![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/892.gif)
(ethene-1,1-diyldisulfonyl)dibenzene | DMSO | E Parameter: -7.50
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/3.gif)
ani(Br)2QM | 0 | E Parameter: -8.63
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/551.gif)
benzylidene-Meldrum's acid | 0 | E Parameter: -9.15
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/192.gif)
benzylidenemalononitrile | 0 | E Parameter: -9.42
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1409.gif)
2-cinnamoyl-3-methyl-1-(perfluorophenyl)-1H-imidazol-3-ium | DMSO | E Parameter: -10.09
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/522.gif)
2-benzylidene-indan-1,3-dione | 0 | E Parameter: -10.11
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/552.gif)
p-(methoxy)benzylidene Meldrum's acid | 0 | E Parameter: -10.28
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/524.gif)
aniBBS | 0 | E Parameter: -10.37
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/527.gif)
dma(S)BBS | 0 | E Parameter: -10.73
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/193.gif)
p-(methoxy)benzylidenemalononitrile | 0 | E Parameter: -10.80
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1194.gif)
maleic anhydride | DMSO | E Parameter: -11.31
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/521.gif)
2-(p-methoxybenzylidene)-indan-1,3-dione | 0 | E Parameter: -11.32
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1411.gif)
2-cinnamoyl-1-mesityl-3-methyl-1H-imidazol-3-ium | DMSO | E Parameter: -11.48
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/928.gif)
2-cinnamoyl-1,3-dimethyl-1H-imidazol-3-ium | DMSO | E Parameter: -11.52
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2012, 51, 5234-5238 DOI: 10.1002/anie.201109042 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1561.gif)
2,6-di-tert-butyl-4-(2,2,2-trifluoroethylidene)cyclohexa-2,5-dien-1-one | DMSO | E Parameter: -11.68
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2020, , 3812-3817 DOI: 10.1002/ejoc.202000295 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/896.gif)
2-benzylidenebenzo[d][1,3]dithiole 1,1,3,3-tetraoxide | DMSO | E Parameter: -11.78
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1412.gif)
2-cinnamoyl-1-(4-methoxyphenyl)-3-methyl-1H-imidazol-3-ium | DMSO | E Parameter: -11.79
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1410.gif)
1-(tert-butyl)-2-cinnamoyl-3-methyl-1H-imidazol-3-ium | DMSO | E Parameter: -11.80
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/611.gif)
2,6-diphenyl-4-benzylidenecyclohexa-2,5-dienone | 0 | E Parameter: -11.87
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/528.gif)
jul(S)BBS | 0 | E Parameter: -11.89
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1413.gif)
2-cinnamoyl-1-(2,6-dimethoxyphenyl)-3-methyl-1H-imidazol-3-ium | DMSO | E Parameter: -12.02
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1309.gif)
ethenesulfonyl fluoride (ESF) | DMSO | E Parameter: -12.09
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2016, 55, 12664-12667 DOI: 10.1002/anie.201601875 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/4.gif)
ani(Ph)2QM | 0 | E Parameter: -12.18
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/836.gif)
4-nitro-<i>trans-beta</i>-nitrostyrene | | E Parameter: -12.37
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/835.gif)
4-cyano-<i>trans-beta</i>-nitrostyrene | | E Parameter: -12.61
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/525.gif)
dmaBBS | 0 | E Parameter: -12.76
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/553.gif)
p-(dimethylamino)benzylidene Meldrum's acid | 0 | E Parameter: -12.76
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/893.gif)
(2-phenylethene-1,1-diyldisulfonyl)dibenzene | DMSO | E Parameter: -12.93
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/897.gif)
2-(4-methoxybenzylidene)benzo[d][1,3]dithiole 1,1,3,3-tetraoxide | DMSO | E Parameter: -13.02
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/686.gif)
1,2-diaza-1,3-diene 1a | DMSO | E Parameter: -13.28
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/194.gif)
p-(dimethylamino)benzylidenemalononitrile | 0 | E Parameter: -13.30
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/834.gif)
4-bromo-<i>trans-beta</i>-nitrostyrene | | E Parameter: -13.37
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/5.gif)
dma(Ph)2QM | 0 | E Parameter: -13.39
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/520.gif)
2-(p-(dimethylamino)benzylidene)-indan-1,3-dione | 0 | E Parameter: -13.56
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/526.gif)
julBBS | 0 | E Parameter: -13.84
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/833.gif)
<i>trans-beta</i>-nitrostyrene | | E Parameter: -13.85
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/894.gif)
(2-(4-methoxyphenyl)ethene-1,1-diyldisulfonyl)dibenzene | DMSO | E Parameter: -13.88
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/687.gif)
1,2-diaza-1,3-diene 1b | DMSO | E Parameter: -13.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/554.gif)
jul Meldrum's acid | 0 | E Parameter: -13.97
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1195.gif)
N-methyl maleimide | DMSO | E Parameter: -14.07
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/832.gif)
4-methyl-<i>trans-beta</i>-nitrostyrene | | E Parameter: -14.23
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/617.gif)
2,6-di-tert.butyl-4-(4-nitrobenzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -14.36
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/616.gif)
2,6-di-tert.butyl-4-(3,5-difluorobenzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -14.50
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/898.gif)
2-(4-methoxybenzylidene)-1,3-dithiane 1,1,3,3-tetraoxide | DMSO | E Parameter: -14.55
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/523.gif)
jul-indan-1,3-dione | 0 | E Parameter: -14.68
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/831.gif)
4-methoxy-<i>trans-beta</i>-nitrostyrene | | E Parameter: -14.70
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/690.gif)
1,2-diaza-1,3-diene 1e | MeOH | E Parameter: -14.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/688.gif)
1,2-diaza-1,3-diene 1c | DMSO | E Parameter: -14.91
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/615.gif)
2,6-di-tert.butyl-4-(3-fluorobenzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -15.03
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1374.gif)
1-phenylprop-2-en-1-one (in DMSO) | DMSO | E Parameter: -15.25
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/691.gif)
1,2-diaza-1,3-diene 1f | MeOH | E Parameter: -15.30
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/689.gif)
1,2-diaza-1,3-diene 1d | DMSO | E Parameter: -15.38
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1196.gif)
fumaronitrile | DMSO | E Parameter: -15.71
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/6.gif)
tol(t-Bu)2QM | 0 | E Parameter: -15.83
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/7.gif)
ani(t-Bu)2QM | | E Parameter: -16.11
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1558.gif)
(E)-2,6-di-tert-butyl-4-(3-(4-nitrophenyl)allylidene)cyclohexa-2,5-dien-1-one | DMSO | E Parameter: -16.25
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/614.gif)
2,6-dimethyl-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -16.36
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/612.gif)
2,6-dimethoxy-4-(4-methoxybenzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -16.38
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/895.gif)
4-(2,2-bis(phenylsulfonyl)vinyl)-N,N-dimethylaniline | DMSO | E Parameter: -16.53
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1683.gif)
butynone | 0 | E Parameter: -16.60
| ![-](/oc/mayr/reaktionsdatenbank/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1310.gif)
2-phenylethene-1-sulfonyl fluoride | DMSO | E Parameter: -16.63
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2016, 55, 12664-12667 DOI: 10.1002/anie.201601875 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1373.gif)
but-3-en-2-one (in DMSO) | DMSO | E Parameter: -16.76
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1557.gif)
E)-2,6-di-tert-butyl-4-(3-(4-chlorophenyl)allylidene)cyclohexa-2,5-dien-1-one | DMSO | E Parameter: -16.84
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1581.gif)
4-phenylbut-3-yn-2-one | 0 | E Parameter: -16.90
| ![-](/oc/mayr/reaktionsdatenbank/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1556.gif)
(E)-2,6-di-tert-butyl-4-(3-phenylallylidene)cyclohexa-2,5-dien-1-one | DMSO | E Parameter: -17.00
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/613.gif)
2,6-dimethoxy-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone | 0 | E Parameter: -17.18
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/8.gif)
dma(t-Bu)2QM | | E Parameter: -17.29
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/653.gif)
bh 6m | | E Parameter: -17.30
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/762.gif)
(E)-3-(4-nitro-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO) | DMSO | E Parameter: -17.33
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1559.gif)
(E)-2,6-di-tert-butyl-4-(3-(4-methoxyphenyl)allylidene)cyclohexa-2,5-dien-1-one | DMSO | E Parameter: -17.42
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/763.gif)
(E)-3-(4-cyano-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO) | DMSO | E Parameter: -17.64
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/566.gif)
diethyl 4-nitrobenzylidene malonate | 0 | E Parameter: -17.67
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1197.gif)
diethyl fumarate | DMSO | E Parameter: -17.79
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/9.gif)
jul(t-Bu)2QM | 0 | E Parameter: -17.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/650.gif)
bh6j | | E Parameter: -17.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1583.gif)
hex-3-yn-2-one | 0 | E Parameter: -17.90
| ![-](/oc/mayr/reaktionsdatenbank/img/symbols/star0.png) | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/567.gif)
diethyl 4-cyano-benzylidene malonate | 0 | E Parameter: -18.06
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/651.gif)
bh 6k | | E Parameter: -18.20
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1371.gif)
ethenylsulfonylbenzene (in DMSO) | DMSO | E Parameter: -18.36
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/647.gif)
bh6a | | E Parameter: -18.60
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1367.gif)
methyl prop-2-enoate (in DMSO) | DMSO | E Parameter: -18.84
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/648.gif)
bh 6f | | E Parameter: -18.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/652.gif)
bh 6l | | E Parameter: -18.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/568.gif)
diethyl 3-chloro-benzylidene malonate | 0 | E Parameter: -18.98
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1372.gif)
acrylonitrile (in DMSO) | DMSO | E Parameter: -19.05
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1368.gif)
ethyl prop-2-enoate (in DMSO) | DMSO | E Parameter: -19.07
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/649.gif)
bh 6i | | E Parameter: -19.10
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/767.gif)
(E)-4,4-dimethyl-1-(4-nitrophenyl)pent-1-en-3-one | DMSO | E Parameter: -19.15
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/766.gif)
(E)-4-methyl-1-(4-nitrophenyl)pent-1-en-3-one (in DMSO) | DMSO | E Parameter: -19.17
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/765.gif)
(E)-4-(4-nitrophenyl)but-3-en-2-one (in DSMO) | DMSO | E Parameter: -19.36
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/764.gif)
(E)-1,3-diphenylprop-2-en-1-one (in DMSO) | DMSO | E Parameter: -19.39
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1551.gif)
3-methylenedihydrofuranone | DMSO | E Parameter: -19.40
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1198.gif)
diethyl maleate | DMSO | E Parameter: -19.49
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1550.gif)
3-methylenetetrahydropyran-2-one | DMSO | E Parameter: -19.50
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1369.gif)
tert-butyl prop-2-enoate (in DMSO) | DMSO | E Parameter: -20.22
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/565.gif)
diethyl benzylidene malonate | 0 | E Parameter: -20.55
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1473.gif)
cyclopentenone | DMSO | E Parameter: -20.60
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1474.gif)
furan-2(5H)-one | DMSO | E Parameter: -20.70
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/569.gif)
diethyl 4-methyl-benzylidene malonate | 0 | E Parameter: -21.11
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/570.gif)
diethyl 4-methoxy-benzylidene malonate | 0 | E Parameter: -21.47
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1549.gif)
dihydro-2H-pyran-2-one | DMSO | E Parameter: -21.80
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1603.gif)
cycloheptenone | DMSO | E Parameter: -22.00
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1472.gif)
2-methylcyclopentenone | DMSO | E Parameter: -22.10
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1548.gif)
cyclohexenone | DMSO | E Parameter: -22.10
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1375.gif)
ethyl 2-methylprop-2-enoate (in DMSO) | DMSO | E Parameter: -22.77
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1365.gif)
(E)-4-phenylbut-3-en-2-one (in DMSO) | DMSO | E Parameter: -23.01
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/571.gif)
diethyl 4-(dimethylamino)benzylidene malonate | 0 | E Parameter: -23.10
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/572.gif)
diethyl 2-((1-methyl-1,2,3,4-tetrahydroquinolin-6-yl)methylene)malonate | 0 | E Parameter: -23.40
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1370.gif)
N,N-dimethylprop-2-enamide (in DMSO) | DMSO | E Parameter: -23.54
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1376.gif)
ethyl (E)-but-2-enoate (in DMSO) | DMSO | E Parameter: -23.59
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/573.gif)
diethyl 2-((julolidine-9-yl)methylene)malonate | 0 | E Parameter: -23.80
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1377.gif)
ethyl cinnamate (in DMSO) | DMSO | E Parameter: -24.52
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1366.gif)
cinnamonitrile (in DMSO) | DMSO | E Parameter: -24.60
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1378.gif)
(E)-1-methyl-4-(styrylsulfonyl)benzene (in DMSO) | DMSO | E Parameter: -24.69
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106 |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1601.gif)
2-methylcyclohexenone | DMSO | E Parameter: -27.50
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1471.gif)
3-methylcyclopentenone | DMSO | E Parameter: -28.90
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |
![image of molecule](/oc/mayr/reaktionsdatenbank/img/molecules/1602.gif)
3-methylcyclohexenone | DMSO | E Parameter: -29.60
| ![*](/oc/mayr/reaktionsdatenbank/img/symbols/star.png) | Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A |