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2007, ISBN 9780471731665, x, 472
Matthew S. Platz, PhD, is Distinguished University Professor at The Ohio State University, with more than 200 research articles and more than a dozen patents... 
Science | Chemistry | Organic | Intermediates (Chemistry) | Chemistry, Organic | Organic chemistry
Book
1992, Oxford chemistry primers., ISBN 0198556721, Volume 8, 89
Book
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2010, Volume 49, Issue 31, pp. 5232 - 5241
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2018, Volume 24, Issue 2, pp. 342 - 346
A general and efficient procedure for C−H alkenylation of arenes with a broad substrate scope catalyzed by Cp*CoIII was demonstrated with alkynes. A highly... 
reaction mechanisms | C−H bond alkenylation | hydroarylation | molecular CpCo catalysts | reactive intermediates | mechanisms | Bonds | Catalysis | Hydrogen bonds | Aromatic compounds | Cobalt | Substrates | Alkynes
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2017, Volume 359, Issue 20, pp. 3503 - 3508
The metal‐free arylative coupling of carboxylic acids using iodosoarenes without the use of a catalyst and base, which is applicable to even a highly‐polar... 
Arylation | Carboxylic acids | Reactive intermediates | Hypervalent compounds | Iodine | IODONIUM SALTS | C-H BOND | CHEMISTRY, ORGANIC | PAIR ELECTRON-TRANSFER | AROMATIC-COMPOUNDS | SENSITIZED PHOTOLYSIS | CROWN-ETHER COMPLEXES | HYPERVALENT IODINE | NEAR-UV PHOTOINITIATOR | CHEMISTRY, APPLIED | ORTHO-BENZOXYLATION | EFFICIENT | Organic acids
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2015, Volume 54, Issue 10, pp. 3065 - 3068
The mechanism of the CuAAC reaction has been investigated by electrospray ionization mass spectrometry (ESI‐MS) using a combination of the neutral reactant... 
dicopper complexes | click chemistry | mass spectrometry | CuAAC reaction | reactive intermediates | Click chemistry | Reactive intermediates | Dicopper complexes | Mass spectrometry | MECHANISM | LIGANDS | GAS-PHASE | REACTIVITY | TERMINAL ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | Copper | Ions | Scientific imaging | Cycloaddition | Catalysts | Ionization | Strategy | Catalysis | Reaction mechanisms
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2008, Volume 47, Issue 36, pp. 6754 - 6756
What is the nature of the gold–carbon bond—double, single? The structure of a crucial intermediate of many gold‐catalyzed reactions has become a matter of... 
gold | carbenes | homogeneous catalysis | reactive intermediates | carbocations | Gold | Carbocations | Reactive intermediates | Carbenes | Homogeneous catalysis | ACTIVATION | COMPLEXES | CYCLOPROPANATION | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | ALKENES | GOLD(III) | CYCLOISOMERIZATION | CYCLIZATION | ENYNES
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