-
1
-
-
0242474000
-
The chemistry of 2H-3 1-benzoxazine-2 ,4(1H)-dione (isatoic anhydride 23 (1) Synthesis of 2-(2-propenyl)-and 2-isopropylanilines
-
Coppola, G. M.; Marsden, C. M. The chemistry of 2H-3,1-benzoxazine-2, 4(1H)-dione (isatoic anhydride), 23 (1): Synthesis of 2-(2-propenyl)-and 2-isopropylanilines. Heterocycl. Commun. 1996, 2, 301-304
-
(1996)
Heterocycl Commun
, vol.2
, pp. 301-304
-
-
Coppola, G.M.1
Marsden, C.M.2
-
2
-
-
0010679653
-
Isatoic anhydrides and their uses in heterocyclic synthesis
-
Kappe, T.; Stadlbauer, W. Isatoic anhydrides and their uses in heterocyclic synthesis. Adv. Heterocycl. Chem. 1981, 28, 127-182
-
(1981)
Adv. Heterocycl. Chem
, vol.28
, pp. 127-182
-
-
Kappe, T.1
Stadlbauer, W.2
-
3
-
-
29744441083
-
New potential anticancer agents based on the anthranilic acid scaffold: Synthesis and evaluation of biological activity
-
Congiu, C.; Cocco, M. T.; Lilliu, V.; Onnis, V. New potential anticancer agents based on the anthranilic acid scaffold: Synthesis and evaluation of biological activity. J. Med. Chem. 2005, 48, 8245-8252
-
(2005)
J. Med. Chem
, vol.48
, pp. 8245-8252
-
-
Congiu, C.1
Cocco, M.T.2
Lilliu, V.3
Onnis, V.4
-
4
-
-
7044235522
-
Synthesis of new N-(2-(trifluoromethyl)pyridin-4-yl)anthranilic acid derivatives and their evaluation as anticancer agents
-
Cocco, M. T.; Congiu, C.; Lilliu, V.; Onnis, V. Synthesis of new N-(2-(trifluoromethyl)pyridin-4-yl)anthranilic acid derivatives and their evaluation as anticancer agents. Bioorg. Med. Chem. Lett. 2004, 14, 5787-5791
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 5787-5791
-
-
Cocco, M.T.1
Congiu, C.2
Lilliu, V.3
Onnis, V.4
-
5
-
-
33747372852
-
Synthesis and biological evaluation of benzamides and benzamidines as selective inhibitors of VEGFR tyrosine kinases
-
Nakamura, H.; Sasaki, Y.; Uno, M.; Yoshikawa, T.; Asano, T.; Ban, H. S.; Fukazawa, H.; Shibuya, M.; Uehara, Y. Synthesis and biological evaluation of benzamides and benzamidines as selective inhibitors of VEGFR tyrosine kinases. Bioorg. Med. Chem. Lett. 2006, 16, 5127-5131
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 5127-5131
-
-
Nakamura, H.1
Sasaki, Y.2
Uno, M.3
Yoshikawa, T.4
Asano, T.5
Ban, H.S.6
Fukazawa, H.7
Shibuya, M.8
Uehara, Y.9
-
6
-
-
63149179306
-
Anthranilamide-based N,N-dialkylbenzamidines as potent and orally bioavailable factor Xa inhibitors: P4 SAR
-
Zhang, P.; Bao, L.; Fan, J.; Jia, Z. J.; Sinha, U.; Wong, P. W.; Park, G.; Hutchaleelaha, A.; Scarborough, R. M.; Zhu, B-Y. Anthranilamide-based N,N-dialkylbenzamidines as potent and orally bioavailable factor Xa inhibitors: P4 SAR. Bioorg. Med. Chem. Lett. 2009, 19, 2186-2189
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, pp. 2186-2189
-
-
Zhang, P.1
Bao, L.2
Fan, J.3
Jia, Z.J.4
Sinha, U.5
Wong, P.W.6
Park, G.7
Hutchaleelaha, A.8
Scarborough, R.M.9
Zhu, B.-Y.10
-
7
-
-
40949140980
-
Synthesis of insecticidal fluorinated anthranilic diamides
-
Clark, D. A.; Lahm, G. P.; Smith, B. K.; Barry, J. D.; Clagg, D. G. Synthesis of insecticidal fluorinated anthranilic diamides. Bioorg. Med. Chem. 2008, 16, 3163-3170
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 3163-3170
-
-
Clark, D.A.1
Lahm, G.P.2
Smith, B.K.3
Barry, J.D.4
Clagg, D.G.5
-
9
-
-
12344268639
-
A novel highly selective chiral auxiliary for the asymmetric synthesis of l-and d-a-amino acid derivatives via a multicomponent ugi reaction
-
Basso, A.; Banfi, L.; Riva, R.; Guanti, G. A novel highly selective chiral auxiliary for the asymmetric synthesis of L-and D-a-amino acid derivatives via a multicomponent Ugi reaction. J. Org. Chem. 2005, 70, 575-579
-
(2005)
J. Org. Chem
, vol.70
, pp. 575-579
-
-
Basso, A.1
Banfi, L.2
Riva, R.3
Guanti, G.4
-
10
-
-
17144366282
-
Asymmetric multicomponent reactions (amcrs): The new frontier
-
Ramó n, D. J.; Yus, M. Asymmetric multicomponent reactions (AMCRs): The new frontier. Angew. Chem., Int. Ed. 2005, 44, 1602-1634
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 1602-1634
-
-
Ramón, D.J.1
Yus, M.2
-
11
-
-
84864232090
-
Multicomponent reactions in unconventional solvents: State of the art
-
Gu, Y. Multicomponent reactions in unconventional solvents: State of the art. Green Chem. 2012, 14, 2091-2128
-
(2012)
Green Chem
, vol.14
, pp. 2091-2128
-
-
Gu, Y.1
-
12
-
-
0039592952
-
One-pot synthesis of tetrasubstituted imidazoles catalyzed by zeolite HY and silica gel under microwave irradiation
-
Balalaie, S.; Arabanian, A. One-pot synthesis of tetrasubstituted imidazoles catalyzed by zeolite HY and silica gel under microwave irradiation. Green Chem. 2000, 2, 274-276
-
(2000)
Green Chem
, vol.2
, pp. 274-276
-
-
Balalaie, S.1
Arabanian, A.2
-
13
-
-
7044235263
-
Domino reactions in organic synthesis
-
Tietze, L. F. Domino reactions in organic synthesis. Chem. Rev. 1996, 96, 115-136
-
(1996)
Chem. Rev
, vol.96
, pp. 115-136
-
-
Tietze, L.F.1
-
14
-
-
31544434530
-
Recent developments in isocyanide-based multicomponent reactions in applied chemistry
-
Dömling, A. Recent developments in isocyanide-based multicomponent reactions in applied chemistry. Chem. Rev. 2006, 106, 17-89
-
(2006)
Chem. Rev
, vol.106
, pp. 17-89
-
-
Dömling, A.1
-
15
-
-
84876926579
-
Chemodivergent multicomponent domino reactions in aqueous media: L-prolinecatalyzed assembly of densely functionalized 4h-pyrano [2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials
-
Prasanna, P.; Perumal, S.; Menéndez, J. C. Chemodivergent, multicomponent domino reactions in aqueous media: L-Prolinecatalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials. Green Chem. 2013, 15, 1292-1299
-
(2013)
Green Chem
, vol.15
, pp. 1292-1299
-
-
Prasanna, P.1
Perumal, S.2
Menéndez, J.C.3
-
16
-
-
31544435491
-
Water-accelerated synthesis of novel bis-2,3-dihydroquinazolin-4(1H)-one derivatives
-
Baghbanzadeh, M.; Salehi, P.; Dabiri, M.; Kozehgary, G. Water-accelerated synthesis of novel bis-2,3-dihydroquinazolin-4(1H)-one derivatives. Synthesis 2006, 344-348
-
(2006)
Synthesis
, pp. 344-348
-
-
Baghbanzadeh, M.1
Salehi, P.2
Dabiri, M.3
Kozehgary, G.4
-
17
-
-
18744388642
-
A novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones
-
Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Baghbanzadeh, M. A novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones. Synlett 2005, 1155-1157
-
(2005)
Synlett
, pp. 1155-1157
-
-
Salehi, P.1
Dabiri, M.2
Zolfigol, M.A.3
Baghbanzadeh, M.4
-
18
-
-
77949343926
-
Synthesis of 2,3-dihydroquinazoline-4(1H)-ones
-
Shaterian, H. R.; Oveisi, A. R.; Honarmand, M. Synthesis of 2,3-dihydroquinazoline-4(1H)-ones. Synth. Commun. 2010, 40, 1231-1242
-
(2010)
Synth. Commun
, vol.40
, pp. 1231-1242
-
-
Shaterian, H.R.1
Oveisi, A.R.2
Honarmand, M.3
-
19
-
-
23244439655
-
Efficient synthesis of mono-and disubstituted 2,3-dihydroquinazolin-4(1H) -ones using KAl(SO4)2 12H2O as a reusable catalyst in water and ethanol
-
Dabiri, M.; Salehi, P.; Otokesh, S.; Baghbanzadeh, M.; Kozehgary, G.; Mohammadi, A. A. Efficient synthesis of mono-and disubstituted 2,3-dihydroquinazolin-4(1H)-ones using KAl(SO4)2 12H2O as a reusable catalyst in water and ethanol. Tetrahedron Lett. 2005, 46, 6123-6126
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 6123-6126
-
-
Dabiri, M.1
Salehi, P.2
Otokesh, S.3
Baghbanzadeh, M.4
Kozehgary, G.5
Mohammadi, A.A.6
-
20
-
-
35649009908
-
Ionic liquid-promoted eco-friendly and efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones
-
Dabiri, M.; Salehi, P.; Baghbanzadeh, M. Ionic liquid-promoted eco-friendly and efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones. Monatsh. Chem. 2007, 138, 1191-1194
-
(2007)
Monatsh. Chem
, vol.138
, pp. 1191-1194
-
-
Dabiri, M.1
Salehi, P.2
Baghbanzadeh, M.3
-
21
-
-
56049088951
-
A novel catalyst zinc(II perfluorooctanoate [Zn(PFO )2]-catalyzed three-component, one-pot reaction: Synthesis of quinazolinone derivatives in aqueous micellar media
-
Wang, L-M.; Hu, L.; Shao, J-H.; Yu, J.; Zhang, L. A novel catalyst zinc(II) perfluorooctanoate [Zn(PFO)2]-catalyzed three-component, one-pot reaction: Synthesis of quinazolinone derivatives in aqueous micellar media. J. Fluorine Chem. 2008, 129, 1139-1145
-
(2008)
J. Fluorine Chem
, vol.129
, pp. 1139-1145
-
-
Wang, L.-M.1
Hu, L.2
Shao, J.-H.3
Yu, J.4
Zhang, L.5
-
22
-
-
43049128809
-
Gallium(III triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)-ones and quinazolin-4(3H)-ones
-
Chen, J.; Wu, D.; He, F.; Liu, M.; Wu, H.; Ding, J.; Su, W. Gallium(III) triflate-catalyzed one-pot selective synthesis of 2,3-dihydroquinazolin-4(1H)- ones and quinazolin-4(3H)-ones. Tetrahedron Lett. 2008, 49, 3814-3818
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 3814-3818
-
-
Chen, J.1
Wu, D.2
He, F.3
Liu, M.4
Wu, H.5
Ding, J.6
Su, W.7
-
23
-
-
0021999825
-
Studies on 4(1H)-quinazolinones 5: Synthesis and anti-inflammatory activity of 4(1H)-quinazolinone derivatives
-
Ozaki, K.; Yamada, Y.; Oine, T.; Ishizuka, T.; Iwasawa, Y. Studies on 4(1H)-quinazolinones, 5: Synthesis and anti-inflammatory activity of 4(1H)-quinazolinone derivatives. J. Med. Chem. 1985, 28, 568-576
-
(1985)
J. Med. Chem
, vol.28
, pp. 568-576
-
-
Ozaki, K.1
Yamada, Y.2
Oine, T.3
Ishizuka, T.4
Iwasawa, Y.5
-
24
-
-
0023157268
-
Synthesis of substituted 2,3-dihydro-1-(b-phenylethyl)-2-aryl and 2,3-diaryl-4(1h)-quinazolinones and their pharmacological activities
-
Sadanandam, Y. S.; Reddy, K. R. M.; Rao, A. B. Synthesis of substituted 2,3-dihydro-1-(b-phenylethyl)-2-aryl and 2,3-diaryl-4(1H)-quinazolinones and their pharmacological activities. Eur. J. Org. Chem. 1987, 22, 169-173
-
(1987)
Eur. J. Org. Chem
, vol.22
, pp. 169-173
-
-
Sadanandam, Y.S.1
Reddy, K.R.M.2
Rao, A.B.3
-
25
-
-
24344488009
-
A new approach to the facile synthesis of mono-and disubstituted quinazolin-4(3H)-ones under solventfree conditions
-
Salehi, P.; Dabiri, M.; Zolfigol, M. A.; Baghbanzadeh, M. A new approach to the facile synthesis of mono-and disubstituted quinazolin-4(3H)-ones under solventfree conditions. Tetrahedron Lett. 2005, 46, 7051-7053
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 7051-7053
-
-
Salehi, P.1
Dabiri, M.2
Zolfigol, M.A.3
Baghbanzadeh, M.4
-
26
-
-
33749365374
-
Nafion-H: An efficient and recyclable heterogeneous catalyst for the one-pot synthesis of 2,3-disubstituted 4-(3H)-quinazolinones under solvent-free microwave irradiation conditions
-
Lingaiah, B. V.; Ezikiel, G.; Yakaiah, T.; Reddy, G. V.; Rao, P. S. Nafion-H: An efficient and recyclable heterogeneous catalyst for the one-pot synthesis of 2,3-disubstituted 4-(3H)-quinazolinones under solvent-free microwave irradiation conditions. Synlett 2006, 2507-2509
-
(2006)
Synlett
, pp. 2507-2509
-
-
Lingaiah, B.V.1
Ezikiel, G.2
Yakaiah, T.3
Reddy, G.V.4
Rao, P.S.5
-
27
-
-
84866647394
-
Synthesis of novel 1,4-benzodiazepine-3,5-dione derivatives: Reaction of 2-aminobenzamides under bargellini reaction conditions
-
Mahdavi, M.; Asadi, M.; Saeedi, M.; Rezaei, Z.; Moghbel, H.; Foroumadi, A.; Shafiee, A. Synthesis of novel 1,4-benzodiazepine-3,5-dione derivatives: Reaction of 2-aminobenzamides under Bargellini reaction conditions. Synlett 2012, 23, 2521-2525
-
(2012)
Synlett
, vol.23
, pp. 2521-2525
-
-
Mahdavi, M.1
Asadi, M.2
Saeedi, M.3
Rezaei, Z.4
Moghbel, H.5
Foroumadi, A.6
Shafiee, A.7
-
28
-
-
84881149530
-
Green synthesis of new boron-containing quinazolinones: Preparation of benzo[d] [1,3,2]diazaborinin-4(1h)one derivatives
-
Mahdavi, M.; Asadi, M.; Saeedi, M.; Tehrani, M. H.; Mirfazli, S. S.; Shafiee, A.; Foroumadi, A. Green synthesis of new boron-containing quinazolinones: Preparation of benzo[d][1,3,2]diazaborinin-4(1H)one derivatives. Synth. Commun. 2013, 43, 2936- 2942
-
(2013)
Synth. Commun
, vol.43
, pp. 2936-2942
-
-
Mahdavi, M.1
Asadi, M.2
Saeedi, M.3
Tehrani, M.H.4
Mirfazli, S.S.5
Shafiee, A.6
Foroumadi, A.7
-
29
-
-
84879076598
-
Reaction of isatoic anhydride, amine, and n,n0-dialkyl carbodiimides under solvent-free conditions: New and efficient synthesis of 3-alkyl-2- (alkylamino) quinazolin-4(3h)-ones
-
Asadi, M.; Ebrahimi, M.; Mahdavi, M.; Saeedi, M.; Ranjbar, P. R.; Yazdani, F.; Shafiee, A.; Foroumadi, A. Reaction of isatoic anhydride, amine, and N,N0-dialkyl carbodiimides under solvent-free conditions: New and efficient synthesis of 3-alkyl-2- (alkylamino) quinazolin-4(3H)-ones. Synth. Commun. 2013, 43, 2385-2392
-
(2013)
Synth. Commun
, vol.43
, pp. 2385-2392
-
-
Asadi, M.1
Ebrahimi, M.2
Mahdavi, M.3
Saeedi, M.4
Ranjbar, P.R.5
Yazdani, F.6
Shafiee, A.7
Foroumadi, A.8
-
30
-
-
5344265115
-
The synthesis of new asymmetric double Schiff bases containing a new o-amino benzoic acid derivative
-
Liang, Y.; Su, B.; Zhao, J.; Sun, W. The synthesis of new asymmetric double Schiff bases containing a new o-amino benzoic acid derivative. Synth. Commun. 2004, 34, 3235-3242
-
(2004)
Synth. Commun
, vol.34
, pp. 3235-3242
-
-
Liang, Y.1
Su, B.2
Zhao, J.3
Sun, W.4
-
31
-
-
28144438533
-
Design synthesis, and biological evaluation of sirtinol analogues as class III histone=protein deacetylase (sirtuin) inhibitors
-
Mai, A.; Massa, S.; Lavu, S.; Pezzi, R.; Simeoni, S.; Ragno, R.; Mariotti, F. R.; Chiani, F.; Camilloni, G.; Sinclair, D. A. Design, synthesis, and biological evaluation of sirtinol analogues as class III histone=protein deacetylase (sirtuin) inhibitors. J. Med. Chem. 2005, 48, 7789-7795
-
(2005)
J. Med. Chem
, vol.48
, pp. 7789-7795
-
-
Mai, A.1
Massa, S.2
Lavu, S.3
Pezzi, R.4
Simeoni, S.5
Ragno, R.6
Mariotti, F.R.7
Chiani, F.8
Camilloni, G.9
Sinclair, D.A.10
-
32
-
-
54049120201
-
Click reaction: Highly efficient synthesis of 2,3-dihydroquinazolin-4(1H) -ones
-
Shaabani, A.; Maleki, A.; Mofakham, H. Click reaction: Highly efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones. Synth. Commun. 2008, 38, 3751-3759
-
(2008)
Synth. Commun
, vol.38
, pp. 3751-3759
-
-
Shaabani, A.1
Maleki, A.2
Mofakham, H.3
-
33
-
-
3142745157
-
One-pot synthesis of 4(3H)-quinazolinones
-
Bhat, B. A.; Sahu, D. P. One-pot synthesis of 4(3H)-quinazolinones. Synth. Commun. 2004, 34, 2169-2176
-
(2004)
Synth. Commun
, vol.34
, pp. 2169-2176
-
-
Bhat, B.A.1
Sahu, D.P.2
-
34
-
-
33750586185
-
Benign and efficient synthesis of 2-substituted 4(3H)-quinazolinones mediated by iron(III) chloride hexahydrate in refluxing water
-
Wang, G-W.; Miao, C-B.; Kang, H. Benign and efficient synthesis of 2-substituted 4(3H)-quinazolinones mediated by iron(III) chloride hexahydrate in refluxing water. Bull. Chem. Soc. Jpn. 2006, 79, 1426-1430
-
(2006)
Bull. Chem. Soc. Jpn
, vol.79
, pp. 1426-1430
-
-
Wang, G.-W.1
Miao, C.-B.2
Kang, H.3
-
35
-
-
1842637263
-
A novel method for the synthesis of 4(3H)-quinazolinones
-
Abdel-Jalil, R. J.; Voelter, W.; Saeed, M. A novel method for the synthesis of 4(3H)-quinazolinones. Tetrahedron Lett. 2004, 45, 3475-3476
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 3475-3476
-
-
Abdel-Jalil, R.J.1
Voelter, W.2
Saeed, M.3
-
36
-
-
0037424799
-
Synthesis of quinazolin-4(3H)-ones and 1,2-dihydroquinazolin-4(3H)-ones with the aid of a low-valent titanium reagent
-
Shi, D.; Rong, L.; Wang, J.; Zhuang, Q.; Wang, X.; Hu, H. Synthesis of quinazolin-4(3H)-ones and 1,2-dihydroquinazolin-4(3H)-ones with the aid of a low-valent titanium reagent. Tetrahedron Lett. 2003, 44, 3199-3201
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 3199-3201
-
-
Shi, D.1
Rong, L.2
Wang, J.3
Zhuang, Q.4
Wang, X.5
Hu, H.6
-
37
-
-
56749163583
-
Direct catalytic asymmetric synthesis of cyclic aminals from aldehydes
-
Cheng, X.; Vellalath, S.; Goddard, R.; List, B. Direct catalytic asymmetric synthesis of cyclic aminals from aldehydes. J. Am. Chem. Soc. 2008, 130, 15786-15787
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 15786-15787
-
-
Cheng, X.1
Vellalath, S.2
Goddard, R.3
List, B.4
-
38
-
-
58349118504
-
Asymmetric Brønsted acid catalysis: Catalytic enantioselective synthesis of highly biologically active dihydroquinazolinones
-
Rueping, M.; Antonchick, A. P.; Sugiono, E.; Grenader, K. Asymmetric Brønsted acid catalysis: Catalytic enantioselective synthesis of highly biologically active dihydroquinazolinones. Angew. Chem., Int. Ed. 2009, 48, 908-910
-
(2009)
Angew. Chem. Int. Ed
, vol.48
, pp. 908-910
-
-
Rueping, M.1
Antonchick, A.P.2
Sugiono, E.3
Grenader, K.4
-
39
-
-
34548215079
-
Eco-friendly synthesis of 2,3-dihydroquinazolin-4(1H)-ones in ionic liquids or ionic liquid-water without additional catalyst
-
Chen, J.; Su, W.; Wu, H.; Liu, M.; Jin, C. Eco-friendly synthesis of 2,3-dihydroquinazolin-4(1H)-ones in ionic liquids or ionic liquid-water without additional catalyst. Green Chem. 2007, 9, 972-975
-
(2007)
Green Chem
, vol.9
, pp. 972-975
-
-
Chen, J.1
Su, W.2
Wu, H.3
Liu, M.4
Jin, C.5
|