Mayr's Database of Reactivity Parameters

Electrophiles

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Name Solvent Reactivity
Parameters
Classification Reference
(title or year)
pfp(Ph)CH+
C13H10F *

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)
C11H14N *
MeCN

E Param.: -9.35

*** J. Am. Chem. Soc. 2013, 135, 6579-6587
10.1021/ja401106x
PhCH=N+(CH2)5 (in MeCN)
C12H16N *
MeCN

E Param.: -9.60

*** J. Am. Chem. Soc. 2013, 135, 6579-6587
10.1021/ja401106x
PhCH=N+Me2 (in MeCN)
C9H12N *
MeCN

E Param.: -9.27

*** J. Am. Chem. Soc. 2013, 135, 6579-6587
10.1021/ja401106x
phenyl isocyanate
C7H5NO *
MeCN

E Param.: -15.38

*** J. Am. Chem. Soc. 2020, 142, 8383-8402
10.1021/jacs.0c01960
phenyl isothiocyanate
C7H5NS *
DMSO

E Param.: -18.15

*** J. Am. Chem. Soc. 2020, 142, 8383-8402
10.1021/jacs.0c01960
pipN+=CH-CH-Ph
C14H18N+ *

E Param.: -10.30

* Angew. Chem. Int. Ed. 2008, 47, 8723-8726
10.1002/anie.200802889
pop(Ph)CH+
C19H15O *

E Param.: 2.90

***** J. Am. Chem. Soc. 2001, 123, 9500-9512
10.1021/ja010890y
pop(tol)CH+
C20H17O *

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)
C10H14N *
MeCN

E Param.: -9.64

*** J. Am. Chem. Soc. 2013, 135, 6579-6587
10.1021/ja401106x
pyrN+=CH-CH-Ph
C13H16N+ *

E Param.: -9.80

*** Angew. Chem. Int. Ed. 2008, 47, 8723-8726
10.1002/anie.200802889
Selectfluor
C7H14ClFN2 *

E Param.: -5.20

*** J. Am. Chem. Soc. 2018, 140, 11474-11486
10.1021/jacs.8b07147
tert-butyl prop-2-enoate (in DMSO)
C7H12O2 *
DMSO

E Param.: -20.22

*** J. Am. Chem. Soc. 2017, 139, 13318-13329
10.1021/jacs.7b05106
thian-4-one (in DMSO)
C5H8OS *
DMSO

E Param.: -16.90

* J. Am. Chem. Soc. 2018, 140, 5500-5515
10.1021/jacs.8b01657
tol(Ph)CH+
C14H13 *

E Param.: 4.43

***** J. Am. Chem. Soc. 2012, 134, 13902-13911
10.1021/ja306522b
tol(t-Bu)2QM
C22H28O *

E Param.: -15.83

**** Angew. Chem. Int. Ed. 2002, 41, 91-95
10.1002/1521-3773(20[...]
tritylium ion (Ph3C+)
C19H15 *

E Param.: 0.51

- J. Am. Chem. Soc. 2003, 125, 286-295
10.1021/ja021010y
tropylium ion
C7H7 *

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
C3H7ClN *

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