-
1
-
-
10744219935
-
SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors
-
L. Liu, J.E. Stelmach, and S.R. Natarajan SAR of 3,4-dihydropyrido[3,2-d] pyrimidone p38 inhibitors Bioorg. Med. Chem. Lett. 13 2003 3979 3982
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3979-3982
-
-
Liu, L.1
Stelmach, J.E.2
Natarajan, S.R.3
-
2
-
-
0035848575
-
Novel p-arylthio cinnamides as antagonists of leukocyte function-Associated antigen-1/intracellular adhesion molecule-1 interaction. 2. Mechanism of inhibition and structure-based improvement of pharmaceutical properties
-
G. Liu, J.R. Huth, and E.T. Olejniczak Novel p-arylthio cinnamides as antagonists of leukocyte function-Associated antigen-1/intracellular adhesion molecule-1 interaction. 2. Mechanism of inhibition and structure-based improvement of pharmaceutical properties J. Med. Chem. 44 2001 1202 1210
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1202-1210
-
-
Liu, G.1
Huth, J.R.2
Olejniczak, E.T.3
-
3
-
-
84979085204
-
Ueber eine neue Darstellungsweise von Phenyläthersalicylsäure
-
F. Ullmann Ueber eine neue Darstellungsweise von Phenylä thersalicylsäure Chem. Ber. 37 1904 853 854
-
(1904)
Chem. Ber.
, vol.37
, pp. 853-854
-
-
Ullmann, F.1
-
4
-
-
0345708168
-
Modern synthetic methods for copper-mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S bond formation
-
S.V. Ley, and A.W. Thomas Modern synthetic methods for copper-mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S bond formation Angew. Chem. Int. Ed. 42 2003 5400 5449
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 5400-5449
-
-
Ley, S.V.1
Thomas, A.W.2
-
5
-
-
9644277114
-
Copper in cross-coupling reactions. The post-Ullmann chemistry
-
I.P. Beletskaya, and A.V. Cheprakov Copper in cross-coupling reactions. The post-Ullmann chemistry Coord. Chem. Rev. 248 2004 2337 2364
-
(2004)
Coord. Chem. Rev.
, vol.248
, pp. 2337-2364
-
-
Beletskaya, I.P.1
Cheprakov, A.V.2
-
6
-
-
0037060980
-
Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophiles
-
D. Prim, J. Campagne, D. Joseph, and B. Andrioletti Palladium-catalysed reactions of aryl halides with soft, non-organometallic nucleophiles Tetrahedron 58 2002 2041 2075
-
(2002)
Tetrahedron
, vol.58
, pp. 2041-2075
-
-
Prim, D.1
Campagne, J.2
Joseph, D.3
Andrioletti, B.4
-
7
-
-
57549097790
-
Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides
-
J.F. Hartwig Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides Acc. Chem. Res. 41 2008 1534 1544
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1534-1544
-
-
Hartwig, J.F.1
-
8
-
-
0037015435
-
A general, efficient, and inexpensive catalyst system for the coupling of aryl iodides and thiols
-
F.Y. Kwong, and S.L. Buchwald A general, efficient, and inexpensive catalyst system for the coupling of aryl iodides and thiols Org. Lett. 4 2002 3420 3517
-
(2002)
Org. Lett.
, vol.4
, pp. 3420-3517
-
-
Kwong, F.Y.1
Buchwald, S.L.2
-
9
-
-
34548455700
-
A general and efficient CuI/BtH catalyzed coupling of aryl halides with thiols
-
A.K. Verma, J. Singh, and R. Chaudhary A general and efficient CuI/BtH catalyzed coupling of aryl halides with thiols Tetrahedron Lett. 48 2007 7199 7202
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 7199-7202
-
-
Verma, A.K.1
Singh, J.2
Chaudhary, R.3
-
10
-
-
64249134236
-
CuO nanoparticles catalyzed CN, CO, and CS cross-coupling reactions: Scope and mechanism
-
S. Jammi, S. Sakthivel, and L. Rout CuO nanoparticles catalyzed CN, CO, and CS cross-coupling reactions: scope and mechanism J. Org. Chem. 74 2009 1971 1976
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1971-1976
-
-
Jammi, S.1
Sakthivel, S.2
Rout, L.3
-
11
-
-
44349176325
-
Iron-catalyzed S-arylation of thiols with aryl iodides
-
A. Correa, A. Carril, and C. Bolm Iron-catalyzed S-arylation of thiols with aryl iodides Angew. Chem. Int. Ed. 47 2008 2880 2883
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 2880-2883
-
-
Correa, A.1
Carril, A.2
Bolm, C.3
-
12
-
-
38649132925
-
Efficient ligand-free nickel-catalyzed CS cross-coupling of thiols with aryl iodides
-
S. Jammi, P. Barua, L. Rout, P. Saha, and T. Punniyamurthy Efficient ligand-free nickel-catalyzed CS cross-coupling of thiols with aryl iodides Tetrahedron Lett. 49 2008 1484 1487
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1484-1487
-
-
Jammi, S.1
Barua, P.2
Rout, L.3
Saha, P.4
Punniyamurthy, T.5
-
13
-
-
33947449188
-
Aromatic nucleophilic substitution reactions
-
J.F. Bunnett, and R.E. Zahler Aromatic nucleophilic substitution reactions Chem. Rev. 49 1951 273 412
-
(1951)
Chem. Rev.
, vol.49
, pp. 273-412
-
-
Bunnett, J.F.1
Zahler, R.E.2
-
14
-
-
1542527790
-
NAr based macrocyclization via biaryl ether formation: Application in natural product synthesis
-
NAr based macrocyclization via biaryl ether formation: application in natural product synthesis Synlett 1997 133 144
-
(1997)
Synlett
, pp. 133-144
-
-
Zhu, J.1
-
15
-
-
0342757538
-
Recent advances in diaryl ether synthesis
-
J.S. Sawyer Recent advances in diaryl ether synthesis Tetrahedron 56 2000 5045 5065
-
(2000)
Tetrahedron
, vol.56
, pp. 5045-5065
-
-
Sawyer, J.S.1
-
16
-
-
0032483549
-
Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6: Expansion of scope and utility
-
J.S. Sawyer, E.A. Schmittling, J.A. Palkowitz, and W.J. Smith III. Synthesis of diaryl ethers, diaryl thioethers, and diarylamines mediated by potassium fluoride-alumina and 18-crown-6: expansion of scope and utility J. Org. Chem. 63 1998 6338 6343
-
(1998)
J. Org. Chem.
, vol.63
, pp. 6338-6343
-
-
Sawyer, J.S.1
Schmittling, E.A.2
Palkowitz, J.A.3
Smith III, W.J.4
-
17
-
-
0000833724
-
Nucleophilic displacement of aromatic nitro groups
-
J.R. Beck Nucleophilic displacement of aromatic nitro groups Tetrahedron 34 1978 2057 2068
-
(1978)
Tetrahedron
, vol.34
, pp. 2057-2068
-
-
Beck, J.R.1
-
18
-
-
32444434695
-
Nucleophilic aromatic substitution reaction of nitroarenes with alkyl- or aryl-thio groups in dimethyl sulfoxide by means of cesium carbonate
-
A. Kondoh, H. Yorimitsu, and K. Oshima Nucleophilic aromatic substitution reaction of nitroarenes with alkyl- or aryl-thio groups in dimethyl sulfoxide by means of cesium carbonate Tetrahedron 62 2006 2357 2360
-
(2006)
Tetrahedron
, vol.62
, pp. 2357-2360
-
-
Kondoh, A.1
Yorimitsu, H.2
Oshima, K.3
-
20
-
-
79953183083
-
The coupling of arylboronic acids with nitroarenes catalyzed by rhodium
-
X. Zheng, J. Ding, and J. Chen The coupling of arylboronic acids with nitroarenes catalyzed by rhodium Org. Lett. 13 2011 1726 1729
-
(2011)
Org. Lett.
, vol.13
, pp. 1726-1729
-
-
Zheng, X.1
Ding, J.2
Chen, J.3
-
22
-
-
79955665891
-
NAr reaction of aryl fluorides and ArSTMS: An efficient synthesis of unsymmetrical diaryl thioethers
-
NAr reaction of aryl fluorides and ArSTMS: an efficient synthesis of unsymmetrical diaryl thioethers Synlett 2011 1143 1148
-
(2011)
Synlett
, pp. 1143-1148
-
-
Liu, C.1
Zang, X.2
Yu, B.3
Yu, X.4
Xu, Q.5
-
23
-
-
52449107816
-
Palladium-catalyzed carbon-ulfur cross-coupling reactions with indium tri(organothiolate) and its application to sequential one-pot processes
-
J.Y. Lee, and P.H. Lee Palladium-catalyzed carbon-ulfur cross-coupling reactions with indium tri(organothiolate) and its application to sequential one-pot processes J. Org. Chem. 73 2008 7413 7416
-
(2008)
J. Org. Chem.
, vol.73
, pp. 7413-7416
-
-
Lee, J.Y.1
Lee, P.H.2
-
24
-
-
33846010734
-
Cobalt-catalyzed arylsulfur bond formation
-
Y.C. Wong, T.T. Jayanth, and C.H. Cheng Cobalt-catalyzed arylsulfur bond formation Org. Lett. 8 2006 5613 5616
-
(2006)
Org. Lett.
, vol.8
, pp. 5613-5616
-
-
Wong, Y.C.1
Jayanth, T.T.2
Cheng, C.H.3
-
25
-
-
0000326398
-
The metalation of some sulfur-containing organic compounds
-
H. Gilman, and F.J. Webb The metalation of some sulfur-containing organic compounds J. Am. Chem. Soc. 71 1949 4062 4066
-
(1949)
J. Am. Chem. Soc.
, vol.71
, pp. 4062-4066
-
-
Gilman, H.1
Webb, F.J.2
-
27
-
-
33846975476
-
Convenient synthesis of unsymmetrical organochalcogenides using organoboronic acids with dichalcogenides via cleavage of the SS, SeSe, or TeTe bond by a copper catalyst
-
N. Taniguchi Convenient synthesis of unsymmetrical organochalcogenides using organoboronic acids with dichalcogenides via cleavage of the SS, SeSe, or TeTe bond by a copper catalyst J. Org. Chem. 72 2007 1241 1245
-
(2007)
J. Org. Chem.
, vol.72
, pp. 1241-1245
-
-
Taniguchi, N.1
-
28
-
-
37049055149
-
The mechanism of displacement reactions. Part III. Kinetics of the reactions of the four 2-halogeno-1,3-dinitrobenzenes and 1,2,3-trinitrobenzene with aniline in ethanol
-
R.E. Parker, and T.O. Read The mechanism of displacement reactions. Part III. Kinetics of the reactions of the four 2-halogeno-1,3-dinitrobenzenes and 1,2,3-trinitrobenzene with aniline in ethanol J. Chem. Soc 1962 3149 3153
-
(1962)
J. Chem. Soc
, pp. 3149-3153
-
-
Parker, R.E.1
Read, T.O.2
|