Electrophiles

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Name	Solvent	Reactivity Parameters	Reference (title or year)
oxan-4-one (in DMSO)	DMSO	E Param.: -17.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657
thian-4-one (in DMSO)	DMSO	E Param.: -16.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657
1,4-dioxaspiro[4.5]decan-8-one (in DMSO)	DMSO	E Param.: -18.20	J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657
pentan-2-one (in DMSO)	DMSO	E Param.: -22.30	J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657
1-methylsulfanylpropan-2-one (in DMSO)	DMSO	E Param.: -15.60	J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657
N-(phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide		E Param.: -6.06	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate		E Param.: -10.46	J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
N-fluoro-2,6-dichloropyridinium tetrafluoroborate		E Param.: -5.29	J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
Selectfluor		E Param.: -5.20	J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
NFSI	MeCN	E Param.: -8.44	J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
N-fluoropyridinium tetrafluoroborate		E Param.: -9.89	J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
N-(trifluoromethyl)thio)phthalimide		E Param.: -11.92	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-(trifluoromethyl)thio)saccharin		E Param.: -6.48	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-(trifluoromethyl)thio)succinimide		E Param.: -12.56	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-(difluoromethyl)thio)phthalimide		E Param.: -11.86	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-methyl-N-((trifluoromethyl)thio)-p-toluenesulfonamide		E Param.: -13.44	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
N-methyl-N-((trifluoromethyl)thio)-aniline		E Param.: -23.32	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
((2-phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane		E Param.: -13.77	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
((2-(2-iodophenyl)propan-2-yl)oxy)(trifluoromethyl)sulfane		E Param.: -14.52	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859
(E)-2,6-di-tert-butyl-4-(3-phenylallylidene)cyclohexa-2,5-dien-1-one	DMSO	E Param.: -17.00	Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...]
E)-2,6-di-tert-butyl-4-(3-(4-chlorophenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Param.: -16.84	Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...]
(E)-2,6-di-tert-butyl-4-(3-(4-nitrophenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Param.: -16.25	Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...]
(E)-2,6-di-tert-butyl-4-(3-(4-methoxyphenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Param.: -17.42	Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...]
2,6-di-tert-butyl-4-(2,2,2-trifluoroethylidene)cyclohexa-2,5-dien-1-one	DMSO	E Param.: -11.68	Eur. J. Org. Chem. 2020, , 3812-3817 10.1002/ejoc.202000295
phenyl isocyanate	MeCN	E Param.: -15.38	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960
p-tosyl isocyanate	MeCN	E Param.: -7.69	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960
phenyl isothiocyanate	DMSO	E Param.: -18.15	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960
p-nitrophenyl isothiocyanate	DMSO	E Param.: -15.89	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960
diphenylcarbodiimide	DMSO	E Param.: -20.14	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960
carbon disulfide	DMSO	E Param.: -17.70	J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960