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Journal of the American Chemical Society, ISSN 0002-7863, 02/2010, Volume 132, Issue 6, pp. 1822 - 1824
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2016, Volume 55, Issue 43, pp. 13571 - 13575
A mixed directing‐group strategy for inexpensive [Co(acac)3]‐catalyzed oxidative C−H/C−H bond arylation of unactivated arenes has been disclosed. This strategy... 
cross-coupling | reaction mechanisms | cobalt | biaryls | arylation | ACTIVATION | ISOQUINOLINES | ANNULATION | SELECTIVE ACCESS | TERMINAL ALKYNES | CARBON-CARBON BONDS | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | MECHANISTIC INSIGHTS | CARBOXYLIC-ACIDS | AMIDES | Pyridine | Catalysis | Cobalt | Bonds | Couplings | Pyridines | Hydrogen bonds | Aromatic compounds | Strategy | Benzamide
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2013, Volume 52, Issue 2, pp. 580 - 584
Doubling up: A chemo‐ and regioselective oxidative cross‐coupling between various N‐heteroarene‐containing arenes and heteroarenes has been carried out by... 
ruthenium | conjugated systems | poly(hetero)aryls | cross‐coupling reaction | rhodium | cross-coupling reaction | Molecular Structure | Catalysis | Benzene Derivatives - chemistry | Ruthenium - chemistry | Rhodium - chemistry | Oxidative Coupling
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2012, Volume 354, Issue 7, pp. 1287 - 1292
An efficient metal‐free oxidative esterification of benzyl CH bonds was developed. Using tetrabutylammonium iodide as catalyst and tert‐butyl hydroperoxide as... 
tetrabutylammonium iodide | benzyl CH bond | protected amino acids | metal‐free catalyst | esterification | metal-free catalyst | benzyl C-H bond | ESTER | CATALYSIS | ACTIVATION | H BOND | ARENES | CHEMISTRY, ORGANIC | benzyl C?H bond | FUNCTIONALIZATION | CHEMISTRY, APPLIED | Synthesis | Iodides | Amino acids | Esters | Carboxylic acids | Bonding | Esterification | Radicals
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2014, Volume 53, Issue 9, pp. 2477 - 2480
Journal Article
Chemical Science, ISSN 2041-6520, 05/2013, Volume 4, Issue 5, pp. 2163 - 2167
We have developed for the first time a general, concise and highly selective method for the C-2-heteroarylation of pyridines and related azines with a broad... 
FUNCTIONALIZATION | AZOLES | ACTIVATION | RH(I)-CATALYZED DIRECT ARYLATION | ALKYLATION | AROMATIC HETEROCYCLES | BONDS | NICKEL/LEWIS ACID CATALYSIS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | REGIOCONTROL
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 33, pp. 6039 - 6046
An effective palladium-catalyzed oxidative C-H/C-H cross-coupling of imidazopyridines with azoles using air as the oxidant has been developed. This protocol... 
SYSTEM | ROOM-TEMPERATURE | 2 HETEROARENES | DIRECT ARYLATION | CHEMISTRY, ORGANIC | BIOLOGICAL-ACTIVITIES | TERMINAL ALKYNES | BOND ACTIVATION | ANTITUMOR AGENT | DERIVATIVES | IMIDAZOHETEROCYCLES | Cross coupling | Azoles | 5-Fluorouracil | Heterocyclic compounds | Lung cancer | Palladium | Tumor cell lines | Coupling | Functional groups
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 32, pp. 9384 - 9388
The use of enaminones as effective synthons for a directed C−H functionalization is reported. Proof‐of‐concept protocols have been developed for the... 
naphthalenes | carbocyclization | C−H activation | enaminones | rhodium | Chemical synthesis | Ketoesters | Alkynes
Journal Article