-
1
-
-
77956191936
-
Synthesis of morpholine containing sulfonamides: Introduction of morpholine moiety on amine functional group
-
Singh, D.; Bansal, G. Synthesis of morpholine containing sulfonamides: Introduction of morpholine moiety on amine functional group. Eur. J. Chem., 2004, 1(2), 164-169.
-
(2004)
Eur. J. Chem
, vol.1
, Issue.2
, pp. 164-169
-
-
Singh, D.1
Bansal, G.2
-
2
-
-
0032509407
-
Deprotection of sulfonyl aziridines
-
Alonso, D. A.; Andersson, P. G. Deprotection of sulfonyl aziridines. J. Org. Chem., 1998, 63(25), 9455-9461.
-
(1998)
J. Org. Chem
, vol.63
, Issue.25
, pp. 9455-9461
-
-
Alonso, D.A.1
Andersson, P.G.2
-
3
-
-
0034895422
-
Deprotection of 2-pyridyl sulfonyl group from pyridine-2-sulfonamides by magnesium in methanol
-
Park, C. S.; Lim, D. S. Deprotection of 2-pyridyl sulfonyl group from pyridine-2-sulfonamides by magnesium in methanol. Synth. Commun., 2001, 31(14), 2209-2214.
-
(2001)
Synth. Commun
, vol.31
, Issue.14
, pp. 2209-2214
-
-
Park, C.S.1
Lim, D.S.2
-
4
-
-
33845492104
-
Discovery of HIV-1 protease inhibitors with picomolar affinities incorporating N-aryl-oxazolidinone-5-carboxamides as novel P2 ligands
-
Ali, A.; Reddy, G. S. K. K.; Cao, H.; Anjum, S. G.; Nalam, M. N. L.; Schiffer, C. A.; Rana, T. M. Discovery of HIV-1 protease inhibitors with picomolar affinities incorporating N-aryl-oxazolidinone-5-carboxamides as novel P2 ligands. J. Med. Chem., 2006, 49, 7342-7356.
-
(2006)
J. Med. Chem
, vol.49
, pp. 7342-7356
-
-
Ali, A.1
Reddy, G.S.K.K.2
Cao, H.3
Anjum, S.G.4
Nalam, M.N.L.5
Schiffer, C.A.6
Rana, T.M.7
-
5
-
-
34147180527
-
Quinols as novel therapeutic agents. 7. 1 Synthesis of antitumor 4-[1-(arylsulfonyl-1H-indol-2-yl)]-4-hydroxycyclohexa-2, 5-dien-1-ones by Sonogashira reactions
-
McCarroll, A. J.; Bradshaw, T. D.; Westwell, A. D.; Matthews, C. S.; Stevens, M. F. G. Quinols as novel therapeutic agents. 7. 1 Synthesis of antitumor 4-[1-(arylsulfonyl-1H-indol-2-yl)]-4-hydroxycyclohexa-2, 5-dien-1-ones by Sonogashira reactions. J. Med. Chem., 2007, 50(7), 1707-1710.
-
(2007)
J. Med. Chem
, vol.50
, Issue.7
, pp. 1707-1710
-
-
McCarroll, A.J.1
Bradshaw, T.D.2
Westwell, A.D.3
Matthews, C.S.4
Stevens, M.F.G.5
-
6
-
-
34147144592
-
Carbonic anhydrase inhibitors: Inhibition of isozymes I, II, and IX with triazole-linked Oglycosides of benzene sulfonamides
-
Wilkinson, B. L.; Bomaghi, L. F.; Houston, T. A.; Innocenti, A.; Vullo, D.; Supuran C. T.; Poulsen, S. A. Carbonic anhydrase inhibitors: Inhibition of isozymes I, II, and IX with triazole-linked Oglycosides of benzene sulfonamides. J. Med. Chem., 2007, 50(7), 1651-1657.
-
(2007)
J. Med. Chem
, vol.50
, Issue.7
, pp. 1651-1657
-
-
Wilkinson, B.L.1
Bomaghi, L.F.2
Houston, T.A.3
Innocenti, A.4
Vullo, D.5
Supuran, C.T.6
Poulsen, S.A.7
-
7
-
-
0034677966
-
Drug discovery: A historical perspective
-
Drews, J. Drug discovery: A historical perspective. Science, 2000, 287(5460), 1960-1964.
-
(2000)
Science
, vol.287
, Issue.5460
, pp. 1960-1964
-
-
Drews, J.1
-
8
-
-
0024272631
-
Sulfonylurea receptors, ion channels, and fruit flies
-
Boyd, A. E. Sulfonylurea receptors, ion channels, and fruit flies. Diabetes, 1988, 37(7), 847-850.
-
(1988)
Diabetes
, vol.37
, Issue.7
, pp. 847-850
-
-
Boyd, A.E.1
-
9
-
-
0034018870
-
Carbonic anhydrase inhibitors and their therapeutic potential
-
Supuran, C. T.; Scozzafava, A. Carbonic anhydrase inhibitors and their therapeutic potential. Exp. Opin. Ther. Patents, 2000, 10(5), 575-600.
-
(2000)
Exp. Opin. Ther. Patents
, vol.10
, Issue.5
, pp. 575-600
-
-
Supuran, C.T.1
Scozzafava, A.2
-
10
-
-
33847145964
-
Synthesis, antimicrobial, and antiinflammatory activities of novel 2-(1-adamantyl)-5-substituted-1, 3, 4-oxadiazoles and 2-(1-adamantylamino)-5-substituted-1, 3, 4-thiadiazoles
-
Kadi, A. A.; El-Brollosy, N. R.; Al-Deeb, O. A.; Habib, E. E.; Ibrahim, T. M.; El-Emam, A. A. Synthesis, antimicrobial, and antiinflammatory activities of novel 2-(1-adamantyl)-5-substituted-1, 3, 4-oxadiazoles and 2-(1-adamantylamino)-5-substituted-1, 3, 4-thiadiazoles. Eur. J. Med. Chem., 2007, 42, 235-242.
-
(2007)
Eur. J. Med. Chem
, vol.42
, pp. 235-242
-
-
Kadi, A.A.1
El-Brollosy, N.R.2
Al-Deeb, O.A.3
Habib, E.E.4
Ibrahim, T.M.5
El-Emam, A.A.6
-
11
-
-
32044439796
-
New 1, 3, 4-thiadiazole derivatives endowed with analgesic and antiinflammatory activities
-
Schenone, S.; Brullo, C.; Bruno, O.; Bondavalli, F.; Ranise, A.; Filippelli, W.; Rinaldi, B.; Capuano, A.; Falcone, G. New 1, 3, 4-thiadiazole derivatives endowed with analgesic and antiinflammatory activities. Bioorg. Med. Chem., 2006, 14(6), 1698-1705.
-
(2006)
Bioorg. Med. Chem
, vol.14
, Issue.6
, pp. 1698-1705
-
-
Schenone, S.1
Brullo, C.2
Bruno, O.3
Bondavalli, F.4
Ranise, A.5
Filippelli, W.6
Rinaldi, B.7
Capuano, A.8
Falcone, G.9
-
12
-
-
80053211227
-
Anticancer and radio-sensitizing evaluation of some new thiazolopyrane and thiazolopyranopyrimidine derivatives bearing a sulfonamide moiety
-
Ghorab, M. M.; Ragab, F. A.; Heiba, H. I.; El-Hazek, R. M. Anticancer and radio-sensitizing evaluation of some new thiazolopyrane and thiazolopyranopyrimidine derivatives bearing a sulfonamide moiety. Eur. J. Med. Chem., 2011, 46(10), 5120-5126.
-
(2011)
Eur. J. Med. Chem
, vol.46
, Issue.10
, pp. 5120-5126
-
-
Ghorab, M.M.1
Ragab, F.A.2
Heiba, H.I.3
El-Hazek, R.M.4
-
13
-
-
34548857118
-
A novel oral indoline-sulfonamide agent, N-[1-(4-methoxybenzenesulfonyl)-2, 3-dihydro-1H-indol-7-yl]-isonicotinamide (J30), exhibits potent activity against human cancer cells in vitro and in vivo through the disruption of microtubule
-
Liou, J. P.; Hsu, K. S.; Kuo, C. C.; Chang, C. Y.; Chang, J. Y. A novel oral indoline-sulfonamide agent, N-[1-(4-methoxybenzenesulfonyl)-2, 3-dihydro-1H-indol-7-yl]-isonicotinamide (J30), exhibits potent activity against human cancer cells in vitro and in vivo through the disruption of microtubule. J. Pharmacol. Exp. Ther., 2007, 323(1), 398-405.
-
(2007)
J. Pharmacol. Exp. Ther
, vol.323
, Issue.1
, pp. 398-405
-
-
Liou, J.P.1
Hsu, K.S.2
Kuo, C.C.3
Chang, C.Y.4
Chang, J.Y.5
-
14
-
-
78650664699
-
Synthesis and antiviral activity of 5-(4-chlorophenyl)-1, 3, 4-thiadiazole sulfonamides
-
Chen, Z.; Xu, W.; Liu, K.; Yang, S.; Fan, H.; Bhadury, P. S.; Hu, D. Y.; Zhang, Y. Synthesis and antiviral activity of 5-(4-chlorophenyl)-1, 3, 4-thiadiazole sulfonamides. Molecules, 2010, 15(2), 9046-9056.
-
(2010)
Molecules
, vol.15
, Issue.2
, pp. 9046-9056
-
-
Chen, Z.1
Xu, W.2
Liu, K.3
Yang, S.4
Fan, H.5
Bhadury, P.S.6
Hu, D.Y.7
Zhang, Y.8
-
15
-
-
0013209248
-
Anticancer and antiviral sulfonamides
-
Scozzafava, A.; Owa, T.; Mastrolorenzo, A.; Supuran, C. T. Anticancer and antiviral sulfonamides. Curr. Med. Chem., 2003, 10(11), 925-953.
-
(2003)
Curr. Med. Chem
, vol.10
, Issue.11
, pp. 925-953
-
-
Scozzafava, A.1
Owa, T.2
Mastrolorenzo, A.3
Supuran, C.T.4
-
16
-
-
0002307325
-
A new preparation of sulfonyl chlorides via pyridiniumsulfonates
-
Barco, A.; Benetti, S.; Pollini, G. P.; Taddia, R. A new preparation of sulfonyl chlorides via pyridiniumsulfonates. Synthesis, 1974, 12, 877-878.
-
(1974)
Synthesis
, vol.12
, pp. 877-878
-
-
Barco, A.1
Benetti, S.2
Pollini, G.P.3
Taddia, R.4
-
18
-
-
0002170503
-
A convenient preparation of arenesulfonyl chlorides from the sodium sulfonates and phosphoryl chloride/sulfolane
-
Fujita, S. A convenient preparation of arenesulfonyl chlorides from the sodium sulfonates and phosphoryl chloride/sulfolane. Synthesis, 1982, 5, 423-424.
-
(1982)
Synthesis
, vol.5
, pp. 423-424
-
-
Fujita, S.1
-
19
-
-
18944362270
-
Synthesis of N-phthalimido α-aminoethanesulfonyl chlorides: The use of thionyl chloride for a simple and efficient synthesis of new peptidosulfonamide building blocks
-
Humljan, J.; Gobec, S. Synthesis of N-phthalimido α-aminoethanesulfonyl chlorides: the use of thionyl chloride for a simple and efficient synthesis of new peptidosulfonamide building blocks. Tetrahedron Lett., 2005, 46(23), 4069-4072.
-
(2005)
Tetrahedron Lett
, vol.46
, Issue.23
, pp. 4069-4072
-
-
Humljan, J.1
Gobec, S.2
-
20
-
-
32144444850
-
A convenient preparation of heteroaryl sulfonamides and sulfonyl fluorides from heteroaryl thiols
-
Wright, S. W.; Hallstrom, K. N. A convenient preparation of heteroaryl sulfonamides and sulfonyl fluorides from heteroaryl thiols. J. Org. Chem., 2006, 71(3), 1080-1084.
-
(2006)
J. Org. Chem
, vol.71
, Issue.3
, pp. 1080-1084
-
-
Wright, S.W.1
Hallstrom, K.N.2
-
21
-
-
0942276310
-
Direct synthesis of sulfonamides and activated sulfonate esters from sulfonic acids
-
Caddick, S.; Wilden, J. D.; Judd, D. B. Direct synthesis of sulfonamides and activated sulfonate esters from sulfonic acids. J. Am. Chem. Soc., 2004, 126, 1024-1025.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 1024-1025
-
-
Caddick, S.1
Wilden, J.D.2
Judd, D.B.3
-
22
-
-
34948815023
-
Novel and efficient synthesis of 1-iodoalkynes
-
Yan, J.; Li, J.; Cheng, D. Novel and efficient synthesis of 1-iodoalkynes. Synlett, 2007, 15, 2442-2444.
-
(2007)
Synlett
, vol.15
, pp. 2442-2444
-
-
Yan, J.1
Li, J.2
Cheng, D.3
-
23
-
-
73149089103
-
Direct conversion of thiols to sulfonyl chlorides and sulfonamides
-
Bahrami, K.; Khodaei M. M.; Soheilizad, M. Direct conversion of thiols to sulfonyl chlorides and sulfonamides. J. Org. Chem., 2009, 74(24), 9287-9291.
-
(2009)
J. Org. Chem
, vol.74
, Issue.24
, pp. 9287-9291
-
-
Bahrami, K.1
Khodaei, M.M.2
Soheilizad, M.3
-
24
-
-
34250316483
-
Convenient one-pot synthesis of sulfonamides from thiols using trichloroisocyanuric acid
-
Bonk, J. D.; Amos, D. T.; Olson, S. J. Convenient one-pot synthesis of sulfonamides from thiols using trichloroisocyanuric acid. Synth. Comm., 2007, 37(12), 2039-2050.
-
(2007)
Synth. Comm
, vol.37
, Issue.12
, pp. 2039-2050
-
-
Bonk, J.D.1
Amos, D.T.2
Olson, S.J.3
-
25
-
-
0142121704
-
Facile one-pot synthesis of aromatic and heteroaromatic sulfonamides
-
Pandya, R.; Murashima, T.; Tedeschi, L.; Barrett, A. G. M. Facile one-pot synthesis of aromatic and heteroaromatic sulfonamides. J. Org. Chem., 2003, 68(21), 8274-8276.
-
(2003)
J. Org. Chem
, vol.68
, Issue.21
, pp. 8274-8276
-
-
Pandya, R.1
Murashima, T.2
Tedeschi, L.3
Barrett, A.G.M.4
-
26
-
-
0035842159
-
Silver(I) oxide-mediated facile and practical sulfonylation of alcohols
-
Bouzide, A.; Leberre, N.; Sauve, G. Silver(I) oxide-mediated facile and practical sulfonylation of alcohols. Tetrahedron Lett., 2001, 42(50), 8781-8783.
-
(2001)
Tetrahedron Lett
, vol.42
, Issue.50
, pp. 8781-8783
-
-
Bouzide, A.1
Leberre, N.2
Sauve, G.3
-
27
-
-
0037033231
-
ChemoselectiveNacylation of amino alcohols promoted by magnesium oxide in aqueous organic solution
-
Kim, D. H.; Rho, H. S.; You, J. W.; Lee, J. C. ChemoselectiveNacylation of amino alcohols promoted by magnesium oxide in aqueous organic solution. Tetrahedron Lett., 2002, 43(2), 277-279.
-
(2002)
Tetrahedron Lett
, vol.43
, Issue.2
, pp. 277-279
-
-
Kim, D.H.1
Rho, H.S.2
You, J.W.3
Lee, J.C.4
-
28
-
-
0035804514
-
A novel method for the mild and selective amidation of diesters and the amidation of monoesters
-
Guo, Z.; Dowdy, E. D.; Li, W. S.; Polniaszek, R.; Delaney, E. A novel method for the mild and selective amidation of diesters and the amidation of monoesters. Tetrahedron Lett., 2001, 42(10), 1843-1845.
-
(2001)
Tetrahedron Lett
, vol.42
, Issue.10
, pp. 1843-1845
-
-
Guo, Z.1
Dowdy, E.D.2
Li, W.S.3
Polniaszek, R.4
Delaney, E.5
-
29
-
-
0041508387
-
Metal oxide in aqueous organic solution promoted chemoselectiveN-sulfonylation of hydrophilic amino alcohols
-
Kang, H. H.; Rho, H. S.; Kim, D. H.; Oh, S-G. Metal oxide in aqueous organic solution promoted chemoselectiveN-sulfonylation of hydrophilic amino alcohols. Tetrahedron Lett., 2003, 44(38), 7225-7227.
-
(2003)
Tetrahedron Lett
, vol.44
, Issue.38
, pp. 7225-7227
-
-
Kang, H.H.1
Rho, H.S.2
Kim, D.H.3
Oh, S.-G.4
-
30
-
-
0742287245
-
Unprecedented observation of sulfonamides in the transesterification of N-unsubstituted carbamates with sulfonyl chlorides
-
Dauvergne, J.; Wellington, K.; Chibale K. Unprecedented observation of sulfonamides in the transesterification of N-unsubstituted carbamates with sulfonyl chlorides. Tetrahedron Lett., 2004, 45(1), 43-47.
-
(2004)
Tetrahedron Lett
, vol.45
, Issue.1
, pp. 43-47
-
-
Dauvergne, J.1
Wellington, K.2
Chibale, K.3
-
31
-
-
79960982559
-
Efficient synthesis of sulfonamide derivatives on solid supports catalyzed using solvent-free and microwave-assisted methods
-
Camargo-Ordoñez, A.; Moreno-Reyes, C.; Olazarán-Santibáñez, F.; Martínez-Hernández, S.; Bocanegra-García, V.; Rivera, G. Efficient synthesis of sulfonamide derivatives on solid supports catalyzed using solvent-free and microwave-assisted methods. Quim. Nova, 2011, 34(5), 787-791.
-
(2011)
Quim. Nova
, vol.34
, Issue.5
, pp. 787-791
-
-
Camargo-Ordoñez, A.1
Moreno-Reyes, C.2
Olazarán-Santibáñez, F.3
Martínez-Hernández, S.4
Bocanegra-García, V.5
Rivera, G.6
-
33
-
-
33847008289
-
A novel approach for the synthesis of alkyl and aryl sulfonamides
-
Shaabani, A.; Soleimani, E.; Rezayan, A. H. A novel approach for the synthesis of alkyl and aryl sulfonamides. Tetrahedron Lett., 2007, 48(12), 2185-2188.
-
(2007)
Tetrahedron Lett
, vol.48
, Issue.12
, pp. 2185-2188
-
-
Shaabani, A.1
Soleimani, E.2
Rezayan, A.H.3
-
34
-
-
43449121552
-
An easy microwave-assisted synthesis of sulfonamides directly from sulfonic acids
-
De Luca, L.; Giacomelli, G. An easy microwave-assisted synthesis of sulfonamides directly from sulfonic acids. J. Org. Chem., 2008, 73, 3967-3969.
-
(2008)
J. Org. Chem
, vol.73
, pp. 3967-3969
-
-
De Luca, L.1
Giacomelli, G.2
-
35
-
-
33947455984
-
Potential metabolic antagonists of orotic acid: 6-uracilsulfonamide and 6-uracil methyl sulfone
-
Greenbaum, S. B. Potential metabolic antagonists of orotic acid: 6-uracilsulfonamide and 6-uracil methyl sulfone. J. Am. Chem. Soc., 1954, 76(23), 6052-6054.
-
(1954)
J. Am. Chem. Soc
, vol.76
, Issue.23
, pp. 6052-6054
-
-
Greenbaum, S.B.1
-
36
-
-
0024420982
-
Topically active carbonic anhydrase inhibitors. 1. O-acyl derivatives of 6-hydroxybenzothiazole-2-sulfonamide
-
Woltersdorf, O. W.; Schwam, H.; Bicking, J. B.; Brown, S. L.; Desolms, S. J.; Fishman, D. R.; Graham, S. L.; Gautheron, P. D.; Hoffman, J. M.; Larson, R. D.; Lee, W. S.; Michelson, S. R.; Robb, C. M.; Share, N. N.; Shepard, K. L.; Smith, A. M.; Smith, R. L.; Sondey, J. M.; Strohmaier, K. M.; Sugrue, M. F.; Viader, M. P. Topically active carbonic anhydrase inhibitors. 1. O-acyl derivatives of 6-hydroxybenzothiazole-2-sulfonamide. J. Med. Chem., 1989, 32(11), 2486-2492.
-
(1989)
J. Med. Chem
, vol.32
, Issue.11
, pp. 2486-2492
-
-
Woltersdorf, O.W.1
Schwam, H.2
Bicking, J.B.3
Brown, S.L.4
Desolms, S.J.5
Fishman, D.R.6
Graham, S.L.7
Gautheron, P.D.8
Hoffman, J.M.9
Larson, R.D.10
Lee, W.S.11
Michelson, S.R.12
Robb, C.M.13
Share, N.N.14
Shepard, K.L.15
Smith, A.M.16
Smith, R.L.17
Sondey, J.M.18
Strohmaier, K.M.19
Sugrue, M.F.20
Viader, M.P.21
more..
-
38
-
-
0025257038
-
Synthesis and antitumor evaluation in mice of certain 7-deazapurine (pyrrolo[2, 3-d]pyrimidine) and 3-deazapurine (imidazo[4, 5-c]pyridine) nucleosides structurally related to sulfenosine, sulfinosine, and sulfonosine
-
Ramasamy, K.; Imamura, N.; Hanna, N. B.; Finch, R. A.; Avery, T. L.; Robins, R. K.; Revankar, G. R. Synthesis and antitumor evaluation in mice of certain 7-deazapurine (pyrrolo[2, 3-d]pyrimidine) and 3-deazapurine (imidazo[4, 5-c]pyridine) nucleosides structurally related to sulfenosine, sulfinosine, and sulfonosine. J. Med. Chem., 1990, 33(4), 1220-1225.
-
(1990)
J. Med. Chem
, vol.33
, Issue.4
, pp. 1220-1225
-
-
Ramasamy, K.1
Imamura, N.2
Hanna, N.B.3
Finch, R.A.4
Avery, T.L.5
Robins, R.K.6
Revankar, G.R.7
-
39
-
-
0025056721
-
Synthesis and in vivo antitumor activity of 2-amino-9H-purine-6-sulfenamide,-sulfinamide, and-sulfonamide and related purine ribonucleosides
-
Revankar, G. R.; Hanna, N. B.; Imamura, N.; Lewis, A. F.; Larson, S. B.; Finch, R. A.; Avery, T. L.; Robins, R. K. Synthesis and in vivo antitumor activity of 2-amino-9H-purine-6-sulfenamide,-sulfinamide, and-sulfonamide and related purine ribonucleosides. J. Med. Chem., 1990, 33(1), 121-128.
-
(1990)
J. Med. Chem
, vol.33
, Issue.1
, pp. 121-128
-
-
Revankar, G.R.1
Hanna, N.B.2
Imamura, N.3
Lewis, A.F.4
Larson, S.B.5
Finch, R.A.6
Avery, T.L.7
Robins, R.K.8
-
40
-
-
0025109420
-
Synthesis and in vivo antitumor and antiviral activities of 2α-deoxyribofuranosyl and arabinofuranosyl nucleosides of certain purine-6-sulfenamides, sulfinamides and sulfonamides
-
Revankar, G. R.; Hanna, N. B.; Ramasamy, K.; Larson, S. B.; Smee, D. F.; Finch, R. A.; Avery, T. L.; Robins, R. K. Synthesis and in vivo antitumor and antiviral activities of 2α-deoxyribofuranosyl and arabinofuranosyl nucleosides of certain purine-6-sulfenamides, sulfinamides and sulfonamides. J. Heterocycl. Chem., 1990, 27(4), 909-918.
-
(1990)
J. Heterocycl. Chem
, vol.27
, Issue.4
, pp. 909-918
-
-
Revankar, G.R.1
Hanna, N.B.2
Ramasamy, K.3
Larson, S.B.4
Smee, D.F.5
Finch, R.A.6
Avery, T.L.7
Robins, R.K.8
-
41
-
-
0344496782
-
Palladium-catalyzed intermolecular coupling of aryl chlorides and sulfonamides under microwave irradiation
-
Burton, G.; Cao, P.; Li, G.; Rivero, R. Palladium-catalyzed intermolecular coupling of aryl chlorides and sulfonamides under microwave irradiation. Org. Lett., 2003, 5(23), 4373-4376.
-
(2003)
Org. Lett
, vol.5
, Issue.23
, pp. 4373-4376
-
-
Burton, G.1
Cao, P.2
Li, G.3
Rivero, R.4
-
42
-
-
33747073729
-
Palladium-catalyzed aromatic aminations with in situ generated aminostannanes
-
Guram, A. S.; Buchwald, S. L. Palladium-catalyzed aromatic aminations with in situ generated aminostannanes. J. Am. Chem. Soc., 1994, 116(17), 7901-7902.
-
(1994)
J. Am. Chem. Soc
, vol.116
, Issue.17
, pp. 7901-7902
-
-
Guram, A.S.1
Buchwald, S.L.2
-
44
-
-
0000499068
-
Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides
-
Paul, F.; Patt, J.; Hartwig, J. F. Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides. J. Am. Chem. Soc., 1994, 116(13), 5969-5970.
-
(1994)
J. Am. Chem. Soc
, vol.116
, Issue.13
, pp. 5969-5970
-
-
Paul, F.1
Patt, J.2
Hartwig, J.F.3
-
45
-
-
0032492942
-
New Nand O-arylations with phenylboronic acids and cupric acetate
-
Chan, D. M. T.; Monaco, K. L.; Wang, R. P.; Winters, M. P. New Nand O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett., 1998, 39(19), 2933-2936.
-
(1998)
Tetrahedron Lett
, vol.39
, Issue.19
, pp. 2933-2936
-
-
Chan, D.M.T.1
Monaco, K.L.2
Wang, R.P.3
Winters, M.P.4
-
46
-
-
0035858723
-
Copper-catalyzed general C-N and C-O bond cross-coupling with arylboronic acid
-
Lam, P. Y. S.; Vincent, G.; Clark, C. G.; Deudon, S.; Jadhav, P. K. Copper-catalyzed general C-N and C-O bond cross-coupling with arylboronic acid. Tetrahedron Lett., 2001, 42(20), 3415-3418.
-
(2001)
Tetrahedron Lett
, vol.42
, Issue.20
, pp. 3415-3418
-
-
Lam, P.Y.S.1
Vincent, G.2
Clark, C.G.3
Deudon, S.4
Jadhav, P.K.5
-
47
-
-
25444455340
-
Coppercatalyzed cross-coupling of sulfonamides with aryl iodides and bromides facilitated by amino acid ligands
-
Deng, W.; Liu, L.; Zhang, C.; Liu, M.; Guo, Q. X. Coppercatalyzed cross-coupling of sulfonamides with aryl iodides and bromides facilitated by amino acid ligands. Tetrahedron Lett., 2005, 46(43), 7295-7298.
-
(2005)
Tetrahedron Lett
, vol.46
, Issue.43
, pp. 7295-7298
-
-
Deng, W.1
Liu, L.2
Zhang, C.3
Liu, M.4
Guo, Q.X.5
-
48
-
-
0348041998
-
Facile N-arylation of amines and sulfonamides
-
Liu, Z. J.; Larock, R. C. Facile N-arylation of amines and sulfonamides. Org. Lett., 2003, 5(24), 4673-4675.
-
(2003)
Org. Lett
, vol.5
, Issue.24
, pp. 4673-4675
-
-
Liu, Z.J.1
Larock, R.C.2
-
49
-
-
33645768327
-
Facile N-arylation of amines and sulfonamides and O-arylation of phenols and arenecarboxylic acids
-
Liu, Z. J.; Larock, R. C. Facile N-arylation of amines and sulfonamides and O-arylation of phenols and arenecarboxylic acids. J. Org. Chem., 2006, 71(8), 3198-3209.
-
(2006)
J. Org. Chem
, vol.71
, Issue.8
, pp. 3198-3209
-
-
Liu, Z.J.1
Larock, R.C.2
-
51
-
-
0344496782
-
Palladium-catalyzed intermolecular coupling of aryl chlorides and sulfonamides under microwave irradiation
-
Burton, G.; Cao, P.; Li, G.; Rivero, R. Palladium-catalyzed intermolecular coupling of aryl chlorides and sulfonamides under microwave irradiation. Org. Lett., 2003, 5(23), 4373-4376.
-
(2003)
Org. Lett
, vol.5
, Issue.23
, pp. 4373-4376
-
-
Burton, G.1
Cao, P.2
Li, G.3
Rivero, R.4
-
52
-
-
33847254407
-
Trichlorophenol (TCP) sulfonate esters: A selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides
-
Wilden, J. D.; Geldeard, L.; Lee, C. C.; Judd, D. B.; Caddick, S. Trichlorophenol (TCP) sulfonate esters: A selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides. Chem. Commun., 2007, 10, 1074-1076.
-
(2007)
Chem. Commun
, vol.10
, pp. 1074-1076
-
-
Wilden, J.D.1
Geldeard, L.2
Lee, C.C.3
Judd, D.B.4
Caddick, S.5
-
53
-
-
0041883689
-
A new route to sulfonamides via intermolecular radical addition to pentafluorophenylvinylsulfonate and subsequent aminolysis
-
Caddick, S.; Wilden, J. D.; Bush, H. D.; Wadman, S. N.; Judd, D. B. A new route to sulfonamides via intermolecular radical addition to pentafluorophenylvinylsulfonate and subsequent aminolysis. Org. Lett., 2002, 4(15), 2549-2551.
-
(2002)
Org. Lett
, vol.4
, Issue.15
, pp. 2549-2551
-
-
Caddick, S.1
Wilden, J.D.2
Bush, H.D.3
Wadman, S.N.4
Judd, D.B.5
-
54
-
-
20744432901
-
Observations on the reactivity of pentafluorophenyl sulfonate esters
-
Caddick, S.; Wilden, J. D.; Judd, D. B. Observations on the reactivity of pentafluorophenyl sulfonate esters. Chem. Comm., 2005, (21), 2727-2728.
-
(2005)
Chem. Comm
, Issue.21
, pp. 2727-2728
-
-
Caddick, S.1
Wilden, J.D.2
Judd, D.B.3
-
56
-
-
12344297434
-
Synthesis of functionalized sulfonamides via microwave assisted displacement of PFP-sulfonates with amines
-
Caddick, S.; Wilden, J. D.; Bush, H. D.; Judd, D. B. Synthesis of functionalized sulfonamides via microwave assisted displacement of PFP-sulfonates with amines. QSAR Comb. Sci., 2004, 23(10), 902-905.
-
(2004)
QSAR Comb. Sci
, vol.23
, Issue.10
, pp. 902-905
-
-
Caddick, S.1
Wilden, J.D.2
Bush, H.D.3
Judd, D.B.4
-
57
-
-
33845988033
-
New synthesis of β-sultams from pentafluorophenylsulfonates
-
Lewis, A. K. D.; Mok, B. J.; Tocher, D. A.; Wilden, J. D.; Caddick, S. New synthesis of β-sultams from pentafluorophenylsulfonates. Org. Lett., 2006, 8(24), 5513-5515.
-
(2006)
Org. Lett
, vol.8
, Issue.24
, pp. 5513-5515
-
-
Lewis, A.K.D.1
Mok, B.J.2
Tocher, D.A.3
Wilden, J.D.4
Caddick, S.5
-
58
-
-
33847254407
-
Trichlorophenol (TCP) sulfonate esters: A selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides
-
Wilden, J. D.; Geldeard, L.; Lee, C. C.; Judd, D. B.; Caddick, S. Trichlorophenol (TCP) sulfonate esters: A selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides. Chem. Comm., 2007, 10, 1074-1076.
-
(2007)
Chem. Comm
, vol.10
, pp. 1074-1076
-
-
Wilden, J.D.1
Geldeard, L.2
Lee, C.C.3
Judd, D.B.4
Caddick, S.5
|