-
1
-
-
0036027120
-
A comparative investigation of supramolecular structures involving copper(II) complexes of imidazolinylalkanimidamides
-
(a)Bishop, M. M.; Lindoy, L. F.; Miller, D. J.; Turner, P. A comparative investigation of supramolecular structures involving copper(II) complexes of imidazolinylalkanimida-mides. J. Chem. Soc., Dalton Trans. 2002, 4128-4133;
-
(2002)
J. Chem. Soc., Dalton Trans.
, pp. 4128-4133
-
-
Bishop, M.M.1
Lindoy, L.F.2
Miller, D.J.3
Turner, P.4
-
2
-
-
0025737509
-
Reactions of carbonic acid diamides with a-hydroxy ketones and a-diketones, part 4: Reactions of substituted biguanides with benzil in ethanol under the influence of sodium ethanolate
-
(b)Schramm, H. W. Reactions of carbonic acid diamides with a-hydroxy ketones and a-diketones, part 4: Reactions of substituted biguanides with benzil in ethanol under the influence of sodium ethanolate. Scientia Pharmaceutica 1991, 59, 123-133;
-
(1991)
Scientia Pharmaceutica
, vol.59
, pp. 123-133
-
-
Schramm, H.W.1
-
3
-
-
0000001411
-
Reaction of guanidines with a-diketones: Syntheses of 45-disubstituted-2-aminoimidazoles and 26-unsymmetrically substituted imidazo[4,5-d]imidazoles
-
(c)Nishimura, T.; Kitajima, K. Reaction of guanidines with a-diketones: Syntheses of 4,5-disubstituted-2-aminoimidazoles and 2,6-unsymmetrically substituted imidazo[4,5-d]imidazoles. J. Org. Chem. 1979, 44, 818-824;
-
(1979)
J. Org. Chem.
, vol.44
, pp. 818-824
-
-
Nishimura, T.1
Kitajima, K.2
-
4
-
-
3543146910
-
New derivatives of 5,5-diphenylhydantoin, II
-
(d)Hoffmann, C. New derivatives of 5,5-diphenylhydantoin, II. Bull. Soc. Chim. Fr. 1950, 659-660.
-
(1950)
Bull. Soc. Chim. Fr.
, pp. 659-660
-
-
Hoffmann, C.1
-
5
-
-
77953715658
-
2,5,5-Triphenylimidazolin-4-one, a new synthesis: Study of its formation by the old synthesis from benzil and benzamidine
-
(a)Rio, G.; Ranjon, A. 2,5,5-Triphenylimidazolin-4-one, a new synthesis: Study of its formation by the old synthesis from benzil and benzamidine. Bull. Soc. Chim. Fr. 1958, 543-551;
-
(1958)
Bull. Soc. Chim. Fr.
, pp. 543-551
-
-
Rio, G.1
Ranjon, A.2
-
6
-
-
33745599323
-
Synthesis and evaluation of 5,5-diphenylimidazolones as potent human neuropeptide Y5 receptor antagonists
-
(b)Gillman, K. W.; Higgins, M. A.; Poindexter, G. S.; Browning, M.; Clarke, W. J.; Flowers, S.; Grace, J. E.; Hogan, J. B.; McGovern, R. T.; Iben, L. G.; Mattson, G. K.; Ortiz, A.; Rassnick, S.; Russell, J. W.; Antal-Zimanyi, I. Synthesis and evaluation of 5,5-diphenylimidazolones as potent human neuropeptide Y5 receptor antagonists. Bioorg. Med. Chem. 2006, 14, 5517-5526.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 5517-5526
-
-
Gillman, K.W.1
Higgins, M.A.2
Poindexter, G.S.3
Browning, M.4
Clarke, W.J.5
Flowers, S.6
Grace, J.E.7
Hogan, J.B.8
McGovern, R.T.9
Iben, L.G.10
Mattson, G.K.11
Ortiz, A.12
Rassnick, S.13
Russell, J.W.14
Antal-Zimanyi, I.15
-
7
-
-
2942519827
-
General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines
-
(a)Zhao, Z.; Wisnoski, D. D.; Wolkenberg, S. E.; Leister, W. H.; Wang, Y.; Lindsley, C. W. General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines. Tetrahedron Lett. 2004, 45, 4873-4876;
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4873-4876
-
-
Zhao, Z.1
Wisnoski, D.D.2
Wolkenberg, S.E.3
Leister, W.H.4
Wang, Y.5
Lindsley, C.W.6
-
8
-
-
38949106966
-
Room-temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid
-
(b)Li, Z.; Li, W.; Sun, Y.; Huang, H.; Ouyang, P. Room-temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid. J. Het. Chem. 2008, 45, 285-288;
-
(2008)
J. Het. Chem.
, vol.45
, pp. 285-288
-
-
Li, Z.1
Li, W.2
Sun, Y.3
Huang, H.4
Ouyang, P.5
-
9
-
-
38149133179
-
Optimization of the heterocyclic core of the quinazolinone-derived CXCR3 antagonists
-
(c)Li, A.-R.; Johnson, M. G.; Liu, J.; Chen, X.; Du, X.; Mihalic, J. T.; Deignan, J.; Gustin, D. J.; Duquette, J.; Fu, Z.; Zhu, L.; Marcus, A. P.; Bergeron, P.; McGee, L. R.; Danao, J.; Lemon, B.; Carabeo, T.; Sullivan, T.; Ma, J.; Tang, L.; Tonn, G.; Collins, T. L.; Medina, J. C. Optimization of the heterocyclic core of the quinazolinone-derived CXCR3 antagonists. Bioorg. Med. Chem. Lett. 2008, 18, 688-693;
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 688-693
-
-
Li, A.-R.1
Johnson, M.G.2
Liu, J.3
Chen, X.4
Du, X.5
Mihalic, J.T.6
Deignan, J.7
Gustin, D.J.8
Duquette, J.9
Fu, Z.10
Zhu, L.11
Marcus, A.P.12
Bergeron, P.13
McGee, L.R.14
Danao, J.15
Lemon, B.16
Carabeo, T.17
Sullivan, T.18
Ma, J.19
Tang, L.20
Tonn, G.21
Collins, T.L.22
Medina, J.C.23
more..
-
10
-
-
34548473308
-
Discovery of 3,3-(2,4-diaminopteridine-6,7-diyl)diphenol as an isozyme-selective inhibitor of PI3 K for the treatment of ischemia reperfusion injury associated with myocardial infarction
-
(d)Palanki, M. S. S.; Dneprovskaia, E.; Doukas, J.; Fine, R. M.; Hood, J.; Kang, X.; Lohse, D.; Martin, M.; Noronha, G.; Soll, R. M.; Wrasidlo, W.; Yee, S.; Zhu, H. Discovery of 3,3-(2,4-diaminopteridine-6,7-diyl)diphenol as an isozyme-selective inhibitor of PI3 K for the treatment of ischemia reperfusion injury associated with myocardial infarction. J. Med. Chem. 2007, 50, 4279-4294;
-
(2007)
J. Med. Chem.
, Issue.50
, pp. 4279-4294
-
-
Palanki, M.S.S.1
Dneprovskaia, E.2
Doukas, J.3
Fine, R.M.4
Hood, J.5
Kang, X.6
Lohse, D.7
Martin, M.8
Noronha, G.9
Soll, R.M.10
Wrasidlo, W.11
Yee, S.12
Zhu, H.13
-
11
-
-
33947585924
-
Quinoxalinylurea derivatives as a novel class of JSP-1 inhibitors
-
(e)Zhang, L.; Qiu, B.; Xiong, B.; Li, X.; Li, J.; Wang, X.; Li, J.; Shen, J. Quinoxalinylurea derivatives as a novel class of JSP-1 inhibitors. Bioorg. Med. Chem. Lett. 2007, 17, 2118-2122;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 2118-2122
-
-
Zhang, L.1
Qiu, B.2
Xiong, B.3
Li, X.4
Li, J.5
Wang, X.6
Li, J.7
Shen, J.8
-
12
-
-
33847037381
-
Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors
-
(f)Rong, F.; Chow, S.; Yan, S.; Larson, G.; Hong, Z.; Wu, J. Structure-activity relationship (SAR) studies of quinoxalines as novel HCV NS5B RNA-dependent RNA polymerase inhibitors. Bioorg. Med. Chem. Lett. 2007, 17, 1663-1666.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 1663-1666
-
-
Rong, F.1
Chow, S.2
Yan, S.3
Larson, G.4
Hong, Z.5
Wu, J.6
-
13
-
-
17144367660
-
Substituted 5,5-diphenyl-2-thioxoimidazo-lidin-4-one as CB1 cannabinoid receptor ligands: Synthesis and pharmacological evaluation
-
(a)Muccioli, G. G.; Martin, D.; Scriba, G. K. E.; Poppitz, W.; Poupaert, J. H.; Wouters, J.; Lambert, D. M. Substituted 5,5-diphenyl-2-thioxoimidazo- lidin-4-one as CB1 cannabinoid receptor ligands: Synthesis and pharmacological evaluation. J. Med. Chem. 2005, 48, 2509-2517;
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2509-2517
-
-
Muccioli, G.G.1
Martin, D.2
Scriba, G.K.E.3
Poppitz, W.4
Poupaert, J.H.5
Wouters, J.6
Lambert, D.M.7
-
14
-
-
34147188545
-
Discovery of diaryl imidazolidin-2-one derivatives, a novel class of muscarinic M3 selective antagonists (part 1)
-
(b)Peretto, I.; Forlani, R.; Fossati, C.; Giardina, G. A. M.; Giardini, A.; Guala, M.; La Porta, E.; Petrillo, P.; Radaelli, S.; Radice, L.; Raveglia, L. F.; Santoro, E.; Scudellaro, R.; Scarpitta, F.; Bigogno, C.; Misiano, P.; Dondio, G. M.; Rizzi, A.; Armani, E.; Amari, G.; Civelli, M.; Villetti, G.; Patacchini, R.; Bergamaschi, M.; Delcanale, M.; Salcedo, C.; Fernandez, A. G.; Imbimbo, B. P. Discovery of diaryl imidazolidin-2-one derivatives, a novel class of muscarinic M3 selective antagonists (part 1). J. Med. Chem. 2007, 50, 1571-1583;
-
(2007)
J. Med. Chem.
, vol.50
, pp. 1571-1583
-
-
Peretto, I.1
Forlani, R.2
Fossati, C.3
Giardina, G.A.M.4
Giardini, A.5
Guala, M.6
La Porta, E.7
Petrillo, P.8
Radaelli, S.9
Radice, L.10
Raveglia, L.F.11
Santoro, E.12
Scudellaro, R.13
Scarpitta, F.14
Bigogno, C.15
Misiano, P.16
Dondio, G.M.17
Rizzi, A.18
Armani, E.19
Amari, G.20
Civelli, M.21
Villetti, G.22
Patacchini, R.23
Bergamaschi, M.24
Delcanale, M.25
Salcedo, C.26
Fernandez, A.G.27
Imbimbo, B.P.28
more..
-
15
-
-
28544451559
-
1-Benzhydryl-3-phenylurea and 1-benzhydryl-3-phenylthiourea derivatives: New templates among the CB1 cannabinoid receptor inverse agonists
-
(c)Muccioli, G. G.; Wouters, J.; Scriba, G. K. E.; Poppitz, W.; Poupaert, J. H.; Lambert, D. M. 1-Benzhydryl-3-phenylurea and 1-benzhydryl-3- phenylthiourea derivatives: New templates among the CB1 cannabinoid receptor inverse agonists. J. Med. Chem. 2005, 48, 7486-7490;
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7486-7490
-
-
Muccioli, G.G.1
Wouters, J.2
Scriba, G.K.E.3
Poppitz, W.4
Poupaert, J.H.5
Lambert, D.M.6
-
16
-
-
0037450446
-
A rapid and efficient microwave-assisted synthesis of hydantoins and thiohydantoins
-
(d)Muccioli, G. G.; Poupaert, J. H.; Wouters, J.; Norberg, B.; Poppitz, W.; Scriba, G. K. E.; Lambert, D. M. A rapid and efficient microwave-assisted synthesis of hydantoins and thiohydantoins. Tetrahedron 2003, 59, 1301-1307.
-
(2003)
Tetrahedron
, vol.59
, pp. 1301-1307
-
-
Muccioli, G.G.1
Poupaert, J.H.2
Wouters, J.3
Norberg, B.4
Poppitz, W.5
Scriba, G.K.E.6
Lambert, D.M.7
-
17
-
-
2442428407
-
Efficient synthesis of imidazoles from aldehydes and 1,2-dike-tones using microwave irradiation
-
(a)Wolkenberg, S. E.; Wisnoski, D. D.; Leister, W. H.; Wang, Y.; Zhao, Z.; Lindsley, C. W. Efficient synthesis of imidazoles from aldehydes and 1,2-dike-tones using microwave irradiation. Org. Lett. 2004, 6, 1453-1456;
-
(2004)
Org. Lett.
, vol.6
, pp. 1453-1456
-
-
Wolkenberg, S.E.1
Wisnoski, D.D.2
Leister, W.H.3
Wang, Y.4
Zhao, Z.5
Lindsley, C.W.6
-
18
-
-
47149103821
-
Synthesis and biological evaluation of trisubstituted imi-dazole derivatives as inhibitors of p38a mitogen-activated protein kinase
-
(b)Kim, D.-K.; Lim, J.-H.; Lee, J. A.; Dewang, P. M. Synthesis and biological evaluation of trisubstituted imi-dazole derivatives as inhibitors of p38a mitogen-activated protein kinase. Bioorg. Med. Chem. Lett. 2008, 18, 4006-4010;
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4006-4010
-
-
Kim, D.-K.1
Lim, J.-H.2
Lee, J.A.3
Dewang, P.M.4
-
19
-
-
77953707498
-
-
(c)Mader, M.; de Dios, A.; Shih, C.; Bonjouklian, R.; Li, T.; White, W.; Lopez de Uralde, B.; Sanchez-Martinez, C.; del Prado, M.; Jaramillo, C.; de Diego, E.; Martin, C., Luisa, M.; Dominguez, C.; Montero, C.;
-
-
-
Mader, M.1
De Dios, A.2
Shih, C.3
Bonjouklian, R.4
Li, T.5
White, W.6
Lopez De Uralde, B.7
Sanchez-Martinez, C.8
Del Prado, M.9
Jaramillo, C.10
De Diego, E.11
Martin, C.12
Luisa, M.13
Dominguez, C.14
Montero, C.15
-
20
-
-
37549052157
-
Imidazolyl benzimidazoles and imida-zo[4,5-b]pyridines as potent p38a MAP kinase inhibitors with excellent in vivo anti-inflammatory properties
-
Shepherd, T.; Dally, R.; Toth, J. E.; Chatterjee, A.; Pleite, S.; Blanco-Urgoiti, J.; Perez, L.; Barberis, M.; Lorite, M. J.; Jambrina, E.; Nevill, C. R.; Lee, P. A.; Schultz, R. C.; Wolos, J. A.; Li, L. C.; Campbell, R. M.; Anderson, B. D. Imidazolyl benzimidazoles and imida-zo[4,5-b]pyridines as potent p38a MAP kinase inhibitors with excellent in vivo anti-inflammatory properties. Bioorg. Med. Chem. Lett. 2008, 18, 179-183;
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 179-183
-
-
Shepherd, T.1
Dally, R.2
Toth, J.E.3
Chatterjee, A.4
Pleite, S.5
Blanco-Urgoiti, J.6
Perez, L.7
Barberis, M.8
Lorite, M.J.9
Jambrina, E.10
Nevill, C.R.11
Lee, P.A.12
Schultz, R.C.13
Wolos, J.A.14
Li, L.C.15
Campbell, R.M.16
Anderson, B.D.17
-
21
-
-
34948893906
-
One-pot efficient synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles and 2,4,5-triaryl-1H-imidazoles using oxalic acid catalyst
-
(d)Kokare, N. D.; Sangshetti, J. N.; Shinde, D. B. One-pot efficient synthesis of 2-aryl-1-arylmethyl-1H-benzimidazoles and 2,4,5-triaryl-1H- imidazoles using oxalic acid catalyst. Synthesis 2007, 2829-2834;
-
(2007)
Synthesis
, pp. 2829-2834
-
-
Kokare, N.D.1
Sangshetti, J.N.2
Shinde, D.B.3
-
22
-
-
34547664793
-
Synthetic small molecules that induce neurogenesis in skeletal muscle
-
(e)Williams, D. R.; Lee, M.-R.; Song, Y. A.; Ko, S.-K.; Kim, G.-H.; Shin, I. Synthetic small molecules that induce neurogenesis in skeletal muscle. J. Am. Chem. Soc. 2007, 129, 9258-9259.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9258-9259
-
-
Williams, D.R.1
Lee, M.-R.2
Song, Y.A.3
Ko, S.-K.4
Kim, G.-H.5
Shin, I.6
-
23
-
-
15044351054
-
Discrimination in the solid-state photodimerization of 1-methyl-5,6-diphenylpyrazin-2-one
-
(a)Kaftory, M.; Shteiman, V.; Lavy, T.; Scheffer, J. R.; Yang, J.; Enkelmann, V. Discrimination in the solid-state photodimerization of 1-methyl-5,6-diphenylpyrazin-2-one. Eur. J. Org. Chem. 2005, 847-853;
-
(2005)
Eur. J. Org. Chem.
, pp. 847-853
-
-
Kaftory, M.1
Shteiman, V.2
Lavy, T.3
Scheffer, J.R.4
Yang, J.5
Enkelmann, V.6
-
24
-
-
19944431003
-
Allosteric Akt (PKB) inhibitors: Discovery and SAR of isozyme selective inhibitors
-
(b)Lindsley, C. W.; Zhao, Z.; Leister, W. H.; Robinson, R. G.; Barnett, S. F.; Defeo-Jones, D.; Jones, R. E.; Hartman, G. D.; Huff, J. R.; Huber, H. E.; Duggan, M. E. Allosteric Akt (PKB) inhibitors: Discovery and SAR of isozyme selective inhibitors. Bioorg. Med. Chem. Lett. 2005, 15, 761-764.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 761-764
-
-
Lindsley, C.W.1
Zhao, Z.2
Leister, W.H.3
Robinson, R.G.4
Barnett, S.F.5
Defeo-Jones, D.6
Jones, R.E.7
Hartman, G.D.8
Huff, J.R.9
Huber, H.E.10
Duggan, M.E.11
-
25
-
-
0037415505
-
Broadening the scope of 1,2,4-triazine synthesis by the application of microwave technology
-
(a)Zhao, Z.; Leister, W. H.; Strauss, K. A.; Wisnoski, D. D.; Lindsley, C. W. Broadening the scope of 1,2,4-triazine synthesis by the application of microwave technology. Tetrahedron Lett. 2003, 44, 1123-1127;
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1123-1127
-
-
Zhao, Z.1
Leister, W.H.2
Strauss, K.A.3
Wisnoski, D.D.4
Lindsley, C.W.5
-
26
-
-
33846984926
-
Efficient synthesis of 3,5,6-trisubstituted-1,2,4-triazines in the Brønsted acidic ionic liquid, 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4)
-
(b)Potewar, T. M.; Lahoti, R. J.; Daniel, T.; Srinivasan, K. V. Efficient synthesis of 3,5,6-trisubstituted-1,2,4-triazines in the Brønsted acidic ionic liquid, 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4). Synth. Commun. 2007, 37, 261-269;
-
(2007)
Synth. Commun.
, vol.37
, pp. 261-269
-
-
Potewar, T.M.1
Lahoti, R.J.2
Daniel, T.3
Srinivasan, K.V.4
-
27
-
-
33646103126
-
Novel one-pot synthesis of substituted 1,2,4-triazines
-
(c)Nongkhlaw, R. L.; Myrboh, B. Novel one-pot synthesis of substituted 1,2,4-triazines. Heterocycl. Commun. 2006, 12, 67-72;
-
(2006)
Heterocycl. Commun.
, vol.12
, pp. 67-72
-
-
Nongkhlaw, R.L.1
Myrboh, B.2
-
28
-
-
0036300983
-
One-pot synthesis of 1,2,4-triazines
-
(d)Rostamizadeh, S.; Sadeghi, K. One-pot synthesis of 1,2,4-triazines. Synth. Commun. 2002, 32, 1899-1902;
-
(2002)
Synth. Commun.
, Issue.32
, pp. 1899-1902
-
-
Rostamizadeh, S.1
Sadeghi, K.2
-
29
-
-
0030791731
-
Dienophilicity of imidazole in inverse electron demand Diels-Alder reactions
-
(e)Neipp, C. E.; Ranslow, P. B.; Wan, Z.; Snyder, J. K. Dienophilicity of imidazole in inverse electron demand Diels-Alder reactions. Tetrahedron Lett. 1997, 38, 7499-7502;
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 7499-7502
-
-
Neipp, C.E.1
Ranslow, P.B.2
Wan, Z.3
Snyder, J.K.4
-
30
-
-
0028062674
-
Studies on anti-platelet agents V: Synthesis and structure-activity relationship of 3-substituted 5,6-bis(4-methoxyphenyl)-1,2,4-triazines
-
(e)Tanaka, A.; Sakai, H.; Ishikawa, T.; Motoyama, Y.; Takasugi, H. Studies on anti-platelet agents, V: Synthesis and structure-activity relationship of 3-substituted 5,6-bis(4-methoxyphenyl)-1,2,4-triazines. Chem. Pharm. Bull. 1994, 42, 1835-1840;
-
(1994)
Chem. Pharm. Bull.
, vol.42
, pp. 1835-1840
-
-
Tanaka, A.1
Sakai, H.2
Ishikawa, T.3
Motoyama, Y.4
Takasugi, H.5
-
31
-
-
0346028862
-
1,2,4-Triazine chemistry, 10: Dihydro-1,2,4-triazines: Structural studies of 5,6-diaryldihydro-1,2,4-triazines through the reactions with dimethyl acetylenedicarboxy-late
-
(f)Sasaki, T.; Minamoto, K.; Harada, K. 1,2,4-Triazine chemistry, 10: Dihydro-1,2,4-triazines: Structural studies of 5,6-diaryldihydro-1,2,4-triazines through the reactions with dimethyl acetylenedicarboxy-late. J. Org. Chem. 1980, 45, 4587-4593;
-
(1980)
J. Org. Chem.
, vol.45
, pp. 4587-4593
-
-
Sasaki, T.1
Minamoto, K.2
Harada, K.3
-
32
-
-
0017681728
-
3-Aryl-as-triazines as potential anti-inflammatory agents
-
(g)O'Rourke, M.; Lang, S. A., Jr.; Cohen, E. 3-Aryl-as-triazines as potential anti-inflammatory agents. J. Med. Chem. 1977, 20, 723-726.
-
(1977)
J. Med. Chem.
, vol.20
, pp. 723-726
-
-
O'Rourke, M.1
Lang Jr., S.A.2
Cohen, E.3
-
33
-
-
34548858716
-
Structure-activity relationship (SAR) investigations of substituted imidazole analogs as TRPV1 antagonists
-
(a)Gore, V. K.; Ma, V. V.; Tamir, R.; Gavva, N. R.; Treanor, J. J. S.; Norman, M. H. Structure-activity relationship (SAR) investigations of substituted imidazole analogs as TRPV1 antagonists. Bioorg. Med. Chem. Lett. 2007, 17, 5825-5830;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 5825-5830
-
-
Gore, V.K.1
Ma, V.V.2
Tamir, R.3
Gavva, N.R.4
Treanor, J.J.S.5
Norman, M.H.6
-
34
-
-
0038065646
-
"One pot" microwave-mediated synthesis of the basic canthine skeleton: Expedient access to unnatural b-carboline alkaloids
-
(a)also see Ref. 1(b)(b). Lindsley, C. W.; Wisnoski, D. D.; Wang, Y.; Leister, W. H.; Zhao, Z. A "one pot" microwave-mediated synthesis of the basic canthine skeleton: Expedient access to unnatural b-carboline alkaloids. Tetrahedron Lett. 2003, 44, 4495-4498;
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 4495-4498
-
-
Lindsley, C.W.1
Wisnoski, D.D.2
Wang, Y.3
Leister, W.H.4
Zhao, Z.A.5
-
35
-
-
15944376218
-
Synthesis and biological evaluation of unnatural canthine alkaloids
-
(b)Lindsley, C. W.; Bogusky, M. J.; Leister, W. H.; McClain, R. T.; Robinson, R. G.; Barnett, S. F.; Defeo-Jones, D.; Ross, C. W., III; Hartman, G. D. Synthesis and biological evaluation of unnatural canthine alkaloids. Tetrahedron Lett. 2005, 46, 2779-2782.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 2779-2782
-
-
Lindsley, C.W.1
Bogusky, M.J.2
Leister, W.H.3
McClain, R.T.4
Robinson, R.G.5
Barnett, S.F.6
Defeo-Jones, D.7
Ross III, C.W.8
Hartman, G.D.9
-
36
-
-
0026703228
-
A convenient preparation of symmetrical and unsymmetrical 1,2-diketones: Application to fluorinated phenytoin synthesis
-
(a)Page, P. C. B.; Graham, A. E.; Park, B. K. A convenient preparation of symmetrical and unsymmetrical 1,2-diketones: Application to fluorinated phenytoin synthesis. Tetrahedron 1992, 48, 7265-7274;
-
(1992)
Tetrahedron
, vol.48
, pp. 7265-7274
-
-
Page, P.C.B.1
Graham, A.E.2
Park, B.K.3
-
37
-
-
0001530618
-
Cyanohydrins as substrates in benzoin condensation: Regiocontrolled mixed benzoin condensation
-
(b)Rozwadowska, M. D. Cyanohydrins as substrates in benzoin condensation: Regiocontrolled mixed benzoin condensation. Tetrahedron 1985, 41, 3135-3140;
-
(1985)
Tetrahedron
, vol.41
, pp. 3135-3140
-
-
Rozwadowska, M.D.1
-
38
-
-
1842580631
-
A convenient and selective synthesis of unsymmetrical benzoins via the cyanide ion-catalyzed cleavage of benzils
-
(c)Demir, A. S.; Reis, O. A convenient and selective synthesis of unsymmetrical benzoins via the cyanide ion-catalyzed cleavage of benzils. Tetrahedron 2004, 60, 3803-3811;
-
(2004)
Tetrahedron
, vol.60
, pp. 3803-3811
-
-
Demir, A.S.1
Reis, O.2
-
39
-
-
28744457017
-
Generation of acyl anion equivalents from acylphosphonates via phosphonate-phosphate rearrangement: A highly practical method for cross-benzoin reaction
-
references therein(d)
-
(d)Demir, A. S.; Reis, O.; Igdir, C.; Esiringu, I.; Eymur, S. Generation of acyl anion equivalents from acylphosphonates via phosphonate-phosphate rearrangement: A highly practical method for cross-benzoin reaction. J. Org. Chem. 2005, 70, 10584-10587, and references therein;
-
(2005)
J. Org. Chem.
, vol.70
, pp. 10584-10587
-
-
Demir, A.S.1
Reis, O.2
Igdir, C.3
Esiringu, I.4
Eymur, S.5
-
40
-
-
13644254491
-
Mechanism and scope of the cyanide-catalyzed cross silyl benzoin reaction
-
(e)Linghu, X.; Bausch, C. C.; Johnson, J. S. Mechanism and scope of the cyanide-catalyzed cross silyl benzoin reaction. J. Am. Chem. Soc. 2005, 127, 1833-1840;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 1833-1840
-
-
Linghu, X.1
Bausch, C.C.2
Johnson, J.S.3
-
41
-
-
84970571837
-
Applications of optically active aryl cyanohydrins in the synthesis of a-hydroxy aldehydes, a-hydroxy ketones, and b-hydroxy amines
-
(f)Jackson, W. R.; Jacobs, H. A.; Jayatilake, G. S.; Matthews, B. R.; Watson, K. G. Applications of optically active aryl cyanohydrins in the synthesis of a-hydroxy aldehydes, a-hydroxy ketones, and b-hydroxy amines. Aust. J. Chem. 1990, 43, 2045-2062;
-
(1990)
Aust. J. Chem.
, vol.43
, pp. 2045-2062
-
-
Jackson, W.R.1
Jacobs, H.A.2
Jayatilake, G.S.3
Matthews, B.R.4
Watson, K.G.5
-
42
-
-
33751158037
-
Photoremovable protecting groups for phosphorylation of chiral alcohols: Asymmetric synthesis of phosphotriesters of (-)-3,5-dimethoxybenzoin
-
references therein(g)
-
(g)Pirrung, M. C.; Shuey, S. W. Photoremovable protecting groups for phosphorylation of chiral alcohols: Asymmetric synthesis of phosphotriesters of (-)-3,5-dimethoxybenzoin. J. Org. Chem. 1994, 59, 3890-3897, and references therein;
-
(1994)
J. Org. Chem.
, vol.59
, pp. 3890-3897
-
-
Pirrung, M.C.1
Shuey, S.W.2
-
43
-
-
0037120881
-
Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: The first asymmetric cross-benzoin condensation
-
(h)Denkelmann, P.; Kolter-Jung, D.; Nitsche, A.; Demir, A. S.; Siegert, P.; Lingen, B.; Baumann, M.; Pohl, M.; Muller, M. Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: The first asymmetric cross-benzoin condensation. J. Am. Chem. Soc. 2002, 124, 12084-12085;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 12084-12085
-
-
Denkelmann, P.1
Kolter-Jung, D.2
Nitsche, A.3
Demir, A.S.4
Siegert, P.5
Lingen, B.6
Baumann, M.7
Pohl, M.8
Muller, M.9
-
44
-
-
0000166235
-
Novel and facile syntheses of alkenyl, alkynyl, and aryl 1,2-diketones
-
(i)Katritzky, A. R.; Wang, Z.; Lang, H.; Feng, D. Novel and facile syntheses of alkenyl, alkynyl, and aryl 1,2-diketones. J. Org. Chem. 1997, 62, 4125-4130;
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4125-4130
-
-
Katritzky, A.R.1
Wang, Z.2
Lang, H.3
Feng, D.4
-
45
-
-
84982070299
-
Trimethylsilyl cyanide as an umpolung reagent, II: Nucleophilic acylation of aldehydes and ketones with anionic 1,4-O,O-silyl group migration
-
(j)Huenig, S.; Wehner, G. Trimethylsilyl cyanide as an umpolung reagent, II: Nucleophilic acylation of aldehydes and ketones with anionic 1,4-O,O-silyl group migration. Chem. Ber. 1979, 112, 2062-2067;
-
(1979)
Chem. Ber.
, vol.112
, pp. 2062-2067
-
-
Huenig, S.1
Wehner, G.2
-
46
-
-
84985109473
-
Nucleophilic acylation with masked acyl anions III: Synthesis of a-hydroxy-ketones
-
(k)Huenig, S.; Wehner, G. Nucleophilic acylation with masked acyl anions, III: Synthesis of a-hydroxy-ketones. Synthesis 1975, 391-392.
-
(1975)
Synthesis
, pp. 391-392
-
-
Huenig, S.1
Wehner, G.2
-
49
-
-
33745205457
-
-
G. Larson (Ed.); JAI: Greenwich, CT
-
(c)Advances in Silicon Chemistry 1, G. Larson (Ed.); JAI: Greenwich, CT 1991;
-
(1991)
Advances in Silicon Chemistry 1
-
-
-
50
-
-
84989438178
-
Synthetic applications of cyanotrimethylsilane, iodotrimethylsilane, azidotrimethylsi-lane, and methylthiotrimethylsilane
-
(d)Groutas, W. C.; Felker, D. Synthetic applications of cyanotrimethylsilane, iodotrimethylsilane, azidotrimethylsi-lane, and methylthiotrimethylsilane. Synthesis 1980, 861-868;
-
(1980)
Synthesis
, pp. 861-868
-
-
Groutas, W.C.1
Felker, D.2
-
51
-
-
0006684831
-
Trimethylsilyl cyanide: Cyanosilation of p-benzoquinone
-
(e)Livinghouse, T. Trimethylsilyl cyanide: Cyanosilation of p-benzoquinone. Org. Synth. Coll. 1990, 7, 517.
-
(1990)
Org. Synth. Coll.
, vol.7
, pp. 517
-
-
Livinghouse, T.1
-
52
-
-
27144444200
-
Cyanosilylation of aldehydes and ketones: Convenient route to cyanohydrin derivatives
-
Evans, D. A.; Truesdale, L. K.; Carroll, G. L. C. Cyanosilylation of aldehydes and ketones: Convenient route to cyanohydrin derivatives. J. Chem. Soc., Chem. Commun. 1973, 55-56.
-
(1973)
J. Chem. Soc. Chem. Commun.
, pp. 55-56
-
-
Evans, D.A.1
Truesdale, L.K.2
Carroll, G.L.C.3
-
53
-
-
0021167197
-
Facile synthesis of a-amino nitriles
-
Mai, K.; Patil, G. Facile synthesis of a-amino nitriles. Tetrahedron Lett. 1984, 25, 4583-4856.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 4583-4856
-
-
Mai, K.1
Patil, G.2
-
54
-
-
0001723378
-
The ultraviolet absorption spectra of alkoxy-and hydroxybenzils
-
Leonard, N. J.; Rapala, R. T.; Herzog, H. L.; Blout, E. R. The ultraviolet absorption spectra of alkoxy-and hydroxybenzils. J. Am. Chem. Soc. 1949, 71, 2997-3002.
-
(1949)
J. Am. Chem. Soc.
, vol.71
, pp. 2997-3002
-
-
Leonard, N.J.1
Rapala, R.T.2
Herzog, H.L.3
Blout, E.R.4
|