SCOPUS 정보 검색 플랫폼

Volumn 4, Issue 95, 2014, Pages 53188-53191

Facile synthesis of azaarene-2-substituted chromanone derivatives via tandem sp3 C-H functionalization/decarboxylation of azaarenes with 4-oxo-4H-chromene-3-carboxylic acid

(5) Shao, Zhuzhou a Wang, Liang a Xu, Lubin a Zhao, Huaili a Xiao, Jian a

a QINGDAO AGRICULTURAL UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

AZAARENES; C-H FUNCTIONALIZATION; CATALYST-FREE; FACILE SYNTHESIS; SINGLE-STEP;

EID: 84908406099 PISSN: None EISSN: 20462069 Source Type: Journal
DOI: 10.1039/c4ra09338k Document Type: Article

Times cited : (31)

References (70)

1
- 2042520924
- F. Cottiglia B. Dhanapal O. Sticher J. Heilmann J. Nat. Prod. 2004 67 537
- (2004) J. Nat. Prod. , vol.67 , pp. 537
- Cottiglia, F.¹ Dhanapal, B.² Sticher, O.³ Heilmann, J.⁴

2
- 33846549175
- X. Yang Y. Sun Q. Xu Z. Guo Org. Biomol. Chem. 2006 4 2483
- (2006) Org. Biomol. Chem. , vol.4 , pp. 2483
- Yang, X.¹ Sun, Y.² Xu, Q.³ Guo, Z.⁴

3
- 33846641683
- P. L. Zhao J. Li G. F. Yang Bioorg. Med. Chem. 2007 15 1888
- (2007) Bioorg. Med. Chem. , vol.15 , pp. 1888
- Zhao, P.L.¹ Li, J.² Yang, G.F.³

4
- 56349150862
- N. Hoettecke S. Rotzoll U. Albrecht M. Lalk C. Fischer P. Langer Bioorg. Med. Chem. 2008 16 10319
- (2008) Bioorg. Med. Chem. , vol.16 , pp. 10319
- Hoettecke, N.¹ Rotzoll, S.² Albrecht, U.³ Lalk, M.⁴ Fischer, C.⁵ Langer, P.⁶

5
- 67249095045
- P. Y. Chen Y. C. Kuo C. H. Chen Y. H. Kuo C. K. Lee Molecules 2009 14 1789
- (2009) Molecules , vol.14 , pp. 1789
- Chen, P.Y.¹ Kuo, Y.C.² Chen, C.H.³ Kuo, Y.H.⁴ Lee, C.K.⁵

6
- 80052189790
- H. Kikuchi M. Isobe M. Sekiya Y. Abe T. Hoshikawa K. Ueda S. Kurata Y. Katou Y. Oshima Org. Lett. 2011 13 4624
- (2011) Org. Lett. , vol.13 , pp. 4624
- Kikuchi, H.¹ Isobe, M.² Sekiya, M.³ Abe, Y.⁴ Hoshikawa, T.⁵ Ueda, K.⁶ Kurata, S.⁷ Katou, Y.⁸ Oshima, Y.⁹

7
- 84890429883
- X. Wu M. Z. Alam L. Feng L. S. Tsutsumi D. Sun J. G. Hurdle J. Appl. Microbiol. 2014 116 23
- (2014) J. Appl. Microbiol. , vol.116 , pp. 23
- Wu, X.¹ Alam, M.Z.² Feng, L.³ Tsutsumi, L.S.⁴ Sun, D.⁵ Hurdle, J.G.⁶

8
- 84903712487
- L. F. Tietze S. Jackenkroll J. Hierold L. Ma B. Waldecker Chem.-Eur. J. 2014 20 8628
- (2014) Chem.-Eur. J. , vol.20 , pp. 8628
- Tietze, L.F.¹ Jackenkroll, S.² Hierold, J.³ Ma, L.⁴ Waldecker, B.⁵

9
- 77956902626
- P. N. Moquist T. Kodama S. E. Schaus Angew. Chem., Int. Ed. 2010 49 7096
- (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 7096
- Moquist, P.N.¹ Kodama, T.² Schaus, S.E.³

10
- 0032544154
- Z.-Q. Xu J. R. W. Buckheit T. L. Stup M. T. Flavin A. Khilevich J. D. Rizzo L. Lin D. E. Zembower Bioorg. Med. Chem. Lett. 1998 8 2179
- (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 2179
- Xu, Z.-Q.¹ Buckheit, J.R.W.² Stup, T.L.³ Flavin, M.T.⁴ Khilevich, A.⁵ Rizzo, J.D.⁶ Lin, L.⁷ Zembower, D.E.⁸

11
- 84903957010
- G. Sudhakar S. Bayya V. D. Kadam J. B. Nanubolu Org. Biomol. Chem. 2014 12 5601
- (2014) Org. Biomol. Chem. , vol.12 , pp. 5601
- Sudhakar, G.¹ Bayya, S.² Kadam, V.D.³ Nanubolu, J.B.⁴

12
- 84881353864
- N. X. Wang Y. Xing Y. J. Wang Curr. Org. Chem. 2013 17 1555
- (2013) Curr. Org. Chem. , vol.17 , pp. 1555
- Wang, N.X.¹ Xing, Y.² Wang, Y.J.³

13
- 84855947965
- A. E. Nibbs K. A. Scheidt Eur. J. Org. Chem. 2012 449
- (2012) Eur. J. Org. Chem. , pp. 449
- Nibbs, A.E.¹ Scheidt, K.A.²

14
- 84863622332
- L. A. Stubbing F. F. Li D. P. Furkert V. E. Caprio M. A. Brimble Tetrahedron 2012 68 6948
- (2012) Tetrahedron , vol.68 , pp. 6948
- Stubbing, L.A.¹ Li, F.F.² Furkert, D.P.³ Caprio, V.E.⁴ Brimble, M.A.⁵

15
- 0001710837
- D. Enders K. Breuer J. Runsink Helv. Chim. Acta 1996 79 1899
- (1996) Helv. Chim. Acta , vol.79 , pp. 1899
- Enders, D.¹ Breuer, K.² Runsink, J.³

16
- 18244367138
- J. R. d. Alaniz T. Rovis J. Am. Chem. Soc. 2005 127 6284
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6284
- Alaniz, J.R.D.¹ Rovis, T.²

17
- 84857598542
- L. R. Domingo R. J. Zaragoza J. A. Saez M. Arno Molecules 2012 17 1335
- (2012) Molecules , vol.17 , pp. 1335
- Domingo, L.R.¹ Zaragoza, R.J.² Saez, J.A.³ Arno, M.⁴

18
- 33750074173
- J. He J. Zheng J. Liu X. She X. Pan Org. Lett. 2006 8 4637
- (2006) Org. Lett. , vol.8 , pp. 4637
- He, J.¹ Zheng, J.² Liu, J.³ She, X.⁴ Pan, X.⁵

19
- 84908396118
- S.-L. You Z.-Q. Rong Y. Li G.-Q. Yang Synlett 2011 2011 1033 1037
- (2011) Synlett , vol.2011 , pp. 1033-1037
- You, S.-L.¹ Rong, Z.-Q.² Li, Y.³ Yang, G.-Q.⁴

20
- 84900440197
- A. Gaspar M. J. Matos J. Garrido E. Uriarte F. Borges Chem. Rev. 2014 114 4960
- (2014) Chem. Rev. , vol.114 , pp. 4960
- Gaspar, A.¹ Matos, M.J.² Garrido, J.³ Uriarte, E.⁴ Borges, F.⁵

21
- 84879048149
- C. Vila V. Hornillos M. Fañanás-Mastral B. L. Feringa Chem. Commun. 2013 49 5933
- (2013) Chem. Commun. , vol.49 , pp. 5933
- Vila, C.¹ Hornillos, V.² Fañanás-Mastral, M.³ Feringa, B.L.⁴

22
- 24044546502
- M. K. Brown S. J. Degrado A. H. Hoveyda Angew. Chem., Int. Ed. 2005 44 5306
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 5306
- Brown, M.K.¹ Degrado, S.J.² Hoveyda, A.H.³

23
- 84880002088
- Ö. Z. Sirin O. Demirkol D. Akbaslar E. S. Giray J. Supercrit. Fluids 2013 81 217
- (2013) J. Supercrit. Fluids , vol.81 , pp. 217
- Sirin Ö., Z.¹ Demirkol, O.² Akbaslar, D.³ Giray, E.S.⁴

24
- 31344454835
- B. Appel N. N. Saleh P. Langer Chem.-Eur. J. 2006 12 1221
- (2006) Chem.-Eur. J. , vol.12 , pp. 1221
- Appel, B.¹ Saleh, N.N.² Langer, P.³

25
- 0642373072
- S. J. Coutts T. W. Wallace Tetrahedron Lett. 1987 28 5195
- (1987) Tetrahedron Lett. , vol.28 , pp. 5195
- Coutts, S.J.¹ Wallace, T.W.²

26
- 80455129182
- J. R. Zimmerman M. Manpadi R. Spatney Green Chem. 2011 13 3103
- (2011) Green Chem. , vol.13 , pp. 3103
- Zimmerman, J.R.¹ Manpadi, M.² Spatney, R.³

27
- 2442657857
- Y.-J. Jang M.-C. Yan Y.-F. Lin C.-F. Yao J. Org. Chem. 2004 69 3961
- (2004) J. Org. Chem. , vol.69 , pp. 3961
- Jang, Y.-J.¹ Yan, M.-C.² Lin, Y.-F.³ Yao, C.-F.⁴

28
- 84886414099
- Y. Wei J. Tang X. Cong X. Zeng Green Chem. 2013 15 3165
- (2013) Green Chem. , vol.15 , pp. 3165
- Wei, Y.¹ Tang, J.² Cong, X.³ Zeng, X.⁴

29
- 79955366218
- C.-H. Tseng R.-W. Lin Y.-L. Chen G.-J. Wang M.-L. Ho C.-C. Tzeng J. Med. Chem. 2011 54 3103
- (2011) J. Med. Chem. , vol.54 , pp. 3103
- Tseng, C.-H.¹ Lin, R.-W.² Chen, Y.-L.³ Wang, G.-J.⁴ Ho, M.-L.⁵ Tzeng, C.-C.⁶

30
- 34247167637
- M. M. Biddle M. Lin K. A. Scheidt J. Am. Chem. Soc. 2007 129 3830
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 3830
- Biddle, M.M.¹ Lin, M.² Scheidt, K.A.³

31
- 84867369146
- A. K. Ghosh X. Cheng B. Zhou Org. Lett. 2012 14 5046
- (2012) Org. Lett. , vol.14 , pp. 5046
- Ghosh, A.K.¹ Cheng, X.² Zhou, B.³

32
- 77955432076
- C. S. López R. Erra-Balsells S. M. Bonesi Tetrahedron Lett. 2010 51 4387
- (2010) Tetrahedron Lett. , vol.51 , pp. 4387
- López, C.S.¹ Erra-Balsells, R.² Bonesi, S.M.³

33
- 84883495351
- E. Jijy P. Prakash M. Shimi P. M. Pihko N. Joseph K. V. Radhakrishnan Chem. Commun. 2013 49 7349
- (2013) Chem. Commun. , vol.49 , pp. 7349
- Jijy, E.¹ Prakash, P.² Shimi, M.³ Pihko, P.M.⁴ Joseph, N.⁵ Radhakrishnan, K.V.⁶

34
- 80051736589
- T.-L. Liu Z.-L. He C.-J. Wang Chem. Commun. 2011 47 9600
- (2011) Chem. Commun. , vol.47 , pp. 9600
- Liu, T.-L.¹ He, Z.-L.² Wang, C.-J.³

35
- 84886421823
- Z. Mao A. Lin Y. Shi H. Mao W. Li Y. Cheng C. Zhu J. Org. Chem. 2013 78 10233
- (2013) J. Org. Chem. , vol.78 , pp. 10233
- Mao, Z.¹ Lin, A.² Shi, Y.³ Mao, H.⁴ Li, W.⁵ Cheng, Y.⁶ Zhu, C.⁷

36
- 35348959557
- M. C. Bagley C. Glover E. A. Merritt Synlett 2007 2459
- (2007) Synlett , pp. 2459
- Bagley, M.C.¹ Glover, C.² Merritt, E.A.³

37
- 3042558198
- G. D. Henry Tetrahedron 2004 60 6043
- (2004) Tetrahedron , vol.60 , pp. 6043
- Henry, G.D.¹

38
- 26844495371
- J. P. Michael Nat. Prod. Rep. 2005 22 627
- (2005) Nat. Prod. Rep. , vol.22 , pp. 627
- Michael, J.P.¹

39
- 78650321875
- B. Qian S. Guo C. Xia H. Huang Adv. Synth. Catal. 2010 352 3195
- (2010) Adv. Synth. Catal. , vol.352 , pp. 3195
- Qian, B.¹ Guo, S.² Xia, C.³ Huang, H.⁴

40
- 79953174314
- H. Komai T. Yoshino S. Matsunaga M. Kanai Org. Lett. 2011 13 1706
- (2011) Org. Lett. , vol.13 , pp. 1706
- Komai, H.¹ Yoshino, T.² Matsunaga, S.³ Kanai, M.⁴

41
- 84908404393
- M. Kanai S. Matsunaga H. Komai T. Yoshino Synthesis 2012 44 2185 2194
- (2012) Synthesis , vol.44 , pp. 2185-2194
- Kanai, M.¹ Matsunaga, S.² Komai, H.³ Yoshino, T.⁴

42
- 84862980843
- J.-J. Jin H.-Y. Niu G.-R. Qu H.-M. Guo J. S. Fossey RSC Adv. 2012 2 5968
- (2012) RSC Adv. , vol.2 , pp. 5968
- Jin, J.-J.¹ Niu, H.-Y.² Qu, G.-R.³ Guo, H.-M.⁴ Fossey, J.S.⁵

43
- 79952150244
- M. Rueping N. Tolstoluzhsky Org. Lett. 2011 13 1095
- (2011) Org. Lett. , vol.13 , pp. 1095
- Rueping, M.¹ Tolstoluzhsky, N.²

44
- 84899452106
- F.-F. Wang C.-P. Luo G. Deng L. Yang Green Chem. 2014 16 2428
- (2014) Green Chem. , vol.16 , pp. 2428
- Wang, F.-F.¹ Luo, C.-P.² Deng, G.³ Yang, L.⁴

45
- 84908423258
- Z. Q. Zhu P. Bai Z. Z. Huang Org. Lett. 2014 16 4881
- (2014) Org. Lett. , vol.16 , pp. 4881
- Zhu, Z.Q.¹ Bai, P.² Huang, Z.Z.³

46
- 84866245574
- J. Y. Liu H. Y. Niu S. Wu G. R. Qu H. M. Guo Chem. Commun. 2012 48 9723
- (2012) Chem. Commun. , vol.48 , pp. 9723
- Liu, J.Y.¹ Niu, H.Y.² Wu, S.³ Qu, G.R.⁴ Guo, H.M.⁵

47
- 77949833074
- B. Qian S. Guo J. Shao Q. Zhu L. Yang C. Xia H. Huang J. Am. Chem. Soc. 2010 132 3650
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 3650
- Qian, B.¹ Guo, S.² Shao, J.³ Zhu, Q.⁴ Yang, L.⁵ Xia, C.⁶ Huang, H.⁷

48
- 84870044777
- S. J. Lou D. Q. Xu D. F. Shen Y. F. Wang Y. K. Liu Z. Y. Xu Chem. Commun. 2012 48 11993
- (2012) Chem. Commun. , vol.48 , pp. 11993
- Lou, S.J.¹ Xu, D.Q.² Shen, D.F.³ Wang, Y.F.⁴ Liu, Y.K.⁵ Xu, Z.Y.⁶

49
- 79956148086
- P. X. Qian Y. Xie H. Huang Org. Lett. 2011 13 2580
- (2011) Org. Lett. , vol.13 , pp. 2580
- Qian, P.X.¹ Xie, Y.² Huang, H.³

50
- 84874279978
- Y. Li F. Guo Z. Zha Z. Wang Chem.-Asian J. 2013 8 534
- (2013) Chem.-Asian J. , vol.8 , pp. 534
- Li, Y.¹ Guo, F.² Zha, Z.³ Wang, Z.⁴

51
- 84869221762
- R. Niu S. Yang J. Xiao T. Liang X. Li Chin. J. Catal. 2012 33 1636
- (2012) Chin. J. Catal. , vol.33 , pp. 1636
- Niu, R.¹ Yang, S.² Xiao, J.³ Liang, T.⁴ Li, X.⁵

52
- 84872171067
- V. B. Graves A. Shaikh Tetrahedron Lett. 2013 54 695
- (2013) Tetrahedron Lett. , vol.54 , pp. 695
- Graves, V.B.¹ Shaikh, A.²

53
- 84867539304
- F. F. Wang C. P. Luo Y. Wang G. Deng L. Yang Org. Biomol. Chem. 2012 10 8605
- (2012) Org. Biomol. Chem. , vol.10 , pp. 8605
- Wang, F.F.¹ Luo, C.P.² Wang, Y.³ Deng, G.⁴ Yang, L.⁵

54
- 84865075151
- S. V. N. Vuppalapati Y. R. Lee Tetrahedron 2012 68 8286
- (2012) Tetrahedron , vol.68 , pp. 8286
- Vuppalapati, S.V.N.¹ Lee, Y.R.²

55
- 84885047516
- A. Kumar L. P. Gupta M. Kumar RSC Adv. 2013 3 18771
- (2013) RSC Adv. , vol.3 , pp. 18771
- Kumar, A.¹ Gupta, L.P.² Kumar, M.³

56
- 84872278893
- H.-Y. Li L.-J. Xing T. Xu P. Wang R.-H. Liu B. Wang Tetrahedron Lett. 2013 54 858
- (2013) Tetrahedron Lett. , vol.54 , pp. 858
- Li, H.-Y.¹ Xing, L.-J.² Xu, T.³ Wang, P.⁴ Liu, R.-H.⁵ Wang, B.⁶

57
- 84862691725
- H. M. Meshram N. Nageswara Rao L. Chandrasekhara Rao N. Satish Kumar Tetrahedron Lett. 2012 53 3963
- (2012) Tetrahedron Lett. , vol.53 , pp. 3963
- Meshram, H.M.¹ Nageswara Rao, N.² Chandrasekhara Rao, L.³ Satish Kumar, N.⁴

58
- 84899825610
- K. Kumari B. K. Allam K. N. Singh RSC Adv. 2014 4 19789
- (2014) RSC Adv. , vol.4 , pp. 19789
- Kumari, K.¹ Allam, B.K.² Singh, K.N.³

59
- 84878564952
- M. Raghu M. Rajasekhar B. Chandra Obula Reddy C. Suresh Reddy B. V. Subba Reddy Tetrahedron Lett. 2013 54 3503
- (2013) Tetrahedron Lett. , vol.54 , pp. 3503
- Raghu, M.¹ Rajasekhar, M.² Chandra Obula Reddy, B.³ Suresh Reddy, C.⁴ Subba Reddy, B.V.⁵

60
- 84904547799
- X. Gao F. Zhang G. Deng L. Yang Org. Lett. 2014 16 3664
- (2014) Org. Lett. , vol.16 , pp. 3664
- Gao, X.¹ Zhang, F.² Deng, G.³ Yang, L.⁴

61
- 84863011225
- R. Niu J. Xiao T. Liang X. Li Org. Lett. 2012 14 676
- (2012) Org. Lett. , vol.14 , pp. 676
- Niu, R.¹ Xiao, J.² Liang, T.³ Li, X.⁴

62
- 84893832052
- L. Xu Z. Shao L. Wang J. Xiao Org. Lett. 2014 16 796
- (2014) Org. Lett. , vol.16 , pp. 796
- Xu, L.¹ Shao, Z.² Wang, L.³ Xiao, J.⁴

63
- 84903362241
- Z. Shao L. Xu L. Wang H. Wei J. Xiao Org. Biomol. Chem. 2014 12 2185
- (2014) Org. Biomol. Chem. , vol.12 , pp. 2185
- Shao, Z.¹ Xu, L.² Wang, L.³ Wei, H.⁴ Xiao, J.⁵

64
- 84858437144
- J. Xiao K. Zhao T. P. Loh Chem. Commun. 2012 48 3548
- (2012) Chem. Commun. , vol.48 , pp. 3548
- Xiao, J.¹ Zhao, K.² Loh, T.P.³

65
- 84859578773
- T. Liang J. Xiao Z. Xiong X. Li J. Org. Chem. 2012 77 3583
- (2012) J. Org. Chem. , vol.77 , pp. 3583
- Liang, T.¹ Xiao, J.² Xiong, Z.³ Li, X.⁴

66
- 84879303041
- X. Yu S. Yu J. Xiao B. Wan X. Li J. Org. Chem. 2013 78 5444
- (2013) J. Org. Chem. , vol.78 , pp. 5444
- Yu, X.¹ Yu, S.² Xiao, J.³ Wan, B.⁴ Li, X.⁵

67
- 84862141663
- X. Li Y. Jiang X. Wang X. Li J. Xiao Synlett 2012 23 1649 1652
- (2012) Synlett , vol.23 , pp. 1649-1652
- Li, X.¹ Jiang, Y.² Wang, X.³ Li, X.⁴ Xiao, J.⁵

68
- 84901265383
- J. Xiao Y. Chen S. Zhu L. Wang L. Xu H. Wei Adv. Synth. Catal. 2014 356 1835 1845
- (2014) Adv. Synth. Catal. , vol.356 , pp. 1835-1845
- Xiao, J.¹ Chen, Y.² Zhu, S.³ Wang, L.⁴ Xu, L.⁵ Wei, H.⁶

69
- 84900443992
- L. Wang J. Xiao T.-P. Loh ChemCatChem 2014 6 1183
- (2014) ChemCatChem , vol.6 , pp. 1183
- Wang, L.¹ Xiao, J.² Loh, T.-P.³

70
- 84869431466
- F. Huang L. Xu J. Xiao Chin. J. Chem. 2012 30 2721
- (2012) Chin. J. Chem. , vol.30 , pp. 2721
- Huang, F.¹ Xu, L.² Xiao, J.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.