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carboxylic amides (2275) 2275
amide formation (468) 468
catalysis, phase‐transfer catalysis (310) 310
amides (307) 307
amines (290) 290
carboxylic acid esters (282) 282
catalysis (246) 246
diastereoselective syntheses, enantioselective syntheses (175) 175
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carboxylic acids (142) 142
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amination, n‐alkylation, n‐arylation (122) 122
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index medicus (65) 65
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alkylation, arylation, dealkylation, dearylation, c‐acylation, olefination (61) 61
e/z‐selectivity (59) 59
furan derivatives (58) 58
hydroxycarboxylic acids (56) 56
cleavage reactions, decomposition reactions, pyrolysis (55) 55
palladium (55) 55
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reduction, hydrogenation (54) 54
alcohols (53) 53
acids (51) 51
copper (51) 51
microwave chemistry, sonochemistry, mechanochemistry (51) 51
aldehydes (50) 50
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aminocarboxylic acids and esters (48) 48
organic chemistry (48) 48
photochemistry, radiation chemistry, chemoluminescence (48) 48
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enantiomers (45) 45
reactions of organo‐metal compounds (45) 45
carbonylation (43) 43
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olefins (42) 42
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pharmacology, medicinal chemistry, vaccines, serums (41) 41
chemistry (40) 40
thio compounds (39) 39
indole derivatives, isoindole derivatives (37) 37
dehydrogenation (36) 36
organic compounds (36) 36
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carboxylic acid derivatives (35) 35
ring opening reactions (35) 35
sulfonamides (34) 34
biochemical syntheses, microbiological syntheses (33) 33
multi‐membered n‐heterocycles (33) 33
oxazole derivatives (33) 33
synthesis (33) 33
urea derivatives (33) 33
esterification, transesterification (32) 32
pyridine (31) 31
carboxylic acids - chemistry (30) 30
chemical reactions (30) 30
hydration (30) 30
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carbonsäuren (29) 29
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alkynes (27) 27
hydroxycarboxylic acids and esters (27) 27
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intermediates (26) 26
chemical synthesis (25) 25
acylation (24) 24
benzene (24) 24
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ethers (24) 24
mercaptans, thioethers (24) 24
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Angewandte Chemie International Edition, ISSN 1433-7851, 09/2017, Volume 56, Issue 38, pp. 11545 - 11548
The first highly enantioselective iridium‐catalyzed allylic alkylation that provides access to products bearing an allylic all‐carbon quaternary stereogenic... 
iridium | quaternary stereocenter | carboxylic acid derivatives | allylic alkylation | umpolung | SUBSTITUTION | REAGENTS | CHEMISTRY, MULTIDISCIPLINARY | CARBON STEREOGENIC CENTERS | DIASTEREO | ORIGINS | STEREOCENTERS | CONSTRUCTION | ESTERS | REGIO | ARYL
Journal Article
Angewandte Chemie, ISSN 0044-8249, 09/2017, Volume 129, Issue 38, pp. 11703 - 11706
The first highly enantioselective iridium‐catalyzed allylic alkylation that provides access to products bearing an allylic all‐carbon quaternary stereogenic... 
Allylische Alkylierungen | Umpolung | Iridium | Quartäre Stereozentren | Carbonsäurederivate | Stereoisomerism | Carboxylic Acids - chemical synthesis | Carboxylic Acids - chemistry | Allyl Compounds - chemistry | Molecular Structure | Catalysis | Iridium - chemistry | Alkylation
Journal Article
ChemInform, ISSN 0931-7597, 03/2016, Volume 47, Issue 13, pp. no - no
Nitration of alkenes (II) and (VII) with LiNO3/TFAA in nitrile solvents provides N‐(β‐nitroalkyl)amides, which undergo Michael addition to acceptors (V). 
carboxylic amides (benzene compounds) | amide formation | nitro compounds (benzene compounds) | nitro compounds (acyclic compounds) | carboxylic amides (acyclic compounds) | nitration | Nitration | Amides
Journal Article
Journal Article
Synthesis, ISSN 0039-7881, 1993, Volume 1993, Issue 12, pp. 1271 - 1290
It is now well established that lithium enolates and analogous derivatives generally exist as complex structures held together by noncovalent bonds... 
feature article | PALYTOXIN CARBOXYLIC-ACID | ACYCLIC STEREOSELECTION | ALPHA-SUBSTITUTED ALKANONES | DIELS-ALDER REACTIONS | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | NUCLEAR MAGNETIC-RESONANCE | 2,3-DISUBSTITUTED 4-NITROKETONES | ORTHO-METALATION | ASYMMETRIC TOTAL SYNTHESIS | POLYSUBSTITUTED AROMATICS
Journal Article
ChemInform, ISSN 0931-7597, 05/2015, Volume 46, Issue 21, pp. no - no
On‐off switchable acyl donors in the form of dihydropyridine alkyl and arylamides are reacting with various primary and secondary aryl, benzyl, and alkyl... 
amines (acyclic compounds) | ketones (benzene compounds) | carboxylic acid esters (acyclic compounds) | mercaptans, thioethers (acyclic compounds) | ketones (acyclic compounds) | Sulfur compounds | Amides | Ketones | Organic compounds
Journal Article
ChemInform, ISSN 0931-7597, 10/2013, Volume 44, Issue 44, pp. no - no
Copper‐catalyzed cross‐coupling reactions of secondary amides with alkyl 2‐iodobenzoates give hindered tertiary amides. 
carboxylic amides (benzene compounds) | amination, N‐alkylation, N‐arylation | catalysis, phase‐transfer catalysis | Copper | Amides
Journal Article
ChemInform, ISSN 0931-7597, 12/2013, Volume 44, Issue 52, pp. no - no
The N‐cyclopropylation of aromatic and aliphatic secondary amines (I), known as poor nucleophiles, is accomplished using a simple and inexpensive copper system. 
carboxylic amides (benzene compounds) | cyclopropane derivatives | amination, N‐alkylation, N‐arylation | Amides | Cyclopropane compounds
Journal Article
ChemInform, ISSN 0931-7597, 11/2013, Volume 44, Issue 45, pp. no - no
Depending on the nature of the amide, diethylzinc‐mediated additions of 2,2‐dibromo‐2‐fluoroacetamides to aldehydes, ketones or imine afford selective access... 
carboxylic amides (acyclic compounds) | halogen compounds (acyclic compounds) | addition reactions
Journal Article
ChemInform, ISSN 0931-7597, 11/2016, Volume 47, Issue 48, pp. no - no
A novel zinc‐catalyzed oxidative reaction of ynamides with phenols, thiophenols, and anilines allows the access to various α‐substituted amides. 
carboxylic amides (benzene compounds) | amide formation | catalysis, phase‐transfer catalysis | carboxylic amides (acyclic compounds)
Journal Article
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