-
1
-
-
0015804139
-
Thiourea derivatives of 2-aminooxazoles showing antibacterial and antifungal activity
-
C. George, N. Martin, and R. Ray Thiourea derivatives of 2-aminooxazoles showing antibacterial and antifungal activity J. Med. Chem. 16 1973 1402 1405
-
(1973)
J. Med. Chem.
, vol.16
, pp. 1402-1405
-
-
George, C.1
Martin, N.2
Ray, R.3
-
2
-
-
25444473651
-
Antimycobacterial natural products: Synthesis and preliminary biological evaluation of the oxazole-containing alkaloid texaline
-
C.G. Anna, I.M.B. Helena, G.F. Scott, E.B. Clifton, and R.C. Brent Antimycobacterial natural products: synthesis and preliminary biological evaluation of the oxazole-containing alkaloid texaline Tetrahedron Lett. 46 2005 7355 7357
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 7355-7357
-
-
Anna, C.G.1
Helena, I.M.B.2
Scott, G.F.3
Clifton, E.B.4
Brent, R.C.5
-
3
-
-
0015151734
-
Derivatives of 2-aminooxazoles showing antiinflammatory activity
-
C. George, and J.F. Michael Derivatives of 2-aminooxazoles showing antiinflammatory activity J. Med. Chem. 14 1971 1075 1077
-
(1971)
J. Med. Chem.
, vol.14
, pp. 1075-1077
-
-
George, C.1
Michael, J.F.2
-
5
-
-
0021923154
-
Synthesis of (+)-antimycin A3. Use of the oxazole ring in protecting and activating functions
-
H.H. Wasserman, and R.J. Gambale Synthesis of (+)-antimycin A3. Use of the oxazole ring in protecting and activating functions J. Am. Chem. Soc. 107 1985 1423 1424
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 1423-1424
-
-
Wasserman, H.H.1
Gambale, R.J.2
-
6
-
-
0012019390
-
The application of N-α-formyl amino acid esters in the enzyme-catalyzed peptide synthesis
-
A. Floersheimer, and M.R. Kula The application of N-α-formyl amino acid esters in the enzyme-catalyzed peptide synthesis Monatsh. Chem. 119 1988 1323 1331
-
(1988)
Monatsh. Chem.
, vol.119
, pp. 1323-1331
-
-
Floersheimer, A.1
Kula, M.R.2
-
8
-
-
0021192532
-
Fluorescent whitening agents - A survey (1974-82)
-
I.H. Leaver, and B. Milligam Fluorescent whitening agents - a survey (1974-82) Dyes Pigm. 5 1984 109 144
-
(1984)
Dyes Pigm.
, vol.5
, pp. 109-144
-
-
Leaver, I.H.1
Milligam, B.2
-
9
-
-
0029943845
-
Total synthesis of dimethyl sulfomycinamate
-
T.R. Kelly, and F. Lang Total synthesis of dimethyl sulfomycinamate J. Org. Chem. 61 1996 4623 4633
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4623-4633
-
-
Kelly, T.R.1
Lang, F.2
-
10
-
-
0035799896
-
Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis
-
P. Wipf, and J.L. Methot Synthetic studies toward diazonamide A. A novel approach for polyoxazole synthesis Org. Lett. 3 2001 1261 1264
-
(2001)
Org. Lett.
, vol.3
, pp. 1261-1264
-
-
Wipf, P.1
Methot, J.L.2
-
12
-
-
0035974239
-
Synthesis and electrochemical study of novel oxazolo-ferrocene derivatives displaying redox-switchable character
-
A. Tarraga, P. Molina, D. Curiel, and M.D. Velasco Synthesis and electrochemical study of novel oxazolo-ferrocene derivatives displaying redox-switchable character Tetrahedron 57 2001 6765 6774
-
(2001)
Tetrahedron
, vol.57
, pp. 6765-6774
-
-
Tarraga, A.1
Molina, P.2
Curiel, D.3
Velasco, M.D.4
-
13
-
-
0003025485
-
Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: Scope and limitations
-
M. Lautens, and A. Roy Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: scope and limitations Org. Lett. 2 2000 555 557
-
(2000)
Org. Lett.
, vol.2
, pp. 555-557
-
-
Lautens, M.1
Roy, A.2
-
14
-
-
0030880842
-
Synthesis and absolute configuration of (-)-normalindine
-
M. Ohba, H. Kubo, T. Fujii, H. Ishibashi, M.V. Sargent, and D. Arbain Synthesis and absolute configuration of (-)-normalindine Tetrahedron Lett. 38 1997 6697 6700
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6697-6700
-
-
Ohba, M.1
Kubo, H.2
Fujii, T.3
Ishibashi, H.4
Sargent, M.V.5
Arbain, D.6
-
15
-
-
0034629166
-
An investigation of imidazole and oxazole syntheses using aryl-substituted TosMIC reagents
-
J. Sisko, A.J. Kassick, M. Mellinger, J.J. Filan, A. Allen, and M.A. Olsen An investigation of imidazole and oxazole syntheses using aryl-substituted TosMIC reagents J. Org. Chem. 65 2000 1516 1524
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1516-1524
-
-
Sisko, J.1
Kassick, A.J.2
Mellinger, M.3
Filan, J.J.4
Allen, A.5
Olsen, M.A.6
-
16
-
-
11144304660
-
Ruthenium- and gold-catalysed sequential reactions: A straightforward synthesis of substituted oxazoles from propargylic alcohols and amides
-
M.D. Milton, Y. Inada, Y. Nishibayashi, and S. Uemura Ruthenium- and gold-catalysed sequential reactions: a straightforward synthesis of substituted oxazoles from propargylic alcohols and amides Chem. Commun. 2004 2712 2713
-
(2004)
Chem. Commun.
, pp. 2712-2713
-
-
Milton, M.D.1
Inada, Y.2
Nishibayashi, Y.3
Uemura, S.4
-
17
-
-
0343081444
-
Mercury(II) p-toluenesulfonate mediated synthesis of oxazoles under microwave irradiation
-
J.C. Lee, and In-Goul Song Mercury(II) p-toluenesulfonate mediated synthesis of oxazoles under microwave irradiation Tetrahedron Lett. 41 2000 5891 5894
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 5891-5894
-
-
Lee, J.C.1
Song, I.-G.2
-
18
-
-
74349112543
-
An efficient ultrasound-promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives
-
H. Zang, Y. Zhang, Y. Zang, and B.W. Cheng An efficient ultrasound-promoted method for the one-pot synthesis of 7,10,11,12- tetrahydrobenzo[c]acridin-8(9H)-one derivatives Ultrason. Sonochem. 17 2010 495 499
-
(2010)
Ultrason. Sonochem.
, vol.17
, pp. 495-499
-
-
Zang, H.1
Zhang, Y.2
Zang, Y.3
Cheng, B.W.4
-
19
-
-
58049137921
-
An efficient synthesis of quinolines derivatives promoted by a room temperature ionic liquid at ambient conditions under ultrasound irradiation via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones
-
M.R.P. Heravi An efficient synthesis of quinolines derivatives promoted by a room temperature ionic liquid at ambient conditions under ultrasound irradiation via the tandem addition/annulation reaction of o-aminoaryl ketones with α-methylene ketones Ultrason. Sonochem. 16 2009 361 366
-
(2009)
Ultrason. Sonochem.
, vol.16
, pp. 361-366
-
-
Heravi, M.R.P.1
-
20
-
-
71649090107
-
Phase transformation of nanostructured titanium dioxide from anatase-to-rutile via combined ultrasound assisted sol-gel technique
-
K. Prasad, D.V. Pinjari, A.B. Pandit, and S.T. Mhaske Phase transformation of nanostructured titanium dioxide from anatase-to-rutile via combined ultrasound assisted sol-gel technique Ultrason. Sonochem. 17 2010 409 415
-
(2010)
Ultrason. Sonochem.
, vol.17
, pp. 409-415
-
-
Prasad, K.1
Pinjari, D.V.2
Pandit, A.B.3
Mhaske, S.T.4
-
22
-
-
71949086423
-
Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa(thia) zoles
-
A. Duarte, W. Cunico, C.M.P. Pereira, A.F.C. Flores, R.A. Freitag, and G.M. Siqueira Ultrasound promoted synthesis of thioesters from 2-mercaptobenzoxa(thia)zoles Ultrason. Sonochem. 17 2010 281 283
-
(2010)
Ultrason. Sonochem.
, vol.17
, pp. 281-283
-
-
Duarte, A.1
Cunico, W.2
Pereira, C.M.P.3
Flores, A.F.C.4
Freitag, R.A.5
Siqueira, G.M.6
-
23
-
-
78149392580
-
Synthesis of chalcone (3-(4-fluorophenyl)-1-(4-methoxyphenyl)prop-2-en-1- one): Advantage of sonochemical method over conventional method
-
K.J. Jarag, D.V. Pinjari, A.B. Pandit, and G.S. Shankarling Synthesis of chalcone (3-(4-fluorophenyl)-1-(4-methoxyphenyl)prop-2-en-1-one): advantage of sonochemical method over conventional method Ultrason. Sonochem. 18 2011 617 623
-
(2011)
Ultrason. Sonochem.
, vol.18
, pp. 617-623
-
-
Jarag, K.J.1
Pinjari, D.V.2
Pandit, A.B.3
Shankarling, G.S.4
-
25
-
-
26444537403
-
Effect of ultrasound in enantioselective hydrogenation of 1-phenyl-1,2-propanedione: Comparison of catalyst activation, solvents and supports
-
B. Toukoniitty, E. Toukoniitty, P. Maki-Arvela, J.-P. Mikkola, T. Salmi, D. Murzim, P. Yu, and J. Kooyman Effect of ultrasound in enantioselective hydrogenation of 1-phenyl-1,2-propanedione: comparison of catalyst activation, solvents and supports Ultrason. Sonochem. 13 2006 68 75
-
(2006)
Ultrason. Sonochem.
, vol.13
, pp. 68-75
-
-
Toukoniitty, B.1
Toukoniitty, E.2
Maki-Arvela, P.3
Mikkola, J.-P.4
Salmi, T.5
Murzim, D.6
Yu, P.7
Kooyman, J.8
-
26
-
-
77956432527
-
Ultrasound promoted synthesis of quinolines using basic ionic liquids in aqueous media as a green procedure
-
E. Kowsari, and M. Mallakmohammadi Ultrasound promoted synthesis of quinolines using basic ionic liquids in aqueous media as a green procedure Ultrason. Sonochem. 18 2011 447 454
-
(2011)
Ultrason. Sonochem.
, vol.18
, pp. 447-454
-
-
Kowsari, E.1
Mallakmohammadi, M.2
-
27
-
-
1642526412
-
Ionic liquid promoted novel and efficient one pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones at ambient temperature under ultrasound irradiation
-
Atul.R. Gholap, K. Venkatesan, T. Daniel, R.J. Lahoti, and K.V. Srinivasan Ionic liquid promoted novel and efficient one pot synthesis of 3,4-dihydropyrimidin-2-(1H)-ones at ambient temperature under ultrasound irradiation Green Chem. 6 2004 147 150
-
(2004)
Green Chem.
, vol.6
, pp. 147-150
-
-
Gholap, A.R.1
Venkatesan, K.2
Daniel, T.3
Lahoti, R.J.4
Srinivasan, K.V.5
-
28
-
-
34147220339
-
Toxicity of ionic liquids
-
D. Zhao, Y. Liao, and Z. Zhang Toxicity of ionic liquids Clean 35 2007 42 48
-
(2007)
Clean
, vol.35
, pp. 42-48
-
-
Zhao, D.1
Liao, Y.2
Zhang, Z.3
-
29
-
-
33745222822
-
Combustible ionic liquids by design: Is laboratory safety another ionic liquid myth?
-
M. Smiglak, W.M. Reichert, J.D. Holbrey, J.S. Wilkes, L. Sun, J.T. Thrasher, K. Kirichenko, S. Singh, A.R. Katritzky, and R.D. Rogers Combustible ionic liquids by design: is laboratory safety another ionic liquid myth? Chem. Commun. 2006 2554 2556
-
(2006)
Chem. Commun.
, pp. 2554-2556
-
-
Smiglak, M.1
Reichert, W.M.2
Holbrey, J.D.3
Wilkes, J.S.4
Sun, L.5
Thrasher, J.T.6
Kirichenko, K.7
Singh, S.8
Katritzky, A.R.9
Rogers, R.D.10
-
30
-
-
0037220832
-
Novel solvent properties of choline chloride/urea mixtures
-
Andrew P. Abbott, Glen Capper, David L. Davies, Raymond K. Rasheed, and Vasuki Tambyrajah Novel solvent properties of choline chloride/urea mixtures Chem. Commun. 2003 70
-
(2003)
Chem. Commun.
, pp. 70
-
-
Abbott, A.P.1
Capper, G.2
Davies, D.L.3
Rasheed, R.K.4
Tambyrajah, V.5
-
31
-
-
26844551807
-
O-acetylation of cellulose and monosaccharides using a zinc based ionic liquid
-
A.P. Abbott, T.J. Bell, S. Handa, and B. Stoddart O-acetylation of cellulose and monosaccharides using a zinc based ionic liquid Green Chem. 7 2005 705 707
-
(2005)
Green Chem.
, vol.7
, pp. 705-707
-
-
Abbott, A.P.1
Bell, T.J.2
Handa, S.3
Stoddart, B.4
-
32
-
-
79651471607
-
Selective N-alkylation of Aromatic Primary Amines Catalyzed by Bio-catalyst or deep eutectic solvent
-
B. Singh, H. Lobo, and G. Shankarling Selective N-alkylation of Aromatic Primary Amines Catalyzed by Bio-catalyst or deep eutectic solvent Catal. Lett. 141 2011 178 182
-
(2011)
Catal. Lett.
, vol.141
, pp. 178-182
-
-
Singh, B.1
Lobo, H.2
Shankarling, G.3
-
33
-
-
84867742494
-
Deep eutectic mixtures and glycerol: A simple, environmentally benign and efficient catalyst/reaction media for synthesis of N-aryl phthalimide derivatives
-
10.1080/17518253.2012.669500
-
H.R. Lobo, B.S. Singh, and G.S. Shankarling Deep eutectic mixtures and glycerol: a simple, environmentally benign and efficient catalyst/reaction media for synthesis of N-aryl phthalimide derivatives Green Chem. Lett. Rev. 2012 10.1080/17518253.2012.669500
-
(2012)
Green Chem. Lett. Rev.
-
-
Lobo, H.R.1
Singh, B.S.2
Shankarling, G.S.3
-
35
-
-
40149099571
-
Sono-electrodeposition (20 and 850 kHz) of copper in aqueous and deep eutectic solvents
-
B.G. Pollet, J.Y. Hihn, and T.J. Mason Sono-electrodeposition (20 and 850 kHz) of copper in aqueous and deep eutectic solvents Electrochimica Acta 53 2008 4248 4256
-
(2008)
Electrochimica Acta
, vol.53
, pp. 4248-4256
-
-
Pollet, B.G.1
Hihn, J.Y.2
Mason, T.J.3
-
37
-
-
0038690524
-
Effect of alpha-halogenation of carbonyl compounds by N-bromosuccinimide and N-chlorosuccinimide
-
J.C. Lee, Y.H. Bae, and S.K. Chang Effect of alpha-halogenation of carbonyl compounds by N-bromosuccinimide and N-chlorosuccinimide Bull. Korean Chem. Soc. 24 2003 407 408
-
(2003)
Bull. Korean Chem. Soc.
, vol.24
, pp. 407-408
-
-
Lee, J.C.1
Bae, Y.H.2
Chang, S.K.3
-
38
-
-
0035823705
-
Preparation of novel, moisture-stable, Lewis-acidic ionic liquids containing quaternary ammonium salts with functional side chains
-
A.P. Abbott, G. Capper, D.L. Davies, H.L. Munro, R.K. Rasheed, and V. Tambyrajah Preparation of novel, moisture-stable, Lewis-acidic ionic liquids containing quaternary ammonium salts with functional side chains Chem. Commun. 2001 2010 2011
-
(2001)
Chem. Commun.
, pp. 2010-2011
-
-
Abbott, A.P.1
Capper, G.2
Davies, D.L.3
Munro, H.L.4
Rasheed, R.K.5
Tambyrajah, V.6
-
39
-
-
84860534571
-
Choline chloride based eutectic solvents: Magical catalytic system for carbon-carbon bond formation in the rapid synthesis of β-hydroxy functionalized derivatives
-
B.S. Singh, H.R. Lobo, and G.S. Shankarling Choline chloride based eutectic solvents: magical catalytic system for carbon-carbon bond formation in the rapid synthesis of β-hydroxy functionalized derivatives Catal. Comm. 24 2012 70 74
-
(2012)
Catal. Comm.
, vol.24
, pp. 70-74
-
-
Singh, B.S.1
Lobo, H.R.2
Shankarling, G.S.3
-
40
-
-
44349168328
-
Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts
-
S.J. Connon Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts Chem. Commun. 2008 2499 2510
-
(2008)
Chem. Commun.
, pp. 2499-2510
-
-
Connon, S.J.1
|