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Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2016, Volume 358, Issue 8, pp. 1219 - 1228
A new visible light‐initiated 1,5‐hydride radical shift strategy has been developed to enable the one‐step functionalization of both a C(sp3)Br bond and a... 
hydride radical shift | visible light | alkyl bromides | enynes | polycyclic hydrocarbons | Synthesis | Hydrocarbons | Strategy | Hydrides | Catalysis | Carbon | Bonding | Radicals
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2014, Volume 136, Issue 47, pp. 16588 - 16593
Journal Article
Organic Letters, ISSN 1523-7060, 08/2016, Volume 18, Issue 16, pp. 4012 - 4015
Reductive cross-coupling has emerged as a direct method for the construction of carbon–carbon bonds. Most cobalt-, nickel-, and palladium-catalyzed reductive... 
VISIBLE-LIGHT | ROOM-TEMPERATURE | UNACTIVATED ALKYL | MERGING PHOTOREDOX | ALLYLIC ACETATES | DECARBOXYLATIVE ARYLATION | LIGHT PHOTOREDOX CATALYSIS | CHEMISTRY, ORGANIC | C-H FUNCTIONALIZATION | SINGLE-ELECTRON TRANSMETALATION | DUAL-CATALYSIS
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 06/2014, Volume 79, Issue 12, pp. 5771 - 5780
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2018, Volume 57, Issue 51, pp. 16857 - 16860
The development of a general, nickel‐catalyzed alkyl‐Mizoroki–Heck reaction of unactivated alkyl bromides is described. The mild reaction proceeds efficiently... 
cross-coupling | radical reactions | nickel | alkyl halides | synthetic methods | HALIDES | ALKENES | SECONDARY | CHEMISTRY, MULTIDISCIPLINARY | ALKENYLATION | CYCLIZATION | Alkenes - chemistry | Cyclization | Nickel - chemistry | Stereoisomerism | Hydrocarbons, Brominated - chemistry | Molecular Structure | Catalysis | Alkenes - chemical synthesis | Palladium | Nickel | Couplings | Regioselectivity | Bromides | Chemical reactions
Journal Article
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, ISSN 0002-7863, 05/2019, Volume 141, Issue 17, pp. 6853 - 6858
Copper oxidative addition into organo-halides is a challenging two-electron process. In contrast, formal oxidative addition of copper to C-sp(2), carbon-... 
CHEMISTRY, MULTIDISCIPLINARY
Journal Article
ACS Catalysis, ISSN 2155-5435, 01/2018, Volume 8, Issue 1, pp. 310 - 313
1,1-Diarylalkanes are important structural frameworks which are widespread in biologically active molecules. Herein, we report a reductive relay cross-coupling... 
alkyl electrophiles | high-valent nickel | 1,1-diarylalkanes | migratory cross-coupling | β-hydride elimination | HALIDES | HYDROCARBONS | NEGISHI ARYLATIONS | UNACTIVATED TERTIARY ALKYL | SECONDARY | CHEMISTRY, PHYSICAL | FUNCTIONALIZATION | beta-hydride elimination | STEREOCENTERS | CARBOXYLATION | REMOTE | ELECTROPHILES
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2016, Volume 22, Issue 36, pp. 12646 - 12650
A practical protocol for a photocatalyzed alkyl‐Heck‐like reaction of unactivated alkyl bromides and different alkenes promoted by dinuclear gold photoredox... 
gold | photoredox catalysis | radicals | alkenes | alkyl halides | HALIDES | EXCITED-STATE | DIFLUOROALKYLATION | PERFLUOROALKYLATION | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | VISIBLE-LIGHT | IODIDES | RADICAL ALKENYLATION | LIGHT PHOTOREDOX CATALYSIS | Catalysis | Organic compounds | Coupling (molecular) | Gold | Hydroxides | Alkenes | Halogens | Bromides | Ethers | Aldehydes
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 09/2018, Volume 13, Issue 17, pp. 2316 - 2332
α‐Carbonyl alkyl bromides are powerful reactive species for the formation of carbon–carbon bonds. Strategies relying on intermolecular C−H functionalization... 
alkenes | enynes | α-carbonyl alkyl bromides | alkynes | coupling reactions
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 09/2018, Volume 13, Issue 17, pp. 2516 - 2521
Regioselective C(2)−H difluoroalkylation of C‐3 unsubstituted indoles with commonly available fluoroalkyl bromides is successfully achieved employing a simple... 
nickel | indoles | fluoroalkylation | regioselective | ROOM-TEMPERATURE | C-H TRIFLUOROETHYLATION | COPPER-MEDIATED DIFLUOROMETHYLATION | OXIDATIVE TRIFLUOROMETHYLATION | ELECTRON-RICH HETEROARENES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ALKYL-HALIDES | ARYL BORONIC ACIDS | LIGHT PHOTOREDOX CATALYSIS | FUNCTIONALIZED DIFLUOROMETHYL BROMIDES | Nickel
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 37, pp. 11207 - 11211
A user‐friendly, nickel‐catalyzed reductive amidation of unactivated primary, secondary, and tertiary alkyl bromides with isocyanates is described. This... 
cross-coupling | nickel | reductive coupling | synthetic methods | HALIDES | CHEMISTRY, MULTIDISCIPLINARY | ALKENES | CROSS-COUPLING REACTIONS | TERTIARY ALKYL | AMINES | OLEFINS | ISOCYANATES | CARBOXYLATION | AMINOCARBONYLATION | AMIDES | Isocyanates | Nickel
Journal Article
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