Che Chun-Bo Liu Xing Wang Ling Liu

In the cation of the title salt, [Ag(C(12)H(6)N(2)O(2))(2)](C(7)H(3)N(2)O(7)), the Ag(I) atom is coordinated in a distorted tetra-hedral geometry by four N atoms from two 1,10-phenanthroline-5,6-dione ligands, while the 3,5-dinitro-salicylate anion has only a short contact [2.847 (6) Å] between one of its O atoms and the Ag(I) atom. The dihedral angle between the two 1,10-phenanthroline-5,6-dio...

Journal: :iranian journal of catalysis 2012
abdolkarim zare roghayyeh khanivar maria merajoddin masoud kazem-rostami mohammad mahdi ahmad-zadeh

brønsted acidic ionic liquid triethylamine-bonded sulfonic acid {[et3n-so3h]cl} efficiently catalyzes the one-pot multi-component condensation of 2-naphthol with arylaldehydes and dimedone (5,5-dimethylcyclohexane-1,3-dione) under solvent-free conditions to afford 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones in high yields and relatively short reaction times.

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