SCOPUS 정보 검색 플랫폼

Volumn 355, Issue 6, 2013, Pages 1185-1192

Copper-catalyzed domino SN2′/coupling reaction: A versatile and facile synthesis of cyclic compounds from baylis-hillman acetates

(8) Niu, Qingsheng a Mao, Hui a Yuan, Guodong a Gao, Jilong a Liu, Haiquan a Tu, Yawei a Wang, Xiaoxia a Lv, Xin a

a ZHEJIANG NORMAL UNIVERSITY (China)

Author keywords

copper; cross coupling; cyclization; domino reactions; nucleophilic substitution

Indexed keywords

EID: 84876473717 PISSN: 16154150 EISSN: 16154169 Source Type: Journal
DOI: 10.1002/adsc.201201033 Document Type: Article

Times cited : (28)

References (48)

1
- 79955004745
- V. R. Solomon, H. Lee, Curr. Med. Chem. 2011, 18, 1488-1508
- (2011) Curr. Med. Chem. , vol.18 , pp. 1488-1508
- Solomon, V.R.¹ Lee, H.²

2
- 77954309291
- K. Kaur, M. Jain, R. P. Reddy, R. Jain, Eur. J. Med. Chem. 2010, 45, 3245-3264
- (2010) Eur. J. Med. Chem. , vol.45 , pp. 3245-3264
- Kaur, K.¹ Jain, M.² Reddy, R.P.³ Jain, R.⁴

3
- 0031449261
- J. P. Michael, Nat. Prod. Rep. 1997, 14, 605-618
- (1997) Nat. Prod. Rep. , vol.14 , pp. 605-618
- Michael, J.P.¹

4
- 0003607021
- (Eds.: A.R. Katritzky, C.W. Rees, E.F.V. Scriven), Pergamon Press, Oxford, pp167- 243
- G. Jones, in: Comprehensive Heterocyclic Chemistry II, (Eds.:, A.R. Katritzky, C.W. Rees, E.F.V. Scriven,), Pergamon Press, Oxford, 1996, Vol. 5, pp167- 243
- (1996) Comprehensive Heterocyclic Chemistry II , pp. 5
- Jones, G.¹

5
- 84986940209
- (Ed.: M.F. Grundon), Royal Society of Chemistry, London, pp99- 121
- M. F. Grundon, M. F. Grundon, Quinoline and Acridone Alkaloids, (Ed.:, M.F. Grundon,), Royal Society of Chemistry, London, 1983, Vol. 13, pp99- 121.
- (1983) Quinoline and Acridone Alkaloids , pp. 13
- Grundon, M.F.¹ Grundon, M.F.²

6
- 84866053734
- F. A. Bassyouni, H. A. Tawfik, A. M. Soliman, M. A. Rehim, Res. Chem. Intermed. 2012, 38, 1291-1310
- (2012) Res. Chem. Intermed. , vol.38 , pp. 1291-1310
- Bassyouni, F.A.¹ Tawfik, H.A.² Soliman, A.M.³ Rehim, M.A.⁴

7
- 84859574809
- J. A. Bull, J. J. Mousseau, G. Pelletier, A. B. Charette, Chem. Rev. 2012, 112, 2642-2713
- (2012) Chem. Rev. , vol.112 , pp. 2642-2713
- Bull, J.A.¹ Mousseau, J.J.² Pelletier, G.³ Charette, A.B.⁴

8
- 80051553376
- P. DiGion, F. Kanefendt, A. Lindauer, M. Scheffler, O. Doroshyenko, U. Fuhr, J. Wolf, U. Jaehde, Clin. Pharmacokinet. 2011, 50, 551-603
- (2011) Clin. Pharmacokinet. , vol.50 , pp. 551-603
- Digion, P.¹ Kanefendt, F.² Lindauer, A.³ Scheffler, M.⁴ Doroshyenko, O.⁵ Fuhr, U.⁶ Wolf, J.⁷ Jaehde, U.⁸

9
- 4544328862
- (Ed.: W.W. Pelletier), Elsevier, New York, pp92
- J. W. Daly, H. M. Garraffo, T. F. Spande, in: Alkaloids: Chemical and Biological Perspectives, (Ed.:, W.W. Pelletier,), Elsevier, New York, 1999, Vol. 13, pp92.
- (1999) Alkaloids: Chemical and Biological Perspectives , pp. 13
- Daly, J.W.¹ Garraffo, H.M.² Spande, T.F.³

10
- 70349234512
- C. H. Lee, K. J. Lee, J. Heterocycl. Chem. 2009, 46, 1023-1027
- (2009) J. Heterocycl. Chem. , vol.46 , pp. 1023-1027
- Lee, C.H.¹ Lee, K.J.²

11
- 0037061594
- W. Quaglia, M. Pigini, A. Piergentili, M. Giannella, F. Gentili, G. Marucci, A. Carrieri, A. Carotti, E. Poggesi, A. Leonardi, C. Melchiorre, J. Med. Chem. 2002, 45, 1633-1643
- (2002) J. Med. Chem. , vol.45 , pp. 1633-1643
- Quaglia, W.¹ Pigini, M.² Piergentili, A.³ Giannella, M.⁴ Gentili, F.⁵ Marucci, G.⁶ Carrieri, A.⁷ Carotti, A.⁸ Poggesi, E.⁹ Leonardi, A.¹⁰ Melchiorre, C.¹¹

12
- 0034721133
- L. A. vanVliet, N. Rodenhuis, D. Dijkstra, H. Wikstrom, J. Med. Chem. 2000, 43, 2871-2882
- (2000) J. Med. Chem. , vol.43 , pp. 2871-2882
- Vanvliet, L.A.¹ Rodenhuis, N.² Dijkstra, D.³ Wikstrom, H.⁴

13
- 84986500874
- H. Nakazumi, Y. Kobara, T. Kitao, J. Heterocycl. Chem. 1992, 29, 135-139
- (1992) J. Heterocycl. Chem. , vol.29 , pp. 135-139
- Nakazumi, H.¹ Kobara, Y.² Kitao, T.³

14
- 0019793937
- J. G. Lombardino, I. G. Otterness, J. Med. Chem. 1981, 24, 830-834.
- (1981) J. Med. Chem. , vol.24 , pp. 830-834
- Lombardino, J.G.¹ Otterness, I.G.²

15
- 84859804224
- Y. X. Wang, X. B. Zhang, J. Zhao, S. Q. Xie, C. J. Wang, J. Med. Chem. 2012, 55, 3502-3512
- (2012) J. Med. Chem. , vol.55 , pp. 3502-3512
- Wang, Y.X.¹ Zhang, X.B.² Zhao, J.³ Xie, S.Q.⁴ Wang, C.J.⁵

16
- 79955876087
- M. Pan, X. M. Lin, G. B. Li, C. Y. Su, Coord. Chem. Rev. 2011, 255, 1921-1936
- (2011) Coord. Chem. Rev. , vol.255 , pp. 1921-1936
- Pan, M.¹ Lin, X.M.² Li, G.B.³ Su, C.Y.⁴

17
- 79952158181
- M. L. Tang, Z. A. Bao, Chem. Mater. 2011, 23, 446-455
- (2011) Chem. Mater. , vol.23 , pp. 446-455
- Tang, M.L.¹ Bao, Z.A.²

18
- 77949488931
- R. S. Upadhayaya, J. K. Vandavasi, R. A. Kardile, S. V. Lahore, S. S. Dixit, H. S. Deokar, P. D. Shinde, M. P. Sarmah, J. Chattopadhyaya, Eur. J. Med. Chem. 2010, 45, 1854-1867
- (2010) Eur. J. Med. Chem. , vol.45 , pp. 1854-1867
- Upadhayaya, R.S.¹ Vandavasi, J.K.² Kardile, R.A.³ Lahore, S.V.⁴ Dixit, S.S.⁵ Deokar, H.S.⁶ Shinde, P.D.⁷ Sarmah, M.P.⁸ Chattopadhyaya, J.⁹

19
- 57349132464
- J. Humljan, M. Kotnik, C. Contreras-Martel, D. Blanot, U. Urleb, A. Dessen, T. Solmajer, S. Gobec, J. Med. Chem. 2008, 51, 7486-7494
- (2008) J. Med. Chem. , vol.51 , pp. 7486-7494
- Humljan, J.¹ Kotnik, M.² Contreras-Martel, C.³ Blanot, D.⁴ Urleb, U.⁵ Dessen, A.⁶ Solmajer, T.⁷ Gobec, S.⁸

20
- 0042291889
- (Ed.: D. Astruc), Wiley-VCH, Weinheim
- A. Suzuki, in: Modern Arene Chemistry, (Ed.:, D. Astruc,), Wiley-VCH, Weinheim, 2002.
- (2002) Modern Arene Chemistry
- Suzuki, A.¹

21
- 77957130705
- D. S. Surry, S. L. Buchwald, Chem. Sci. 2010, 1, 13-31
- (2010) Chem. Sci. , vol.1 , pp. 13-31
- Surry, D.S.¹ Buchwald, S.L.²

22
- 70350607555
- F. Monnier, M. Taillefer, Angew. Chem. 2009, 121, 7088-7105
- (2009) Angew. Chem. , vol.121 , pp. 7088-7105
- Monnier, F.¹ Taillefer, M.²

23
- 70349786460
- Angew. Chem. Int. Ed. 2009, 48, 6954-6971
- (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6954-6971

24
- 51049095122
- G. Evano, N. Blanchard, M. Toumi, Chem. Rev. 2008, 108, 3054-3131
- (2008) Chem. Rev. , vol.108 , pp. 3054-3131
- Evano, G.¹ Blanchard, N.² Toumi, M.³

25
- 49549087576
- F. Monnier, M. Taillefer, Angew. Chem. 2008, 120, 3140-3143
- (2008) Angew. Chem. , vol.120 , pp. 3140-3143
- Monnier, F.¹ Taillefer, M.²

26
- 47749142816
- Angew. Chem. Int. Ed. 2008, 47, 3096-3099
- (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3096-3099

27
- 57549098954
- D. W. Ma, Q. Cai, Acc. Chem. Res. 2008, 41, 1450-1460.
- (2008) Acc. Chem. Res. , vol.41 , pp. 1450-1460
- Ma, D.W.¹ Cai, Q.²

28
- 84862574375
- Y. Liu, J. P. Wan, Chem. Asian J. 2012, 7, 1488-1501
- (2012) Chem. Asian J. , vol.7 , pp. 1488-1501
- Liu, Y.¹ Wan, J.P.²

29
- 84862938638
- F. Wang, P. Zhao, C. J. Xi, Heterocycles 2012, 84, 209-221
- (2012) Heterocycles , vol.84 , pp. 209-221
- Wang, F.¹ Zhao, P.² Xi, C.J.³

30
- 80053318791
- Y. Liu, J. P. Wan, Org. Biomol. Chem. 2011, 9, 6873-6894.
- (2011) Org. Biomol. Chem. , vol.9 , pp. 6873-6894
- Liu, Y.¹ Wan, J.P.²

31
- 84863116621
- Z. M. Xia, K. Wang, J. N. Zheng, Z. Y. Ma, Z. G. Jiang, X. X. Wang, X. Lv, Org. Biomol. Chem. 2012, 10, 1602-1611
- (2012) Org. Biomol. Chem. , vol.10 , pp. 1602-1611
- Xia, Z.M.¹ Wang, K.² Zheng, J.N.³ Ma, Z.Y.⁴ Jiang, Z.G.⁵ Wang, X.X.⁶ Lv, X.⁷

32
- 78651480581
- Q. Liao, L. Y. Zhang, S. T. Li, C. J. Xi, Org. Lett. 2011, 13, 228-231
- (2011) Org. Lett. , vol.13 , pp. 228-231
- Liao, Q.¹ Zhang, L.Y.² Li, S.T.³ Xi, C.J.⁴

33
- 51649124289
- A. Minatti, S. L. Buchwald, Org. Lett. 2008, 10, 2721-2724.
- (2008) Org. Lett. , vol.10 , pp. 2721-2724
- Minatti, A.¹ Buchwald, S.L.²

34
- 82955190421
- D. Basavaiah, G. Veeraraghavaiah, Chem. Soc. Rev. 2012, 41, 68-78
- (2012) Chem. Soc. Rev. , vol.41 , pp. 68-78
- Basavaiah, D.¹ Veeraraghavaiah, G.²

35
- 77956464073
- D. Basavaiah, B. S. Reddy, S. S. Badsara, Chem. Rev. 2010, 110, 5447-5674
- (2010) Chem. Rev. , vol.110 , pp. 5447-5674
- Basavaiah, D.¹ Reddy, B.S.² Badsara, S.S.³

36
- 59649098742
- V. Declerck, J. Martinez, F. Lamaty, Chem. Rev. 2009, 109, 1-48
- (2009) Chem. Rev. , vol.109 , pp. 1-48
- Declerck, V.¹ Martinez, J.² Lamaty, F.³

37
- 41649086484
- V. Singh, S. Batra, Tetrahedron 2008, 64, 4511-4574.
- (2008) Tetrahedron , vol.64 , pp. 4511-4574
- Singh, V.¹ Batra, S.²

38
- 0000984929
- J. N. Kim, H. J. Lee, K. Y. Lee, H. S. Kim, Tetrahedron Lett. 2001, 42, 3737-3740
- (2001) Tetrahedron Lett. , vol.42 , pp. 3737-3740
- Kim, J.N.¹ Lee, H.J.² Lee, K.Y.³ Kim, H.S.⁴

39
- 0035538832
- Y. M. Chung, H. J. Lee, S. S. Hwang, J. N. Kim, Bull. Korean Chem. Soc. 2001, 22, 799-800
- (2001) Bull. Korean Chem. Soc. , vol.22 , pp. 799-800
- Chung, Y.M.¹ Lee, H.J.² Hwang, S.S.³ Kim, J.N.⁴

40
- 0035908278
- J. N. Kim, Y. J. Im, J. H. Gong, K. Y. Lee, Tetrahedron Lett. 2001, 42, 4195-4197
- (2001) Tetrahedron Lett. , vol.42 , pp. 4195-4197
- Kim, J.N.¹ Im, Y.J.² Gong, J.H.³ Lee, K.Y.⁴

41
- 0000975007
- J. N. Kim, K. Y. Lee, H. S. Kim, T. Y. Kim, Org. Lett. 2000, 2, 343-345.
- (2000) Org. Lett. , vol.2 , pp. 343-345
- Kim, J.N.¹ Lee, K.Y.² Kim, H.S.³ Kim, T.Y.⁴

42
- 80053931202
- It was found that N-alkyl-1,4-dihydroquinolines could be obtained in moderate yields during the synthesis of N-substituted quinolones from some ortho-halo B-H acetates. Dichloro and trifluoro substrates were used in many cases; and long reaction times were generally required
- It was found that N-alkyl-1,4-dihydroquinolines could be obtained in moderate yields during the synthesis of N-substituted quinolones from some ortho-halo B-H acetates. Dichloro and trifluoro substrates were used in many cases; and long reaction times were generally required:, J. V. Napoleon, M. K. Manheri, Synthesis 2011, 3379-3388
- (2011) Synthesis , pp. 3379-3388
- Napoleon, J.V.¹ Manheri, M.K.²

43
- 34547934800
- 2. An N-aryldihydroquinoline could be prepared through the Pd-catalyzed one-pot reaction, but the expensive Pd catalyst was used, and no systematic study of the domino reaction was demonstrated therein
- 2. An N-aryldihydroquinoline could be prepared through the Pd-catalyzed one-pot reaction, but the expensive Pd catalyst was used, and no systematic study of the domino reaction was demonstrated therein:, Y. S. Park, M. Y. Cho, Y. B. Kwon, B. W. Yoo, C. M. Yoon, Synth. Commun. 2007, 37, 2677-2685.
- (2007) Synth. Commun. , vol.37 , pp. 2677-2685
- Park, Y.S.¹ Cho, M.Y.² Kwon, Y.B.³ Yoo, B.W.⁴ Yoon, C.M.⁵

44
- 0035210846
- P. T. Kaye, X. W. Nocanda, Synthesis 2001, 2389-2392.
- (2001) Synthesis , pp. 2389-2392
- Kaye, P.T.¹ Nocanda, X.W.²

45
- 38949213023
- M. J. Cha, Y. S. Song, E. G. Han, K. J. Lee, J. Heterocycl. Chem. 2008, 45, 235-240.
- (2008) J. Heterocycl. Chem. , vol.45 , pp. 235-240
- Cha, M.J.¹ Song, Y.S.² Han, E.G.³ Lee, K.J.⁴

46
- 77955706565
- D. B. Chen, Z. J. Wang, W. L. Bao, J. Org. Chem. 2010, 75, 5768-5771.
- (2010) J. Org. Chem. , vol.75 , pp. 5768-5771
- Chen, D.B.¹ Wang, Z.J.² Bao, W.L.³

47
- 79955383449
- C. C. Malakar, D. Schmidt, J. Conrad, U. Beifuss, Org. Lett. 2011, 13, 1972-1975
- (2011) Org. Lett. , vol.13 , pp. 1972-1975
- Malakar, C.C.¹ Schmidt, D.² Conrad, J.³ Beifuss, U.⁴

48
- 0037189133
- Y. J. Im, K. Y. Lee, T. H. Kim, J. N. Kim, Tetrahedron Lett. 2002, 43, 4675-4678.
- (2002) Tetrahedron Lett. , vol.43 , pp. 4675-4678
- Im, Y.J.¹ Lee, K.Y.² Kim, T.H.³ Kim, J.N.⁴

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