SCOPUS 정보 검색 플랫폼

Volumn 11, Issue 36, 2013, Pages 6029-6035

AgOTf-catalyzed reactions of naphthols/substituted phenols with 2-hydroxychalcones: Facile synthesis of di-aromatic ring-fused [3.3.1]bicyclic compounds

(2) Rao, Yin a Yin, Guodong a

a HUBEI NORMAL UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

PHENOLS;

BICYCLIC COMPOUNDS; DOMINO PROCESS; FACILE SYNTHESIS; FRIEDEL-CRAFTS ALKYLATION; FUNCTIONALIZED; ONE POT; SILVER TRIFLATE;

CATALYSIS;

2' HYDROXYCHALCONE; 2'-HYDROXYCHALCONE; BICYCLO COMPOUND; CHALCONE DERIVATIVE; MESYLIC ACID DERIVATIVE; NAPHTHOL DERIVATIVE; PHENOL DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

BICYCLO COMPOUNDS; CATALYSIS; CHALCONES; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; MESYLATES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; NAPHTHOLS; PHENOLS;

EID: 84883018777 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c3ob40860d Document Type: Article

Times cited : (38)

References (56)

1
- 79959399727
- M. Ruiz P. López-Alvarado G. Giorgi J. C. Menéndez Chem. Soc. Rev. 2011 40 3445 3454
- (2011) Chem. Soc. Rev. , vol.40 , pp. 3445-3454
- Ruiz, M.¹ López-Alvarado, P.² Giorgi, G.³ Menéndez, J.C.⁴

2
- 80052400158
- J. T. Njardarson Tetrahedron 2011 67 7631 7666
- (2011) Tetrahedron , vol.67 , pp. 7631-7666
- Njardarson, J.T.¹

3
- 77949649590
- W.-Y. Zhao Chem. Rev. 2010 110 1706 1745
- (2010) Chem. Rev. , vol.110 , pp. 1706-1745
- Zhao, W.-Y.¹

4
- 0035207263
- E. Butkus Synlett 2001 1827 1835
- (2001) Synlett , pp. 1827-1835
- Butkus, E.¹

5
- 84872251535
- M. Presset Y. Coquerel J. Rodriguez Chem. Rev. 2013 113 525 595
- (2013) Chem. Rev. , vol.113 , pp. 525-595
- Presset, M.¹ Coquerel, Y.² Rodriguez, J.³

6
- 70549087907
- F. M. Moghaddam Z. Mirjafary H. Saeidian S. Taheri M. Doulabi M. Kiamehr Tetrahedron 2010 66 134 138
- (2010) Tetrahedron , vol.66 , pp. 134-138
- Moghaddam, F.M.¹ Mirjafary, Z.² Saeidian, H.³ Taheri, S.⁴ Doulabi, M.⁵ Kiamehr, M.⁶

7
- 69849115537
- Y.-F. Wang S. Chiba J. Am. Chem. Soc. 2009 131 12570 12572
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 12570-12572
- Wang, Y.-F.¹ Chiba, S.²

8
- 0034629316
- E. Butkus U. Berg J. Malinauskiene J. Sandström J. Org. Chem. 2000 65 1353 1358
- (2000) J. Org. Chem. , vol.65 , pp. 1353-1358
- Butkus, E.¹ Berg, U.² Malinauskiene, J.³ Sandström, J.⁴

9
- 77950287608
- C. J. Wallentin T. Wixe O. F. Wendt K. E. Bergquist K. Wärnmark Chem.-Eur. J. 2010 16 3994 4002
- (2010) Chem.-Eur. J. , vol.16 , pp. 3994-4002
- Wallentin, C.J.¹ Wixe, T.² Wendt, O.F.³ Bergquist, K.E.⁴ Wärnmark, K.⁵

10
- 77955898850
- A. Mendoza P. Pardo F. Rodríguez F. J. Fañanás Chem.-Eur. J. 2010 16 9758 9762
- (2010) Chem.-Eur. J. , vol.16 , pp. 9758-9762
- Mendoza, A.¹ Pardo, P.² Rodríguez, F.³ Fañanás, F.J.⁴

11
- 77954558393
- T. Enomoto Y. Yasui Y. Takemoto J. Org. Chem. 2010 75 4876 4879
- (2010) J. Org. Chem. , vol.75 , pp. 4876-4879
- Enomoto, T.¹ Yasui, Y.² Takemoto, Y.³

12
- 78449241433
- K. Vervisch M. D'hooghe K. W. Törnroos N. de Kimpe J. Org. Chem. 2010 75 7734 7744
- (2010) J. Org. Chem. , vol.75 , pp. 7734-7744
- Vervisch, K.¹ D'Hooghe, M.² Törnroos, K.W.³ De Kimpe, N.⁴

13
- 79951622667
- I. N. Michaelides B. Darses D. J. Dixon Org. Lett. 2011 13 664 667
- (2011) Org. Lett. , vol.13 , pp. 664-667
- Michaelides, I.N.¹ Darses, B.² Dixon, D.J.³

14
- 77950602163
- F. M. Moghaddam S. Taheri Z. Mirjafary H. Saeidian Synlett 2010 123 127
- (2010) Synlett , pp. 123-127
- Moghaddam, F.M.¹ Taheri, S.² Mirjafary, Z.³ Saeidian, H.⁴

15
- 84868089500
- H.-L. Ren C.-R. Wu X.-X. Ding X.-G. Chen F. Shi Org. Biomol. Chem. 2012 10 8975 8984
- (2012) Org. Biomol. Chem. , vol.10 , pp. 8975-8984
- Ren, H.-L.¹ Wu, C.-R.² Ding, X.-X.³ Chen, X.-G.⁴ Shi, F.⁵

16
- 77956447079
- T.-M. Teng A. Das D. B. Huple R.-S. Liu J. Am. Chem. Soc. 2010 132 12565 12567
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 12565-12567
- Teng, T.-M.¹ Das, A.² Huple, D.B.³ Liu, R.-S.⁴

17
- 67149105797
- Y. Kuninobu J. Morita M. Nishi A. Kawata K. Takai Org. Lett. 2009 11 2535 2537
- (2009) Org. Lett. , vol.11 , pp. 2535-2537
- Kuninobu, Y.¹ Morita, J.² Nishi, M.³ Kawata, A.⁴ Takai, K.⁵

18
- 35549008171
- C.-L. Cao X.-L. Sun Y.-B. Kang Y. Tang Org. Lett. 2007 9 4151 4154
- (2007) Org. Lett. , vol.9 , pp. 4151-4154
- Cao, C.-L.¹ Sun, X.-L.² Kang, Y.-B.³ Tang, Y.⁴

19
- 27744454658
- J. M. Aurrecoechea J. M. Gorgojo C. Saornil J. Org. Chem. 2005 70 9640 9643
- (2005) J. Org. Chem. , vol.70 , pp. 9640-9643
- Aurrecoechea, J.M.¹ Gorgojo, J.M.² Saornil, C.³

20
- 53849129256
- N. R. Norcross J. P. Melbardis M. Ferris-Solera M. A. Sephton C. Kilner L. N. Zakharov P. C. Astles S. L. Warriner P. R. Blakemore J. Org. Chem. 2008 73 7939 7951
- (2008) J. Org. Chem. , vol.73 , pp. 7939-7951
- Norcross, N.R.¹ Melbardis, J.P.² Ferris-Solera, M.³ Sephton, M.A.⁴ Kilner, C.⁵ Zakharov, L.N.⁶ Astles, P.C.⁷ Warriner, S.L.⁸ Blakemore, P.R.⁹

21
- 27144522621
- P. R. Blakemore C. Kilner N. R. Norcross P. C. Astles Org. Lett. 2005 7 4721 4724
- (2005) Org. Lett. , vol.7 , pp. 4721-4724
- Blakemore, P.R.¹ Kilner, C.² Norcross, N.R.³ Astles, P.C.⁴

22
- 3543120754
- N. K. Garg D. D. Caspi B. M. Stoltz J. Am. Chem. Soc. 2004 126 9552 9553
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 9552-9553
- Garg, N.K.¹ Caspi, D.D.² Stoltz, B.M.³

23
- 0037420315
- L. N. Mander M. M. McLachlan J. Am. Chem. Soc. 2003 125 2400 2401
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 2400-2401
- Mander, L.N.¹ McLachlan, M.M.²

24
- 77953529895
- Y.-Q. Sun B.-X. Yu X.-L. Wang S.-B. Tang X.-G. She X.-F. Pan J. Org. Chem. 2010 75 4224 4229
- (2010) J. Org. Chem. , vol.75 , pp. 4224-4229
- Sun, Y.-Q.¹ Yu, B.-X.² Wang, X.-L.³ Tang, S.-B.⁴ She, X.-G.⁵ Pan, X.-F.⁶

25
- 0000212607
- D. Solé E. Peidró J. Bonjoch Org. Lett. 2000 2 2225 2228
- (2000) Org. Lett. , vol.2 , pp. 2225-2228
- Solé, D.¹ Peidró, E.² Bonjoch, J.³

26
- 0036167206
- K. Kadota T. Taniguchi K. Ogasawara Synlett 2002 334 336
- (2002) Synlett , pp. 334-336
- Kadota, K.¹ Taniguchi, T.² Ogasawara, K.³

27
- 0030781058
- A. Arnone G. Nasini O. V. de Pava J. Nat. Prod. 1997 60 971 975
- (1997) J. Nat. Prod. , vol.60 , pp. 971-975
- Arnone, A.¹ Nasini, G.² De Pava, O.V.³

28
- 2542523876
- V. Dumontet N. van Hung M. T. Adeline C. Riche A. Chiaroni T. Sévenet F. Guéritte J. Nat. Prod. 2004 67 858 862
- (2004) J. Nat. Prod. , vol.67 , pp. 858-862
- Dumontet, V.¹ Van Hung, N.² Adeline, M.T.³ Riche, C.⁴ Chiaroni, A.⁵ Sévenet, T.⁶ Guéritte, F.⁷

29
- 70349792634
- M. Xu L. Shen K. Wang Fitoterapia 2009 80 461 464
- (2009) Fitoterapia , vol.80 , pp. 461-464
- Xu, M.¹ Shen, L.² Wang, K.³

30
- 70350521052
- K. I. Nakashima N. Abe F. Kamiya T. Ito M. Oyama M. Iinuma Helv. Chim. Acta 2009 92 1999 2008
- (2009) Helv. Chim. Acta , vol.92 , pp. 1999-2008
- Nakashima, K.I.¹ Abe, N.² Kamiya, F.³ Ito, T.⁴ Oyama, M.⁵ Iinuma, M.⁶

31
- 0017394276
- W. R. Porter W. F. Trager J. Heterocycl. Chem. 1977 14 319 320
- (1977) J. Heterocycl. Chem. , vol.14 , pp. 319-320
- Porter, W.R.¹ Trager, W.F.²

32
- 84985257113
- L. Jurd J. Heterocycl. Chem. 1981 18 429 430
- (1981) J. Heterocycl. Chem. , vol.18 , pp. 429-430
- Jurd, L.¹

33
- 0029063981
- I. Manolov N. D. Danche Eur. J. Med. Chem. 1995 30 531 535
- (1995) Eur. J. Med. Chem. , vol.30 , pp. 531-535
- Manolov, I.¹ Danche, N.D.²

34
- 18144423865
- D.-U. Chen P.-Y. Kuo D.-Y. Yang Bioorg. Med. Chem. Lett. 2005 15 2665 2668
- (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 2665-2668
- Chen, D.-U.¹ Kuo, P.-Y.² Yang, D.-Y.³

35
- 33646529881
- I. Manolov C. Maichle-Moessmer E. Z. Niquet Z. Naturforsch 2006 61b 207 212
- (2006) Z. Naturforsch , vol.61 , pp. 207-212
- Manolov, I.¹ Maichle-Moessmer, C.² Niquet, E.Z.³

36
- 36849023139
- I. Kim S. G. Kim J. Choi G. H. Lee Tetrahedron 2008 64 664 671
- (2008) Tetrahedron , vol.64 , pp. 664-671
- Kim, I.¹ Kim, S.G.² Choi, J.³ Lee, G.H.⁴

37
- 65349193802
- D. B. Ramachary R. Sakthidevi Chem.-Eur. J. 2009 15 4516 4522
- (2009) Chem.-Eur. J. , vol.15 , pp. 4516-4522
- Ramachary, D.B.¹ Sakthidevi, R.²

38
- 84876539585
- F.-J. Wang F. Chen M.-L. Qu T. Li Y.-L. Liu M. Shi Chem. Commun. 2013 3360 3362
- (2013) Chem. Commun. , pp. 3360-3362
- Wang, F.-J.¹ Chen, F.² Qu, M.-L.³ Li, T.⁴ Liu, Y.-L.⁵ Shi, M.⁶

39
- 84875953113
- N. C. Ganguly P. Mondal S. Roy Tetrahedron Lett. 2013 54 2386 2390
- (2013) Tetrahedron Lett. , vol.54 , pp. 2386-2390
- Ganguly, N.C.¹ Mondal, P.² Roy, S.³

40
- 84878499424
- M. F. Polat L. Hettmanczyk W. Zhang Z. Szabo J. Franzén ChemCatChem 2013 5 1334 1339
- (2013) ChemCatChem , vol.5 , pp. 1334-1339
- Polat, M.F.¹ Hettmanczyk, L.² Zhang, W.³ Szabo, Z.⁴ Franzén, J.⁵

41
- 84875944749
- G.-D. Yin T.-B. Ren Y. Rao Y.-F. Zhou Z.-X. Li W.-M. Shu A.-X. Wu J. Org. Chem. 2013 78 3132 3141
- (2013) J. Org. Chem. , vol.78 , pp. 3132-3141
- Yin, G.-D.¹ Ren, T.-B.² Rao, Y.³ Zhou, Y.-F.⁴ Li, Z.-X.⁵ Shu, W.-M.⁶ Wu, A.-X.⁷

42
- 84873334224
- W.-M. Shu Y. Yang D.-X. Zhang L.-M. Wu Y.-P. Zhu G.-D. Yin A.-X. Wu Org. Lett. 2013 15 456 459
- (2013) Org. Lett. , vol.15 , pp. 456-459
- Shu, W.-M.¹ Yang, Y.² Zhang, D.-X.³ Wu, L.-M.⁴ Zhu, Y.-P.⁵ Yin, G.-D.⁶ Wu, A.-X.⁷

43
- 77957347790
- Y. Sohtome B. Shin N. Horitsugi R. Takagi K. Noguchi K. Nagasawa Angew. Chem., Int. Ed. 2010 49 7299 7303
- (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 7299-7303
- Sohtome, Y.¹ Shin, B.² Horitsugi, N.³ Takagi, R.⁴ Noguchi, K.⁵ Nagasawa, K.⁶

44
- 80051724270
- Y. Sohtome B. Shin N. Horitsugi K. Noguchi K. Nagasawa Chem.-Asian J. 2011 6 2463 2470
- (2011) Chem.-Asian J. , vol.6 , pp. 2463-2470
- Sohtome, Y.¹ Shin, B.² Horitsugi, N.³ Noguchi, K.⁴ Nagasawa, K.⁵

45
- 34249803216
- T.-Y. Liu H.-L. Cui Q. Chai J. Long B.-J. Li Y. Wu L.-S. Ding Y.-C. Chen Chem. Commun. 2007 2228 2230
- (2007) Chem. Commun. , pp. 2228-2230
- Liu, T.-Y.¹ Cui, H.-L.² Chai, Q.³ Long, J.⁴ Li, B.-J.⁵ Wu, Y.⁶ Ding, L.-S.⁷ Chen, Y.-C.⁸

46
- 77953005442
- H. Zhang Y.-H. Liao W.-C. Yuan X. M. Zhang Eur. J. Org. Chem. 2010 3215 3218
- (2010) Eur. J. Org. Chem. , pp. 3215-3218
- Zhang, H.¹ Liao, Y.-H.² Yuan, W.-C.³ Zhang, X.M.⁴

47
- 77749249116
- J. Lv X. Li L. Zhong S.-Z. Luo J.-P. Cheng Org. Lett. 2010 12 1096 1099
- (2010) Org. Lett. , vol.12 , pp. 1096-1099
- Lv, J.¹ Li, X.² Zhong, L.³ Luo, S.-Z.⁴ Cheng, J.-P.⁵

48
- 84864978468
- S. Bai X.-H. Liu Z. Wang W.-D. Cao L.-L. Lin X.-M. Feng Adv. Synth. Catal. 2012 354 2096 2100
- (2012) Adv. Synth. Catal. , vol.354 , pp. 2096-2100
- Bai, S.¹ Liu, X.-H.² Wang, Z.³ Cao, W.-D.⁴ Lin, L.-L.⁵ Feng, X.-M.⁶

49
- 84872973870
- G.-D. Yin H.-Q. Shi L.-Q.-Y. Xu X.-H. Wei Q. Tao Synthesis 2013 334 340
- (2013) Synthesis , pp. 334-340
- Yin, G.-D.¹ Shi, H.-Q.² Xu, L.-Q.-Y.³ Wei, X.-H.⁴ Tao, Q.⁵

50
- 84873734194
- G.-D. Yin T.-T. Lai Z.-S. Yan H. Chen J. Zheng Q. Tao Tetrahedron 2013 69 2430 2435
- (2013) Tetrahedron , vol.69 , pp. 2430-2435
- Yin, G.-D.¹ Lai, T.-T.² Yan, Z.-S.³ Chen, H.⁴ Zheng, J.⁵ Tao, Q.⁶

51
- 84868021857
- G.-D. Yin L. Fan T.-B. Ren C.-Y. Zheng Q. Tao A.-X. Wu N.-F. She Org. Biomol. Chem. 2012 10 8877 8883
- (2012) Org. Biomol. Chem. , vol.10 , pp. 8877-8883
- Yin, G.-D.¹ Fan, L.² Ren, T.-B.³ Zheng, C.-Y.⁴ Tao, Q.⁵ Wu, A.-X.⁶ She, N.-F.⁷

52
- 78650374372
- L. Hao Y.-M. Pan T. Wang M. Lin L. Chen Z.-P. Zhan Adv. Synth. Catal. 2010 352 3215 3222
- (2010) Adv. Synth. Catal. , vol.352 , pp. 3215-3222
- Hao, L.¹ Pan, Y.-M.² Wang, T.³ Lin, M.⁴ Chen, L.⁵ Zhan, Z.-P.⁶

53
- 60849101850
- 934870
- M. Bandini A. Eichholzer P. Kotrusz M. Tragni S. Troisi A. Umani-Ronchi Adv. Synth. Catal. 2009 351 319 324
- (2009) Adv. Synth. Catal. , vol.351 , pp. 319-324
- Bandini, M.¹ Eichholzer, A.² Kotrusz, P.³ Tragni, M.⁴ Troisi, S.⁵ Umani-Ronchi, A.⁶

54
- 69249092514
- S.-L. You Q. Cai M. Zeng Chem. Soc. Rev. 2009 38 2190 2201
- (2009) Chem. Soc. Rev. , vol.38 , pp. 2190-2201
- You, S.-L.¹ Cai, Q.² Zeng, M.³

55
- 69549126459
- L. Hong L. Wang W.-S. Sun K. Wong R. Wang J. Org. Chem. 2009 74 6881 6884
- (2009) J. Org. Chem. , vol.74 , pp. 6881-6884
- Hong, L.¹ Wang, L.² Sun, W.-S.³ Wong, K.⁴ Wang, R.⁵

56
- 84862907638
- X.-M. Wang Z.-B. Han Z. Wang K.-L. Ding Angew. Chem., Int. Ed. 2012 51 936 940
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 936-940
- Wang, X.-M.¹ Han, Z.-B.² Wang, Z.³ Ding, K.-L.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.