-
1
-
-
0842304432
-
Discovery of a new class of anilinoquinazoline inhibitors with high affinity and specificity for the tyrosine kinase domain of c-Src
-
P.A. Plé, T.P. Green, L.F. Hennequin, and et al. Discovery of a new class of anilinoquinazoline inhibitors with high affinity and specificity for the tyrosine kinase domain of c-Src J. Med. Chem. 47 2004 871 887
-
(2004)
J. Med. Chem.
, vol.47
, pp. 871-887
-
-
Plé, P.A.1
Green, T.P.2
Hennequin, L.F.3
-
2
-
-
0345688604
-
Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2)
-
L.A. Doyle, and D.D. Ross Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2) Oncogene 22 2003 7340 7358
-
(2003)
Oncogene
, vol.22
, pp. 7340-7358
-
-
Doyle, L.A.1
Ross, D.D.2
-
3
-
-
0035445139
-
Influence of the replacement of the oxo function with the thioxo group on the antimycobacterial activity of 3-aryl-6,8-dichloro-2H-1,3-benzoxazine-2,4(3H)-diones and 3-arylquinazoline-2,4(1H,3H)-diones
-
K. Waisser, J. Gregor, H. Dostál, and et al. Influence of the replacement of the oxo function with the thioxo group on the antimycobacterial activity of 3-aryl-6,8-dichloro-2H-1,3-benzoxazine-2,4(3H)-diones and 3-arylquinazoline-2,4(1H,3H)-diones Farmaco 56 2001 803 807
-
(2001)
Farmaco
, vol.56
, pp. 803-807
-
-
Waisser, K.1
Gregor, J.2
Dostál, H.3
-
4
-
-
38849111840
-
Quinoline, quinazoline and acridone alkaloids
-
J.P. Michael Quinoline, quinazoline and acridone alkaloids Nat. Prod. Rep. 25 2008 166 187
-
(2008)
Nat. Prod. Rep.
, vol.25
, pp. 166-187
-
-
Michael, J.P.1
-
5
-
-
33749328794
-
Structural investigation of the 7-chloro-3-hydroxy-1H-quinazoline-2,4-dione scaffold to obtain AMPA and kainate receptor selective antagonists. Synthesis, pharmacological, and molecular modeling studies
-
V. Colotta, D. Catarzi, F. Varano, and et al. Structural investigation of the 7-chloro-3-hydroxy-1H-quinazoline-2,4-dione scaffold to obtain AMPA and kainate receptor selective antagonists. Synthesis, pharmacological, and molecular modeling studies J. Med. Chem. 49 2006 6015 6026
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6015-6026
-
-
Colotta, V.1
Catarzi, D.2
Varano, F.3
-
6
-
-
0037405042
-
Recent developments in the field of quinazoline chemistry
-
A. Witt, and J. Bergman Recent developments in the field of quinazoline chemistry Curr. Org. Chem. 7 2003 659 677
-
(2003)
Curr. Org. Chem.
, vol.7
, pp. 659-677
-
-
Witt, A.1
Bergman, J.2
-
7
-
-
25144475990
-
Synthesis of quinazolinones and quinazolines
-
D.J. Connolly, D. Cusack, T.P. O'Sullivan, and et al. Synthesis of quinazolinones and quinazolines Tetrahedron 61 2005 10153 10202
-
(2005)
Tetrahedron
, vol.61
, pp. 10153-10202
-
-
Connolly, D.J.1
Cusack, D.2
O'Sullivan, T.P.3
-
8
-
-
64049109957
-
A new and facile synthesis of quinazoline-2,4(1H,3H)-diones
-
L. Jiarong, C. Xian, S. Daxin, and et al. A new and facile synthesis of quinazoline-2,4(1H,3H)-diones Org. Lett. 11 2009 1193 1196
-
(2009)
Org. Lett.
, vol.11
, pp. 1193-1196
-
-
Jiarong, L.1
Xian, C.2
Daxin, S.3
-
9
-
-
0028970007
-
Quinazoline antifolate thymidylate synthase inhibitors: Replacement of glutamic acid in the C2-methyl series
-
P.R. Marsham, A.L. Jackman, A.J. Barker, and et al. Quinazoline antifolate thymidylate synthase inhibitors: replacement of glutamic acid in the C2-methyl series J. Med. Chem. 38 1995 994 1004
-
(1995)
J. Med. Chem.
, vol.38
, pp. 994-1004
-
-
Marsham, P.R.1
Jackman, A.L.2
Barker, A.J.3
-
10
-
-
77953576195
-
A simple and efficient approach to the synthesis of 2-phenylquinazolines via sp3 C-H functionalization
-
J. Zhang, D. Zhu, C. Yu, and et al. A simple and efficient approach to the synthesis of 2-phenylquinazolines via sp3 C-H functionalization Org. Lett. 12 2010 2841 2843
-
(2010)
Org. Lett.
, vol.12
, pp. 2841-2843
-
-
Zhang, J.1
Zhu, D.2
Yu, C.3
-
11
-
-
77954691447
-
A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles
-
J. Zhang, C. Yu, S. Wang, and et al. A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles Chem. Commun. 46 2010 5244 5246
-
(2010)
Chem. Commun.
, vol.46
, pp. 5244-5246
-
-
Zhang, J.1
Yu, C.2
Wang, S.3
-
12
-
-
80051586717
-
Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity
-
Y. Yan, and Z. Wang Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity Chem. Commun. 47 2011 9513 9515
-
(2011)
Chem. Commun.
, vol.47
, pp. 9513-9515
-
-
Yan, Y.1
Wang, Z.2
-
13
-
-
84864758851
-
Selective iodine-catalyzed intermolecular oxidative amination of C (sp3)-H bonds with ortho-carbonyl-substituted anilines to give quinazolines
-
Y. Yan, Y. Zhang, C. Feng, and et al. Selective iodine-catalyzed intermolecular oxidative amination of C (sp3)-H bonds with ortho-carbonyl-substituted anilines to give quinazolines Angew. Chem. Int. Ed. 51 2012 8077 8081
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 8077-8081
-
-
Yan, Y.1
Zhang, Y.2
Feng, C.3
-
14
-
-
79952464191
-
Microwave-promoted efficient synthesis of dihydroquinazolines
-
R. Sarma, and D. Prajapati Microwave-promoted efficient synthesis of dihydroquinazolines Green Chem. 13 2011 718 722
-
(2011)
Green Chem.
, vol.13
, pp. 718-722
-
-
Sarma, R.1
Prajapati, D.2
-
15
-
-
84860429043
-
Catalyst-free synthesis of quinazoline derivatives using low melting sugar-urea-salt mixture as a solvent
-
Z.H. Zhang, X.N. Zhang, L.P. Mo, and et al. Catalyst-free synthesis of quinazoline derivatives using low melting sugar-urea-salt mixture as a solvent Green Chem. 14 2012 1502 1506
-
(2012)
Green Chem.
, vol.14
, pp. 1502-1506
-
-
Zhang, Z.H.1
Zhang, X.N.2
Mo, L.P.3
-
16
-
-
84887936713
-
Unexpected copper-catalyzed cascade synthesis of quinazoline derivatives
-
Z. Chen, J. Chen, M. Liu, and et al. Unexpected copper-catalyzed cascade synthesis of quinazoline derivatives J. Org. Chem. 78 2013 11342 11348
-
(2013)
J. Org. Chem.
, vol.78
, pp. 11342-11348
-
-
Chen, Z.1
Chen, J.2
Liu, M.3
-
17
-
-
79959784065
-
Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C-H bond amination catalyzed by 4-hydroxyO
-
B. Han, C. Wang, R.F. Han, and et al. Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C-H bond amination catalyzed by 4-hydroxyO Chem. Commun. 47 2011 7818 7820
-
(2011)
Chem. Commun.
, vol.47
, pp. 7818-7820
-
-
Han, B.1
Wang, C.2
Han, R.F.3
-
18
-
-
84879947615
-
One-pot synthesis of quinazoline derivatives via [2 + 2+ 2] cascade annulation of diaryliodonium salts and two nitriles
-
X. Su, C. Chen, Y. Wang, and et al. One-pot synthesis of quinazoline derivatives via [2 + 2+ 2] cascade annulation of diaryliodonium salts and two nitriles Chem. Commun. 49 2013 6752 6754
-
(2013)
Chem. Commun.
, vol.49
, pp. 6752-6754
-
-
Su, X.1
Chen, C.2
Wang, Y.3
-
19
-
-
84885345680
-
One-pot synthesis of multiply substituted quinoline and quinazoline derivatives via [2 + 2+ 2] cascade annulation with diaryliodonium salts
-
Y. Wang, X. Su, and C. Chen One-pot synthesis of multiply substituted quinoline and quinazoline derivatives via [2 + 2+ 2] cascade annulation with diaryliodonium salts Synlett 24 2013 2619 2623
-
(2013)
Synlett
, vol.24
, pp. 2619-2623
-
-
Wang, Y.1
Su, X.2
Chen, C.3
-
20
-
-
84922818481
-
Potassium iodide-catalyzed three-component synthesis of 2-arylquinazolines via amination of benzylic C-H bonds of methylarenes
-
D. Zhao, Q. Shen, and J.-X. Li Potassium iodide-catalyzed three-component synthesis of 2-arylquinazolines via amination of benzylic C-H bonds of methylarenes Adv. Synth. Catal. 357 2015 339 344
-
(2015)
Adv. Synth. Catal.
, vol.357
, pp. 339-344
-
-
Zhao, D.1
Shen, Q.2
Li, J.-X.3
-
21
-
-
84896778047
-
Palladium-catalyzed unactivated C (sp3)-H bond activation and intramolecular amination of carboxamides: A new approach to β-lactams
-
W.W. Sun, P. Cao, R.Q. Mei, and et al. Palladium-catalyzed unactivated C (sp3)-H bond activation and intramolecular amination of carboxamides: a new approach to β-lactams Org. Lett. 16 2013 480 483
-
(2013)
Org. Lett.
, vol.16
, pp. 480-483
-
-
Sun, W.W.1
Cao, P.2
Mei, R.Q.3
-
22
-
-
84868355610
-
CuI controlled C-C and C-N bond formation of heteroaromatics through C (sp3)-H activation
-
R. Xia, H.Y. Niu, G.R. Qu, and et al. CuI controlled C-C and C-N bond formation of heteroaromatics through C (sp3)-H activation Org. Lett. 14 2012 5546 5549
-
(2012)
Org. Lett.
, vol.14
, pp. 5546-5549
-
-
Xia, R.1
Niu, H.Y.2
Qu, G.R.3
-
23
-
-
84867357072
-
Stereoselective radical amination of electron-deficient C (sp3)-H bonds by Co(II)-based metalloradical catalysis: Direct synthesis of α-amino acid derivatives via α-C-H amination
-
H. Lu, Y. Hu, H. Jiang, and et al. Stereoselective radical amination of electron-deficient C (sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination Org. Lett. 14 2012 5158 5161
-
(2012)
Org. Lett.
, vol.14
, pp. 5158-5161
-
-
Lu, H.1
Hu, Y.2
Jiang, H.3
-
24
-
-
80054764821
-
Intermolecular oxidative C-N bond formation under metal-free conditions: Control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation
-
H.J. Kim, J. Kim, S.H. Cho, and et al. Intermolecular oxidative C-N bond formation under metal-free conditions: control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation J. Am. Chem. Soc. 133 2011 16382 16385
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 16382-16385
-
-
Kim, H.J.1
Kim, J.2
Cho, S.H.3
-
25
-
-
84877649939
-
Iodine-mediated intramolecular amination of ketones: The synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups
-
W.C. Gao, S. Jiang, R.L. Wang, and et al. Iodine-mediated intramolecular amination of ketones: the synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups Chem. Commun. 49 2013 4890 4892
-
(2013)
Chem. Commun.
, vol.49
, pp. 4890-4892
-
-
Gao, W.C.1
Jiang, S.2
Wang, R.L.3
-
26
-
-
33746071928
-
Intermolecular amidation of unactivated sp2 and sp3 CH bonds via palladium-catalyzed cascade CH activation/nitrene insertion
-
H.Y. Thu, W.Y. Yu, and C.M. Che Intermolecular amidation of unactivated sp2 and sp3 CH bonds via palladium-catalyzed cascade CH activation/nitrene insertion J. Am. Chem. Soc. 128 2006 9048 9049
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 9048-9049
-
-
Thu, H.Y.1
Yu, W.Y.2
Che, C.M.3
-
27
-
-
84855643302
-
Heterocycle synthesis via direct C-H/N-H coupling
-
E.T. Nadres, and O. Daugulis Heterocycle synthesis via direct C-H/N-H coupling J. Am. Chem. Soc. 134 2012 7 10
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 7-10
-
-
Nadres, E.T.1
Daugulis, O.2
-
28
-
-
84896496785
-
Iridium-catalyzed intermolecular amidation of sp3 C-H bonds: Late-stage functionalization of an unactivated methyl group
-
T. Kang, Y. Kim, D. Lee, and et al. Iridium-catalyzed intermolecular amidation of sp3 C-H bonds: late-stage functionalization of an unactivated methyl group J. Am. Chem. Soc. 136 2014 4141 4144
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 4141-4144
-
-
Kang, T.1
Kim, Y.2
Lee, D.3
-
29
-
-
84862908390
-
Highly efficient syntheses of azetidines, pyrrolidines, and indolines via palladium catalyzed intramolecular amination of C (sp3)-H and C (sp2)-H bonds at γ and δ positions
-
G. He, Y. Zhao, S. Zhang, and et al. Highly efficient syntheses of azetidines, pyrrolidines, and indolines via palladium catalyzed intramolecular amination of C (sp3)-H and C (sp2)-H bonds at γ and δ positions J. Am. Chem. Soc. 134 2012 3 6
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 3-6
-
-
He, G.1
Zhao, Y.2
Zhang, S.3
-
30
-
-
75749085640
-
Palladium-katalysierte amidierung nichtaktivierter C (sp3)-H-bindungen: Von anilinen zu indolinen
-
J.J. Neumann, S. Rakshit, T. Dröge, and et al. Palladium-katalysierte amidierung nichtaktivierter C (sp3)-H-bindungen: von anilinen zu indolinen Angew. Chem. Int. Ed. 121 2009 7024 7027
-
(2009)
Angew. Chem. Int. Ed.
, vol.121
, pp. 7024-7027
-
-
Neumann, J.J.1
Rakshit, S.2
Dröge, T.3
-
31
-
-
80052459625
-
Palladium (0)-catalyzed intermolecular amination of unactivated C sp3-H bonds
-
J. Pan, M. Suand, and S.L. Buchwald Palladium (0)-catalyzed intermolecular amination of unactivated C sp3-H bonds Angew. Chem. Int. Ed. 50 2011 8647 8651
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 8647-8651
-
-
Pan, J.1
Suand, M.2
Buchwald, S.L.3
-
32
-
-
33846430525
-
Catalytic intermolecular amination of C-H bonds: Method development and mechanistic insights
-
K.W. Fiori, and J. Du Bois Catalytic intermolecular amination of C-H bonds: method development and mechanistic insights J. Am. Chem. Soc. 129 2007 562 568
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 562-568
-
-
Fiori, K.W.1
Du Bois, J.2
-
33
-
-
0005159543
-
A Rh-catalyzed C-H insertion reaction for the oxidative conversion of carbamates to oxazolidinones
-
C.G. Espino, and J. Du Bois A Rh-catalyzed C-H insertion reaction for the oxidative conversion of carbamates to oxazolidinones Angew. Chem. Int. Ed. 113 2001 618 620
-
(2001)
Angew. Chem. Int. Ed.
, vol.113
, pp. 618-620
-
-
Espino, C.G.1
Du Bois, J.2
-
34
-
-
84886778961
-
1,2,3-Triazoles as versatile directing group for selective sp2 and sp3 C-H activation: Cyclization vs substitution
-
X. Ye, Z. He, T. Ahmed, and et al. 1,2,3-Triazoles as versatile directing group for selective sp2 and sp3 C-H activation: cyclization vs substitution Chem. Sci. 4 2013 3712 3716
-
(2013)
Chem. Sci.
, vol.4
, pp. 3712-3716
-
-
Ye, X.1
He, Z.2
Ahmed, T.3
-
35
-
-
84890477776
-
Stereoselective synthesis of chiral α-amino-β-lactams through palladium(II)-catalyzed sequential monoarylation/amidation of C (sp3)-H bonds
-
Q. Zhang, K. Chen, W. Rao, and et al. Stereoselective synthesis of chiral α-amino-β-lactams through palladium(II)-catalyzed sequential monoarylation/amidation of C (sp3)-H bonds Angew. Chem. Int. Ed. 52 2013 13588 13592
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 13588-13592
-
-
Zhang, Q.1
Chen, K.2
Rao, W.3
-
36
-
-
84885447016
-
Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C (sp3)-H bonds
-
G. He, S.Y. Zhang, W.A. Nack, and et al. Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C (sp3)-H bonds Angew. Chem. Int. Ed. 52 2013 11124 11128
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 11124-11128
-
-
He, G.1
Zhang, S.Y.2
Nack, W.A.3
-
37
-
-
84902000334
-
Palladium-catalysed CH activation of aliphatic amines to give strained nitrogen heterocycles
-
A. McNally, B. Haffemayer, B.S.L. Collins, and et al. Palladium-catalysed CH activation of aliphatic amines to give strained nitrogen heterocycles Nature 510 2014 129 133
-
(2014)
Nature
, vol.510
, pp. 129-133
-
-
McNally, A.1
Haffemayer, B.2
Collins, B.S.L.3
-
38
-
-
84907342206
-
Silver-catalysed direct amination of unactivated C-H bonds of functionalized molecules
-
M. Yang, B. Su, Y. Wang, and et al. Silver-catalysed direct amination of unactivated C-H bonds of functionalized molecules Nat. Commun. 5 2014 4707 4712
-
(2014)
Nat. Commun.
, vol.5
, pp. 4707-4712
-
-
Yang, M.1
Su, B.2
Wang, Y.3
-
39
-
-
69849109789
-
Oxaziridine-mediated intramolecular amination of sp3-hybridized C-H bonds
-
C.P. Allen, T. Benkovics, A.K. Turek, and et al. Oxaziridine-mediated intramolecular amination of sp3-hybridized C-H bonds J. Am. Chem. Soc. 131 2009 12560 12561
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 12560-12561
-
-
Allen, C.P.1
Benkovics, T.2
Turek, A.K.3
-
40
-
-
84856714142
-
Intermolecular Ritter-type C-H amination of unactivated sp3 carbons
-
Q. Michaudel, D. Thevenet, and P.S. Baran Intermolecular Ritter-type C-H amination of unactivated sp3 carbons J. Am. Chem. Soc. 134 2012 2547 2550
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 2547-2550
-
-
Michaudel, Q.1
Thevenet, D.2
Baran, P.S.3
-
41
-
-
84904571201
-
Copper-catalyzed aerobic oxidative amination of sp3 C-H bonds: Efficient synthesis of 2-hetarylquinazolin-4(3H)-ones
-
Q. Li, Y. Huang, T. Chen, and et al. Copper-catalyzed aerobic oxidative amination of sp3 C-H bonds: efficient synthesis of 2-hetarylquinazolin-4(3H)-ones Org. Lett. 16 2014 3672 3675
-
(2014)
Org. Lett.
, vol.16
, pp. 3672-3675
-
-
Li, Q.1
Huang, Y.2
Chen, T.3
-
42
-
-
84894146819
-
Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes
-
B.L. Tran, B. Li, M. Driess, and et al. Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes J. Am. Chem. Soc. 136 2014 2555 2563
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 2555-2563
-
-
Tran, B.L.1
Li, B.2
Driess, M.3
-
43
-
-
84897408695
-
Copper-catalyzed site-selective intramolecular amidation of unactivated C (sp3)-H bonds
-
X. Wu, Y. Zhao, G. Zhang, and et al. Copper-catalyzed site-selective intramolecular amidation of unactivated C (sp3)-H bonds Angew. Chem. Int. Ed. 53 2014 3706 3710
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 3706-3710
-
-
Wu, X.1
Zhao, Y.2
Zhang, G.3
-
45
-
-
84896441672
-
Copper-catalyzed intramolecular C. H and C (sp2)-H amidation by oxidative cyclization
-
Z. Wang, J. Ni, Y. Kuninobu, and et al. Copper-catalyzed intramolecular C. H and C (sp2)-H amidation by oxidative cyclization Angew. Chem. Int. Ed. 53 2014 3496 3499
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 3496-3499
-
-
Wang, Z.1
Ni, J.2
Kuninobu, Y.3
-
46
-
-
79953899217
-
An efficient method for the N-arylation of phenylurea via copper catalyzed amidation
-
S.N. Gavade, R.S. Balaskar, M.S. Mane, and et al. An efficient method for the N-arylation of phenylurea via copper catalyzed amidation Chin. Chem. Lett. 22 2011 675 678
-
(2011)
Chin. Chem. Lett.
, vol.22
, pp. 675-678
-
-
Gavade, S.N.1
Balaskar, R.S.2
Mane, M.S.3
-
47
-
-
84901385901
-
Copper-catalyzed N-arylation of 2-arylindoles with aryl halides
-
W. Liu, L.Y. Hai, R.L. Liu, and et al. Copper-catalyzed N-arylation of 2-arylindoles with aryl halides Chin. Chem. Lett. 25 2014 1240 1243
-
(2014)
Chin. Chem. Lett.
, vol.25
, pp. 1240-1243
-
-
Liu, W.1
Hai, L.Y.2
Liu, R.L.3
-
48
-
-
57249094142
-
Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives
-
C. Huang, Y. Fu, H. Fu, and et al. Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives Chem. Commun. 47 2008 6333 6335
-
(2008)
Chem. Commun.
, vol.47
, pp. 6333-6335
-
-
Huang, C.1
Fu, Y.2
Fu, H.3
-
49
-
-
58249100136
-
A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions
-
X. Liu, H. Fu, Y. Jiang, and Y. Zhao A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions Angew. Chem. Int. Ed. 48 2009 348 351
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 348-351
-
-
Liu, X.1
Fu, H.2
Jiang, Y.3
Zhao, Y.4
-
50
-
-
77951687153
-
Efficient copper-catalyzed synthesis of 4-aminoquinazoline and 2,4-diaminoquinazoline derivatives
-
X. Yang, H. Liu, H. Fu, and et al. Efficient copper-catalyzed synthesis of 4-aminoquinazoline and 2,4-diaminoquinazoline derivatives Synlett 1 2010 101 106
-
(2010)
Synlett
, vol.1
, pp. 101-106
-
-
Yang, X.1
Liu, H.2
Fu, H.3
-
51
-
-
72149116698
-
Mild and efficient ligand-free copper-catalyzed condensation for the synthesis of quinazolines
-
V.L. Truong, and M. Morrow Mild and efficient ligand-free copper-catalyzed condensation for the synthesis of quinazolines Tetrahedron Lett. 51 2010 758 760
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 758-760
-
-
Truong, V.L.1
Morrow, M.2
-
52
-
-
84867076904
-
Copper-catalyzed three-component one-pot synthesis of quinazolines
-
J. Ju, R. Hua, and J. Su Copper-catalyzed three-component one-pot synthesis of quinazolines Tetrahedron 68 2012 9364 9370
-
(2012)
Tetrahedron
, vol.68
, pp. 9364-9370
-
-
Ju, J.1
Hua, R.2
Su, J.3
-
53
-
-
79955148862
-
Direct electrochemical imidation of aliphatic aminesvia anodic oxidation
-
L. Zhang, J.H. Su, S. Wang, and et al. Direct electrochemical imidation of aliphatic aminesvia anodic oxidation Chem. Commun. 47 2011 5488 5490
-
(2011)
Chem. Commun.
, vol.47
, pp. 5488-5490
-
-
Zhang, L.1
Su, J.H.2
Wang, S.3
-
54
-
-
84891009821
-
Electrochemical synthesis of the aryl α-ketoesters from acetophenones mediated by KI
-
Z. Zhang, J. Su, Z. Zha, and et al. Electrochemical synthesis of the aryl α-ketoesters from acetophenones mediated by KI Chem. Eur. J. 19 2013 17711 17714
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 17711-17714
-
-
Zhang, Z.1
Su, J.2
Zha, Z.3
|