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chemistry, multidisciplinary (18) 18
chemistry, organic (13) 13
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Chemical Communications, ISSN 1359-7345, 2013, Volume 49, Issue 41, pp. 4634 - 4636
We have discovered that phenyl tosylates can be used to arylate pyridines at the C3-position using a Pd(OAc)(2)-1,10-phenanthroline catalyst system. We also... 
ARYL TOSYLATES | ACTIVATION | ELECTRON-DEFICIENT POLYFLUOROARENES | AROMATIC HETEROCYCLES | ARENES | N-OXIDES | HETEROAROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | SUZUKI-MIYAURA | ARYLBORONIC ACIDS
Journal Article
Catal. Sci. Technol, ISSN 2044-4753, 2013, Volume 3, Issue 3, pp. 562 - 571
Journal Article
Catalysis Science and Technology, ISSN 2044-4753, 2/2013, Volume 3, Issue 3, pp. 562 - 571
Significant progress has been accomplished in direct C-H bond arylations of arenes and heteroarenes with readily accessible, inexpensive phenol derivatives.... 
ARYL TOSYLATES | CROSS-COUPLING REACTIONS | INTRAMOLECULAR ARYLATION | NATURAL-PRODUCTS | RUTHENIUM(II) CARBOXYLATE | CHEMISTRY, PHYSICAL | CARBON-CARBON BONDS | CATALYZED DIRECT ARYLATIONS | HETEROAROMATIC-COMPOUNDS | PROTON-ABSTRACTION MECHANISM | UNACTIVATED ALKYL-HALIDES
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2016, Volume 55, Issue 50, pp. 15544 - 15548
This work emphasizes the synthesis of substituted vinyl arenes by reductive coupling of aryl halides with vinyl bromides under mild and easy‐to‐operate... 
cross-coupling | reaction mechanisms | nickel | arenes | alkenes | Arenes | Nickel | Cross-coupling | Alkenes | Reaction mechanisms | INSERTION | MECHANISM | PHOTOREDOX | COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES | TOSYLATES | IODIDES | CHLORIDES | DUAL CATALYSIS | ELECTROPHILES | Halides
Journal Article
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, ISSN 0002-7863, 04/2011, Volume 133, Issue 15, pp. 6061 - 6071
A new technique for the ex situ generation of carbon monoxide (CO) and its efficient incorporation in palladium catalyzed carbonylation reactions was achieved... 
CROSS-COUPLING REACTIONS | ARYL BORONIC ACIDS | CARBONYLATION REACTIONS | CARBON-MONOXIDE | MICROWAVE-PROMOTED AMINOCARBONYLATION | CONVENIENT METHOD | PYRIDINE HALIDES | ELECTRON-RICH OLEFINS | CHEMISTRY, MULTIDISCIPLINARY | ATMOSPHERIC-PRESSURE | HETEROAROMATIC TOSYLATES
Journal Article
Synlett, ISSN 0936-5214, 02/2012, Volume 2012, Issue 3, pp. 478 - 479
Nobutaka Yamaoka was born in Gifu, Japan. He received his M.Sc. (2011) in chemistry from Ritsumeikan University. Currently, he is working toward his D.Sc.... 
spotlight | PHENYLATION | HETEROAROMATIC IODONIUM SALTS | HYPERVALENT IODINE | ACIDS | ESTERS | CHEMISTRY, ORGANIC | CONVENIENT | EFFICIENT | TOSYLATES | WATER
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 10/2012, Volume 2012, Issue 30, pp. 6021 - 6032
Aza‐Nazarov reactions starting from 1‐azapenta‐1,4‐dien‐3‐ones offer an attractive route to five‐membered nitrogen heterocycles such as N‐substituted pyrroles.... 
Aza‐Nazarov reaction | Ab initio calculations | Nitrogen heterocycles | Superacidic systems | Reaction mechanisms | Electrocyclic reactions | Aza-Nazarov reaction | NITROGENOUS HETEROAROMATIC-COMPOUNDS | ACID-CATALYZED CYCLIZATION | 1-AZAPENTADIENYL | FUNCTIONALIZED ARYLAZO TOSYLATES | CHEMISTRY, ORGANIC | HYDRAZINES | BOND-CLEAVAGE | AMINATION | CHROMOPHORES | CHEMISTRY | DERIVATIVES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2017, Volume 359, Issue 3, pp. 419 - 425
An efficient method for the carbonylation of (hetero) aryl pentafluorobenzenesulfonates and triflates under exceptionally mild conditions using... 
chemoselectivity | palladium | cobalt | carbonylation | bimetallic catalysis | Palladium catalysts | Palladium | Catalysis | Carbon monoxide | Cobalt | Deactivation | Catalysts | Carbon dioxide | Insertion | Substrates | Bimetals | Aromatic compounds | Activated carbon | Bromides | Room temperature | Carbonyls | Chlorides
Journal Article
by Zhao, BT and Wang, CB and Wu, SJ and Ye, BX
CHINESE JOURNAL OF ORGANIC CHEMISTRY, ISSN 0253-2786, 08/2010, Volume 30, Issue 8, pp. 1212 - 1219
Five 2-(2-heterocycle-2-ylthioethoxy)ethanols 1a similar to 1e were prepared by the reaction of 2-(2-chloroethoxy)ethanol and 2-mercapto-heterocycles using... 
synthesis | RECOGNITION | crystal structure | CHEMISTRY, ORGANIC | calixarene | 2-mercapto-heteroaromatic compound | CALIXARENES | Synthesis | Calixarene | Crystal structure
Journal Article