-
4
-
-
0034746865
-
-
Baldwin, J. E.; Pritchard, G. J.; Rathmell, R. E. J. Chem. Soc, Perkin Trans. 1 2001, 2906.
-
(2001)
J. Chem. Soc, Perkin Trans. 1
, pp. 2906
-
-
Baldwin, J.E.1
Pritchard, G.J.2
Rathmell, R.E.3
-
5
-
-
0034618258
-
-
Adlington, R. M.; Baldwin, J. E.; Catterick, D.; Pritchard, G. J.; Tang, L. T. J. Chem. Soc., Perkin Trans. 1 2000, 2311.
-
(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 2311
-
-
Adlington, R.M.1
Baldwin, J.E.2
Catterick, D.3
Pritchard, G.J.4
Tang, L.T.5
-
6
-
-
0001674667
-
-
Adlington, R. M.; Baldwin, J. E.; Catterick, D.; Pritchard, G. J. J. Chem. Soc, Perkin Trans. 1 1999, 855.
-
(1999)
J. Chem. Soc, Perkin Trans. 1
, pp. 855
-
-
Adlington, R.M.1
Baldwin, J.E.2
Catterick, D.3
Pritchard, G.J.4
-
7
-
-
0034639905
-
-
(a) Bagley, M. C.; Bashford, K. E.; Hesketh, C. L.; Moody, C. J. J. Am. Chem. Soc. 2000, 122, 3301.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 3301
-
-
Bagley, M.C.1
Bashford, K.E.2
Hesketh, C.L.3
Moody, C.J.4
-
9
-
-
13844306055
-
-
(c) Bagley, M. C.; Dale, J. W.; Merritt, E. A.; Xiong, X. Chem. Rev. 2005, 105, 685.
-
(2005)
Chem. Rev
, vol.105
, pp. 685
-
-
Bagley, M.C.1
Dale, J.W.2
Merritt, E.A.3
Xiong, X.4
-
10
-
-
28844437779
-
-
Davis, J. M.; Truong, A.; Hamilton, A. D. Org. Lett. 2005, 7, 5405.
-
(2005)
Org. Lett
, vol.7
, pp. 5405
-
-
Davis, J.M.1
Truong, A.2
Hamilton, A.D.3
-
11
-
-
0018723551
-
-
Schroeder, E.; Lehmann, M.; Boettcher, I. Eur. J. Med. Chem. 1979, 14, 309.
-
(1979)
Eur. J. Med. Chem
, vol.14
, pp. 309
-
-
Schroeder, E.1
Lehmann, M.2
Boettcher, I.3
-
12
-
-
0013021290
-
-
Bagley, M. C.; Dale, J. W.; Ohnesorge, M.; Xiong, X.; Bower, J. J. Comb. Chem. 2003, 5, 41.
-
(2003)
J. Comb. Chem
, vol.5
, pp. 41
-
-
Bagley, M.C.1
Dale, J.W.2
Ohnesorge, M.3
Xiong, X.4
Bower, J.5
-
13
-
-
0037450398
-
-
Bashford, K. E.; Burton, M. B.; Cameron, S.; Cooper, A. L.; Hogg, R. D.; Kane, P. D.; MacManus, D. A.; Matrunola, C. A.; Moody, C. J.; Robertson, A. A. B.; Warne, M. R. Tetrahedron Lett. 2003, 44, 1627.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1627
-
-
Bashford, K.E.1
Burton, M.B.2
Cameron, S.3
Cooper, A.L.4
Hogg, R.D.5
Kane, P.D.6
MacManus, D.A.7
Matrunola, C.A.8
Moody, C.J.9
Robertson, A.A.B.10
Warne, M.R.11
-
14
-
-
12344308011
-
-
Bagley, M. C.; Hughes, D. D.; Lubinu, M. C.; Merritt, E. A.; Taylor, P. H.; Tomkinson, N. C. O. QSAR Comb. Sci. 2004, 23, 859.
-
(2004)
QSAR Comb. Sci
, vol.23
, pp. 859
-
-
Bagley, M.C.1
Hughes, D.D.2
Lubinu, M.C.3
Merritt, E.A.4
Taylor, P.H.5
Tomkinson, N.C.O.6
-
16
-
-
0034817380
-
-
Bagley, M. C.; Dale, J. W.; Hughes, D. D.; Ohnesorge, M.; Phillips, N. G.; Bower, J. Synlett 2001, 1523.
-
(2001)
Synlett
, pp. 1523
-
-
Bagley, M.C.1
Dale, J.W.2
Hughes, D.D.3
Ohnesorge, M.4
Phillips, N.G.5
Bower, J.6
-
17
-
-
0037064517
-
-
Bagley, M. C.; Lunn, R.; Xiong, X. Tetrahedron Lett. 2002, 43, 8331.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 8331
-
-
Bagley, M.C.1
Lunn, R.2
Xiong, X.3
-
18
-
-
3142745109
-
-
Bagley, M. C.; Chapaneri, K.; Xiong, X. Tetrahedron Lett. 2004, 45, 6121.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 6121
-
-
Bagley, M.C.1
Chapaneri, K.2
Xiong, X.3
-
20
-
-
0035996944
-
-
Bagley, M. C.; Brace, C.; Dale, J. W.; Ohnesorge, M.; Phillips, N. G.; Xiong, X.; Bower, J. J. Chem. Soc., Perkin Trans. 1 2002, 1663.
-
(2002)
J. Chem. Soc., Perkin Trans. 1
, pp. 1663
-
-
Bagley, M.C.1
Brace, C.2
Dale, J.W.3
Ohnesorge, M.4
Phillips, N.G.5
Xiong, X.6
Bower, J.7
-
22
-
-
1942489365
-
-
Bagley, M. C.; Glover, C.; Merritt, E. A.; Xiong, X. Synlett 2004, 811.
-
(2004)
Synlett
, pp. 811
-
-
Bagley, M.C.1
Glover, C.2
Merritt, E.A.3
Xiong, X.4
-
25
-
-
0035840392
-
-
Bagley, M. C.; Hughes, D. D.; Lloyd, R.; Powers, V. E. C. Tetrahedron Lett. 2001, 42, 6585.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 6585
-
-
Bagley, M.C.1
Hughes, D.D.2
Lloyd, R.3
Powers, V.E.C.4
-
31
-
-
33751158531
-
-
(a) Cablewski, T.; Faux, A. F.; Strauss, C. R. J. Org. Chem. 1994, 59, 3408.
-
(1994)
J. Org. Chem
, vol.59
, pp. 3408
-
-
Cablewski, T.1
Faux, A.F.2
Strauss, C.R.3
-
32
-
-
0034712151
-
-
(b) Kabza, K. G.; Chapados, B. R.; Gestwicki, J. E.; McGrath, J. L. J. Org. Chem. 2000, 65, 1210.
-
(2000)
J. Org. Chem
, vol.65
, pp. 1210
-
-
Kabza, K.G.1
Chapados, B.R.2
Gestwicki, J.E.3
McGrath, J.L.4
-
34
-
-
0342656971
-
-
(d) Esveld, E.; Chemat, F.; van Haveren, J. Chem. Eng. Technol. 2000, 23, 279.
-
(2000)
Chem. Eng. Technol
, vol.23
, pp. 279
-
-
Esveld, E.1
Chemat, F.2
van Haveren, J.3
-
35
-
-
0034180026
-
-
(e) Esveld, E.; Chemat, F.; van Haveren, J. Chem. Eng. Technol. 2000, 23, 429.
-
(2000)
Chem. Eng. Technol
, vol.23
, pp. 429
-
-
Esveld, E.1
Chemat, F.2
van Haveren, J.3
-
36
-
-
0037025725
-
-
(f) Shieh, W.-C.; Dell, S.; Repi, O. Tetrahedron Lett. 2002, 43, 5607.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5607
-
-
Shieh, W.-C.1
Dell, S.2
Repi, O.3
-
38
-
-
23644454820
-
-
Bagley, M. C.; Jenkins, R. L.; Lubinu, M. C.; Mason, C.; Wood, R. J. Org. Chem. 2005, 70, 7003.
-
(2005)
J. Org. Chem
, vol.70
, pp. 7003
-
-
Bagley, M.C.1
Jenkins, R.L.2
Lubinu, M.C.3
Mason, C.4
Wood, R.5
-
39
-
-
33947728988
-
-
13C NMR, IR, MS and HRMS.
-
13C NMR, IR, MS and HRMS.
-
-
-
-
40
-
-
33947715787
-
-
1H NMR spectrum of both pyrazole regioisomers. The 5-ethyl-trisubstituted pyrazole (entry 4) showed NOESY effects between the aryl ortho-methine resonances and the methylene protons.
-
1H NMR spectrum of both pyrazole regioisomers. The 5-ethyl-trisubstituted pyrazole (entry 4) showed NOESY effects between the aryl ortho-methine resonances and the methylene protons.
-
-
-
-
41
-
-
33947725019
-
-
1,3-Diphenylpyrazole (3, mp 81-83°C (lit.35 mp 84-85°C, Rf, 0.61 (CH2Cl2, HRMS: m/z [MH, calcd for C15H13N2: 221.1073; found: 221.1074 [MH, IR(nujol, νmax, 1598, 1526, 1504, 1360, 1264, 1114, 1061, 1046, 954, 755, 686 cm-1. UV (CH2Cl2, λmax (ε, 284 (17959, 224 (6189) nm. 1H NMR (400 MHz, CDCl3, δ, 7.89 (1 H, d, J, 2.5 Hz, 5-H, 7.85 (2 H, m, PhH, 7.71 (2 H, m, PhH, 7.38 (4 H, PhH, 7.24 (2 H, m, PhH, 6.71 (1 H, d, J, 2.5 Hz, 4-H) ppm. 13C NMR (100 MHz, CDCl3, δ, 153.3 (C, 140.6 (C, 133.5 (C, 129.8 (CH, 129.1 (CH, 128.5 (CH, 128.4 (CH, 126.7 (CH, 126.2 (CH, 119.5 (CH, 105.4 (CH) ppm. MS(APCI, m/z, 221 (100, MH, 194(5, 118 10
-
+], 194(5), 118 (10).
-
-
-
-
42
-
-
33947724566
-
-
1,5-Diphenylpyrazole (4, mp 52-55°C (lit.35 mp 55-56°C, Rf, 0.18 (CH2Cl2, HRMS: m/z [MH, calcd for C15H13N2: 221.1073; found: 221.1072 [MH, IR(nujol, νmax, 1596, 1541, 1502, 1450, 1385, 1224, 1158, 1130, 1068, 960, 761, 695 cm -1. UV (CH2Cl2, λmax (ε, 252 (14493, 1H NMR (400 MHz, CDCl3, δ, 7.66 (1 H, d, J, 1.5 Hz, 3-H, 7.28-7.22 (8 H, PhH, 7.19-7.15 (2 H, m, PhH, 6.45 (1 H, d, J, 1.5 Hz, 4-H) ppm. 13C NMR (100 MHz, CDCl3, δ, 143.0 (C, 140.3 (CH, 140.1 (C, 130.6 (CH, 128.9 (CH, 128.8 (CH, 128.5 (CH, 128.2 (CH, 127.4 (CH, 125.2 (CH, 107.9 (CH) ppm. MS (APCI, m/z, 221 (100, MH, 194 (10, 152 (5, 103 5
-
+], 194 (10), 152 (5), 103 (5).
-
-
-
|