Electrophiles
| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
pfp(Ph)CH+ ![]() |
E Param.: 5.20 |
J. Am. Chem. Soc. 2012, 134, 13902-13911 10.1021/ja306522b |
||
Ph2C=C=N(+)Me2 ![]() |
E Param.: -1.90 |
Synthesis 2025, 57, 3251-3262 10.1055/a-2649-1999 |
||
PhCH=N+(CH2)4 (in MeCN) ![]() |
MeCN | E Param.: -9.35 |
J. Am. Chem. Soc. 2013, 135, 6579-6587 10.1021/ja401106x |
|
PhCH=N+(CH2)5 (in MeCN) ![]() |
MeCN | E Param.: -9.60 |
J. Am. Chem. Soc. 2013, 135, 6579-6587 10.1021/ja401106x |
|
PhCH=N+Me2 (in MeCN) ![]() |
MeCN | E Param.: -9.27 |
J. Am. Chem. Soc. 2013, 135, 6579-6587 10.1021/ja401106x |
|
phenyl isocyanate ![]() |
MeCN | E Param.: -15.38 |
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 |
|
pipN+=CH-CH-Ph ![]() |
E Param.: -10.30 |
Angew. Chem. Int. Ed. 2008, 47, 8723-8726 10.1002/anie.200802889 |
||
pop(Ph)CH+ ![]() |
E Param.: 2.90 |
J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y |
||
pop(tol)CH+ ![]() |
E Param.: 2.16, Deviation: ±0.03 |
Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c |
||
propyn-1-ylium-Co2(CO)6 ![]() |
E Param.: -0.84, Deviation: ±0.36 |
Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c |
||
pTolCH=N+CH2 (in MeCN) ![]() |
MeCN | E Param.: -9.64 |
J. Am. Chem. Soc. 2013, 135, 6579-6587 10.1021/ja401106x |
|
pyrN+=CH-CH-Ph ![]() |
E Param.: -9.80 |
Angew. Chem. Int. Ed. 2008, 47, 8723-8726 10.1002/anie.200802889 |
||
Selectfluor ![]() |
E Param.: -5.20 |
J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
||
tert-butyl prop-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -20.22 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
thian-4-one (in DMSO) ![]() |
DMSO | E Param.: -16.90 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
|
tol(Ph)CH+ ![]() |
E Param.: 4.43 |
J. Am. Chem. Soc. 2012, 134, 13902-13911 10.1021/ja306522b |
||
tol(t-Bu)2QM ![]() |
E Param.: -15.83 |
Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] |
||
tritylium ion (Ph3C+) ![]() |
E Param.: 0.51 |
J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y |
||
tropylium ion ![]() |
E Param.: -3.72, Deviation: ±0.03 |
Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c |
||
Umemoto I (tetrafluoroborate) ![]() |
E Param.: -13.39 |
Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
||
Umemoto I (triflate) ![]() |
E Param.: -13.08 |
Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
||
Umemoto II (triflate) ![]() |
E Param.: -12.80 |
Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 |
||
Vilsmeier ion ![]() |
E Param.: -5.77 |
Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c |
||
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = 3,5-difluorophenyl) ![]() |
E Param.: -14.21 |
Organometallics 2012, 31, 2416-2424 10.1021/om3000357 |
||
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = 4-(dimethylamino)phenyl) ![]() |
E Param.: -14.46 |
Organometallics 2012, 31, 2416-2424 10.1021/om3000357 |
||
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = Ph) ![]() |
E Param.: -14.14 |
Organometallics 2012, 31, 2416-2424 10.1021/om3000357 |

