Arenes

For reactivities of structurally related compounds go to: Nucleophiles » C-Nucleophiles

Found 42 Molecules.

Molecule	Solvent	Reactivity Parameters	Reference (sort by title or year)
1,2-dimethylindole	dichloromethane	N Parameter: 6.54 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
pyrrole	dichloromethane	N Parameter: 4.63 s_N Parameter: 1.00	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
2-(trimethylsilyl)furan	dichloromethane	N Parameter: 2.16 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(triethylsilyl)furan	dichloromethane	N Parameter: 2.20 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylsilyl)furan	dichloromethane	N Parameter: 2.37 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
thiophene	dichloromethane	N Parameter: -1.01 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsilyl)thiophene	dichloromethane	N Parameter: -0.80 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylstannyl)furan	dichloromethane	N Parameter: 3.63 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylstannyl)thiophene	dichloromethane	N Parameter: 1.53 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
5-amino-indole	MeCN	N Parameter: 7.22 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-hydroxy-indole	MeCN	N Parameter: 6.44 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-methyl-indole	MeCN	N Parameter: 6.00 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-chloro-indole	MeCN	N Parameter: 4.42 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-bromo-indole	MeCN	N Parameter: 4.38 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-cyano-indole	MeCN	N Parameter: 2.83 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
1H-indole-5-carboxylic acid	MeCN	N Parameter: 3.97 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-methoxy-2-methylindole	MeCN	N Parameter: 7.26 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
2,5-dimethylindole	MeCN	N Parameter: 7.22 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
2-methylindole	MeCN	N Parameter: 6.91 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-chloro-2-methylindole	MeCN	N Parameter: 6.08 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
4-methoxy-indole	MeCN	N Parameter: 5.41 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
7-azaindole	MeCN	N Parameter: 3.87 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
anisole	dichloromethane	N Parameter: -1.18 s_N Parameter: 1.20	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-methylanisole	dichloromethane	N Parameter: 0.13 s_N Parameter: 1.27	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
N-(triisopropylsilyl)pyrrole	dichloromethane	N Parameter: 3.12 s_N Parameter: 0.93	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
Indole	dichloromethane	N Parameter: 5.55 s_N Parameter: 1.09	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
N-methylindole	dichloromethane	N Parameter: 5.75 s_N Parameter: 1.23	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-methoxy-indole	dichloromethane	N Parameter: 6.22 s_N Parameter: 1.12	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
2,5-dimethylpyrrole	MeCN	N Parameter: 8.01 s_N Parameter: 0.96	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
1,2,5-trimethylpyrrole	MeCN	N Parameter: 8.69 s_N Parameter: 1.07	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
2,4-dimethylpyrrole	MeCN	N Parameter: 10.67 s_N Parameter: 0.91	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
3-ethyl-2,4-dimethylpyrrole	MeCN	N Parameter: 11.63 s_N Parameter: 0.95	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
azulene	MeCN	N Parameter: 6.66 s_N Parameter: 1.02	Eur. J. Org. Chem. 2009, , 1202-1206 DOI: 10.1002/ejoc.200801099
tert-butyl indole-1-carboxylate	MeCN	N Parameter: 1.68 s_N Parameter: 1.26	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
3-methoxythiophene	MeCN	N Parameter: 3.06 s_N Parameter: 1.19	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
toluene	dichloromethane	N Parameter: -4.36 s_N Parameter: 1.77	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
m-xylene	dichloromethane	N Parameter: -3.57 s_N Parameter: 2.08	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methylthiophene	dichloromethane	N Parameter: 1.35 s_N Parameter: 0.99	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
1,3-dimethoxybenzene	dichloromethane	N Parameter: 2.48 s_N Parameter: 1.09	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methylfuran	dichloromethane	N Parameter: 3.61 s_N Parameter: 1.11	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
N-methylpyrrole	dichloromethane	N Parameter: 5.85 s_N Parameter: 1.03	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
furan	dichloromethane	N Parameter: 1.33 s_N Parameter: 1.29	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b