X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (11104) 11104
Book Chapter (145) 145
Dissertation (15) 15
Magazine Article (6) 6
Publication (6) 6
Book Review (4) 4
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chemistry, organic (4494) 4494
aryl chlorides (3423) 3423
chemistry, multidisciplinary (3361) 3361
palladium (3114) 3114
catalysis (2413) 2413
aryl halides (1697) 1697
cross-coupling reactions (1663) 1663
chlorides (1564) 1564
halides (1502) 1502
aryl (1444) 1444
chemistry, inorganic & nuclear (1393) 1393
ligands (1376) 1376
complexes (1211) 1211
derivatives (1175) 1175
chemistry (1137) 1137
catalysts (1036) 1036
aromatic compounds (1027) 1027
arylboronic acids (998) 998
bromides (968) 968
cross-coupling (958) 958
arylation (918) 918
chemistry, applied (878) 878
efficient (769) 769
synthesis (735) 735
amination (690) 690
ligand (687) 687
coupling reactions (683) 683
palladium catalysts (676) 676
chemistry, physical (664) 664
activation (645) 645
chemical reactions (637) 637
copper (633) 633
room-temperature (626) 626
organic chemistry (606) 606
molecular structure (584) 584
bond formation (571) 571
heck reaction (565) 565
reagents (548) 548
analysis (534) 534
animals (508) 508
water (504) 504
aryl bromides (496) 496
homogeneous catalysis (495) 495
chemical properties (489) 489
amines (477) 477
nanoparticles (472) 472
nickel (472) 472
cross‐coupling (464) 464
humans (461) 461
chemical synthesis (455) 455
organic-synthesis (450) 450
palladium - chemistry (428) 428
suzuki-miyaura (417) 417
ketones (415) 415
iodides (406) 406
heterocycles (404) 404
reactivity (399) 399
oxidative addition (392) 392
c-c (386) 386
esters (385) 385
boronic acids (381) 381
alkynes (370) 370
palladium complexes (366) 366
acids (359) 359
coupling (358) 358
c-h activation (349) 349
terminal alkynes (348) 348
n-heterocyclic carbenes (345) 345
highly efficient (343) 343
cyclization (341) 341
alkenes (333) 333
cross coupling (333) 333
oxidation (326) 326
c-n (323) 323
research (322) 322
grignard-reagents (320) 320
mechanism (319) 319
functionalization (317) 317
one-pot synthesis (313) 313
cross-coupling reaction (306) 306
efficient synthesis (305) 305
polymer science (303) 303
n-heterocyclic carbene (301) 301
chemical sciences (300) 300
carbon (299) 299
aldehydes (298) 298
alcohols (284) 284
male (283) 283
aryl iodides (277) 277
inhibitors (273) 273
pharmacology & pharmacy (272) 272
heterogeneous catalysis (271) 271
synthetic methods (270) 270
heck (269) 269
suzuki (267) 267
biaryls (262) 262
carbonylation (256) 256
polymers (255) 255
biochemistry & molecular biology (254) 254
amides (250) 250
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (11177) 11177
Japanese (121) 121
Chinese (109) 109
German (53) 53
French (15) 15
Portuguese (8) 8
Russian (6) 6
Turkish (4) 4
Arabic (1) 1
Croatian (1) 1
Norwegian (1) 1
Polish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Angewandte Chemie (International ed.), ISSN 1433-7851, 2016, Volume 55, Issue 47, pp. 14752 - 14755
...‐pipecolinic acid enables the analogous transformation with aryl chlorides. The key advantage of this broadly applicable transformation is the use of an inexpensive... 
ruthenium | aryl halides | benzoic acids | biaryls | C−H arylation | ACTIVATION | FUNCTIONALIZATIONS | STRATEGY | BIARYL COMPOUNDS | BOND FORMATION | C-H arylation | CHEMISTRY, MULTIDISCIPLINARY | DIRECTING GROUPS | CROSS-COUPLING REACTIONS | ORGANIC HALIDES | ALKENYLATION | CARBOXYLIC-ACIDS | Benzoic acid | Amino acids | Dichloropropane | Ruthenium | Chlorides | Transformation | Catalysts | Aromatic compounds | Phosphine | Bromides | Carboxylates
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2019, Volume 58, Issue 19, pp. 6391 - 6395
...‐coupling of primary heteroarylamines and (hetero)aryl chlorides, while sought‐after given the ubiquity of unsymmetrical di(hetero... 
cross-coupling | ligand design | nickel | amination | bisphosphines | ARYLATION | ARYL | LIGAND | CHEMISTRY, MULTIDISCIPLINARY | Nickel | Dichloropropane | Catalysis | Metal catalysts | Chlorides | Coupling (molecular) | Couplings | Catalysts | Aromatic compounds | Pharmacology | Palladium | Substrates | PharmacoPhores
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 05/2016, Volume 138, Issue 19, pp. 6139 - 6142
.... This method allows access to primary, secondary, and tertiary boronic esters from the parent chlorides, which were previously inaccessible as coupling partners... 
HALIDES | PALLADIUM | SUBSTITUTION | REAGENTS | CROSS-COUPLING REACTION | SECONDARY | ALKYLBORONIC ESTERS | ELECTROPHILES | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | ARYL CHLORIDES | Chemical properties | Catalysis | Chemical compounds | Analysis
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2013, Volume 52, Issue 38, pp. 10035 - 10039
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 2016, Volume 358, Issue 23, pp. 3700 - 3705
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 03/2015, Volume 357, Issue 5, pp. 907 - 911
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2018, Volume 57, Issue 51, pp. 16871 - 16876
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2016, Volume 55, Issue 21, pp. 6211 - 6215
Couplings between (hetero)aryl chlorides and phenols can be effectively promoted by CuI in combination with an N‐aryl‐N′‐alkyl... 
cross-coupling | copper | ligand screen | (hetero)aryl chlorides | biaryl ethers | HALIDES | PALLADIUM | C-O BOND | ARYLATION | CHEMISTRY, MULTIDISCIPLINARY | MILD | VERSATILE | PRODUCTS | LIGAND | EFFICIENT | ARYL CHLORIDES | Phenols | Chlorides | Dichloropropane | Substitutes | Couplings | Aromatic compounds | Ligands | Electrons
Journal Article
Chemistry, an Asian journal, ISSN 1861-4728, 2018, Volume 13, Issue 17, pp. 2543 - 2548
A sulfonylation of benzylic C−H bonds of aryl(o‐tolyl)methanones with arylsulfonyl hydrazides or arylsulfonyl chlorides has been developed... 
radical reactions | reaction mechanisms | UV irradiation | sulfonylation | synthetic methods | PHOTOCHEMICAL GENERATION | INSERTION | SULFUR-DIOXIDE | ARYL SULFONES | CHEMISTRY, MULTIDISCIPLINARY | SULFINIC ACIDS | RADICAL CYCLIZATION | LIGHT PHOTOREDOX CATALYSIS | SELECTIVE SYNTHESIS | MULTICOMPONENT REACTION | O-QUINODIMETHANES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 08/2017, Volume 359, Issue 16, pp. 2890 - 2894
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2017, Volume 56, Issue 49, pp. 15693 - 15697
.... A dual catalytic cycle merging retro‐hydrocyanation and cross‐coupling enables the conversion of a broad array of aryl chlorides and aryl/vinyl triflates into their corresponding nitriles... 
cross-coupling | aryl chlorides | cyanation | aryl triflate | retro-hydrocyanation | HALIDES | PALLADIUM | COMPLEXES | CONVENIENT | ALKYNES | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | MILD | SHUTTLE CATALYSIS | NITRILES | CYANIDE | Nitriles | Nickel | Dichloropropane | Chlorides | Cyanide | Salts | Cross coupling | Halides | Aromatic compounds | Cyanides | Catalytic converters
Journal Article