X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
alkenylation (1192) 1192
chemistry, organic (962) 962
chemistry, multidisciplinary (652) 652
catalysis (493) 493
functionalization (449) 449
activation (446) 446
palladium (337) 337
c-h activation (333) 333
arylation (305) 305
derivatives (301) 301
index medicus (272) 272
alkylation (249) 249
alkenes (246) 246
alkynes (240) 240
arenes (239) 239
direct arylation (228) 228
indoles (186) 186
bond activation (170) 170
olefination (169) 169
molecular structure (160) 160
cyclization (148) 148
heterocycles (147) 147
olefins (147) 147
cross-coupling reactions (138) 138
c-h functionalization (137) 137
c-h bonds (127) 127
rhodium (118) 118
selective alkenylation (114) 114
complexes (108) 108
halides (105) 105
aldehydes (104) 104
chemistry, applied (104) 104
stereoisomerism (100) 100
synthesis (99) 99
carbon-hydrogen bonds (98) 98
ketones (98) 98
room-temperature (98) 98
chemical properties (97) 97
chemistry (97) 97
organic-synthesis (97) 97
bond formation (95) 95
catalysts (94) 94
ligands (94) 94
aromatic compounds (92) 92
organic chemistry (88) 88
palladium - chemistry (88) 88
directing group (86) 86
ortho-alkenylation (86) 86
hydroarylation (85) 85
ruthenium (82) 82
copper (81) 81
efficient synthesis (81) 81
h bond activation (81) 81
funktionalisierung (80) 80
aryl (79) 79
functionalisation (79) 79
regioselectivity (79) 79
chemistry, physical (78) 78
chemical reactions (75) 75
annulation (74) 74
alkenes - chemistry (73) 73
analysis (73) 73
cleavage (72) 72
coupling reactions (72) 72
heck reaction (69) 69
nickel (68) 68
oxidation (68) 68
pyridine (68) 68
cross-coupling (67) 67
friedel-crafts alkenylation (67) 67
c-h bond (66) 66
efficient (66) 66
coupling reaction (64) 64
alkene (62) 62
bond functionalization (62) 62
esters (62) 62
mechanism (62) 62
carboxylic-acids (60) 60
reagents (60) 60
amides (58) 58
one-pot synthesis (58) 58
terminal alkynes (58) 58
chemical synthesis (57) 57
c–h activation (57) 57
chemistry, inorganic & nuclear (56) 56
grignard-reagents (56) 56
stereoselective-synthesis (56) 56
alkynylation (55) 55
bromides (55) 55
homogeneous catalysis (53) 53
katalyse (53) 53
c−h activation (52) 52
alcohols (51) 51
directing groups (51) 51
internal alkynes (51) 51
selectivity (51) 51
oxidation-reduction (50) 50
pyridines (50) 50
acids (49) 49
article (49) 49
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1805) 1805
Chinese (18) 18
Japanese (9) 9
German (3) 3
Korean (2) 2
Czech (1) 1
French (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Tetrahedron, ISSN 0040-4020, 07/2018, Volume 74, Issue 29, pp. 3947 - 3954
The dual role of the (2-pyridyl)sulfonyl unit as directing functionality and readily removable -protecting group has enabled an efficient and practical... 
Benzopyrrolizidine | Benzazepinone | Heterocycles | Pyridine directing group | Palladium | C[sbnd]H alkenylation | Pyrrolidine | C–H alkenylation | ACTIVATION | LATE-STAGE DIVERSIFICATION | ARYLATION | C-H OLEFINATION | INDOLINES | CHEMISTRY, ORGANIC | INDOLES | DIRECTING GROUPS | FUNCTIONALIZATION | C-H alkenylation | BONDS | ALKENYLATION | Pyridine
Journal Article
by Liu, WJ and Wang, SH and Zhang, Q and Yu, JW and Li, JH and Xie, ZW and Cao, H
CHEMISTRY-AN ASIAN JOURNAL, ISSN 1861-4728, 09/2014, Volume 9, Issue 9, pp. 2436 - 2439
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 12/2018, Volume 59, Issue 52, pp. 4562 - 4565
The treatment of bromo homoallyl pyrrolyl/indolyl ketone derivatives with Pd(OAc) in the presence of PPh and Cs CO in DMF resulted in the formation of... 
Palladium | C[sbnd]H alkenylation | Tetrahydrocarbazolone | Tetrahydroindolone | C–H alkenylation | FUNCTIONALIZATION | C-H alkenylation | ENANTIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | ALLYLIC DEAROMATIZATION | DERIVATIVES | INDOLES | SPIRO | HYDROARYLATION | Acetates
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2014, Volume 20, Issue 17, pp. 4896 - 4900
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2018, Volume 360, Issue 20, pp. 3820 - 3820
The inside cover picture , provided by Cirujano and co‐workers, illustrates the results of their work on recycling catalytic amounts of Pd(OAc) 2 in the... 
Palladium | MOFs | Uracil | Alkenylation | Indole
Journal Article
Chemical Communications, ISSN 1359-7345, 8/2017, Volume 53, Issue 64, pp. 8931 - 8947
The transition-metal-catalyzed chelation-assisted alkenylation at the inert C-H bond of aromatics with alkenes is one of the efficient methods to synthesize... 
DIRECT ORTHO-ALKENYLATION | DIRECTING GROUP | ASYMMETRIC 1,4-ADDITION | RUTHENIUM-CATALYZED CYCLIZATION | COUPLING REACTION | BOND ACTIVATION | ARYL KETONES | INTERNAL ALKYNES | HECK REACTION | CHEMISTRY, MULTIDISCIPLINARY | OXIDATIVE ALKENYLATION
Journal Article
Angewandte Chemie - International Edition, 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
Angewandte Chemie - International Edition, ISSN 1433-7851, 04/2012, Volume 51, Issue 15, pp. 3638 - 3641
Journal Article
ACS Catalysis, ISSN 2155-5435, 01/2019, Volume 9, Issue 1, pp. 431 - 441
Nickel-catalyzed regioselective C-H bond alkenylation of indoles and related heteroarenes with alkenyl bromides is accomplished under relatively mild... 
alkenylation | nickel | single-electron transfer | indoles | C-H activation | mechanism | DIRECT C2-OLEFINATION | NATURAL-PRODUCTS | BOND FUNCTIONALIZATIONS | CHEMISTRY, PHYSICAL | C-2 ALKENYLATION | SELECTIVE ALKENYLATION | TRANSITION-METALS | CARBON-HYDROGEN | DIRECT ALKYLATION | EFFICIENT ACCESS | COUPLING REACTIONS
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2013, Volume 2013, Issue 10, pp. 1950 - 1962
Two pathways that can be used to access ortho ‐olefinated phenol carbamate, including a ruthenium(II)‐catalyzed oxidative olefination of phenol carbamate with... 
C‐H activation | Ruthenium | Rhodium | Olefination | Protecting groups | C-H activation | ROOM-TEMPERATURE | ACTIVATION | ARENES | CHEMISTRY, ORGANIC | CIS-ADDITION | SELECTIVE ALKENYLATION | ALKYNES | ALKENES | CATALYZED ALKENYLATION | DERIVATIVES | OXIDATIVE ALKENYLATION | Carbamates | Phenols | Acrylates
Journal Article
Tetrahedron, ISSN 0040-4020, 09/2019, Volume 75, Issue 39, p. 130534
A novel method for the synthesis of -amino alkenyl-substituted hydrazone derivatives was disclosed through silver-catalyzed reaction of sulfonyl hydrazones... 
Ynamide | Enamide | Silver catalysis | Hydrazone | Alkenylation
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
Tetrahedron Letters, ISSN 0040-4039, 11/2013, Volume 54, Issue 48, pp. 6507 - 6510
An efficient Fe(acac) -catalyzed decarboxylative C(sp )-C(sp ) coupling reaction via oxidation of C-H bond adjacent to an oxygen atom has been developed... 
Fe(acac) | Decarboxylative | Oxidation | Coupling | Alkenylation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 8, pp. 2418 - 2422
Both E ‐ and Z ‐ N ′‐alkenyl urea derivatives of imidazolidinones may be formed selectively from enantiopure α‐amino acids. Generation of their enolate... 
α-alkenylation | stereodivergence | quaternary amino acids | DFT calculations | rearrangement | ENANTIOSELECTIVE SYNTHESIS | ALKYLATION | ARYLATION | CHEMISTRY, MULTIDISCIPLINARY | MICHAEL ADDITION | VINYL | alpha-alkenylation | INHIBITORS | METHIONINE | Geometry | Urea | Quaternary | Migration | Absolute configuration | Amino acids | Derivatives
Journal Article
by Wang, H and Fu, WQ and Zhang, L and Shen, RS and Cai, GR and Chen, Q and Tang, TD
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, ISSN 0888-5885, 05/2019, Volume 58, Issue 17, pp. 7014 - 7024
Development of a high-efficiency heterogeneous catalyst for modern organic synthesis is greatly important. Herein, a nanosized ETS-10 zeolite (ETS-10-N) with... 
ENGINEERING, CHEMICAL | SELECTIVITY | ZEOLITE | ALKENYLATION | CARBOXYLIC-ACIDS
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.