-
1
-
-
0020052842
-
-
Shutske G.M., Setescak L.L., Allen R.C., Davis L., Effland R.C., Ranbom K., Kitzen J.M., Wilker J.C., and Novick Jr. W.J. J. Med. Chem. 25 (1982) 36-44
-
(1982)
J. Med. Chem.
, vol.25
, pp. 36-44
-
-
Shutske, G.M.1
Setescak, L.L.2
Allen, R.C.3
Davis, L.4
Effland, R.C.5
Ranbom, K.6
Kitzen, J.M.7
Wilker, J.C.8
Novick Jr., W.J.9
-
3
-
-
73649143268
-
Improved Process for the Preparation of Intermediates Useful for the Preparation of Zonisamide. WO 2005/030738, Sep 29, 2003
-
Veera Reddy, A.; Rajendiran, C.; Vaishali, N. Improved Process for the Preparation of Intermediates Useful for the Preparation of Zonisamide. WO 2005/030738, Sep 29, 2003; Chem. Abstr. 2005, 142, 33849.
-
(2005)
Chem. Abstr
, vol.142
, pp. 33849
-
-
Veera Reddy, A.1
Rajendiran, C.2
Vaishali, N.3
-
4
-
-
0021808398
-
-
Struczewski J.T., Allen R.C., Gardner B.A., Schmid B.L., Glamkovski E.J., Jones M.C., Ellis D.B., Huger F.P., and Dunn R.W. J. Med. Chem. 28 (1985) 761-769
-
(1985)
J. Med. Chem.
, vol.28
, pp. 761-769
-
-
Struczewski, J.T.1
Allen, R.C.2
Gardner, B.A.3
Schmid, B.L.4
Glamkovski, E.J.5
Jones, M.C.6
Ellis, D.B.7
Huger, F.P.8
Dunn, R.W.9
-
6
-
-
73649145272
-
-
note
-
NAr.
-
-
-
-
9
-
-
17144375265
-
-
Liu K., Xu L., Berger J.P., MacNaul L.L., Zhou G., Doebbler T.W., Forrst M.J., Moller D.E., and Jones A.B. J. Med. Chem. 48 (2005) 2262-2265
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2262-2265
-
-
Liu, K.1
Xu, L.2
Berger, J.P.3
MacNaul, L.L.4
Zhou, G.5
Doebbler, T.W.6
Forrst, M.J.7
Moller, D.E.8
Jones, A.B.9
-
14
-
-
26844443331
-
-
Cvetovich R.J., Chung J.Y.L., Kress M.H., Amato J.S., Matty L., Weingarten M.D., Tsay F.-R., Li Z., and Zhou G. J. Org. Chem. 70 (2005) 8560-8563
-
(2005)
J. Org. Chem.
, vol.70
, pp. 8560-8563
-
-
Cvetovich, R.J.1
Chung, J.Y.L.2
Kress, M.H.3
Amato, J.S.4
Matty, L.5
Weingarten, M.D.6
Tsay, F.-R.7
Li, Z.8
Zhou, G.9
-
19
-
-
4744376265
-
-
Malamas M.S., Manas E.S., McDewitt R.E., Gunawan I., Xu Z.B., Collini M.D., Miller C.P., Dinh T., Henderson R.A., Keith, Jr J.C., and Harris H.A. J. Med. Chem. 47 (2004) 5021-5040
-
(2004)
J. Med. Chem.
, vol.47
, pp. 5021-5040
-
-
Malamas, M.S.1
Manas, E.S.2
McDewitt, R.E.3
Gunawan, I.4
Xu, Z.B.5
Collini, M.D.6
Miller, C.P.7
Dinh, T.8
Henderson, R.A.9
Keith10
Jr, J.C.11
Harris, H.A.12
-
22
-
-
0343334869
-
-
For some recent examples in which fluoride is utilized as a leaving group, see:
-
For some recent examples in which fluoride is utilized as a leaving group, see:. Bunnett J.F., and Yih S.Y. J. Am. Chem. Soc. 83 (1961) 3805-3807
-
(1961)
J. Am. Chem. Soc.
, vol.83
, pp. 3805-3807
-
-
Bunnett, J.F.1
Yih, S.Y.2
-
23
-
-
51349121840
-
-
Kunz R.K., Rumfelt S., Chen N., Zhang D., Tasker A.S., Bürli R., Hungate R., Yu V., Nguyen Y., Whittington D.A., Meagher K.L., Plant M., Tudor Y., Schrag M., Xu Y., Ng G.Y., and Hu E. Bioorg. Med. Chem. Lett. 18 (2008) 5115-5117
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5115-5117
-
-
Kunz, R.K.1
Rumfelt, S.2
Chen, N.3
Zhang, D.4
Tasker, A.S.5
Bürli, R.6
Hungate, R.7
Yu, V.8
Nguyen, Y.9
Whittington, D.A.10
Meagher, K.L.11
Plant, M.12
Tudor, Y.13
Schrag, M.14
Xu, Y.15
Ng, G.Y.16
Hu, E.17
-
24
-
-
39149136212
-
-
Gopalsamy A., Shi M., Golas J., Vogan E., Jacob J., Johnson M., Lee F., Nilakantan R., Petersen R., Svenson K., Chopra R., Tam M.S., Wen Y., Ellingboe J., Arndt K., and Boschelli F. J. Med. Chem. 51 (2008) 373-375
-
(2008)
J. Med. Chem.
, vol.51
, pp. 373-375
-
-
Gopalsamy, A.1
Shi, M.2
Golas, J.3
Vogan, E.4
Jacob, J.5
Johnson, M.6
Lee, F.7
Nilakantan, R.8
Petersen, R.9
Svenson, K.10
Chopra, R.11
Tam, M.S.12
Wen, Y.13
Ellingboe, J.14
Arndt, K.15
Boschelli, F.16
-
25
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33748631210
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-
For some recent examples in which chloride is utilized as a leaving group, see:
-
For some recent examples in which chloride is utilized as a leaving group, see:. King J.F., and Durst T. Can. J. Chem. 40 (1962) 882-889
-
(1962)
Can. J. Chem.
, vol.40
, pp. 882-889
-
-
King, J.F.1
Durst, T.2
-
27
-
-
0025896058
-
-
Sato H., Dan T., Onuma E., Haruko A., and Bunya K. Chem. Pharm. Bull. 39 (1991) 1760-1772
-
(1991)
Chem. Pharm. Bull.
, vol.39
, pp. 1760-1772
-
-
Sato, H.1
Dan, T.2
Onuma, E.3
Haruko, A.4
Bunya, K.5
-
28
-
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0017872205
-
-
For some recent examples in which bromide is utilized as a leaving group, see:
-
For some recent examples in which bromide is utilized as a leaving group, see:. Tidwell R.R., and Geratz. J. Med. Chem. 21 (1978) 613-623
-
(1978)
J. Med. Chem.
, vol.21
, pp. 613-623
-
-
Tidwell, R.R.1
Geratz2
-
30
-
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33847802171
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-
For some recent examples in which a nitro group is utilized as a leaving group, see:
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For some recent examples in which a nitro group is utilized as a leaving group, see:. Kemp D.S., and Paul K.G. J. Am. Chem. Soc. 97 (1975) 7305-7312
-
(1975)
J. Am. Chem. Soc.
, vol.97
, pp. 7305-7312
-
-
Kemp, D.S.1
Paul, K.G.2
-
31
-
-
0028058926
-
-
Hrib N.J., Jurcak J.G., Burgher K.L., Conway P.G., Hartman H.B., Kerman L.L., Roehr J.E., and Woods A.T. J. Med. Chem. 37 (1994) 2308-2314
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2308-2314
-
-
Hrib, N.J.1
Jurcak, J.G.2
Burgher, K.L.3
Conway, P.G.4
Hartman, H.B.5
Kerman, L.L.6
Roehr, J.E.7
Woods, A.T.8
-
36
-
-
33846930164
-
-
Inamoto K., Katsuno M., Yoshino T., Arai Y., Hiroya K., and Sakamoto T. Tetrahedron 63 (2007) 2695-2711
-
(2007)
Tetrahedron
, vol.63
, pp. 2695-2711
-
-
Inamoto, K.1
Katsuno, M.2
Yoshino, T.3
Arai, Y.4
Hiroya, K.5
Sakamoto, T.6
-
40
-
-
0037179113
-
-
Pavlischchuk V., Birkelbach F., Weyhermüller T., Wieghardt K., and Chaudhuri P. Inorg. Chem. 41 (2002) 4405-4416
-
(2002)
Inorg. Chem.
, vol.41
, pp. 4405-4416
-
-
Pavlischchuk, V.1
Birkelbach, F.2
Weyhermüller, T.3
Wieghardt, K.4
Chaudhuri, P.5
-
41
-
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73649108678
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note
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Maitra reported that Na,K-tartrate was needed to prevent the Cu(II)-catalyzed deoximation, for details see: Ref. 15b.
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42
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23644447718
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For copper-catalyzed formation of C-O-bonds, see:
-
For copper-catalyzed formation of C-O-bonds, see:. Chem C., and Dormer P.G. J. Org. Chem. 70 (2005) 6964-6967
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6964-6967
-
-
Chem, C.1
Dormer, P.G.2
-
51
-
-
37049056629
-
-
Heating may induce isomerization under basic conditions. For details, see:
-
Heating may induce isomerization under basic conditions. For details, see:. Smith N.H.P. J. Chem. Soc. (1961) 4209-4211
-
(1961)
J. Chem. Soc.
, pp. 4209-4211
-
-
Smith, N.H.P.1
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