SCOPUS 정보 검색 플랫폼

RSC Advances

Volumn 3, Issue 18, 2013, Pages 6278-6281

Efficient copper-catalyzed domino synthesis of tetrazoloisoquinolines

(5) Shi, Liangliang a Wang, Ruji a Yang, Haijun a Jiang, Yuyang b Fu, Hua a,b

a Tsinghua University (China)

b TSINGHUA UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER IODIDE; DOMINO REACTIONS; INTERNAL ALKYNES; INTRAMOLECULAR ADDITIONS; ISOQUINOLINES; SONOGASHIRA CROSS-COUPLING; TETRAZOLES;

CATALYSIS; HYDROCARBONS; REACTION KINETICS;

COPPER;

EID: 84878037369 PISSN: None EISSN: 20462069 Source Type: Journal
DOI: 10.1039/c3ra23230a Document Type: Article

Times cited : (11)

References (68)

1
- 0003607021
- ed. A. R. Katritzky, C. W. Rees, Pergamon, New York
- J. K. Landquist in Comprehensive Heterocyclic Chemistry, ed., A. R. Katritzky, C. W. Rees, Pergamon, New York, 1984
- (1984) Comprehensive Heterocyclic Chemistry
- Landquist, J.K.¹

2
- 0003607021
- ed. A. R. Katritzky, C. W. Rees, Pergamon, New York
- P. J. Crowley in Comprehensive Heterocyclic Chemistry, ed., A. R. Katritzky, C. W. Rees, Pergamon, New York, 1984
- (1984) Comprehensive Heterocyclic Chemistry
- Crowley, P.J.¹

3
- 0003655764
- Academic Press, San Diego, CA, and others in this series
- The Alkaloids: Chemistry and Biology, ed., G. A. Cordell, Academic Press, San Diego, CA, 2000, Vol. 54, and others in this series
- (2000) The Alkaloids: Chemistry and Biology , vol.54
- Cordell, G.A.¹

4
- 84878041643
- PCT Int. Appl. WO 2005-JP2974, 2005, 266938
- M. Seki, Y. Tarao, K. Yamada, A. Nakao, Y. Usui and Y. Komatsu, PCT Int. Appl. WO 2005-JP2974, 2005, Chem. Abstr., 2005, 143, 266938
- (2005) Chem. Abstr. , vol.143
- Seki, M.¹ Tarao, Y.² Yamada, K.³ Nakao, A.⁴ Usui, Y.⁵ Komatsu, Y.⁶

5
- 84878028155
- U.S. Pat. Appl. Publ. US 2005153877, 2005;, 153709
- Z. Miao, Y. Sun, S. Nakajima, D. Tang, F. Wu, G. Xu, Y. S. Or and Z. Wang, U.S. Pat. Appl. Publ. US 2005153877, 2005; Chem. Abstr., 2005, 143, 153709
- (2005) Chem. Abstr. , vol.143
- Miao, Z.¹ Sun, Y.² Nakajima, S.³ Tang, D.⁴ Wu, F.⁵ Xu, G.⁶ Or, Y.S.⁷ Wang, Z.⁸

6
- 84878068758
- PCT Int. Appl. WO 2004-JP19843, 2005;, 153371
- K. Nonoshita, Y. Ogino, M. Ishikawa, F. Sakai, H. Nakashima, Y. Nagae, D. Tsukahara, K. Arakawa, T. Nishimura and J. Eiki, PCT Int. Appl. WO 2004-JP19843, 2005; Chem. Abstr., 2005, 143, 153371
- (2005) Chem. Abstr. , vol.143
- Nonoshita, K.¹ Ogino, Y.² Ishikawa, M.³ Sakai, F.⁴ Nakashima, H.⁵ Nagae, Y.⁶ Tsukahara, D.⁷ Arakawa, K.⁸ Nishimura, T.⁹ Eiki, J.¹⁰

7
- 84878070636
- PCT Int. Appl. WO 2004-US40721, 2005;, 78091
- G. Luo, L. Chen, A. P. Degnan, G. M. Dubowchik, J. E. Macor, G. O. Tora and P. V. Chaturvedula, PCT Int. Appl. WO 2004-US40721, 2005; Chem. Abstr., 2005, 143, 78091
- (2005) Chem. Abstr. , vol.143
- Luo, G.¹ Chen, L.² Degnan, A.P.³ Dubowchik, G.M.⁴ Macor, J.E.⁵ Tora, G.O.⁶ Chaturvedula, P.V.⁷

8
- 33745165041
- ed. R. C. Storr and T. L. Gilchrist, Thieme, Stuttgart, Germany
- A. F. Brigas, In Science of Synthesis, ed., R. C. Storr and T. L. Gilchrist, Thieme, Stuttgart, Germany, 2004, Vol. 13, p. 861
- (2004) In Science of Synthesis , vol.13 , pp. 861
- Brigas, A.F.¹

9
- 73449128687
- M. Špulák R. Lubojacký P. Šenel J. KuneŠ M. Pour J. Org. Chem. 2010 75 241
- (2010) J. Org. Chem. , vol.75 , pp. 241
- Špulák, M.¹ Lubojacký, R.² Šenel, P.³ Kuneš, J.⁴ Pour, M.⁵

10
- 0003947866
- Hardwood Academic, Amsterdam
- K. W. Bentley, The Isoquinoline Alkaloids, Vol. 1, Hardwood Academic, Amsterdam, 1998
- (1998) The Isoquinoline Alkaloids , vol.1
- Bentley, K.W.¹

11
- 0036784031
- F. Dzierszinski A. Coppin M. Mortuaire E. Dewally C. Slomianny J.-C. Ameisen F. DeBels S. Tomavo Antimicrob. Agents Chemother. 2002 46 3197
- (2002) Antimicrob. Agents Chemother. , vol.46 , pp. 3197
- Dzierszinski, F.¹ Coppin, A.² Mortuaire, M.³ Dewally, E.⁴ Slomianny, C.⁵ Ameisen, J.-C.⁶ Debels, F.⁷ Tomavo, S.⁸

12
- 2342633234
- D. Kletsas W. Li Z. Han V. Papadopoulos Biochem. Pharmacol. 2004 67 1927
- (2004) Biochem. Pharmacol. , vol.67 , pp. 1927
- Kletsas, D.¹ Li, W.² Han, Z.³ Papadopoulos, V.⁴

13
- 3242655533
- U. R. Mach A. E. Hackling S. Perachon S. Ferry C. G. Wermuth J.-C. Schwartz P. Sokoloff H. Stark ChemBioChem 2004 5 508
- (2004) ChemBioChem , vol.5 , pp. 508
- Mach, U.R.¹ Hackling, A.E.² Perachon, S.³ Ferry, S.⁴ Wermuth, C.G.⁵ Schwartz, J.-C.⁶ Sokoloff, P.⁷ Stark, H.⁸

14
- 0038494029
- D. E. Muscarella K. A. O'Brian A. T. Lemley S. E. Bloom Toxicol. Sci. 2003 74 66
- (2003) Toxicol. Sci. , vol.74 , pp. 66
- Muscarella, D.E.¹ O'Brian, K.A.² Lemley, A.T.³ Bloom, S.E.⁴

15
- 44449123579
- W. Yu E. Wang R. J. Voll A. H. Miller M. M. Goodman Bioorg. Med. Chem. 2008 16 6145
- (2008) Bioorg. Med. Chem. , vol.16 , pp. 6145
- Yu, W.¹ Wang, E.² Voll, R.J.³ Miller, A.H.⁴ Goodman, M.M.⁵

16
- 33845368736
- B. W. Trotter K. K. Nanda N. R. Kett C. P. Regan J. J. Lynch G. L. Stump L. Kiss J. Wang R. H. Spencer S. A. Kane R. B. White R. Zhang K. D. Anderson N. J. Liverton C. J. McIntyre D. C. Beshore G. D. Hartman C. J. Dinsmore J. Med. Chem. 2006 49 6954
- (2006) J. Med. Chem. , vol.49 , pp. 6954
- Trotter, B.W.¹ Nanda, K.K.² Kett, N.R.³ Regan, C.P.⁴ Lynch, J.J.⁵ Stump, G.L.⁶ Kiss, L.⁷ Wang, J.⁸ Spencer, R.H.⁹ Kane, S.A.¹⁰ White, R.B.¹¹ Zhang, R.¹² Anderson, K.D.¹³ Liverton, N.J.¹⁴ McIntyre, C.J.¹⁵ Beshore, D.C.¹⁶ Hartman, G.D.¹⁷ Dinsmore, C.J.¹⁸

17
- 84981419171
- H. Reimlinger Chem. Ber. 1970 103 1900
- (1970) Chem. Ber. , vol.103 , pp. 1900
- Reimlinger, H.¹

18
- 0242582193
- H. Reimlinger W. R. F. Lingier J. J. M. Vandewalle Chem. Ber. 1975 108 3780
- (1975) Chem. Ber. , vol.108 , pp. 3780
- Reimlinger, H.¹ Lingier, W.R.F.² Vandewalle, J.J.M.³

19
- 84860012589
- B. Stanovnik M. Tisler D. Gabrijelcic M. Kunaver J. Zmitek J. Heterocycl. Chem. 1979 16 1567
- (1979) J. Heterocycl. Chem. , vol.16 , pp. 1567
- Stanovnik, B.¹ Tisler, M.² Gabrijelcic, D.³ Kunaver, M.⁴ Zmitek, J.⁵

20
- 0000756589
- C. Wentrup H. W. Winter J. Am. Chem. Soc. 1980 102 6159
- (1980) J. Am. Chem. Soc. , vol.102 , pp. 6159
- Wentrup, C.¹ Winter, H.W.²

21
- 0008788896
- A. Messmer A. Gelleri G. Hajos Tetrahedron 1986 42 4827
- (1986) Tetrahedron , vol.42 , pp. 4827
- Messmer, A.¹ Gelleri, A.² Hajos, G.³

22
- 33846468799
- B. H. Bhide V. D. Akolkar D. I. Brahmbhatt Indian J. Chem., Section B: Orga. Chem. Incl. Med. Chem. 1993 32B 675
- (1993) Indian J. Chem., Section B: Orga. Chem. Incl. Med. Chem. , vol.32 , pp. 675
- Bhide, B.H.¹ Akolkar, V.D.² Brahmbhatt, D.I.³

23
- 37049085968
- S. Donnelly J. Grimshaw J. Trocha-Grimshaw J. Chem. Soc., Chem. Commun. 1994 2171
- (1994) J. Chem. Soc., Chem. Commun. , pp. 2171
- Donnelly, S.¹ Grimshaw, J.² Trocha-Grimshaw, J.³

24
- 4344654759
- L. W. Deady S. M. Devine J. Heterocycl. Chem. 2004 41 549
- (2004) J. Heterocycl. Chem. , vol.41 , pp. 549
- Deady, L.W.¹ Devine, S.M.²

25
- 58149331052
- J. K. Laha G. D. Cuny Synthesis 2008 4002
- (2008) Synthesis , pp. 4002
- Laha, J.K.¹ Cuny, G.D.²

26
- 33845520080
- J. M. Keith J. Org. Chem. 2006 71 9540
- (2006) J. Org. Chem. , vol.71 , pp. 9540
- Keith, J.M.¹

27
- 69249173342
- C.-W. Tsai S.-C. Yang Y.-M. Liu M.-J. Wu Tetrahedron 2009 65 8367
- (2009) Tetrahedron , vol.65 , pp. 8367
- Tsai, C.-W.¹ Yang, S.-C.² Liu, Y.-M.³ Wu, M.-J.⁴

28
- 0345708168
- S. V. Ley A. W. Thomas Angew. Chem., Int. Ed. 2003 42 5400
- (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400
- Ley, S.V.¹ Thomas, A.W.²

29
- 0346749657
- K. Kunz U. Scholz D. Ganzer Synlett 2003 2428
- (2003) Synlett , pp. 2428
- Kunz, K.¹ Scholz, U.² Ganzer, D.³

30
- 9644277114
- I. P. Beletskaya A. V. Cheprakov Coord. Chem. Rev. 2004 248 2337
- (2004) Coord. Chem. Rev. , vol.248 , pp. 2337
- Beletskaya, I.P.¹ Cheprakov, A.V.²

31
- 51049095122
- G. Evano N. Blanchard M. Toumi Chem. Rev. 2008 108 3054
- (2008) Chem. Rev. , vol.108 , pp. 3054
- Evano, G.¹ Blanchard, N.² Toumi, M.³

32
- 57549098954
- D. Ma Q. Cai Acc. Chem. Res. 2008 41 1450
- (2008) Acc. Chem. Res. , vol.41 , pp. 1450
- Ma, D.¹ Cai, Q.²

33
- 70349786460
- F. Monnier M. Taillefer Angew. Chem., Int. Ed. 2009 48 6954
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6954
- Monnier, F.¹ Taillefer, M.²

34
- 77957130705
- D. S. Surry S. L. Buchwald Chem. Sci. 2010 1 13
- (2010) Chem. Sci. , vol.1 , pp. 13
- Surry, D.S.¹ Buchwald, S.L.²

35
- 79953028268
- references cited therein
- H. Rao H. Fu Synlett 2011 745
- (2011) Synlett , pp. 745
- Rao, H.¹ Fu, H.²

36
- 33751386131
- K. Okuro M. Furuune M. Enna M. Miura M. Nomura J. Org. Chem. 1993 58 4716
- (1993) J. Org. Chem. , vol.58 , pp. 4716
- Okuro, K.¹ Furuune, M.² Enna, M.³ Miura, M.⁴ Nomura, M.⁵

37
- 0001572402
- R. K. Gujadhur C. G. Bates D. Venkataraman Org. Lett. 2001 3 4315
- (2001) Org. Lett. , vol.3 , pp. 4315
- Gujadhur, R.K.¹ Bates, C.G.² Venkataraman, D.³

38
- 0242712817
- S. Cacchi G. Fabrizi L. M. Parisi Org. Lett. 2003 5 3843
- (2003) Org. Lett. , vol.5 , pp. 3843
- Cacchi, S.¹ Fabrizi, G.² Parisi, L.M.³

39
- 4444227434
- G. A. Slough V. Krchňák P. Helquist S. M. Canham Org. Lett. 2004 6 2909
- (2004) Org. Lett. , vol.6 , pp. 2909
- Slough, G.A.¹ Krchňák, V.² Helquist, P.³ Canham, S.M.⁴

40
- 2342583283
- M. B. Thathagar J. Beckers G. Rothenberg Green Chem. 2004 6 215
- (2004) Green Chem. , vol.6 , pp. 215
- Thathagar, M.B.¹ Beckers, J.² Rothenberg, G.³

41
- 5044240208
- D. Ma F. Liu Chem. Commun. 2004 1934
- (2004) Chem. Commun. , pp. 1934
- Ma, D.¹ Liu, F.²

42
- 22244450348
- P. Saejueng C. G. Bates D. Venkataraman Synthesis 2005 1706
- (2005) Synthesis , pp. 1706
- Saejueng, P.¹ Bates, C.G.² Venkataraman, D.³

43
- 33947202279
- J.-H. Li J.-L. Li D.-P. Wang S.-F. Pi Y.-X. Xie M.-B. Zhang X.-C. Hu J. Org. Chem. 2007 72 2053
- (2007) J. Org. Chem. , vol.72 , pp. 2053
- Li, J.-H.¹ Li, J.-L.² Wang, D.-P.³ Pi, S.-F.⁴ Xie, Y.-X.⁵ Zhang, M.-B.⁶ Hu, X.-C.⁷

44
- 34250876277
- F. Liu D. Ma J. Org. Chem. 2007 72 4844
- (2007) J. Org. Chem. , vol.72 , pp. 4844
- Liu, F.¹ Ma, D.²

45
- 49649083069
- H. Jiang H. Fu R. Qiao Y. Jiang Y. Zhao Synthesis 2008 2417
- (2008) Synthesis , pp. 2417
- Jiang, H.¹ Fu, H.² Qiao, R.³ Jiang, Y.⁴ Zhao, Y.⁵

46
- 57249094142
- C. Huang Y. Fu H. Fu Y. Jiang Y. Zhao Chem. Commun. 2008 6333
- (2008) Chem. Commun. , pp. 6333
- Huang, C.¹ Fu, Y.² Fu, H.³ Jiang, Y.⁴ Zhao, Y.⁵

47
- 53049096302
- D. Yang H. Fu L. Hu Y. Jiang Y. Zhao J. Org. Chem. 2008 73 7841
- (2008) J. Org. Chem. , vol.73 , pp. 7841
- Yang, D.¹ Fu, H.² Hu, L.³ Jiang, Y.⁴ Zhao, Y.⁵

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

49
- 68949149911
- D. Yang H. Liu H. Yang H. Fu L. Hu Y. Jiang Y. Zhao Adv. Synth. Catal. 2009 351 1999
- (2009) Adv. Synth. Catal. , vol.351 , pp. 1999
- Yang, D.¹ Liu, H.² Yang, H.³ Fu, H.⁴ Hu, L.⁵ Jiang, Y.⁶ Zhao, Y.⁷

50
- 66149167196
- F. Wang H. Liu H. Fu Y. Jiang Y. Zhao Org. Lett. 2009 11 2469
- (2009) Org. Lett. , vol.11 , pp. 2469
- Wang, F.¹ Liu, H.² Fu, H.³ Jiang, Y.⁴ Zhao, Y.⁵

51
- 77953184051
- J. Lu X. Gong H. Yang H. Fu Chem. Commun. 2010 46 4172
- (2010) Chem. Commun. , vol.46 , pp. 4172
- Lu, J.¹ Gong, X.² Yang, H.³ Fu, H.⁴

52
- 77952474057
- H. Zhao H. Fu R. Qiao J. Org. Chem. 2010 75 3311
- (2010) J. Org. Chem. , vol.75 , pp. 3311
- Zhao, H.¹ Fu, H.² Qiao, R.³

53
- 77951169071
- X. Yang H. Fu R. Qiao Y. Jiang Y. Zhao Adv. Synth. Catal. 2010 352 1033
- (2010) Adv. Synth. Catal. , vol.352 , pp. 1033
- Yang, X.¹ Fu, H.² Qiao, R.³ Jiang, Y.⁴ Zhao, Y.⁵

54
- 77954559372
- X. Gong H. Yang H. Liu Y. Jiang Y. Zhao H. Fu Org. Lett. 2010 12 3128
- (2010) Org. Lett. , vol.12 , pp. 3128
- Gong, X.¹ Yang, H.² Liu, H.³ Jiang, Y.⁴ Zhao, Y.⁵ Fu, H.⁶

55
- 79955165110
- S. Xu J. Lu H. Fu Chem. Commun. 2011 47 5596
- (2011) Chem. Commun. , vol.47 , pp. 5596
- Xu, S.¹ Lu, J.² Fu, H.³

56
- 79957943706
- T. Liu R. Wang H. Yang H. Fu Chem.-Eur. J. 2011 17 6765
- (2011) Chem.-Eur. J. , vol.17 , pp. 6765
- Liu, T.¹ Wang, R.² Yang, H.³ Fu, H.⁴

57
- 84863123198
- D. Yang Y. Wang H. Yang T. Liu H. Fu Adv. Synth. Catal. 2012 354 477
- (2012) Adv. Synth. Catal. , vol.354 , pp. 477
- Yang, D.¹ Wang, Y.² Yang, H.³ Liu, T.⁴ Fu, H.⁵

58
- 84865726470
- X. Yang Y. Luo Y. Jin H. Liu Y. Jiang H. Fu RSC Adv. 2012 2 8258
- (2012) RSC Adv. , vol.2 , pp. 8258
- Yang, X.¹ Luo, Y.² Jin, Y.³ Liu, H.⁴ Jiang, Y.⁵ Fu, H.⁶

59
- 12344278958
- G. Altenhoff F. Glorius Adv. Synth. Catal. 2004 346 1661
- (2004) Adv. Synth. Catal. , vol.346 , pp. 1661
- Altenhoff, G.¹ Glorius, F.²

60
- 33644643208
- G. Evindar R. A. Batey J. Org. Chem. 2006 71 1802
- (2006) J. Org. Chem. , vol.71 , pp. 1802
- Evindar, G.¹ Batey, R.A.²

61
- 33750623389
- R. Martin M. R. Rivero S. L. Buchwald Angew. Chem., Int. Ed. 2006 45 7079
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 7079
- Martin, R.¹ Rivero, M.R.² Buchwald, S.L.³

62
- 33749023851
- F. Bonnaterre M. Bois-Choussy J. Zhu Org. Lett. 2006 8 4351
- (2006) Org. Lett. , vol.8 , pp. 4351
- Bonnaterre, F.¹ Bois-Choussy, M.² Zhu, J.³

63
- 36649030328
- Y. Chen X. Xie D. Ma J. Org. Chem. 2007 72 9329
- (2007) J. Org. Chem. , vol.72 , pp. 9329
- Chen, Y.¹ Xie, X.² Ma, D.³

64
- 34250839461
- B. Zou Q. Yuan D. Ma Angew. Chem., Int. Ed. 2007 46 2598
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 2598
- Zou, B.¹ Yuan, Q.² Ma, D.³

65
- 33846972345
- X. Yuan X. Xu X. Zhou J. Yuan L. Mai Y. Li J. Org. Chem. 2007 72 1510
- (2007) J. Org. Chem. , vol.72 , pp. 1510
- Yuan, X.¹ Xu, X.² Zhou, X.³ Yuan, J.⁴ Mai, L.⁵ Li, Y.⁶

66
- 51649116660
- B. Wang B. Lu Y. Jiang Y. Zhang D. Ma Org. Lett. 2008 10 2761
- (2008) Org. Lett. , vol.10 , pp. 2761
- Wang, B.¹ Lu, B.² Jiang, Y.³ Zhang, Y.⁴ Ma, D.⁵

67
- 84866041300
- references cited therein
- T. Liu H. Fu Synthesis 2012 44 2805
- (2012) Synthesis , vol.44 , pp. 2805
- Liu, T.¹ Fu, H.²

68
- 70749147617
- Q. Wang S. L. Schreiber Org. Lett. 2009 11 5178
- (2009) Org. Lett. , vol.11 , pp. 5178
- Wang, Q.¹ Schreiber, S.L.²

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