SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 66, 2015, Pages 13113-13116

Organocatalytic cascade reaction for the asymmetric synthesis of novel chroman-fused spirooxindoles that potently inhibit cancer cell proliferation

(9) Zhou, Rui a Wu, Qinjie a Guo, Mingrui a Huang, Wei b He, Xianghong b Yang, Lei b Peng, Fu c He, Gu a Han, Bo b

a SICHUAN UNIVERSITY (China)

b CHENGDU UNIVERSITY OF TRADITIONAL CHINESE MEDICINE (China)

c THE UNIVERSITY OF HONG KONG (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CASPASE; CHROMAN DERIVATIVE; NUTLIN 3; OXINDOLE; PROTEIN MDM2; PROTEIN P21; PROTEIN P53; SPIRO COMPOUND; SPIROOXINDOLE DERIVATIVE; UNCLASSIFIED DRUG; INDOLE DERIVATIVE;

ANTIPROLIFERATIVE ACTIVITY; APOPTOSIS; ARTICLE; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; CANCER INHIBITION; CELL CYCLE ARREST; CELL PROLIFERATION; CHIRALITY; CONTROLLED STUDY; DRUG EFFICACY; DRUG POTENCY; DRUG SYNTHESIS; ENANTIOSELECTIVITY; HUMAN; HUMAN CELL; MCF 7 CELL LINE; MICHAEL ADDITION; MOLECULAR DOCKING; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; STRUCTURE ACTIVITY RELATION; CATALYSIS; CELL CYCLE CHECKPOINT; CHEMICAL STRUCTURE; CHEMISTRY; DRUG EFFECTS; METABOLISM; PROTEIN CONFORMATION; SYNTHESIS;

ANTINEOPLASTIC AGENTS; APOPTOSIS; CATALYSIS; CELL CYCLE CHECKPOINTS; CELL PROLIFERATION; CHEMISTRY TECHNIQUES, SYNTHETIC; CHROMANS; HUMANS; INDOLES; MCF-7 CELLS; MODELS, MOLECULAR; PROTEIN CONFORMATION; PROTO-ONCOGENE PROTEINS C-MDM2; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84938852043 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c5cc04968g Document Type: Article

Times cited : (84)

References (50)

1
- 33947198541
- D. Enders C. Grondal M. R. M. Hüttl Angew. Chem., Int. Ed. 2007 46 1570
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 1570
- Enders, D.¹ Grondal, C.² Hüttl, M.R.M.³

2
- 34347335758
- A. M. Walji D. W. C. MacMillan Synlett 2007 1477
- (2007) Synlett , pp. 1477
- Walji, A.M.¹ MacMillan, D.W.C.²

3
- 80051716582
- A. Moyano R. Rios Chem. Rev. 2011 111 4703
- (2011) Chem. Rev. , vol.111 , pp. 4703
- Moyano, A.¹ Rios, R.²

4
- 84855432965
- A. Grossmann D. Enders Angew. Chem., Int. Ed. 2012 51 314
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 314
- Grossmann, A.¹ Enders, D.²

5
- 84857258027
- H. Pellissier Adv. Synth. Catal. 2012 354 237
- (2012) Adv. Synth. Catal. , vol.354 , pp. 237
- Pellissier, H.¹

6
- 84897671012
- C. M. R. Volla L. Atodiresei M. Rueping Chem. Rev. 2014 114 2390
- (2014) Chem. Rev. , vol.114 , pp. 2390
- Volla, C.M.R.¹ Atodiresei, L.² Rueping, M.³

7
- 34250684250
- R. M. de Figueiredo M. Christmann Eur. J. Org. Chem. 2007 2575
- (2007) Eur. J. Org. Chem. , pp. 2575
- De Figueiredo, R.M.¹ Christmann, M.²

8
- 79953701945
- C. Vaxelaire P. Winter M. Christmann Angew. Chem., Int. Ed. 2011 50 3605
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 3605
- Vaxelaire, C.¹ Winter, P.² Christmann, M.³

9
- 84865343822
- L.-Q. Lu J.-R. Chen W.-J. Xiao Acc. Chem. Res. 2012 45 1278
- (2012) Acc. Chem. Res. , vol.45 , pp. 1278
- Lu, L.-Q.¹ Chen, J.-R.² Xiao, W.-J.³

10
- 84874052662
- P. Kumar N. Dwivedi Acc. Chem. Res. 2013 46 289
- (2013) Acc. Chem. Res. , vol.46 , pp. 289
- Kumar, P.¹ Dwivedi, N.²

11
- 33750977591
- K. C. Nicolaou D. J. Edmonds P. G. Bulger Angew. Chem., Int. Ed. 2006 45 7134
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 7134
- Nicolaou, K.C.¹ Edmonds, D.J.² Bulger, P.G.³

12
- 77649087999
- C. Grondal M. Jeanty D. Enders Nat. Chem. 2010 2 167
- (2010) Nat. Chem. , vol.2 , pp. 167
- Grondal, C.¹ Jeanty, M.² Enders, D.³

13
- 77954827954
- E. Marqués-López R. P. Herrera M. Christmann Nat. Prod. Rep. 2010 27 1138
- (2010) Nat. Prod. Rep. , vol.27 , pp. 1138
- Marqués-López, E.¹ Herrera, R.P.² Christmann, M.³

14
- 8344250171
- D. B. Ramachary C. F. Barbas III Chem.-Eur. J. 2004 10 5323
- (2004) Chem.-Eur. J. , vol.10 , pp. 5323
- Ramachary, D.B.¹ Barbas, C.F.²

15
- 20444500603
- D. Tejedor D. González-Cruz A. Santos-Expósito J. J. Marrero-Tellado P. de Armas F. García-Tellado Chem.-Eur. J. 2005 11 3502
- (2005) Chem.-Eur. J. , vol.11 , pp. 3502
- Tejedor, D.¹ González-Cruz, D.² Santos-Expósito, A.³ Marrero-Tellado, J.J.⁴ De Armas, P.⁵ García-Tellado, F.⁶

16
- 46849107496
- D. B. Ramachary M. Kishor Y. V. Reddy Eur. J. Org. Chem. 2008 975
- (2008) Eur. J. Org. Chem. , pp. 975
- Ramachary, D.B.¹ Kishor, M.² Reddy, Y.V.³

17
- 84915758781
- A. Grossmann S. Bartlett M. Janecek J. T. Hodgkinson D. R. Spring Angew. Chem., Int. Ed. 2014 53 13093
- (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 13093
- Grossmann, A.¹ Bartlett, S.² Janecek, M.³ Hodgkinson, J.T.⁴ Spring, D.R.⁵

18
- 84871997136
- references therein
- J. Alemán S. Cabrera Chem. Soc. Rev. 2013 42 774
- (2013) Chem. Soc. Rev. , vol.42 , pp. 774
- Alemán, J.¹ Cabrera, S.²

19
- 57749085320
- P. Kotame B.-C. Hong J.-H. Liao Tetrahedron Lett. 2009 50 704
- (2009) Tetrahedron Lett. , vol.50 , pp. 704
- Kotame, P.¹ Hong, B.-C.² Liao, J.-H.³

20
- 62349132506
- H.-H. Lu H. Liu W. Wu X.-F. Wang L.-Q. Lu W.-J. Xiao Chem.-Eur. J. 2009 15 2742
- (2009) Chem.-Eur. J. , vol.15 , pp. 2742
- Lu, H.-H.¹ Liu, H.² Wu, W.³ Wang, X.-F.⁴ Lu, L.-Q.⁵ Xiao, W.-J.⁶

21
- 76849107394
- B.-C. Hong P. Kotame C.-W. Tsai J.-H. Liao Org. Lett. 2010 12 776
- (2010) Org. Lett. , vol.12 , pp. 776
- Hong, B.-C.¹ Kotame, P.² Tsai, C.-W.³ Liao, J.-H.⁴

22
- 80054737705
- Y. Lee S. W. Seo S.-G. Kim Adv. Synth. Catal. 2011 353 2671
- (2011) Adv. Synth. Catal. , vol.353 , pp. 2671
- Lee, Y.¹ Seo, S.W.² Kim, S.-G.³

23
- 81555226814
- D.-F. Yu Y. Wang P.-F. Xu Adv. Synth. Catal. 2011 353 2960
- (2011) Adv. Synth. Catal. , vol.353 , pp. 2960
- Yu, D.-F.¹ Wang, Y.² Xu, P.-F.³

24
- 84863171707
- K.-S. Choi S.-G. Kim Eur. J. Org. Chem. 2012 1119
- (2012) Eur. J. Org. Chem. , pp. 1119
- Choi, K.-S.¹ Kim, S.-G.²

25
- 84857455190
- D. Enders G. Urbanietz R. Hahn G. Raabe Synthesis 2012 773
- (2012) Synthesis , pp. 773
- Enders, D.¹ Urbanietz, G.² Hahn, R.³ Raabe, G.⁴

26
- 84857832758
- M. Rueping J. Dufour M. S. Maji Chem. Commun. 2012 48 3406
- (2012) Chem. Commun. , vol.48 , pp. 3406
- Rueping, M.¹ Dufour, J.² Maji, M.S.³

27
- 84913580492
- Z.-C. Geng S.-Y. Zhang N.-K. Li N. Li J. Chen H.-Y. Li X.-W. Wang J. Org. Chem. 2014 79 10772
- (2014) J. Org. Chem. , vol.79 , pp. 10772
- Geng, Z.-C.¹ Zhang, S.-Y.² Li, N.-K.³ Li, N.⁴ Chen, J.⁵ Li, H.-Y.⁶ Wang, X.-W.⁷

28
- 84901368637
- A.-B. Xia C. Wu T. Wang Y.-P. Zhang X.-H. Du A.-G. Zhong D.-Q. Xu Z.-Y. Xu Adv. Synth. Catal. 2014 356 1753
- (2014) Adv. Synth. Catal. , vol.356 , pp. 1753
- Xia, A.-B.¹ Wu, C.² Wang, T.³ Zhang, Y.-P.⁴ Du, X.-H.⁵ Zhong, A.-G.⁶ Xu, D.-Q.⁷ Xu, Z.-Y.⁸

29
- 84862864632
- N. R. Ball-Jones J. J. Badillo A. K. Franz Org. Biomol. Chem. 2012 10 5165
- (2012) Org. Biomol. Chem. , vol.10 , pp. 5165
- Ball-Jones, N.R.¹ Badillo, J.J.² Franz, A.K.³

30
- 84876492985
- L. Hong R. Wang Adv. Synth. Catal. 2013 355 1023
- (2013) Adv. Synth. Catal. , vol.355 , pp. 1023
- Hong, L.¹ Wang, R.²

31
- 84896786583
- D. J. Cheng Y. Ishihara B. Tan C. F. Barbas III ACS Catal. 2014 4 743
- (2014) ACS Catal. , vol.4 , pp. 743
- Cheng, D.J.¹ Ishihara, Y.² Tan, B.³ Barbas, C.F.⁴

32
- 11144239577
- Q. Jiang J. Wong H. Fyrst J. D. Saba B. N. Ames Proc. Natl. Acad. Sci. U. S. A. 2004 101 17825
- (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , pp. 17825
- Jiang, Q.¹ Wong, J.² Fyrst, H.³ Saba, J.D.⁴ Ames, B.N.⁵

33
- 21444438990
- I. M. Lee N. R. Cook J. M. Gaziano D. Gordon P. M. Ridker J. E. Manson C. H. Hennekens J. E. Buring JAMA, J. Am. Med. Assoc. 2005 294 56
- (2005) JAMA, J. Am. Med. Assoc. , vol.294 , pp. 56
- Lee, I.M.¹ Cook, N.R.² Gaziano, J.M.³ Gordon, D.⁴ Ridker, P.M.⁵ Manson, J.E.⁶ Hennekens, C.H.⁷ Buring, J.E.⁸

34
- 33846998312
- K. S. Ahn G. Sethi K. Krishnan B. B. Aggarwal J. Biol. Chem. 2007 282 809
- (2007) J. Biol. Chem. , vol.282 , pp. 809
- Ahn, K.S.¹ Sethi, G.² Krishnan, K.³ Aggarwal, B.B.⁴

35
- 47049121032
- C. Constantinou A. Papas A. I. Constantinou Int. J. Cancer 2008 123 739
- (2008) Int. J. Cancer , vol.123 , pp. 739
- Constantinou, C.¹ Papas, A.² Constantinou, A.I.³

36
- 77957909450
- B. B. Aggarwal C. Sundaram S. Prasad R. Kannappan Biochem. Pharmacol. 2010 80 1613
- (2010) Biochem. Pharmacol. , vol.80 , pp. 1613
- Aggarwal, B.B.¹ Sundaram, C.² Prasad, S.³ Kannappan, R.⁴

37
- 84908148515
- S. Wang W. Sun Y. Zhao D. McEachern I. Meaux C. Barrière J. A. Stuckey J. L. Meagher L. C. Bai L. Liu C.-G. Hoffman-Luca J. Lu S. Shangary S. Yu D. Bernard A. Aguilar O. Dos-Santos L. Besret S. Guerif P. Pannier D. Gorge-Bernat L. Debussche Cancer Res. 2014 74 5855
- (2014) Cancer Res. , vol.74 , pp. 5855
- Wang, S.¹ Sun, W.² Zhao, Y.³ McEachern, D.⁴ Meaux, I.⁵ Barrière, C.⁶ Stuckey, J.A.⁷ Meagher, J.L.⁸ Bai, L.C.⁹ Liu, L.¹⁰ Hoffman-Luca, C.-G.¹¹ Lu, J.¹² Shangary, S.¹³ Yu, S.¹⁴ Bernard, D.¹⁵ Aguilar, A.¹⁶ Dos-Santos, O.¹⁷ Besret, L.¹⁸ Guerif, S.¹⁹ Pannier, P.²⁰ more..

38
- 84882750879
- H. Mao A. Lin Y. Tang Y. Shi H. Hu Y. Cheng C. Zhu Org. Lett. 2013 15 4062
- (2013) Org. Lett. , vol.15 , pp. 4062
- Mao, H.¹ Lin, A.² Tang, Y.³ Shi, Y.⁴ Hu, H.⁵ Cheng, Y.⁶ Zhu, C.⁷

39
- 84899897142
- Y. Huang C. Zheng Z. Chai G. Zhao Adv. Synth. Catal. 2014 356 579
- (2014) Adv. Synth. Catal. , vol.356 , pp. 579
- Huang, Y.¹ Zheng, C.² Chai, Z.³ Zhao, G.⁴

40
- 84890811789
- D. B. Ramachary M. S. Prasad S. V. Laxmi R. Madhavachary Org. Biomol. Chem. 2014 12 574
- (2014) Org. Biomol. Chem. , vol.12 , pp. 574
- Ramachary, D.B.¹ Prasad, M.S.² Laxmi, S.V.³ Madhavachary, R.⁴

41
- 84867298005
- X. Xie C. Peng G. He H.-J. Leng B. A. Wang W. Huang B. Han Chem. Commun. 2012 48 10487
- (2012) Chem. Commun. , vol.48 , pp. 10487
- Xie, X.¹ Peng, C.² He, G.³ Leng, H.-J.⁴ Wang, B.A.⁵ Huang, W.⁶ Han, B.⁷

42
- 84883324923
- X. Li L. Yang C. Peng X. Xie H.-J. Leng B. Wang Z.-W. Tang G. He L. Ouyang W. Huang B. Han Chem. Commun. 2013 49 8692
- (2013) Chem. Commun. , vol.49 , pp. 8692
- Li, X.¹ Yang, L.² Peng, C.³ Xie, X.⁴ Leng, H.-J.⁵ Wang, B.⁶ Tang, Z.-W.⁷ He, G.⁸ Ouyang, L.⁹ Huang, W.¹⁰ Han, B.¹¹

43
- 84915750399
- B. Han X. Xie W. Huang X. Li L. Yang C. Peng Adv. Synth. Catal. 2014 356 3676
- (2014) Adv. Synth. Catal. , vol.356 , pp. 3676
- Han, B.¹ Xie, X.² Huang, W.³ Li, X.⁴ Yang, L.⁵ Peng, C.⁶

44
- 84903820428
- G. He F. B. Wu W. Huang R. Zhou L. Ouyang B. Han Adv. Synth. Catal. 2014 356 2311
- (2014) Adv. Synth. Catal. , vol.356 , pp. 2311
- He, G.¹ Wu, F.B.² Huang, W.³ Zhou, R.⁴ Ouyang, L.⁵ Han, B.⁶

45
- 85027933836
- 1001245
- B. Han W. Huang W. Ren G. He J.-H. Wang C. Peng Adv. Synth. Catal. 2015 357 561
- (2015) Adv. Synth. Catal. , vol.357 , pp. 561
- Han, B.¹ Huang, W.² Ren, W.³ He, G.⁴ Wang, J.-H.⁵ Peng, C.⁶

46
- 84867458226
- W. Wang Y. Hu Med. Res. Rev. 2012 32 1159
- (2012) Med. Res. Rev. , vol.32 , pp. 1159
- Wang, W.¹ Hu, Y.²

47
- 84922813362
- Y. Zhao A. Aguilar D. Bernard S. Wang J. Med. Chem. 2015 58 1038
- (2015) J. Med. Chem. , vol.58 , pp. 1038
- Zhao, Y.¹ Aguilar, A.² Bernard, D.³ Wang, S.⁴

48
- 84955652007
- W. Huang L. Cai C. Chen X. Xie Q. Zhao X. Zhao H. Zhou B. Han C. Peng J. Biomol. Struct. Dyn. 2015 10.1080/07391102.2015.1031178
- (2015) J. Biomol. Struct. Dyn.
- Huang, W.¹ Cai, L.² Chen, C.³ Xie, X.⁴ Zhao, Q.⁵ Zhao, X.⁶ Zhou, H.⁷ Han, B.⁸ Peng, C.⁹

49
- 84924419827
- Z. Liu Z. Miao J. Li K. Fang C. Zhuang L. Du C. Sheng M. Li Chem. Biol. Drug Des. 2015 85 411
- (2015) Chem. Biol. Drug Des. , vol.85 , pp. 411
- Liu, Z.¹ Miao, Z.² Li, J.³ Fang, K.⁴ Zhuang, C.⁵ Du, L.⁶ Sheng, C.⁷ Li, M.⁸

50
- 84927144395
- B. Liu L. Fu C. Zhang L. Zhang Y. Zhang L. Ouyang G. He J. Huang Oncotarget 2015 6 6762
- (2015) Oncotarget , vol.6 , pp. 6762
- Liu, B.¹ Fu, L.² Zhang, C.³ Zhang, L.⁴ Zhang, Y.⁵ Ouyang, L.⁶ He, G.⁷ Huang, J.⁸

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.