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alkenylation (339) 339
catalysis (101) 101
science & technology (87) 87
chemistry (86) 86
physical sciences (84) 84
palladium (75) 75
alkenylierung (48) 48
c-h activation (48) 48
arylation (46) 46
alkenes (45) 45
alkylation (44) 44
aromatic compounds (37) 37
organic chemistry (34) 34
alkynes (32) 32
rhodium (32) 32
catalysts (30) 30
chemistry, physical (29) 29
c–h activation (29) 29
functionalisation (29) 29
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chemistry, multidisciplinary (28) 28
c−h activation (27) 27
alkene (25) 25
chemistry, organic (24) 24
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indoles (23) 23
ch activation (22) 22
ruthenium (22) 22
chemical reactions (21) 21
katalyse (21) 21
regioselectivity (21) 21
activation (19) 19
alkynylation (19) 19
amides (19) 19
cobalt (19) 19
cross-coupling (19) 19
olefins (19) 19
functional groups (18) 18
heterocycles (18) 18
indole (18) 18
ligands (18) 18
selectivity (18) 18
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alkine (15) 15
copper (15) 15
nitrogen heterocycles (15) 15
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chemical synthesis (14) 14
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homogeneous catalysis (13) 13
oxidant (13) 13
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aldehydes (12) 12
chemical sciences (12) 12
c–h functionalization (12) 12
esters (12) 12
ketones (12) 12
regioselektivität (12) 12
transition metals (12) 12
c-h functionalization (11) 11
dehydrogenation (11) 11
heterogeneous catalysis (11) 11
palladium catalysis (11) 11
reaction-condition (11) 11
reaktionsbedingung (11) 11
amide (10) 10
bonding (10) 10
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hydrogen bonds (10) 10
indol (10) 10
iron (10) 10
letter (10) 10
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reaction-mechanism (10) 10
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acetates (9) 9
amination (9) 9
asymmetric catalysis (9) 9
boron (9) 9
life sciences & biomedicine (9) 9
organocatalysis (9) 9
oxidation (9) 9
phenols (9) 9
pyridine (9) 9
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[chim]chemical sciences (8) 8
carbonylation (8) 8
coupling (8) 8
halides (8) 8
molecular structure (8) 8
organic compounds (8) 8
oxygen (8) 8
quinoline (8) 8
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acids (7) 7
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Chemical science (Cambridge), ISSN 2041-6520, 2013, Volume 4, Issue 3, pp. 886 - 896
Significant progress has been accomplished in direct olefinations through twofold C-H bond functionalization of arenes and heteroarenes employing readily... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Ruthenium | Catalysis | Catalysts | Styrenes | Bonding | Decoration
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 03/2010, Volume 49, Issue 12, pp. 2202 - 2205
Breaking the Si‐lence: The direct cross‐coupling of heteroarenes with aryl‐ or alkenylsilanes proceeds efficiently, in the presence of a nickel catalyst, to... 
alkenylation | silanes | nickel | heterocycles | arylation | Silanes | Arylation | Heterocycles | Nickel | Alkenylation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2012, Volume 51, Issue 15, pp. 3638 - 3641
Ni made it! A novel Heck‐type reaction of secondary and tertiary α‐carbonyl alkyl bromides, most likely involving a radical process, was achieved through the... 
α alkenylation | Heck reaction | radical reactions | nickel | alkyl bromides | α alkenylation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 18, pp. 5091 - 5095
A hydroxy group chelation-assisted stereospecific oxidative cross-coupling reaction between alkenes was developed under mild reaction conditions. In the... 
alkenylation | cross-coupling | palladium | C−H activation
Journal Article
Catalysis science & technology, ISSN 2044-4753, 2013, Volume 3, Issue 3, pp. 562 - 571
Significant progress has been accomplished in direct C-H bond arylations of arenes and heteroarenes with readily accessible, inexpensive phenol derivatives.... 
Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2015, Volume 71, Issue 26-27, pp. 4552 - 4556
The utility of Cp∗Co(III)-catalysts was expanded to oxidative C–C bond-forming reaction. In situ-generated Cp∗Co(III)-catalyst, rather than a preformed... 
C–H activation | Oxidation | Catalysis | Cobalt | Alkenylation | C-H activation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2011, Volume 50, Issue 22, pp. 5192 - 5196
Hats off to the director: High levels of regio‐ and stereoselectivity were observed for a broad range of amine substrates with aryl and vinyl iodide coupling... 
alkenylation | CH activation | palladium | directing groups | arylation | C-H activation
Journal Article
ACS catalysis, ISSN 2155-5435, 2015, Volume 5, Issue 5, pp. 2822 - 2825
Isoindolinone derivatives were prepared in a step-economical fashion by a C–H/N–H functionalization process with a catalytic system composed of Co­(OAc)2 and... 
alkenylation | cobalt | C-H activation | mechanism | oxidative annulation | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2009, Volume 48, Issue 35, pp. 6511 - 6515
Easy on, easy off: The N‐(2‐pyridyl)sulfonyl group controls the direct PdII‐catalyzed alkenylation of indoles, affording the corresponding products in good... 
alkenylation | CH activation | palladium | sulfonyl protecting groups | heterocycles | C.-h. Activation | Heterocycles | Palladium | Alkenylation | Sulfonyl protecting groups
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 12/2018, Volume 140, Issue 48, pp. 16387 - 16391
Unprecedented hydroxy-alkynylation and -alkenylation reactions of arylalkenes have been developed through electrochemically enabled addition of an... 
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2010, Volume 49, Issue 33, pp. 5792 - 5797
A highly regioselective direct cross‐coupling of internal alkenes of α‐oxoketene dithioacetals with terminal alkenes has been successfully realized by... 
alkenylation | CH activation | palladium | alkenes | heterocycles | Heterocycles | Palladium | C-H activation | Alkenes | Alkenylation
Journal Article
European journal of organic chemistry, ISSN 1434-193X, 07/2020, Volume 2020, Issue 35, pp. 5729 - 5734
We have developed a Pd(II) catalyzed direct modification of dihydropyrrolo[2,1‐a]isoquinoline derivatives with various alkenes including acrylates, acrylamide,... 
Heterocycles | Palladium | Oxidative coupling | Alkenylation | Dihydroisoquinoline
Journal Article