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Journal of the American Chemical Society, ISSN 0002-7863, 11/2014, Volume 136, Issue 44, pp. 15509 - 15512
Oxidative coupling between C((sp2)))-H bonds and C((sp3)))-H bonds is achieved by the Ni(II)-catalyzed reaction of benzamides containing an 8-aminoquinoline... 
H BOND ACTIVATION | FUNCTIONALIZATION | CATALYZED ORTHO-ARYLATION | FLUOROALKYLATION | C-C | PERFLUOROALKYL IODIDES | CHEMISTRY, MULTIDISCIPLINARY | SIMPLE ARENES | ALKYL-HALIDES
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 01/2014, Volume 136, Issue 3, pp. 898 - 901
The Ni-catalyzed, direct arylation of C(sp(3))-H (methyl and methylene) bonds in aliphatic amides containing an 8-aminoquinoline moiety as a bidentate... 
C(SP)-H BONDS | ACID DERIVATIVES | PALLADIUM | C-H BOND | AROMATIC AMIDES | INTRAMOLECULAR AMINATION | NATURAL-PRODUCTS | UNACTIVATED C(SP)-H | CARBON-HYDROGEN BONDS | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES | Usage | Analysis | Chemical bonds | Amides | Chemical reactions | Nickel | Research
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 12/2014, Volume 79, Issue 24, pp. 11933 - 11939
The Ni(II)-catalyzed direct arylation of C(sp(3))-H (methyl and methylene) bonds in aliphatic amides containing an 8-aminoquinoline moiety as the directing... 
BIDENTATE-CHELATION ASSISTANCE | PALLADIUM | DIRECT ETHYNYLATION | ACTIVATION | NATURAL-PRODUCTS | CHEMISTRY, ORGANIC | CARBON-HYDROGEN BONDS | C-H BONDS | CARBOXYLIC-ACID DERIVATIVES | SIMPLE ARENES | ALKYL-HALIDES | Arylation | Nickel compounds | Chemical reactions | Chemical properties | Catalysis | Research
Journal Article
Chemistry Letters, ISSN 0366-7022, 10/2015, Volume 44, Issue 10, pp. 1365 - 1367
The chelation-assisted cross dehydrogenative coupling of C(sp3)–H bonds is achieved by the Pd(II)-catalyzed reaction of aliphatic amides that contain a... 
Catalytic C-H Activation | DIRECTING GROUPS | FUNCTIONALIZATION | PALLADIUM | ACTIVATION | ARENES | C(SP)-H | CHEMISTRY, MULTIDISCIPLINARY | Chelating | Iodides | Dehydrogenation | Toluene | Amides | Joining | Derivatives | Aliphatic compounds
Journal Article
ACS CATALYSIS, ISSN 2155-5435, 07/2016, Volume 6, Issue 7, pp. 4323 - 4329
The first example of the nickel(II)-catalyzed reaction of amides using inexpensive and milder molecular iodine (I-2) as an iodinating reagent is reported. The... 
nickel | PALLADIUM | ACTIVATION | iodination | CHEMISTRY, PHYSICAL | oxidative cyclization | DIRECT THIOLATION | MOLECULAR I-2 | ALIPHATIC AMIDES | DIRECTING GROUPS | ORTHO-HALOGENATION | C-H activation | ORTHO-BROMINATION | AROMATIC AMIDES | REGIOSELECTIVE HALOGENATION | bidentate directing group
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 12/2014, Volume 79, Issue 24, pp. 11922 - 11932
Arylation via the cleavage of the ortho CH bonds by a nickel-catalyzed reaction of aromatic amides containing an 8-aminoquinoline moiety with aryl iodides is... 
BIDENTATE-CHELATION ASSISTANCE | ALIPHATIC AMIDES | UNACTIVATED C(SP)-H BONDS | ACID-DERIVATIVES | ORTHO AMINATION | NATURAL-PRODUCTS | ARYL HALIDES | RUTHENIUM-CATALYZED CARBONYLATION | CHEMISTRY, ORGANIC | CARBON-HYDROGEN BONDS | ALKYL-HALIDES | Arylation | Aromatic amines | Nickel compounds | Catalysis | Research | Chemical properties | Chemical synthesis
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2016, Volume 22, Issue 4, pp. 1362 - 1367
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2015, Volume 137, Issue 43, pp. 13776 - 13779
Journal Article
Chemical Science, ISSN 2041-6520, 02/2013, Volume 4, Issue 2, pp. 664 - 670
Arylation of ortho C-H bonds is achieved by a ruthenium-catalyzed reaction of aromatic amides having an 8-aminoquinoline moiety with aryl bromides. The... 
FUNCTIONALIZATION | UNACTIVATED C(SP)-H BONDS | C(SP)-H BONDS | PALLADIUM | ACTIVATION | CROSS-COUPLING REACTION | ORTHO-C(SP)-H BONDS | ORGANIC HALIDES | CHEMISTRY, MULTIDISCIPLINARY | CARBOXYLIC-ACID DERIVATIVES | ARYL CHLORIDES | Bromides | Chemical bonds | Electronics | Amides | Aromatic compounds | Functional groups
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2017, Volume 56, Issue 7, pp. 1877 - 1880
Journal Article
Chemical Communications, ISSN 1359-7345, 2016, Volume 52, Issue 66, pp. 10129 - 10132
The cobalt-catalyzed chelation assisted ortho C-H allylation of aromatic amides with unactivated aliphatic alkenes is reported. The reaction proceeds in air... 
FUNCTIONALIZATION | ALLYLIC CARBONATES | NATURAL-PRODUCTS | ALKYLATION | BOND ACTIVATION | NUCLEOPHILIC-ADDITION | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | ALIPHATIC ALKENES | RHODIUM CATALYSIS | MOLECULES | Alkenes | Olefins | Chelation | Amides | Chemical reactions | Tolerances | Allyl compounds | Aliphatic compounds
Journal Article
PHYSICAL REVIEW LETTERS, ISSN 0031-9007, 01/2012, Volume 108, Issue 3
We report the first observations of the spin-singlet bottomonium states h(b)(1P) and h(b)(2P). The states are produced in the reaction e(+)e(-) -->... 
PHYSICS, MULTIDISCIPLINARY
Journal Article
Bulletin of the Chemical Society of Japan, ISSN 0009-2673, 3/2015, Volume 88, Issue 3, pp. 438 - 446
Journal Article
Physical Review Letters, ISSN 0031-9007, 01/2012, Volume 108, Issue 3
We report the first observation of the spin-singlet bottomonium states h_b(1P) and h_b(2P) produced in the reaction e+e- --> hb(nP)pi+pi- using a 121.4fb-1... 
Physics - High Energy Physics - Experiment
Journal Article
PHYSICAL REVIEW LETTERS, ISSN 0031-9007, 12/2012, Volume 109, Issue 23
We report the first evidence for the eta(b)(2S) using the h(b)(2P) -> eta(b)(2S)gamma transition and the first observation of the h(b)(1P) -> eta(b)(1S)gamma... 
PHYSICS, MULTIDISCIPLINARY | ANNIHILATION | QUARK-MODEL | HADRON DECAY PROCESSES
Journal Article
PHYSICAL REVIEW LETTERS, ISSN 0031-9007, 09/2015, Volume 115, Issue 14
Using a sample of 771.6 x 10(6) Upsilon Upsilon(4S) decays collected by the Belle experiment at the KEKB e(+)e(-) collider, we observe, for the first time, the... 
STATES | QCD | SPECTROSCOPY | PHYSICS, MULTIDISCIPLINARY | CHARMONIUM | SHORT-DISTANCE ANALYSIS | HEAVY-QUARK SYSTEMS
Journal Article