oxan-4-one (in DMSO) |
DMSO | E Param.: -17.90 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
thian-4-one (in DMSO) |
DMSO | E Param.: -16.90 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
pentan-2-one (in DMSO) |
DMSO | E Param.: -22.30 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
1-methylsulfanylpropan-2-one (in DMSO) |
DMSO | E Param.: -15.60 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
N-(phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide |
| E Param.: -6.06 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate |
| E Param.: -10.46 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
N-fluoro-2,6-dichloropyridinium tetrafluoroborate |
| E Param.: -5.29 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
Selectfluor |
| E Param.: -5.20 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
NFSI |
MeCN | E Param.: -8.44 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
N-fluoropyridinium tetrafluoroborate |
| E Param.: -9.89 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
N-(trifluoromethyl)thio)phthalimide |
| E Param.: -11.92 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-(trifluoromethyl)thio)saccharin |
| E Param.: -6.48 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-(trifluoromethyl)thio)succinimide |
| E Param.: -12.56 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-(difluoromethyl)thio)phthalimide |
| E Param.: -11.86 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-methyl-N-((trifluoromethyl)thio)-p-toluenesulfonamide |
| E Param.: -13.44 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
N-methyl-N-((trifluoromethyl)thio)-aniline |
| E Param.: -23.32 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
((2-phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane |
| E Param.: -13.77 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 |
3-methylcyclopentenone |
DMSO | E Param.: -28.90 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
2-methylcyclopentenone |
DMSO | E Param.: -22.10 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
cyclopentenone |
DMSO | E Param.: -20.60 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
furan-2(5H)-one |
DMSO | E Param.: -20.70 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
2-methylcyclohexenone |
DMSO | E Param.: -27.50 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
cyclohexenone |
DMSO | E Param.: -22.10 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
dihydro-2H-pyran-2-one |
DMSO | E Param.: -21.80 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
3-methylenetetrahydropyran-2-one |
DMSO | E Param.: -19.50 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
3-methylenedihydrofuranone |
DMSO | E Param.: -19.40 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
(E)-2,6-di-tert-butyl-4-(3-phenylallylidene)cyclohexa-2,5-dien-1-one |
DMSO | E Param.: -17.00 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | 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 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Eur. J. Org. Chem. 2020, , 3812-3817 10.1002/ejoc.202000295 |
ethyl 3-nitro-1H-indole-1-carboxylate |
| E Param.: -14.10 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j |
3-nitro-1-tosyl-1H-indole |
| E Param.: -14.87 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j |
4-bromo-3-nitro-1-tosyl-1H-indole |
| E Param.: -14.60 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j |
phenyl isocyanate |
MeCN | E Param.: -15.38 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
p-tosyl isocyanate |
MeCN | E Param.: -7.69 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
phenyl isothiocyanate |
DMSO | E Param.: -18.15 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
p-nitrophenyl isothiocyanate |
DMSO | E Param.: -15.89 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
diphenylcarbodiimide |
DMSO | E Param.: -20.14 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
carbon disulfide |
DMSO | E Param.: -17.70 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
3-methylcyclohexenone |
DMSO | E Param.: -29.60 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
3,6-dinitro-1-tosyl-1H-indole |
| E Param.: -12.90 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j |
4-phenylbut-3-yn-2-one |
| E Param.: -16.90 | ![-](/oc/mayr/reaktionsdatenbank2/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 |
hex-3-yn-2-one |
| E Param.: -17.90 | ![-](/oc/mayr/reaktionsdatenbank2/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 |
cycloheptenone |
DMSO | E Param.: -22.00 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
methyl diazoacetate |
| E Param.: -18.50 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
dimethyl diazomalonate |
| E Param.: -18.20 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
(p-nitrophenyl)diazomethane |
| E Param.: -18.30 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
diphenyldiazomethane |
| E Param.: -21.40 | ![-](/oc/mayr/reaktionsdatenbank2/img/symbols/star0.png) | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
butynone |
| E Param.: -16.60 | ![-](/oc/mayr/reaktionsdatenbank2/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 |
Umemoto I (triflate) |
| E Param.: -13.08 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
Umemoto I (tetrafluoroborate) |
| E Param.: -13.39 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
Umemoto II (triflate) |
| E Param.: -12.80 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
(E)-6-(4-nitrobenzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -13.15 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(4-(trifluoromethyl)benzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -13.54 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(3-fluorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -14.00 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(4-chlorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -13.99 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-benzylidenebenzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -14.47 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(4-methylbenzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -14.85 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(4-methoxybenzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -15.20 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(4-(dimethylamino)benzylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -16.07 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Chem. Eur. J. 2024, , e202403785 10.1002/chem.202403785 |
(E)-6-(furan-2-ylmethylene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -15.73 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Org. Biomol. Chem. 2024, , accepted 10.1039/D4OB01855A |
(E)-6-((1-methyl-1H-pyrrol-2-yl)methylene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -17.03 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Org. Biomol. Chem. 2024, , accepted 10.1039/D4OB01855A |
(E)-6-((1-methyl-1H-indol-2-yl)methylene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -15.55 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Org. Biomol. Chem. 2024, , accepted 10.1039/D4OB01855A |
(E)-6-((E)-3-phenylallylidene)benzo[d][1,3]dioxol-5(6H)-one |
| E Param.: -16.00 | ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank2/img/symbols/star.png) | Org. Biomol. Chem. 2024, , accepted 10.1039/D4OB01855A |