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Angewandte Chemie International Edition, ISSN 1433-7851, 12/2018, Volume 57, Issue 49, pp. 15948 - 15982
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2016, Volume 55, Issue 16, pp. 5053 - 5057
A user‐friendly Ni‐catalyzed reductive carboxylation of benzylic C−N bonds with CO 2 is described. This procedure outperforms state‐of‐the‐art techniques for... 
carboxylation | nickel | homogeneous catalysis | reductive coupling | C−N activation | C-N activation | KETONE FORMATION | AMMONIUM-SALTS | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES | REDUCTIVE CARBOXYLATION | CROSS-COUPLING REACTIONS | ANILINE DERIVATIVES | UNACTIVATED PRIMARY | ARYL | METAL | CARBON-DIOXIDE | Nickel | Catalysis
Journal Article
ACS Catalysis, ISSN 2155-5435, 10/2016, Volume 6, Issue 10, pp. 6739 - 6749
The recent years have witnessed the development of metal-catalyzed reductive carboxylation of organic (pseudo)halides with CO2 as C1 source, representing... 
cross-coupling | carbon dioxide | nickel | catalysis | carboxylic acid | O BOND | CHEMISTRY, PHYSICAL | C-H BONDS | REDUCTIVE CARBOXYLATION | ALKYL-HALIDES | PROMOTED CARBOXYLATION | ARYL BROMIDES | CROSS-COUPLING REACTIONS | UNACTIVATED PRIMARY | CARBON-DIOXIDE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2017, Volume 56, Issue 23, pp. 6558 - 6562
A switchable site‐selective catalytic carboxylation of allylic alcohols has been developed in which CO 2 is used with dual roles, both facilitating C−OH... 
regioselectivity | cross-coupling | carbon dioxide | nickel | synthetic methods | ACTIVATION | REDUCTIVE ALLYLATION | OXIDATIVE ADDITION | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES | CROSS-COUPLING REACTIONS | C-N BONDS | TERTIARY ALKYL | ETHERS | UNACTIVATED PRIMARY | ORGANIC HALIDES | Carboxylation | Alcohol | Ligands | Reagents | Carbon dioxide | Alcohols
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2017, Volume 139, Issue 35, pp. 12161 - 12164
A catalytic protocol that reliably predicts and controls the site-selective incorporation of CO, to a wide range of unsaturated hydrocarbons utilizing water as... 
FUNCTIONALIZATION | ALCOHOLS | ALKENES | ACIDS | ESTERS | REMOTE | BUILDING-BLOCK | ALKYNES | CARBON-DIOXIDE | CHEMISTRY, MULTIDISCIPLINARY | REDUCTIVE CARBOXYLATION
Journal Article
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, ISSN 0002-7863, 08/2014, Volume 136, Issue 32, pp. 11212 - 11215
A Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2 at atmospheric pressure is described. The method is characterized by... 
ARYL BROMIDES | TRANSFORMATION | CROSS-COUPLING REACTIONS | REAGENTS | ACIDS | ZINC HALIDES | BONDS | CARBON-DIOXIDE | ELECTROPHILES | CHEMISTRY, MULTIDISCIPLINARY | REDUCTIVE CARBOXYLATION
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 07/2017, Volume 139, Issue 28, pp. 9467 - 9470
A highly useful, visible-light-driven carboxylation of aryl bromides and chlorides with CO2 was realized using a combination of Pd(OAc)(2) as a carboxylation... 
UNACTIVATED ALKYL | C-H ARYLATION | TEMPERATURE | CO2 | CHLORIDES | MERGING PALLADIUM | PHOTOCARBOXYLATION | CARBON-DIOXIDE | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | REDUCTIVE CARBOXYLATION | Usage | Catalysts | Metal catalysts | Halides | Aromatic compounds | Carboxylation | Oxidation-reduction reaction | Palladium | Chemical properties | Research | Photochemistry
Journal Article
Coordination Chemistry Reviews, ISSN 0010-8545, 11/2018, Volume 374, pp. 439 - 463
Journal Article