Acceptor-Substituted Ethylenes
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« Back Forward » Found 129 molecules, displaying page 6 of 7 Results per page
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Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
dma(Ph)2QM![]() ![]() |
E Param.: -13.39 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
dma(S)BBS![]() ![]() |
E Param.: -10.73 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
dma(t-Bu)2QM![]() ![]() |
E Param.: -17.29 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
dmaBBS![]() ![]() |
E Param.: -12.76 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
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.[...] |
ethenesulfonyl fluoride (ESF)![]() ![]() |
DMSO | E Param.: -12.09 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2016, 55, 12664-12667 10.1002/anie.201601875 |
ethenylsulfonylbenzene (in DMSO)![]() ![]() |
DMSO | E Param.: -18.36 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
ethyl (E)-but-2-enoate (in DMSO)![]() ![]() |
DMSO | E Param.: -23.59 | ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
ethyl 2-methylprop-2-enoate (in DMSO)![]() ![]() |
DMSO | E Param.: -22.77 | ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
ethyl cinnamate (in DMSO)![]() ![]() |
DMSO | E Param.: -24.52 | ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
ethyl prop-2-enoate (in DMSO)![]() ![]() |
DMSO | E Param.: -19.07 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
fumaronitrile![]() ![]() |
DMSO | E Param.: -15.71 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
furan-2(5H)-one![]() ![]() |
DMSO | E Param.: -20.70 | ![]() ![]() ![]() | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
hex-3-yn-2-one![]() ![]() |
E Param.: -17.90 | ![]() | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | |
jul Meldrum's acid![]() ![]() |
E Param.: -13.97 | ![]() ![]() ![]() | J. Org. Chem. 2008, 73, 2738-2745 10.1021/jo702590s | |
jul(S)BBS![]() ![]() |
E Param.: -11.89 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
jul(t-Bu)2QM![]() ![]() |
E Param.: -17.90 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
jul-indan-1,3-dione![]() ![]() |
E Param.: -14.68 | ![]() ![]() ![]() | Org. Biomol. Chem. 2007, 5, 3020-3026 10.1039/b708025e | |
julBBS![]() ![]() |
E Param.: -13.84 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
maleic anhydride![]() ![]() |
DMSO | E Param.: -11.31 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |