SCOPUS 정보 검색 플랫폼

Chemical Communications

Volumn 46, Issue 29, 2010, Pages 5244-5246

A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles

(5) Zhang, Jintang a Yu, Chenmin a Wang, Sujing a Wan, Changfeng a Wang, Zhiyong a

a UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA (China)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOBENZOPHENONE DERIVATIVE; AMINE; BENZOPHENONE DERIVATIVE; BENZYLIC AMINE DERIVATIVE; COPPER OXIDE; KAOLIN; METAL NANOPARTICLE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DRUG SYNTHESIS; SEPARATION TECHNIQUE;

EID: 77954691447 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/c002454f Document Type: Article

Times cited : (113)

References (36)

1
- 0034867043
- R. M. Crooks M. Q. Zhao L. Sun V. Chechik L. K. Yeung Acc. Chem. Res. 2001 34 181
- (2001) Acc. Chem. Res. , vol.34 , pp. 181
- Crooks, R.M.¹ Zhao, M.Q.² Sun, L.³ Chechik, V.⁴ Yeung, L.K.⁵

2
- 0037436556
- A. T. Bell Science 2003 299 1688
- (2003) Science , vol.299 , pp. 1688
- Bell, A.T.¹

3
- 29244458383
- D. Astruc F. Lu J. R. Aranzaes Angew. Chem., Int. Ed. 2005 44 7852
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 7852
- Astruc, D.¹ Lu, F.² Aranzaes, J.R.³

4
- 59349085767
- N. R. Shiju V. V. Guliants Appl. Catal., A 2009 356 1
- (2009) Appl. Catal., A , vol.356 , pp. 1
- Shiju, N.R.¹ Guliants, V.V.²

5
- 70350754662
- S. J. Wang Z. Y. Wang Z. G. Zha Dalton Trans. 2009 9363
- (2009) Dalton Trans. , pp. 9363
- Wang, S.J.¹ Wang, Z.Y.² Zha, Z.G.³

6
- 0036592824
- M. Haruta CATTECH 2002 6 102
- (2002) CATTECH , vol.6 , pp. 102
- Haruta, M.¹

7
- 0035851967
- M. Králik A. Biffis J. Mol. Catal. A: Chem. 2001 177 113
- (2001) J. Mol. Catal. A: Chem. , vol.177 , pp. 113
- Králik, M.¹ Biffis, A.²

8
- 34948902040
- B. Gallon R. Kojima R. Kaner P. Diaconescu Angew. Chem., Int. Ed. 2007 46 7251
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 7251
- Gallon, B.¹ Kojima, R.² Kaner, R.³ Diaconescu, P.⁴

9
- 0037184451
- B. M. Choudary S. Madhi N. S. Chowdari M. L. Kantam B. Sreedhar J. Am. Chem. Soc. 2002 124 14127
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 14127
- Choudary, B.M.¹ Madhi, S.² Chowdari, N.S.³ Kantam, M.L.⁴ Sreedhar, B.⁵

10
- 0037668129
- R. Narayanan M. A. El-Sayed J. Am. Chem. Soc. 2003 125 8340
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 8340
- Narayanan, R.¹ El-Sayed, M.A.²

11
- 4544234366
- J. Huang T. Jiang H. X. Gao B. X. Han Z. M. Liu W. Z. Wu Y. H. Chang G. Y. Zhao Angew. Chem., Int. Ed. 2004 43 1397
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 1397
- Huang, J.¹ Jiang, T.² Gao, H.X.³ Han, B.X.⁴ Liu, Z.M.⁵ Wu, W.Z.⁶ Chang, Y.H.⁷ Zhao, G.Y.⁸

12
- 4344602894
- K. Mori T. Hara T. Mizugaki K. Ebitani K. Kaneda J. Am. Chem. Soc. 2004 126 10657
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 10657
- Mori, K.¹ Hara, T.² Mizugaki, T.³ Ebitani, K.⁴ Kaneda, K.⁵

13
- 17644366510
- S. Carrettin J. Guzman A. Corma Angew. Chem., Int. Ed. 2005 44 2242
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 2242
- Carrettin, S.¹ Guzman, J.² Corma, A.³

14
- 25444436715
- P. D. Stevens G. Li J. Fan M. Yen Y. Gao Chem. Commun. 2005 4435
- (2005) Chem. Commun. , pp. 4435
- Stevens, P.D.¹ Li, G.² Fan, J.³ Yen, M.⁴ Gao, Y.⁵

15
- 34948904946
- T. Ishida M. Haruta Angew. Chem., Int. Ed. 2007 46 7154
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 7154
- Ishida, T.¹ Haruta, M.²

16
- 34548391350
- M. L. Kantam J. Yadav S. Laha B. Sreedhar S. Jha Adv. Synth. Catal. 2007 349 1938
- (2007) Adv. Synth. Catal. , vol.349 , pp. 1938
- Kantam, M.L.¹ Yadav, J.² Laha, S.³ Sreedhar, B.⁴ Jha, S.⁵

17
- 34548152778
- L. Rout S. Jammi T. Punniyamurthy Org. Lett. 2007 9 3397
- (2007) Org. Lett. , vol.9 , pp. 3397
- Rout, L.¹ Jammi, S.² Punniyamurthy, T.³

18
- 34547163805
- L. Rout T. K. Sen T. Punniyamurthy Angew. Chem., Int. Ed. 2007 46 5583
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 5583
- Rout, L.¹ Sen, T.K.² Punniyamurthy, T.³

19
- 55049092392
- J. T. Zhang Z. H. Zhang Y. Wang X. Q. Zheng Z. Y. Wang Eur. J. Org. Chem. 2008 5112
- (2008) Eur. J. Org. Chem. , pp. 5112
- Zhang, J.T.¹ Zhang, Z.H.² Wang, Y.³ Zheng, X.Q.⁴ Wang, Z.Y.⁵

20
- 62749122280
- V. P. Reddy A. V. Kumar K. Swapna K. R. Rao Org. Lett. 2009 11 951
- (2009) Org. Lett. , vol.11 , pp. 951
- Reddy, V.P.¹ Kumar, A.V.² Swapna, K.³ Rao, K.R.⁴

21
- 33748602640
- S. B. Mhaske N. P. Argade Tetrahedron 2006 62 9787
- (2006) Tetrahedron , vol.62 , pp. 9787
- Mhaske, S.B.¹ Argade, N.P.²

22
- 38849111840
- J. P. Michael Nat. Prod. Rep. 2008 25 166
- (2008) Nat. Prod. Rep. , vol.25 , pp. 166
- Michael, J.P.¹

23
- 0037405042
- A. Witt J. Bergman Curr. Org. Chem. 2003 7 659
- (2003) Curr. Org. Chem. , vol.7 , pp. 659
- Witt, A.¹ Bergman, J.²

24
- 25144475990
- D. J. Connolly D. Cusack T. P. O'Sullivan P. J. Guiry Tetrahedron 2005 61 10153
- (2005) Tetrahedron , vol.61 , pp. 10153
- Connolly, D.J.¹ Cusack, D.² O'Sullivan, T.P.³ Guiry, P.J.⁴

25
- 64049109957
- J. R. Li X. Chen D. X. Shi S. L. Ma Q. Li Q. Zhang J. H. Tang Org. Lett. 2009 11 1193
- (2009) Org. Lett. , vol.11 , pp. 1193
- Li, J.R.¹ Chen, X.² Shi, D.X.³ Ma, S.L.⁴ Li, Q.⁵ Zhang, Q.⁶ Tang, J.H.⁷

26
- 0028970007
- P. R. Marsham A. L. Jackman A. J. Barker F. T. Boyle S. J. Pegg J. M. Wardleworth R. Kimbell B. M. O'Connor A. H. Calvert L. R. Hughes J. Med. Chem. 1995 38 994
- (1995) J. Med. Chem. , vol.38 , pp. 994
- Marsham, P.R.¹ Jackman, A.L.² Barker, A.J.³ Boyle, F.T.⁴ Pegg, S.J.⁵ Wardleworth, J.M.⁶ Kimbell, R.⁷ O'Connor, B.M.⁸ Calvert, A.H.⁹ Hughes, L.R.¹⁰

27
- 72149116698
- V. L. Truong M. Morrow Tetrahedron Lett. 2010 51 758
- (2010) Tetrahedron Lett. , vol.51 , pp. 758
- Truong, V.L.¹ Morrow, M.²

28
- 77951687153
- X. B. Yang H. X. Liu H. Fu R. Z. Qiao Y. Y. Jiang Y. F. Zhao Synlett 2010 101
- (2010) Synlett , pp. 101
- Yang, X.B.¹ Liu, H.X.² Fu, H.³ Qiao, R.Z.⁴ Jiang, Y.Y.⁵ Zhao, Y.F.⁶

29
- 70449396611
- X. H. Huang H. J. Yang H. Fu R. Z. Qiao Y. F. Zhao Synthesis 2009 2679
- (2009) Synthesis , pp. 2679
- Huang, X.H.¹ Yang, H.J.² Fu, H.³ Qiao, R.Z.⁴ Zhao, Y.F.⁵

30
- 57249094142
- C. Huang Y. Fu H. Fu Y. Y. Jiang Y. F. Zhao Chem. Commun. 2008 6333
- (2008) Chem. Commun. , pp. 6333
- Huang, C.¹ Fu, Y.² Fu, H.³ Jiang, Y.Y.⁴ Zhao, Y.F.⁵

31
- 58249100136
- X. W. Liu H. Fu Y. Y. Jiang Y. F. Zhao Angew. Chem., Int. Ed. 2009 48 348
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 348
- Liu, X.W.¹ Fu, H.² Jiang, Y.Y.³ Zhao, Y.F.⁴

32
- 33749005084
- Z. H. Zhang Z. Y. Wang J. Org. Chem. 2006 71 7485
- (2006) J. Org. Chem. , vol.71 , pp. 7485
- Zhang, Z.H.¹ Wang, Z.Y.²

33
- 33748907768
- K. B. Zhou R. P. Wang B. Q. Xu Y. D. Li Nanotechnology 2006 17 3939
- (2006) Nanotechnology , vol.17 , pp. 3939
- Zhou, K.B.¹ Wang, R.P.² Xu, B.Q.³ Li, Y.D.⁴

34
- 77954732817
- CCDC- 757569 contains the supplementary crystallographic data for this paper
- CCDC- 757569 Contains the Supplementary Crystallographic Data for This Paper

35
- 4644355479
- Z. P. Li C. J. Li J. Am. Chem. Soc. 2004 126 11810
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 11810
- Li, Z.P.¹ Li, C.J.²

36
- 15744372304
- Compound A was also synthesized, and could be converted to 3aa in quantative yield under the reaction conditions
- Z. P. Li C. J. Li J. Am. Chem. Soc. 2005 127 3672
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 3672
- Li, Z.P.¹ Li, C.J.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.