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chemistry, organic (305) 305
trifluoromethylthiolation (262) 262
chemistry, multidisciplinary (165) 165
fluorine (155) 155
oxidative trifluoromethylthiolation (128) 128
aryl boronic acids (112) 112
catalysis (95) 95
alpha-fluorinated ethers (91) 91
hypervalent iodine reagent (80) 80
copper (79) 79
electrophilic trifluoromethylthiolation (79) 79
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copper-catalyzed trifluoromethylthiolation (73) 73
reagents (73) 73
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index medicus (68) 68
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silver trifluoromethanethiolate (49) 49
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fluorides (44) 44
aromatic compounds (43) 43
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catalyzed trifluoromethylthiolation (41) 41
fluorination (41) 41
hypervalent iodonium ylide (41) 41
elemental sulfur (40) 40
chemical sciences (36) 36
enantioselective trifluoromethylthiolation (36) 36
carbonyl-compounds (35) 35
fluor (35) 35
chemistry, applied (34) 34
halides (34) 34
room-temperature (32) 32
chemistry, inorganic & nuclear (31) 31
convenient synthesis (31) 31
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electrophilic trifluoromethanesulfanylation (30) 30
terminal alkynes (30) 30
indoles (29) 29
amines (28) 28
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efficient synthesis (28) 28
molecular structure (28) 28
trifluoromethylation (28) 28
ethers (27) 27
mild (27) 27
acids (26) 26
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esters (26) 26
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thiols (26) 26
difluorocarbene (25) 25
organic-synthesis (25) 25
trifluoromethylthiolation reactions (25) 25
mediated oxidative trifluoromethylthiolation (24) 24
ketones (23) 23
chemical tests and reagents (22) 22
chlorides (22) 22
difluoromethylthiolation (22) 22
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nucleophilic trifluoromethylation (22) 22
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sodium trifluoromethanesulfinate (20) 20
trifluoromethanesulfenamide (20) 20
direct trifluoromethylthiolation (19) 19
hydrocarbons, fluorinated - chemistry (19) 19
reactivity (19) 19
stereoisomerism (19) 19
aldehydes (18) 18
iodides (18) 18
sulfenylation (18) 18
trifluoromethanesulfenyl chloride (18) 18
carboxylic-acids (17) 17
chemical properties (17) 17
fluorinated ethers (17) 17
sulfur compounds (17) 17
unactivated alkenes (17) 17
activation (16) 16
arenes (16) 16
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Chemical Communications, ISSN 1359-7345, 11/2014, Volume 50, Issue 91, pp. 14157 - 14160
A general method to form a C(SP3)-SCF3 bond via copper-mediated oxidative trifluoromethylthiolation of unactivated alkenes with stable nucleophilic AgSCF3 was... 
NUCLEOPHILIC TRIFLUOROMETHYLTHIOLATION | ROOM-TEMPERATURE | ARYL BORONIC ACIDS | ELECTROPHILIC TRIFLUOROMETHYLTHIOLATION | HYPERVALENT IODINE REAGENT | ALPHA-FLUORINATED ETHERS | ENANTIOSELECTIVE TRIFLUOROMETHYLTHIOLATION | CATALYZED TRIFLUOROMETHYLTHIOLATION | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | ALLYLIC BROMIDES
Journal Article
Organic Letters, ISSN 1523-7060, 02/2017, Volume 19, Issue 4, pp. 934 - 937
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 10/2014, Volume 50, Issue 91, pp. 14157 - 14160
A general method to form a C(SP super(3))-SCF sub(3) bond viacopper-mediated oxidative trifluoromethylthiolation of unactivated alkenes with stable... 
Tolerances | Terminals | Alkenes | Bonding | Functional groups
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2015, Volume 54, Issue 49, pp. 14965 - 14969
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2014, Volume 2014, Issue 12, pp. 2415 - 2428
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 7/2016, Volume 14, Issue 3, pp. 715 - 7182
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 07/2016, Volume 14, Issue 30, pp. 7150 - 7182
Substitution by the CF3S group allows for an increase in lipophilicity and electron-withdrawing properties along with an improvement in the bioavailability of... 
Journal Article