Indexed keywords
1 CHLORO 4 NITROBENZENE;
1,3 DINITROBENZENE;
2 CHLORO 3 NITROPYRIDINE;
2 CHLORO 3,4 DINITROPYRIDINE;
2 CHLORO 3,5 DINITROPYRIDINE;
2 CHLORO 5 NITROPYRIDINE;
2 CHLORO 6 NITROPYRAZINE;
2 NITRO 3,4,5,6 TETRACHLOROPYRIDINE;
2 NITRO 3,5,6 TRIFLUOROPYRIDINE;
2,3 DINITROPYRIDINE;
2,3,5,6 TETRAFLUOROPYRIDINE;
2,4 DICHLORO 6 (N PROPOXY) S TRIAZINE;
2,4 DICHLOROPYRIMIDINE;
2,4,5,6 TETRACHLOROPYRIMIDINE;
2,4,6 TRICHLOROPYRIMIDINE;
2,6 DICHLOROPYRAZINE;
4 CHLORO 6 NITROPYRIMIDINE;
4 NITRO 2,3,5,6 TETRACHLOROPYRIDINE;
4 NITRO 2,3,5,6 TETRAFLUOROPYRIDINE;
AROMATIC COMPOUND;
AROMATIC NITRO COMPOUND;
BENZYL CHLORIDE;
N BENZYLTRIPHENYLPHOSPHINIMINE;
PENTACHLOROPYRIDINE;
PENTAFLUOROPYRIDINE;
PYRAZINE DERIVATIVE;
PYRIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
CHEMICAL STRUCTURE;
CONFERENCE PAPER;
NITRATION;
OXIDATION;
SUBSTITUTION REACTION;
SYNTHESIS;
5
0003480901
VCH Publishers Inc
See, for instance, Olah, G. A., Malhotra, R., Narang, S. C., Nitration: Methods and Mechanisms; VCH Publishers Inc. 1989.
(1989)
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Olah, G.A.1
Malhotra, R.2
Narang, S.C.3
6
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Albright, L. F., Carr, R. V. C., Schmitt, R. J. (Eds.), Nitration: Recent Laboratory & Industrial Developments; A.C.S. Symposium Series 623, American Chemical Society 1996.
(1996)
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Albright, L.F.1
Carr, R.V.C.2
Schmitt, R.J.3
12
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See ref. 5, page 96. Also, a report (Baik, W., Yun, S., Rhee, U. J. & Russell, G. A., J Chem. Soc. Perkin Trans. 1 1996, 1777) has indicated that, under special conditions (DMSO solvent) isoquinolines may be nitrated in the 2-position in yields of around 30%, but no assessment was made of the applicability of this method to other heterocyclic systems.
(1996)
J. Chem. Soc. Perkin Trans. 1
, pp. 1777
Baik, W.1
Yun, S.2
Rhee, U.J.3
Russell, G.A.4
13
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Taylor, E. C., Tseng, C.-P., Rampal, J. B., J. Org. Chem. 1982, 47, 552.
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Tseng, C.-P.2
Rampal, J.B.3
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Corey, E. J., Samuelsson, B., Luzzio, F. A., J. Am. Chem. Soc. 1984, 106, 3682.
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Samuelsson, B.2
Luzzio, F.A.3
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Rakitin, O. A., Vlasova, O. G., Khmelnitski, L. I., Khim. Geterotsikl. Soedin. 1990, 11, 1536.
(1990)
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Rakitin, O.A.1
Vlasova, O.G.2
Khmelnitski, L.I.3
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Rakitin, O. A., Obruchnikova, N. V., Khmelnitski, L. I., Phosphorus Sulphur, 1993, 78, 309.
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Obruchnikova, N.V.2
Khmelnitski, L.I.3
19
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Rakitin, O. A., Vlasova, O. G., Khmelnitski, L. I., Org. Prep. Proced. Int. 1994, 26 331.
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Vlasova, O.G.2
Khmelnitski, L.I.3
21
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See ref. 20, page 527
See ref. 20, page 527.
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Tamura, Y., Sumoto, K., Matusushima, H., Taniguchi, H., Ikeda, M., J. Org. Chem. 1973, 38, 4324.
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Ikeda, M.5
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Sandall, J. P. B., C. Thompson, C., Steel, N. J. D., J Chem. Soc. Perkin Trans. 2 1997, 513-6.
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Sandall, J.P.B.1
Thompson, C.C.2
Steel, N.J.D.3
24
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For further details, see Claridge, R. P., Millar, R. W., Sandall, J. P. B., C. Thompson, C., J Chem. Res.(S) 1999, 520, J Chem. Res.(M) 1999, 1952-1969.
(1999)
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Millar, R.W.2
Sandall, J.P.B.3
Thompson, C.C.4
25
3242722750
For further details, see Claridge, R. P., Millar, R. W., Sandall, J. P. B., C. Thompson, C., J Chem. Res.(S) 1999, 520, J Chem. Res.(M) 1999, 1952-1969.
(1999)
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26
0001394911
Makosza, M., Winiarski, J., Acc. Chem. Res. 1987, 20, 282.
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Acc. Chem. Res.
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Winiarski, J.2
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Thompson, C.4
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For a recent review, see: Curci, R., Dinoi, A., Rubino, M. F., Pure Appl. Chem. 1995, 67, 811.
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(1992)
Organic Peroxides
Ando, W.1
31
3242682069
note
2 in trifluoroacetic acid are capable of cleaving the N-S bond in sulphoximines (M. D. Coburn, personal communication).
32
3242731752
note
This effect was first reported by Coburn (see refs. 15 and 16).
33
3242706424
Aldrich Chemical Co. Inc
nd Edit.; Vol. 1, Aldrich Chemical Co. Inc. 1983.
(1983)
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Nissan, R.A.2
Wilson, W.S.3