-
11
-
-
0034712242
-
-
(d) Adam, W.; Ma̧kosza, M.; Zhao, C. G.; Surowiec, M. J. Org. Chem. 2000, 65, 1099.
-
(2000)
J. Org. Chem
, vol.65
, pp. 1099
-
-
Adam, W.1
Ma̧kosza, M.2
Zhao, C.G.3
Surowiec, M.4
-
20
-
-
0001411961
-
-
(a) Stern, M. K.; Hileman, F. D.; Bashkin, J. K. J. Am. Chem. Soc. 1992, 114, 9237.
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 9237
-
-
Stern, M.K.1
Hileman, F.D.2
Bashkin, J.K.3
-
21
-
-
34347395386
-
-
US Patent 6388136
-
(b) Beska, E.; Toman, P.; Fiedler, K.; Hronec, M.; Pinter, J. US Patent 6388136, 2002.
-
(2002)
-
-
Beska, E.1
Toman, P.2
Fiedler, K.3
Hronec, M.4
Pinter, J.5
-
22
-
-
0032770630
-
-
Lipilin, D. L.; Churakov, A. M.; Ioffe, S. L.; Strelenko, Y. A.; Tartakowsky, V. A. Eur. J. Org. Chem. 1999, 29.
-
(1999)
Eur. J. Org. Chem
, pp. 29
-
-
Lipilin, D.L.1
Churakov, A.M.2
Ioffe, S.L.3
Strelenko, Y.A.4
Tartakowsky, V.A.5
-
23
-
-
0037715306
-
-
Lemek, T.; Ma̧kosza, M.; Stephenson, D. S.; Mayr, H. Angew. Chem. Int. Ed. 2003, 42, 2793.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 2793
-
-
Lemek, T.1
Ma̧kosza, M.2
Stephenson, D.S.3
Mayr, H.4
-
24
-
-
1642603924
-
-
Błażej, S.; Kwast, A.; Ma̧kosza, M. Tetrahedron Lett. 2004, 45, 3193.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 3193
-
-
Błażej, S.1
Kwast, A.2
Ma̧kosza, M.3
-
26
-
-
37049107949
-
-
(b) Bartoli, G.; Leardini, R.; Medici, A.; Rosini, G. J. Chem. Soc., Perkin Trans. 1 1978, 692.
-
(1978)
J. Chem. Soc., Perkin Trans. 1
, pp. 692
-
-
Bartoli, G.1
Leardini, R.2
Medici, A.3
Rosini, G.4
-
27
-
-
34347374507
-
-
Melting points are uncorrected. 1H and 13C NMR spectra were recorded on a Varian Mercury 400 instrument (400 MHz for 1H NMR and 100 MHz for 13C NMR spectra) in CDCl 3 Chemical shifts (δ) are expressed in ppm referred to TMS, and coupling constants are given in Hz. 15N GHMBC experiment was performed on a Bruker 500 instrument in CDCl3 at 273 K. Mass spectra (EI, 70 eV) were obtained on an AMD-604 spectrometer. Silica gel Merck 60 (230-400 mesh) was used for column chromatography. 2-Chloro-4- trifluoromethylonitrobenzene20 (2d) and 4-chloro-2- methoxynitrobenzene21 (2e) were obtained according to the literature. All other reagents are commercially available. Preparation of 2-Nitroso-N-arylanilines 3a-i; General Procedure To a cooled solution of t-BuOK (6 mmol, 672 mg) in DMF (2 mL) was added dropwise at -60°C a solution of aniline 1 2 m
-
2 at r.t. for 30 min. The catalyst was filtered off and the solution was evaporated to dryness. ...
-
-
-
-
28
-
-
0041664457
-
-
(a) Fasani, E.; Pietra, S.; Albini, A. Heterocycles 1992, 33, 573.
-
(1992)
Heterocycles
, vol.33
, pp. 573
-
-
Fasani, E.1
Pietra, S.2
Albini, A.3
-
29
-
-
37049079979
-
-
(b) Fasani, E.; Mella, M.; Albini, A. J. Chem. Soc., Perkin Trans. 1 1992, 2689.
-
(1992)
Chem. Soc., Perkin Trans. 1
, pp. 2689
-
-
Fasani, E.1
Mella, M.2
Albini, A.J.3
-
31
-
-
5644273896
-
-
(d) Okubo, M.; Inatomi, Y.; Taniguchi, N.; Imamura, K. Bull. Chem. Soc. Jpn. 1988, 61, 3581.
-
(1988)
Bull. Chem. Soc. Jpn
, vol.61
, pp. 3581
-
-
Okubo, M.1
Inatomi, Y.2
Taniguchi, N.3
Imamura, K.4
-
32
-
-
0242576820
-
-
Holschbach, M. H.; Sanz, D.; Claramunt, R. M.; Infantes, L.; Motherwell, S.; Raithby, P. R.; Jimeno, M. L.; Herrero, D.; Alkorta, I.; Jagerovic, N.; Elguero, J. J. Org. Chem. 2003, 68, 8831.
-
(2003)
J. Org. Chem
, vol.68
, pp. 8831
-
-
Holschbach, M.H.1
Sanz, D.2
Claramunt, R.M.3
Infantes, L.4
Motherwell, S.5
Raithby, P.R.6
Jimeno, M.L.7
Herrero, D.8
Alkorta, I.9
Jagerovic, N.10
Elguero, J.11
-
33
-
-
34347376541
-
-
Urbelis, G.; Susvilo, I.; Tumkevicius, S. J. Mol. Model. 2007, 13, 219.
-
(2007)
J. Mol. Model
, vol.13
, pp. 219
-
-
Urbelis, G.1
Susvilo, I.2
Tumkevicius, S.3
-
34
-
-
84971062505
-
-
Buckley, P. D.; Furness, A. R.; Jolley, K. W.; Pinder, D. N. Austr. J. Chem. 1974, 27, 21.
-
(1974)
Austr. J. Chem
, vol.27
, pp. 21
-
-
Buckley, P.D.1
Furness, A.R.2
Jolley, K.W.3
Pinder, D.N.4
-
35
-
-
0026761625
-
-
Tsui, K.; Nakamura, K.; Konishi, N.; Okumura, H.; Matsuo, M. Chem. Pharm. Bull. 1992, 40, 2399.
-
(1992)
Chem. Pharm. Bull
, vol.40
, pp. 2399
-
-
Tsui, K.1
Nakamura, K.2
Konishi, N.3
Okumura, H.4
Matsuo, M.5
-
36
-
-
34347394556
-
-
Barluenga, J.; Fananas, F. J.; Sanz, R.; Fernandez, Y. Chem. Eur. J. 1965, 397.
-
(1965)
Chem. Eur. J
, pp. 397
-
-
Barluenga, J.1
Fananas, F.J.2
Sanz, R.3
Fernandez, Y.4
|