Mayr's Database Of Reactivity Parameters
AK Prof. Mayr

Arenes

For reactivities of structurally related compounds go to: Nucleophiles » C-Nucleophiles
Found 42 Molecules.
Molecule Solvent Reactivity Parameters Classification Reference (sort by title or year)
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toluene
dichloromethaneN  Parameter: -4.36
sN Parameter: 1.77
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

m-xylene
dichloromethaneN  Parameter: -3.57
sN Parameter: 2.08
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

anisole
dichloromethaneN  Parameter: -1.18
sN Parameter: 1.20
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

thiophene
dichloromethaneN  Parameter: -1.01
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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2-(trimethylsilyl)thiophene
dichloromethaneN  Parameter: -0.80
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

3-methylanisole
dichloromethaneN  Parameter: 0.13
sN Parameter: 1.27
***J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
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furan
dichloromethaneN  Parameter: 1.33
sN Parameter: 1.29
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2-methylthiophene
dichloromethaneN  Parameter: 1.35
sN Parameter: 0.99
*****J. Am. Chem. Soc. 2012, 134, 13902-13911
DOI: 10.1021/ja306522b
image of molecule

2-(tributylstannyl)thiophene
dichloromethaneN  Parameter: 1.53
sN Parameter: 1.00
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

tert-butyl indole-1-carboxylate
MeCNN  Parameter: 1.68
sN Parameter: 1.26
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
image of molecule

2-(trimethylsilyl)furan
dichloromethaneN  Parameter: 2.16
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(triethylsilyl)furan
dichloromethaneN  Parameter: 2.20
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

2-(tributylsilyl)furan
dichloromethaneN  Parameter: 2.37
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
image of molecule

1,3-dimethoxybenzene
dichloromethaneN  Parameter: 2.48
sN Parameter: 1.09
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
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5-cyano-indole
MeCNN  Parameter: 2.83
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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3-methoxythiophene
MeCNN  Parameter: 3.06
sN Parameter: 1.19
***J. Am. Chem. Soc. 2013, 135, 6317-6324
DOI: 10.1021/ja4017655
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N-(triisopropylsilyl)pyrrole
dichloromethaneN  Parameter: 3.12
sN Parameter: 0.93
***Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
image of molecule

2-methylfuran
dichloromethaneN  Parameter: 3.61
sN Parameter: 1.11
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

2-(tributylstannyl)furan
dichloromethaneN  Parameter: 3.63
sN Parameter: 1.10
*Acc. Chem. Res. 2003, 36, 66-77
DOI: 10.1021/ar020094c
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7-azaindole
MeCNN  Parameter: 3.87
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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1H-indole-5-carboxylic acid
MeCNN  Parameter: 3.97
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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5-bromo-indole
MeCNN  Parameter: 4.38
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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5-chloro-indole
MeCNN  Parameter: 4.42
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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pyrrole
dichloromethaneN  Parameter: 4.63
sN Parameter: 1.00
*Chem. Eur. J. 2003, 9, 2209-2218
DOI: 10.1002/chem.200204666
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4-methoxy-indole
MeCNN  Parameter: 5.41
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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Indole
dichloromethaneN  Parameter: 5.55
sN Parameter: 1.09
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

N-methylindole
dichloromethaneN  Parameter: 5.75
sN Parameter: 1.23
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

N-methylpyrrole
dichloromethaneN  Parameter: 5.85
sN Parameter: 1.03
*****J. Am. Chem. Soc. 2001, 123, 9500-9512
DOI: 10.1021/ja010890y
image of molecule

5-methyl-indole
MeCNN  Parameter: 6.00
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-chloro-2-methylindole
MeCNN  Parameter: 6.08
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-methoxy-indole
dichloromethaneN  Parameter: 6.22
sN Parameter: 1.12
***J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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5-hydroxy-indole
MeCNN  Parameter: 6.44
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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1,2-dimethylindole
dichloromethaneN  Parameter: 6.54
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
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azulene
MeCNN  Parameter: 6.66
sN Parameter: 1.02
***Eur. J. Org. Chem. 2009, , 1202-1206
DOI: 10.1002/ejoc.200801099
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2-methylindole
MeCNN  Parameter: 6.91
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-amino-indole
MeCNN  Parameter: 7.22
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

2,5-dimethylindole
MeCNN  Parameter: 7.22
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

5-methoxy-2-methylindole
MeCNN  Parameter: 7.26
sN Parameter: 1.10
*J. Org. Chem. 2006, 71, 9088-9095
DOI: 10.1021/jo0614339
image of molecule

2,5-dimethylpyrrole
MeCNN  Parameter: 8.01
sN Parameter: 0.96
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

1,2,5-trimethylpyrrole
MeCNN  Parameter: 8.69
sN Parameter: 1.07
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

2,4-dimethylpyrrole
MeCNN  Parameter: 10.67
sN Parameter: 0.91
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092
image of molecule

3-ethyl-2,4-dimethylpyrrole
MeCNN  Parameter: 11.63
sN Parameter: 0.95
***Eur. J. Org. Chem. 2008, , 2369-2374
DOI: 10.1002/ejoc.200800092