-
1
-
-
0028057975
-
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitors
-
10.1126/science.8278812
-
P. Lam P.K. Jadhav C.J. Eyermann C.N. Hodge Y. Ru L.T. Bacheler J.L. Meek M. Otto M.M. Rayner Y.N. Wong C.H. Chang P.C. Weber D.A. Jackson T.R. Sharp S. Erickson-Viitanen 1994 Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitors Science 263 380 384 10.1126/science. 8278812
-
(1994)
Science
, vol.263
, pp. 380-384
-
-
Lam, P.1
Jadhav, P.K.2
Eyermann, C.J.3
Hodge, C.N.4
Ru, Y.5
Bacheler, L.T.6
Meek, J.L.7
Otto, M.8
Rayner, M.M.9
Wong, Y.N.10
Chang, C.H.11
Weber, P.C.12
Jackson, D.A.13
Sharp, T.R.14
Erickson-Viitanen, S.15
-
2
-
-
0345848837
-
Substituted ureas. Methods of synthesis and applications
-
10.1070/RC1985v054n03ABEH003022
-
T.P. Vishnyakova I.A. Golubeva E.V. Glebova 1985 Substituted ureas. Methods of synthesis and applications Russ Chem Rev 54 429 449 10.1070/RC1985v054n03ABEH003022
-
(1985)
Russ Chem Rev
, vol.54
, pp. 429-449
-
-
Vishnyakova, T.P.1
Golubeva, I.A.2
Glebova, E.V.3
-
3
-
-
45449122598
-
Oxidative carbonylation of aniline over Pd/C catalyst: Effect of promoters, solvents, and reaction conditions
-
10.1016/0021-9517(88)90028-0
-
S.P. Gupte R.V. Chaudhari 1988 Oxidative carbonylation of aniline over Pd/C catalyst: Effect of promoters, solvents, and reaction conditions J Catal 114 246 258 10.1016/0021-9517(88)90028-0
-
(1988)
J Catal
, vol.114
, pp. 246-258
-
-
Gupte, S.P.1
Chaudhari, R.V.2
-
4
-
-
33751157494
-
A safe and efficient method for preparation of N, N′- unsymmetrically disubstituted ureas utilizing triphosgene
-
10.1021/jo00086a061
-
P. Majer R.S. Randad 1994 A safe and efficient method for preparation of N, N′-unsymmetrically disubstituted ureas utilizing triphosgene J Org Chem 59 1937 1938 10.1021/jo00086a061
-
(1994)
J Org Chem
, vol.59
, pp. 1937-1938
-
-
Majer, P.1
Randad, R.S.2
-
5
-
-
1642415730
-
A new simplified method for the preparation of N, N′-diphenylurea
-
10.1080/00304940409355373
-
K. Tran D. Berlin 2004 A new simplified method for the preparation of N, N′-diphenylurea Org Prep Proced Int 36 71 74 10.1080/00304940409355373
-
(2004)
Org Prep Proced Int
, vol.36
, pp. 71-74
-
-
Tran, K.1
Berlin, D.2
-
6
-
-
33745905312
-
Kamni. Synthesis, X-ray structure and N-H⋯O interactions in 1,3-diphenyl-urea
-
10.1007/BF02706491
-
D. Rajnikant M.B. Deshmukh 2006 Kamni. Synthesis, X-ray structure and N-H⋯O interactions in 1,3-diphenyl-urea Bull Mater Sci 29 239 242 10.1007/BF02706491
-
(2006)
Bull Mater Sci
, vol.29
, pp. 239-242
-
-
Rajnikant, D.1
Deshmukh, M.B.2
-
7
-
-
0032764585
-
A novel method for the synthesis of disubstituted ureas and thioureas under microwave irradiation
-
Mojtahedi MM, Saidi MR, Bolourtchian M. A novel method for the synthesis of disubstituted ureas and thioureas under microwave irradiation. J Chem Res (s), 1999, 710-711
-
(1999)
J Chem Res (S)
, pp. 710-711
-
-
Mojtahedi, M.M.1
Saidi, M.R.2
Bolourtchian, M.3
-
8
-
-
0037057021
-
Soluble and polymer-anchored rhodium catalyst for carbonylation reaction: Kinetics and mechanism of diphenylurea formation
-
10.1006/jcat.2002.3665
-
D.K. Mukherjee C.R. Saha 2002 Soluble and polymer-anchored rhodium catalyst for carbonylation reaction: Kinetics and mechanism of diphenylurea formation J Catal 210 255 262 10.1006/jcat.2002.3665
-
(2002)
J Catal
, vol.210
, pp. 255-262
-
-
Mukherjee, D.K.1
Saha, C.R.2
-
9
-
-
15044347515
-
Silica gel confined ionic liquid + metal complexes for oxygen-free carbonylation of amines and nitrobenzene to ureas
-
DOI 10.1002/adsc.200404242
-
F. Shi Q.H. Zhang Y.L. Gu Y.Q. Deng 2005 Silica gel confined ionic liquid+ metal complexes for oxygen-free carbonylation of amines and nitrobenzene to ureas Adv Synth Catal 347 225 230 10.1002/adsc.200404242 (Pubitemid 40380368)
-
(2005)
Advanced Synthesis and Catalysis
, vol.347
, Issue.2-3
, pp. 225-230
-
-
Shi, F.1
Zhang, Q.2
Gu, Y.3
Deng, Y.4
-
10
-
-
0037450229
-
Reusable polymer-anchored catalyst for carbonylation reaction: Kinetics and mechanism for diphenylurea formation
-
10.1016/S1381-1169(02)00458-2
-
D.K. Mukherjee C.R. Saha 2003 Reusable polymer-anchored catalyst for carbonylation reaction: kinetics and mechanism for diphenylurea formation J Mol Catal A 193 41 50 10.1016/S1381-1169(02)00458-2
-
(2003)
J Mol Catal A
, vol.193
, pp. 41-50
-
-
Mukherjee, D.K.1
Saha, C.R.2
-
11
-
-
34447102805
-
Transformation of carbon dioxide
-
DOI 10.1021/cr068357u
-
T. Sakakura J.C. Choi H. Yasuda 2007 Transformation of carbon dioxide Chem Rev 107 2365 2387 10.1021/cr068357u (Pubitemid 47029097)
-
(2007)
Chemical Reviews
, vol.107
, Issue.6
, pp. 2365-2387
-
-
Sakakura, T.1
Choi, J.-C.2
Yasuda, H.3
-
12
-
-
0001458108
-
Homogeneous Hydrogenation of carbon dioxide
-
10.1021/cr00034a001
-
P.G. Jessop T. Ikariya R. Noyori 1995 Homogeneous Hydrogenation of carbon dioxide Chem Rev 95 259 272 10.1021/cr00034a001
-
(1995)
Chem Rev
, vol.95
, pp. 259-272
-
-
Jessop, P.G.1
Ikariya, T.2
Noyori, R.3
-
13
-
-
34249002571
-
Carbon dioxide fixation into chemicals (methyl formate) at high yields by surface coupling over a Pd/Cu/ZnO nanocatalyst
-
DOI 10.1021/ja0706302
-
K.M.K. Yu C.M.Y. Yeung S.C. Tsang 2007 Carbon dioxide fixation into chemicals (methyl formate) at high yields by surface coupling over a Pd/Cu/ZnO nanocatalyst J Am Chem Soc 129 6360 6361 10.1021/ja0706302 (Pubitemid 46799318)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.20
, pp. 6360-6361
-
-
Yu, K.M.K.1
Yeung, C.M.Y.2
Shik, C.T.3
-
15
-
-
0023362440
-
Preparation of cyclic ureas from carbon dioxide and diamines catalyzed by triphenylstibine oxide
-
10.1021/ie00066a002
-
R. Nomura M. Yamamoto H. Matsuda 1987 Preparation of cyclic ureas from carbon dioxide and diamines catalyzed by triphenylstibine oxide Ind Eng Chem Res 26 1056 1059 10.1021/ie00066a002
-
(1987)
Ind Eng Chem Res
, vol.26
, pp. 1056-1059
-
-
Nomura, R.1
Yamamoto, M.2
Matsuda, H.3
-
17
-
-
0037525419
-
Synthesis of cyclic ureas and urethanes from alkylene diamines and amino alcohols with pressurized carbon dioxide in the absence of catalysts
-
10.1039/b300778b
-
B.M. Bhanage S.I. Fujita Y. Ikushima M. Arai 2003 Synthesis of cyclic ureas and urethanes from alkylene diamines and amino alcohols with pressurized carbon dioxide in the absence of catalysts Green Chem 5 340 342 10.1039/b300778b
-
(2003)
Green Chem
, vol.5
, pp. 340-342
-
-
Bhanage, B.M.1
Fujita, S.I.2
Ikushima, Y.3
Arai, M.4
-
18
-
-
0001553531
-
Ruthenium-catalyzed synthesis of symmetrical N, N′-dialkylureas directly from carbon dioxide and amines
-
10.1021/jo00014a024
-
J. Fournier C. Bruneau P.H. Dixneuf S. Lecolier 1991 Ruthenium-catalyzed synthesis of symmetrical N, N′-dialkylureas directly from carbon dioxide and amines J Org Chem 56 4456 4458 10.1021/jo00014a024
-
(1991)
J Org Chem
, vol.56
, pp. 4456-4458
-
-
Fournier, J.1
Bruneau, C.2
Dixneuf, P.H.3
Lecolier, S.4
-
19
-
-
85067409412
-
A convenient direct synthesis of ureas from carbon dioxide and amines
-
Ogura H, Takeda K, Tokue R, Kobayashi T. A convenient direct synthesis of ureas from carbon dioxide and amines. Synthesis, 1978, 394-396
-
(1978)
Synthesis
, pp. 394-396
-
-
Ogura, H.1
Takeda, K.2
Tokue, R.3
Kobayashi, T.4
-
21
-
-
0000302218
-
Carbonylation of amines by carbon dioxide in the presence of an organoantimony catalyst
-
10.1021/jo00052a060
-
R. Nomura Y. Hasegawa M. Ishimoto T. Toyosaki H. Matsuda 1992 Carbonylation of amines by carbon dioxide in the presence of an organoantimony catalyst J Org Chem 57 7339 7342 10.1021/jo00052a060
-
(1992)
J Org Chem
, vol.57
, pp. 7339-7342
-
-
Nomura, R.1
Hasegawa, Y.2
Ishimoto, M.3
Toyosaki, T.4
Matsuda, H.5
-
22
-
-
0000172113
-
Carbonylation of amines with carbon dioxide under atmospheric conditions
-
10.1016/S0040-4039(01)82442-4
-
N. Yamazaki F. Higashi T. Iguchi 1974 Carbonylation of amines with carbon dioxide under atmospheric conditions Tetrahedron lett 15 1191 1194 10.1016/S0040-4039(01)82442-4
-
(1974)
Tetrahedron Lett
, vol.15
, pp. 1191-1194
-
-
Yamazaki, N.1
Higashi, F.2
Iguchi, T.3
-
23
-
-
0028999976
-
A simple one-pot procedure for preparing symmetrical diarylureas from carbon dioxide and aromatic amines
-
10.1080/00397919508015452
-
C.F. Cooper S.J. Falcone 1995 A simple one-pot procedure for preparing symmetrical diarylureas from carbon dioxide and aromatic amines Synth Commun 25 2467 2474 10.1080/00397919508015452
-
(1995)
Synth Commun
, vol.25
, pp. 2467-2474
-
-
Cooper, C.F.1
Falcone, S.J.2
-
24
-
-
0042267239
-
Alternatives to phosgene and carbon monoxide: Synthesis of symmetric urea derivatives with carbon dioxide in ionic liquids
-
DOI 10.1002/anie.200351098
-
F. Shi Y.Q. Deng T.L. SiMa J.J. Peng Y.L. Gu B.T. Qiao 2003 Alternatives to phosgene and carbon monoxide: synthesis of symmetric urea derivatives with carbon dioxide in ionic liquids Angew Chem Int Ed 42 3257 3260 10.1002/anie.200351098 (Pubitemid 36917170)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.28
, pp. 3257-3260
-
-
Shi, F.1
Deng, Y.2
SiMa, T.3
Peng, J.4
Gu, Y.5
Qiao, B.6
-
25
-
-
32844467938
-
The distillation and volatility of ionic liquids
-
DOI 10.1038/nature04451, PII NATURE04451
-
M.J. Earle J.M.S.S. Esperanca M.A. Gilea J.N.C. Lopes L.P.N. Rebelo J.W. Magee K.R. Seddon J.A. Widegren 2006 The distillation and volatility of ionic liquids Nature 439 831 834 10.1038/nature04451 (Pubitemid 43256743)
-
(2006)
Nature
, vol.439
, Issue.7078
, pp. 831-834
-
-
Earle, M.J.1
Esperanca, J.M.S.S.2
Gilea, M.A.3
Lopes, J.N.C.4
Rebelo, L.P.N.5
Magee, J.W.6
Seddon, K.R.7
Widegren, J.A.8
-
26
-
-
34249708781
-
Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids
-
Wilkes JS, Zaworotko MJ. Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids. J Chem Soc, Chem Commun, 1992, 965-967
-
(1992)
J Chem Soc, Chem Commun
, pp. 965-967
-
-
Wilkes, J.S.1
Zaworotko, M.J.2
-
28
-
-
0000661241
-
Room-temperature molten salts based on the quaternary ammonium ion
-
10.1021/jp981159p
-
J. Sun M. Forsyth D.R. Macfarlane 1998 Room-temperature molten salts based on the quaternary ammonium ion J Phys Chem B 102 8858 8864 10.1021/jp981159p
-
(1998)
J Phys Chem B
, vol.102
, pp. 8858-8864
-
-
Sun, J.1
Forsyth, M.2
MacFarlane, D.R.3
-
30
-
-
67649317291
-
Existence of nearly-free hydrogen bonds in an ionic liquid, N, N-diethyl-N-methyl-N-(2-methoxyethyl) ammonium tetrafluoroborate-water at 77 K
-
10.1021/jp902125f
-
Y. Yoshimura T. Goto H. Abe Y. Imai 2009 Existence of nearly-free hydrogen bonds in an ionic liquid, N, N-diethyl-N-methyl-N-(2-methoxyethyl) ammonium tetrafluoroborate-water at 77 K J Phys Chem B 113 8091 8095 10.1021/jp902125f
-
(2009)
J Phys Chem B
, vol.113
, pp. 8091-8095
-
-
Yoshimura, Y.1
Goto, T.2
Abe, H.3
Imai, Y.4
-
31
-
-
2142643682
-
Hydroxylation of alkyl halides with water in ionic liquid: Significantly enhanced nucleophilicity of water
-
DOI 10.1021/jo035563i
-
D.W. Kim D.J. Hong J.W. Seo H.S. Kim H.K. Kim C.E. Song D.Y. Chi 2004 Hydroxylation of alkyl halides with water in ionic liquid: significantly enhanced nucleophilicity of water J Org Chem 69 3186 3189 10.1021/jo035563i (Pubitemid 38542575)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.9
, pp. 3186-3189
-
-
Kim, D.W.1
Hong, D.J.2
Seo, J.W.3
Kim, H.S.4
Kim, H.K.5
Song, C.E.6
Chi, D.Y.7
-
32
-
-
25444520789
-
2-expanded liquid media. in situ generation of carbamates as a strategy for reactions of amines in supercritical carbon dioxide
-
2-expanded liquid media. In situ generation of carbamates as a strategy for reactions of amines in supercritical carbon dioxide. Chem Commun, 2005, 4465-4467
-
(2005)
Chem Commun
, pp. 4465-4467
-
-
Dunetz, J.R.1
Ciccolini, R.P.2
Froling, M.3
Paap, S.M.4
Allen, A.J.5
Holmes, A.B.6
Tester, J.W.7
Danheiser, R.L.8
-
33
-
-
34249993173
-
A non-phosgene route for the synthesis of methyl N-Phenyl carbamate derived from CO2 under mild conditions
-
10.1039/b614229j
-
J.J. Gao H.Q. Li Y.F. Zhang Y. Zhang 2007 A non-phosgene route for the synthesis of methyl N-Phenyl carbamate derived from CO2 under mild conditions Green Chem 9 572 576 10.1039/b614229j
-
(2007)
Green Chem
, vol.9
, pp. 572-576
-
-
Gao, J.J.1
Li, H.Q.2
Zhang, Y.F.3
Zhang, Y.4
-
34
-
-
0037452818
-
2 catalysts for oxidative carbonylation of aniline with methanol
-
10.1016/S1381-1169(02)00550-2
-
2 catalysts for oxidative carbonylation of aniline with methanol J Mol Catal A 195 37 45 10.1016/S1381-1169(02)00550-2
-
(2003)
J Mol Catal A
, vol.195
, pp. 37-45
-
-
Chen, B.1
Chuang, S.S.C.2
-
35
-
-
1242295229
-
A phosgene-free process for the synthesis of methyl N-Phenyl carbamate by the reaction of aniline with methyl carbamate
-
10.1016/j.molcata.2003.11.002
-
Q.F. Li J.W. Wang W.S. Dong M.Q. Kang X.K. Wang S.Y. Peng 2004 A phosgene-free process for the synthesis of methyl N-Phenyl carbamate by the reaction of aniline with methyl carbamate J Mol Catal A 212 99 105 10.1016/j.molcata.2003.11.002
-
(2004)
J Mol Catal A
, vol.212
, pp. 99-105
-
-
Li, Q.F.1
Wang, J.W.2
Dong, W.S.3
Kang, M.Q.4
Wang, X.K.5
Peng, S.Y.6
|