-
1
-
-
84987276636
-
-
[1a] R. S. Foxe, C. F. Beam, and C. R. Hauser, J. Heterocyclic Chem., 7, 589 (1970);
-
(1970)
J. Heterocyclic Chem.
, vol.7
, pp. 589
-
-
Foxe, R.S.1
Beam, C.F.2
Hauser, C.R.3
-
3
-
-
84980213404
-
-
[c] C. P. Beam, R. S. Foote, and C. R. Hauser, J. Heterocyclic Chem., 9, 183 (1972);
-
(1972)
J. Heterocyclic Chem.
, vol.9
, pp. 183
-
-
Beam, C.P.1
Foote, R.S.2
Hauser, C.R.3
-
4
-
-
0009998221
-
-
[d] C. F. Beam, D. C. Reames, C. E. Harris, L. W. Dasher, W. M. Hollinger, N. L. Shealy, R. M. Saodifer, M. Perkios, and C. R. Hauser, J. Org Chem., 40, 514 (1975);
-
(1975)
J. Org Chem.
, vol.40
, pp. 514
-
-
Beam, C.F.1
Reames, D.C.2
Harris, C.E.3
Dasher, L.W.4
Hollinger, W.M.5
Shealy, N.L.6
Saodifer, R.M.7
Perkios, M.8
Hauser, C.R.9
-
5
-
-
0010732054
-
-
[e] C. F. Beam, R. M. Saodifer, R. S. Foote, and C. R. Hauser, Synth. Commun., 6, 5 (1976);
-
(1976)
Synth. Commun.
, vol.6
, pp. 5
-
-
Beam, C.F.1
Saodifer, R.M.2
Foote, R.S.3
Hauser, C.R.4
-
6
-
-
0000463903
-
-
[f] T. D. Pulmer, M. L. Livingstoo, L. P. Dasher, B. L. Bobb, J. D. Wilson, K. L. Sides, and C. F. Beam, J. Heterocyclic Chem., 17, 799 (1980);
-
(1980)
J. Heterocyclic Chem.
, vol.17
, pp. 799
-
-
Pulmer, T.D.1
Livingstoo, M.L.2
Dasher, L.P.3
Bobb, B.L.4
Wilson, J.D.5
Sides, K.L.6
Beam, C.F.7
-
7
-
-
84985219471
-
-
[g] M. J. Livingston, M. F. Chick, E. O. Shealy, D. J. Park, T. D. Fulmer, and C. F. Beam, J. Heterocyclic Chem., 19, 215 (1982);
-
(1982)
J. Heterocyclic Chem.
, vol.19
, pp. 215
-
-
Livingston, M.J.1
Chick, M.F.2
Shealy, E.O.3
Park, D.J.4
Fulmer, T.D.5
Beam, C.F.6
-
8
-
-
0001451524
-
-
[h] C. F. Beam, H. L. Hall, A. M. Huff, R. C. Tummons, S. A. O'Grady, J. Heterocyclic Chem., 21, 1897 (1984);
-
(1984)
J. Heterocyclic Chem.
, vol.21
, pp. 1897
-
-
Beam, C.F.1
Hall, H.L.2
Huff, A.M.3
Tummons, R.C.4
O'Grady, S.A.5
-
10
-
-
0000075374
-
-
[j] M. L. Mazat, C. F. Beam, and M. A. Hines, Synth. Commun., 20, 253 (1990);
-
(1990)
Synth. Commun.
, vol.20
, pp. 253
-
-
Mazat, M.L.1
Beam, C.F.2
Hines, M.A.3
-
11
-
-
84986467804
-
-
[k] D. C. Duncan, T. A. Trumbo, C. D. Almquist, T. A. Lentz, and C. F. Beam, J. Heterocyclic Chem., 24, 555 (1987);
-
(1987)
J. Heterocyclic Chem.
, vol.24
, pp. 555
-
-
Duncan, D.C.1
Trumbo, T.A.2
Almquist, C.D.3
Lentz, T.A.4
Beam, C.F.5
-
12
-
-
0029788412
-
-
[l] A. C. Church, M. U. Koller, M. A. Hines, and C. F. Beam, Synth. Commun., 26, 3659 (1996);
-
(1996)
Synth. Commun.
, vol.26
, pp. 3659
-
-
Church, A.C.1
Koller, M.U.2
Hines, M.A.3
Beam, C.F.4
-
13
-
-
0029898204
-
-
A. C. Church, M. U. Koller, S. A. O'Grady, and C. F. Beam, Synth. Commun., 26, 2603 (1996).
-
(1996)
Synth. Commun.
, vol.26
, pp. 2603
-
-
Church, A.C.1
Koller, M.U.2
O'Grady, S.A.3
Beam, C.F.4
-
14
-
-
1542554618
-
-
R. H. Wiley, ed, John Wiley and Sons, Inc., New York, N. Y., Chapter 3.
-
See R. Fusco, The Chemistry of Heterocyclic Compounds, Vol 22, R. H. Wiley, ed, John Wiley and Sons, Inc., New York, N. Y., 2967, Chapter 3.
-
The Chemistry of Heterocyclic Compounds
, vol.22
, pp. 2967
-
-
Fusco, R.1
-
17
-
-
0000873893
-
-
K. N. Zelenin, O. V. Solod, and A. B. Tomchin, Zh. Obshch. Khim., 57, 584 (1987).
-
(1987)
Zh. Obshch. Khim.
, vol.57
, pp. 584
-
-
Zelenin, K.N.1
Solod, O.V.2
Tomchin, A.B.3
-
20
-
-
1542554614
-
-
[6a] N. S. Vul'fson, Sbnorik Statei, Nauch-Issledovatel Inst. Org. Poluprovd. i Krasitelei, 2, 128 (1961); Chem. Abstr., 56, 10031c (1962);
-
(1961)
Sbnorik Statei, Nauch-Issledovatel Inst. Org. Poluprovd. i Krasitelei
, vol.2
, pp. 128
-
-
VuL'Fson, N.S.1
-
21
-
-
26744479322
-
-
[6a] N. S. Vul'fson, Sbnorik Statei, Nauch-Issledovatel Inst. Org. Poluprovd. i Krasitelei, 2, 128 (1961); Chem. Abstr., 56, 10031c (1962);
-
(1962)
Chem. Abstr.
, vol.56
-
-
-
22
-
-
0018575383
-
-
[b] D. N. Ridge, J. W. Hanifin, L. A. Harten, B. D. Johnson, J. Menschik, G. Nicolau, A. E. Sloboda, and D. E. Watts, J. Med. Chem., 22, 1385 (1979);
-
(1979)
J. Med. Chem.
, vol.22
, pp. 1385
-
-
Ridge, D.N.1
Hanifin, J.W.2
Harten, L.A.3
Johnson, B.D.4
Menschik, J.5
Nicolau, G.6
Sloboda, A.E.7
Watts, D.E.8
-
27
-
-
33748992815
-
-
[g] G. Ege and P. Arnold, Angew. Chem., 86, 237 (1974); Angew. Chem. Int. Ed Engl., 13, 206 (1974);
-
(1974)
Angew. Chem.
, vol.86
, pp. 237
-
-
Ege, G.1
Arnold, P.2
-
28
-
-
84982356545
-
-
[g] G. Ege and P. Arnold, Angew. Chem., 86, 237 (1974); Angew. Chem. Int. Ed Engl., 13, 206 (1974);
-
(1974)
Angew. Chem. Int. Ed Engl.
, vol.13
, pp. 206
-
-
-
30
-
-
1542450083
-
-
[i] P. Kurtz, H. Gold, and H. Disselknotter, Liebig S. Vuli'fson Sbornik Statei, Nauch-Issledovatel Inst. Org. Poluprovd. i Krasiteli, 2, 128 (1961).
-
(1961)
Liebig S. Vuli'fson Sbornik Statei, Nauch-Issledovatel Inst. Org. Poluprovd. i Krasiteli
, vol.2
, pp. 128
-
-
Kurtz, P.1
Gold, H.2
Disselknotter, H.3
-
31
-
-
1542554609
-
-
[7a] E. Ajello, S. Plescia, and G. Dattolo, Atti Accad. Sci. Lett. Arti Palermo, 33, 297 (1974);
-
(1974)
Atti Accad. Sci. Lett. Arti Palermo
, vol.33
, pp. 297
-
-
Ajello, E.1
Plescia, S.2
Dattolo, G.3
-
36
-
-
1542764951
-
-
There is considerable literature precedent for testing new pyrazoles as insecticides, fungicides, bacterocides, herbicides, and plant growth enhancers
-
There is considerable literature precedent for testing new pyrazoles as insecticides, fungicides, bacterocides, herbicides, and plant growth enhancers.
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37
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1542554613
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Five percent excess base and ester; 0.015 mole entry compound 0.063 mole LDA: 0.0158 mole ester for approximate ratio of entry compound: base: ester of 1:4:1.
-
Five percent excess base and ester; 0.015 mole entry compound 0.063 mole LDA: 0.0158 mole ester for approximate ratio of entry compound: base: ester of 1:4:1.
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-
-
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38
-
-
0028792333
-
-
+ ion; see also: [a] L. Orsatti, R. Seragila, P. Traldi, G. Diamantini, G. Tarzia, and A. Tontiai, J. Mass Spectrom., 30, 1567 (1995);
-
(1995)
J. Mass Spectrom.
, vol.30
, pp. 1567
-
-
Orsatti, L.1
Seragila, R.2
Traldi, P.3
Diamantini, G.4
Tarzia, G.5
Tontiai, A.6
-
40
-
-
84989023315
-
-
[c] K. Harada, K. Masuda and M. Suzuki, H. Oka, Y. Ikai, and J. Hayakawa, Org. Mass. Spectrom., 28, 1512 (1993).
-
(1993)
Org. Mass. Spectrom.
, vol.28
, pp. 1512
-
-
Harada, K.1
Masuda, K.2
Suzuki, M.3
Oka, H.4
Ikai, Y.5
Hayakawa, J.6
-
41
-
-
0001118231
-
-
NRCVAX, An Interactive Program System for Structure Analysis. See: E. J. Gabe, Y. Le Page, J.-P. Charland, P. L. Lee, and P. S. White, J. Appl. Cryst., 22, 384 (1989); [b] Further data are available on request from the authors C. R. M. or W. T. P.
-
(1989)
J. Appl. Cryst.
, vol.22
, pp. 384
-
-
Gabe, E.J.1
Le Page, Y.2
Charland, J.-P.3
Lee, P.L.4
White, P.S.5
-
42
-
-
1542659696
-
-
Further data are available on request from the authors C. R. M. or W. T. P
-
NRCVAX, An Interactive Program System for Structure Analysis. See: E. J. Gabe, Y. Le Page, J.-P. Charland, P. L. Lee, and P. S. White, J. Appl. Cryst., 22, 384 (1989); [b] Further data are available on request from the authors C. R. M. or W. T. P.
-
-
-
-
44
-
-
0017316415
-
-
[b] M. H. Elnagdi, M. R. H. El-Moghayar, D. H. Fleita, E. A. A. Hafez, and S. M. Fahmy, J. Org. Chem., 41, 3781 (1976);
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3781
-
-
Elnagdi, M.H.1
El-Moghayar, M.R.H.2
Fleita, D.H.3
Hafez, E.A.A.4
Fahmy, S.M.5
-
45
-
-
0025314467
-
-
[c] A. Costanzo, F. Bruni, A. Auzzi, S. Sellen and L. P. Vettori, J. Hetemcyclic Chem., 27, 695 (1990).
-
(1990)
J. Hetemcyclic Chem.
, vol.27
, pp. 695
-
-
Costanzo, A.1
Bruni, F.2
Auzzi, A.3
Sellen, S.4
Vettori, L.P.5
-
46
-
-
1542764837
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-
13C high field nmr studies. Instrumentation for such spectra will be available in this department in several months
-
13C high field nmr studies. Instrumentation for such spectra will be available in this department in several months,
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47
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1542659694
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X-ray crystallographic analysis are necessary before reporting the condensation/cyclization of polylithiated acetophenone semicarbazone with lithiated ethyl benzoylacetate
-
[b] X-ray crystallographic analysis are necessary before reporting the condensation/cyclization of polylithiated acetophenone semicarbazone with lithiated ethyl benzoylacetate.
-
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48
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1542554610
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1H nmr integration ratios for NH and OH intensities were variable
-
1H nmr integration ratios for NH and OH intensities were variable.
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-
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51
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1542659697
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In an earlier investigation, methyl isonicotinate was an ester used in a condensation/cyclizatioo with dilithiated phenylhydrazones. See also: ref [1f]
-
In an earlier investigation, methyl isonicotinate was an ester used in a condensation/cyclizatioo with dilithiated phenylhydrazones. See also: ref [1f]
-
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52
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1542659698
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The ratio initially used was different from 1:4:1, which is part of the developing general experimental procedure
-
The ratio initially used was different from 1:4:1, which is part of the developing general experimental procedure.
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-
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-
55
-
-
0025734242
-
-
[c] S. D. Larsen, C. H. Spilman, P. P. Bell, D. M. Dinh, E. Martinborough, and G. J. Wilson, J. Med. Chem., 34, 1721 (1991).
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1721
-
-
Larsen, S.D.1
Spilman, C.H.2
Bell, P.P.3
Dinh, D.M.4
Martinborough, E.5
Wilson, G.J.6
-
57
-
-
0027196915
-
-
[b] P. Bruni, A. Costazo, S. Selleri, G. Guerrini, R. Fontozzi, R. Pirisino, and S. Brunelleschi, J. Pharm. Sci., 82, 480 (1993).
-
(1993)
J. Pharm. Sci.
, vol.82
, pp. 480
-
-
Bruni, P.1
Costazo, A.2
Selleri, S.3
Guerrini, G.4
Fontozzi, R.5
Pirisino, R.6
Brunelleschi, S.7
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