نتایج جستجو برای: 14 aryl 14h dibenzoxanthene

تعداد نتایج: 373509  

Journal: :organic chemistry research 2015
dariush saberi khodabakhsh niknam farhad panahi mohammad reza hormozi-nezhad

silica-grafted n-propyl-diaza-15-crown-5 (sgpdc) with immobilized palladium nanoparticles was found as an efficient heterogeneous catalytic system for the heck and suzuki coupling reactions and satisfied results were obtained. different derivatives of aryl halides and alkenes under the heck reaction were converted to the corresponding products with good efficiency. the presence of electron-dona...

2012
Haruyasu Asahara Peter Mayer Herbert Mayr

The title compound, C(15)H(12)O(5)S(2), crystallizes with two mol-ecules in the asymmetric unit. In both mol-ecules, the 1,3-benzodithiole plane and the aryl ring of the anisyl group are not quite coplanar; the corresponding dihedral angles are 20.4 (1) and 18.0 (1)°. π-Stacking [with centroid-centroid distances between 3.5440 (14) and 3.8421 (14) Å] takes place along [100] between the alternat...

2017
Aniket Kumar Lipeeka Rout Lakkoji Satish Kumar Achary Rajendra. S. Dhaka Priyabrat Dash

A facile, efficient and environmentally-friendly protocol for the synthesis of xanthenes by graphene oxide based nanocomposite (GO-CuFe2O4) has been developed by one-pot condensation route. The nanocomposite was designed by decorating copper ferrite nanoparticles on graphene oxide (GO) surface via a solution combustion route without the use of template. The as-synthesized GO-CuFe2O4 composite w...

2005
Guisheng Deng Baihua Xu Jianbo Wang

2-Cyclopenten-1-one-5-carboxylic ester derivatives 14 are synthesized in a four-step-reaction sequence starting from alkynyl aldehydes 9 via 4Z-b-vinyl-a-diazo b-ketoesters intermediate 8. The synthetic method for 8 is described. When the d substituent is an alkyl group, Rh(II)-mediated decomposition of the diazo compounds 8 led to an intramolecular C–H insertion to afford 2-cyclopenten-1-one-5...

2005
William Michael Seganish Philip DeShong Ian Mather Steve Rokita

Title of Dissertation: DEVELOPMENT OF ARYL SILOXANE CROSSCOUPLING TECHNOLOGY AND ITS APPLICATION TO THE SYNTHESIS OF COLCHICINE AND ALLOCOLCHICINE DERIVATIVES William Michael Seganish, Doctor of Philosophy, 2005 Dissertation directed by: Professor Philip DeShong Department of Chemistry and Biochemistry One of the most versatile methods for the formation of aryl-aryl bonds is the palladium-catal...

2008
B. Thimme Gowda Miroslav Tokarčík Jozef Kožíšek K. S. Babitha Hartmut Fuess

The crystal structure of the title compound (24DMPBA), C(15)H(14)O(2), resembles those of 4-methyl-phenyl benzoate, 2,3-dimethyl-phenyl benzoate and other aryl benzoates, with similar bond parameters. The central -O-C-O- group in 24DMPBA makes dihedral angles of 85.81 (5) and 5.71 (13)°, respectively, with the benzoyl and phenyl rings, while the two aromatic rings form a dihedral angle of 80.25...

Journal: :Chemical communications 2013
Nanase Uchiyama Eiji Shirakawa Tamio Hayashi

The mechanism of the previously developed cross-coupling reaction of aryl Grignard reagents with aryl halides was explored in more detail. Single electron transfer from an aryl Grignard reagent to an aryl halide initiates a radical chain by giving an anion radical of the aryl halide. The following propagation cycle consists entirely of anion radical intermediates.

2014
Shaozhong Ge Wojciech Chaładaj John F. Hartwig

We report the Pd-catalyzed α-arylation of α,α-difluoroketones with aryl and heteroaryl bromides and chlorides catalyzed by an air- and moisture-stable palladacyclic complex containing P(t-Bu)Cy2 as ligand. The combination of this Pd-catalyzed arylation and base-induced cleavage of the acyl-aryl C-C bond within the α-aryl-α,α-difluoroketone constitutes a one-pot, two-step procedure to synthesize...

Journal: :European journal of biochemistry 1981
S T George A S Balasubramanian

Human serum aryl acylamidase associated with serum cholinesterase was purified to homogeneity. Evidence for the identity of the two enzymes was based on co-elution profiles, co-purification in the different steps including affinity chromatography with constant ratios of specific activity and percentage recoveries, co-migration on gel electrophoresis, parallel inhibition by typical cholinesteras...

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