X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (15188) 15188
Publication (164) 164
Book Review (64) 64
Book Chapter (46) 46
Dissertation (27) 27
Conference Proceeding (5) 5
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
alkylation, arylation, dealkylation, dearylation, c‐acylation, olefination (10431) 10431
olefination (3012) 3012
stereochemistry (2083) 2083
chemistry, organic (2069) 2069
chemistry, multidisciplinary (950) 950
catalysis, phase‐transfer catalysis (885) 885
ring closure reactions (756) 756
ketones (735) 735
carboxylic acid esters (699) 699
alcohols (644) 644
catalysis (635) 635
aldehydes (577) 577
alkenes (569) 569
reactions of organo‐metal compounds (536) 536
derivatives (534) 534
pyridine derivatives (479) 479
cyclohexane derivatives (463) 463
palladium (459) 459
index medicus (440) 440
activation (437) 437
furan derivatives (407) 407
amines (360) 360
functionalization (352) 352
organic chemistry, review (352) 352
amino acids, peptides (332) 332
pyrrole derivatives (322) 322
carbohydrates (315) 315
stereoselective-synthesis (314) 314
polyphenylalkene derivatives (310) 310
hydrocarbons (304) 304
arylation (303) 303
chemistry (292) 292
synthesis (287) 287
esters (274) 274
nitriles (272) 272
wittig olefination (272) 272
reduction, hydrogenation (257) 257
indole derivatives, isoindole derivatives (256) 256
molecular structure (254) 254
c-h activation (244) 244
halogen compounds (241) 241
pharmacology, medicinal chemistry, vaccines, serums (241) 241
cyclopentane derivatives (236) 236
arenes (228) 228
carbonyl-compounds (225) 225
e/z‐selectivity (218) 218
stereoisomerism (218) 218
polyphenyl derivatives (212) 212
organic-synthesis (207) 207
alkaloids (205) 205
thiophene derivatives (203) 203
substitution reactions (200) 200
cyclization (197) 197
alkynes (194) 194
olefins (190) 190
rearrangements (184) 184
mechanism (183) 183
alkenylation (182) 182
fused pyridine derivatives (177) 177
addition reactions (176) 176
cleavage reactions, decomposition reactions, pyrolysis (175) 175
terpenes (172) 172
alkylation (170) 170
organic chemistry (170) 170
chemistry, inorganic & nuclear (168) 168
efficient (167) 167
antibiotics (164) 164
reagents (158) 158
enantioselective synthesis (153) 153
imidazole derivatives (153) 153
bond activation (152) 152
rhodium (152) 152
carboxylic amides (149) 149
chemical properties (149) 149
c‐c bond formation (146) 146
oxidation, dehydrogenation, ozonolysis (145) 145
polyphenylalkane derivatives (145) 145
efficient synthesis (143) 143
quinoline derivatives (143) 143
acid (141) 141
acids (140) 140
benzopyran derivatives (140) 140
direct arylation (140) 140
letter (140) 140
ethers (139) 139
organo‐silicon compounds, acyclic c derivatives (138) 138
oxazole derivatives (138) 138
pyran derivatives (138) 138
diphenylmethane derivatives (137) 137
oxidation (137) 137
alkenes - chemistry (134) 134
cycloaddition reactions (134) 134
intermediates (133) 133
chemistry, physical (132) 132
cross-coupling reactions (132) 132
chemistry, applied (131) 131
carboxylic-acids (130) 130
complexes (129) 129
photochemistry, radiation chemistry, chemoluminescence (128) 128
catalysts (127) 127
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (15168) 15168
Japanese (50) 50
Chinese (37) 37
French (23) 23
German (23) 23
Russian (4) 4
Czech (1) 1
Dutch (1) 1
Hungarian (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Angewandte Chemie International Edition, ISSN 1433-7851, 02/2011, Volume 50, Issue 5, pp. 1064 - 1067
A good neighborhood! The metal‐catalyzed oxidative CH functionalization of electron‐rich arenes is well‐established, but analogous reactions of electron‐poor... 
Heck reaction | stilbenes | amination | olefination | rhodium | ROOM-TEMPERATURE | ACTIVATION | DIRECT ARYLATION | PD(II)-CATALYZED OLEFINATION | AROMATIC KETONES | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | FUNCTIONALIZATION | ARYL KETONES | BENZOIC-ACIDS
Journal Article
Helvetica Chimica Acta, ISSN 0018-019X, 05/2015, Volume 98, Issue 5, pp. 650 - 656
Journal Article
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, ISSN 1433-7851, 07/2018, Volume 57, Issue 29, pp. 9131 - 9135
Catalysis with earth-abundant transition metals is an option to help save our rare noble-metal resources and is especially interesting when novel reactivity or... 
METHANOL | ALPHA-OLEFINATION | NOBEL LECTURE | SUSTAINABLE SYNTHESIS | TRANSFER HYDROGENATION | alcohols | N-heteroarenes | manganese | CHEMISTRY, MULTIDISCIPLINARY | KETONES | COUPLING REACTIONS | AMINES | PNP PINCER COMPLEXES | dehydrogenation | EFFICIENT | olefination | Dehydrogenation | Cobalt | Alcohols
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2014, Volume 136, Issue 39, pp. 13602 - 13605
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki–Heck reaction) is one of the most popular reactions for synthesizing complex organic... 
BIDENTATE-CHELATION ASSISTANCE | OXIDATIVE OLEFINATION | ACID-DERIVATIVES | OXIDIZING DIRECTING GROUP | CROSS-COUPLING REACTIONS | DIRECT ARYLATION | CONJUGATED POLYMERS | PD(II)-CATALYZED OLEFINATION | CARBON-HYDROGEN BONDS | HECK REACTION | CHEMISTRY, MULTIDISCIPLINARY | Palladium | Chemical properties | Hydrogen | Carbon compounds
Journal Article
ACS Catalysis, ISSN 2155-5435, 03/2018, Volume 8, Issue 3, pp. 2473 - 2478
Ruthenium­(II) pincer-catalyzed α-olefination of nitriles is reported. This simple protocol provides a transformation for the catalytic synthesis of... 
acceptorless dehydrogenation | ruthenium | alcohols | nitriles | α-olefination | green synthesis | BORROWING HYDROGEN | ALKYLATION | CHEMISTRY, PHYSICAL | TERMINAL ALKYNES | METAL-LIGAND COOPERATION | CARBONYL OLEFINATION | H-2 | alpha-olefination | COUPLING REACTIONS | PINCER COMPLEXES | ALPHA,BETA-UNSATURATED NITRILES
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 12/2013, Volume 54, Issue 50, pp. 6871 - 6873
In the olefination reaction of ester carbonyl with ynolate, an α-hetero (N, O, S)-substituent on the substrates was found to markedly improve the yields of... 
Polar Felkin–Anh | Olefination | Ynolate | Tetrasubstituted olefin | Polar Felkin-Anh | STEREOSELECTIVE OLEFINATION | KETONES | ENOL ETHERS | SELECTIVE OLEFINATION | CONSTRUCTION | CHEMISTRY, ORGANIC | Tetrasubstituted Olefin | TORQUOSELECTIVE OLEFINATION | TETRASUBSTITUTED OLEFINS
Journal Article
by Yang, X and Sun, R and Zhang, CC and Zheng, XL and Yuan, ML and Fu, HY and Li, RX and Chen, H
ORGANIC LETTERS, ISSN 1523-7060, 02/2019, Volume 21, Issue 4, pp. 1002 - 1006
The first iridium-catalyzed oxidative alkeynylation of benzylamines with acrylates enabled by a new directing group pentafluorobenzoyl has been developed. The... 
OXIDATIVE OLEFINATION | FUNCTIONALIZATION | ACTIVATION | SELECTIVE OLEFINATION | ARYLATION | CHEMISTRY, ORGANIC | SWITCH | AROMATIC-SUBSTITUTION | ANILIDES | DERIVATIVES | HYDROARYLATION
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 05/2012, Volume 41, Issue 9, pp. 3651 - 3678
Rhodium(III)-catalyzed direct functionalization of C-H bonds under oxidative conditions leading to C-C, C-N, and C-O bond formation is reviewed. Various arene... 
FUNCTIONALIZATION | RHODIUM | OLEFINATION | COUPLING REACTIONS | INTERNAL ALKYNES | INTRAMOLECULAR ALKANE ARYLATION | CLEAVAGE | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | BENZOIC-ACIDS
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 9/2014, Volume 43, Issue 2, pp. 696 - 6919
The use of coordinating moieties as directing groups for the functionalisation of aromatic carbon-hydrogen (C-H) bonds has become an efficient strategy for the... 
ORTHO-HALOGENATION | ACTIVATION | AMINATION | OLEFINATION | ACID | ARYLATION | BOND FORMATION | ORTHO-TRIFLUOROMETHYLATION | ALKYNYLATION | CHEMISTRY, MULTIDISCIPLINARY | ALKYL-HALIDES
Journal Article
Chemical Science, ISSN 2041-6520, 03/2015, Volume 6, Issue 3, pp. 1923 - 1927
The oxidative olefination of a broad array of arenes and heteroarenes with a variety of activated and unactivated olefins has be achieved via a... 
OXIDATIVE OLEFINATION | ELECTRON | PD(II)-CATALYZED OLEFINATION | CATALYZED OXIDATION | COMPLEXES | DEHYDROGENATIVE HECK REACTIONS | BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | CYCLIZATION | MOLECULAR-OXYGEN
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 04/2012, Volume 10, Issue 14, pp. 2862 - 2869
Carbonyl compounds react with organozinc reagents in the presence of diphenyl phosphite to give the corresponding olefins. Avariety of 1,3-dienes and... 
COUPLING REACTIONS | SELECTIVE OLEFINATION | PORPHYRIN-CATALYZED OLEFINATION | EFFICIENT SYNTHESIS | WITTIG OLEFINATION | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | PHOSPHORUS YLIDES | ALDEHYDE-OLEFINATION | CARBENE COMPLEXES | ETHYL DIAZOACETATE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2012, Volume 51, Issue 29, pp. 7242 - 7245
Journal Article
Angewandte Chemie International Edition in English, ISSN 0570-0833, 09/1995, Volume 34, Issue 17, pp. 1844 - 1848
The catalytic CC coupling of chloroarenes by both the Heck and the Suzuki reactions has been achieved for the first time with new palladacycles of type 1, in... 
Heck olefination | catalysis | palladacycles | Palladacycles | Catalysis
Journal Article
Synthesis, ISSN 0039-7881, 09/2014, Volume 46, Issue 17, pp. 2353 - 2361
Abstract A one-pot procedure for the synthesis of trisubstituted alkenes from N -tosylhydrazones and alcohols is reported. This procedure combines the aerobic... 
paper | Wittig reaction | alkenes | diazo compounds | hydrazones | olefination | ENANTIOSELECTIVE SYNTHESIS | SELECTIVE OLEFINATION | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | PHOSPHORUS YLIDES | ETHYL DIAZOACETATE | GENERATED DIAZO-COMPOUNDS | PORPHYRIN-CATALYZED OLEFINATION | ALDEHYDE-OLEFINATION | STEREOSELECTIVE-SYNTHESIS | EPOXIDATION-ISOMERIZATION
Journal Article
Organic Letters, ISSN 1523-7060, 03/2016, Volume 18, Issue 5, pp. 900 - 903
A previously unexplored palladium-catalyzed C-3 selective alkenylation of 7-azaindoles, performed in the presence of Pd­(OAc)2 as the catalyst, PPh3 as the... 
DIRECTING GROUP | ACTIVATION | FUNCTIONALIZED CARBAZOLES | PALLADIUM-CATALYZED OLEFINATION | C-H OLEFINATION | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | HECK REACTIONS | KINASE INHIBITORS | FUJIWARA-MORITANI REACTION | INDOLES
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 09/2019, Volume 60, Issue 37, p. 151027
[Display omitted] •An efficient approach for synthesis of Balticolid is reported.•The synthesis was accomplished from the known and Cost-effective starting... 
12-Membered macrolides | Wittig olefination | Yamaguchi macrolactonization | Sharpless asymmetric epoxidation | 12-MEMBERED MACROLIDE | FUNGUS | Wittg olefination | CHEMISTRY, ORGANIC | (+)-PATULOLIDE C
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2014, Volume 79, Issue 17, pp. 8278 - 8287
Rh(III)-catalyzed ortho C–H olefination of aryl sulfonamide directed by the SO2NHAc group is reported. This oxidative coupling process is achieved highly... 
ALKENES | RHODIUM(III)-CATALYZED OXIDATIVE OLEFINATION | LATE-STAGE DIVERSIFICATION | SELECTIVE OLEFINATION | COUPLING REACTION | ARENES | CHEMISTRY, ORGANIC | RUTHENIUM | CLEAVAGE | ALKYNES | ORTHO-ALKENYLATION | Chemical properties | Hydrogen | Carbon compounds | Olefins | Analysis
Journal Article