SCOPUS 정보 검색 플랫폼

Volumn 2015, Issue 20, 2015, Pages 4374-4382

Asymmetric Dearomatization of 1-Aminonaphthalene Derivatives through C-C Bond Formation with Electron-Rich Heterocycles as Nucleophiles

(4) Baba, Takafumi a Oka, Junko a Noguchi, Keiichi a Tanaka, Ken a,b,c

a TOKYO UNIVERSITY OF AGRICULTURE AND TECHNOLOGY (Japan)

b TOKYO INSTITUTE OF TECHNOLOGY (Japan)

c JAPAN SCIENCE AND TECHNOLOGY AGENCY (Japan)

Author keywords

Arenes; Asymmetric catalysis; Dearomatization; Enantioselectivity; Gold; Heterocycles

Indexed keywords

EID: 85027949848 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201500486 Document Type: Article

Times cited : (14)

References (86)

1
- 84905838008
- C.-X. Zhuo, C. Zheng, S.-L. You, Acc. Chem. Res. 2014, 47, 2558.
- (2014) Acc. Chem. Res. , vol.47 , pp. 2558
- Zhuo, C.-X.¹ Zheng, C.² You, S.-L.³

2
- 84890123981
- A. Parra, S. Reboredo, Chem. Eur. J. 2013, 19, 17244.
- (2013) Chem. Eur. J. , vol.19 , pp. 17244
- Parra, A.¹ Reboredo, S.²

3
- 84871616516
- Q. Ding, Y. Ye, R. Fan, Synthesis 2013, 45, 1.
- (2013) Synthesis , vol.45 , pp. 1
- Ding, Q.¹ Ye, Y.² Fan, R.³

4
- 84870989113
- Angew. Chem. 2012, 124, 12834.
- C.-X. Zhuo, W. Zhang, S.-L. You, Angew. Chem. Int. Ed. 2012, 51, 12662; Angew. Chem. 2012, 124, 12834.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12662
- Zhuo, C.-X.¹ Zhang, W.² You, S.-L.³

5
- 83455208461
- Angew. Chem. 2011, 123, 12051.
- H. Liang, M. A. Ciufolini, Angew. Chem. Int. Ed. 2011, 50, 11849; Angew. Chem. 2011, 123, 12051.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 11849
- Liang, H.¹ Ciufolini, M.A.²

6
- 79955397100
- J. A. Porco Jr., Angew. Chem. 2011, 123, 4154.
- S. P. Roche, J. A. Porco Jr., Angew. Chem. Int. Ed. 2011, 50, 4068; Angew. Chem. 2011, 123, 4154.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4068
- Roche, S.P.¹

7
- 40949135163
- S. Quideau, L. Pouységu, D. Deffieux, Synlett 2008, 467.
- (2008) Synlett , pp. 467
- Quideau, S.¹ Pouységu, L.² Deffieux, D.³

8
- 85028192557
- For the transition-metal-catalyzed asymmetric oxidative dearomatization of phenols, see
- For the transition-metal-catalyzed asymmetric oxidative dearomatization of phenols, see

9
- 78049517379
- T. Nemoto, Y. Ishige, M. Yoshida, Y. Kohno, M. Kanematsu, Y. Hamada, Org. Lett. 2010, 12, 5020.
- (2010) Org. Lett. , vol.12 , pp. 5020
- Nemoto, T.¹ Ishige, Y.² Yoshida, M.³ Kohno, Y.⁴ Kanematsu, M.⁵ Hamada, Y.⁶

10
- 79955488982
- Angew. Chem. 2011, 123, 4547.
- Q.-F. Wu, W.-B. Liu, C.-X. Zhuo, Z.-Q. Rong, K.-Y. Ye, S.-L. You, Angew. Chem. Int. Ed. 2011, 50, 4455; Angew. Chem. 2011, 123, 4547.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4455
- Wu, Q.-F.¹ Liu, W.-B.² Zhuo, C.-X.³ Rong, Z.-Q.⁴ Ye, K.-Y.⁵ You, S.-L.⁶

11
- 79959203841
- M. A. D. A. Sanchez.
- S. Rousseaux, J. García-Fortanet, M. A. D. A. Sanchez, S. L. Buchwald, J. Am. Chem. Soc. 2011, 133, 9282.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 9282
- Rousseaux, S.¹ García-Fortanet, J.² Buchwald, S.L.³

12
- 84864211395
- M. Yoshida, T. Nemoto, Z. Zhao, Y. Ishige, Y. Hamada, Tetrahedron: Asymmetry 2012, 23, 859.
- (2012) Tetrahedron: Asymmetry , vol.23 , pp. 859
- Yoshida, M.¹ Nemoto, T.² Zhao, Z.³ Ishige, Y.⁴ Hamada, Y.⁵

13
- 84873930949
- Angew. Chem. 2013, 125, 2273.
- T. Nemoto, Z. Zhao, T. Yokosaka, Y. Suzuki, R. Wu, Y. Hamada, Angew. Chem. Int. Ed. 2013, 52, 2217; Angew. Chem. 2013, 125, 2273.
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 2217
- Nemoto, T.¹ Zhao, Z.² Yokosaka, T.³ Suzuki, Y.⁴ Wu, R.⁵ Hamada, Y.⁶

14
- 84884245585
- Angew. Chem. 2013, 125, 10240.
- C.-X. Zhuo, S.-L. You, Angew. Chem. Int. Ed. 2013, 52, 10056; Angew. Chem. 2013, 125, 10240.
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 10056
- Zhuo, C.-X.¹ You, S.-L.²

15
- 84902474433
- C.-X. Zhuo, S.-L. You, Adv. Synth. Catal. 2014, 356, 2020.
- (2014) Adv. Synth. Catal. , vol.356 , pp. 2020
- Zhuo, C.-X.¹ You, S.-L.²

16
- 84908626401
- R.-Q. Xu, Q. Gu, W.-T. Wu, Z.-A. Zhao, S.-L. You, J. Am. Chem. Soc. 2014, 136, 15469.
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 15469
- Xu, R.-Q.¹ Gu, Q.² Wu, W.-T.³ Zhao, Z.-A.⁴ You, S.-L.⁵

17
- 67650550449
- For the transition-metal-catalyzed asymmetric oxidative dearomatization of anilines, see.
- For the transition-metal-catalyzed asymmetric oxidative dearomatization of anilines, see:, J. García-Fortanet, F. Kessler, S. L. Buchwald, J. Am. Chem. Soc. 2009, 131, 6676.
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 6676
- García-Fortanet, J.¹ Kessler, F.² Buchwald, S.L.³

18
- 85028228052
- For other recent examples of transition-metal-catalyzed asymmetric dearomatizations, see
- For other recent examples of transition-metal-catalyzed asymmetric dearomatizations, see

19
- 84900296522
- C.-X. Zhuo, Y. Zhuo, S.-L. You, J. Am. Chem. Soc. 2014, 136, 6590.
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 6590
- Zhuo, C.-X.¹ Zhuo, Y.² You, S.-L.³

20
- 84903158938
- Angew. Chem. 2014, 126, 7106.
- Z.-P. Yang, Q.-F. Wu, S.-L. You, Angew. Chem. Int. Ed. 2014, 53, 6986; Angew. Chem. 2014, 126, 7106.
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 6986
- Yang, Z.-P.¹ Wu, Q.-F.² You, S.-L.³

21
- 84873970915
- Y. Liu, H. Du, Org. Lett. 2013, 15, 740.
- (2013) Org. Lett. , vol.15 , pp. 740
- Liu, Y.¹ Du, H.²

22
- 84893442757
- X. Zhang, L. Han, S.-L. You, Chem. Sci. 2014, 5, 1059.
- (2014) Chem. Sci. , vol.5 , pp. 1059
- Zhang, X.¹ Han, L.² You, S.-L.³

23
- 84883321327
- K.-J. Wu, L.-X. Dai, S.-L. You, Chem. Commun. 2013, 49, 8620.
- (2013) Chem. Commun. , vol.49 , pp. 8620
- Wu, K.-J.¹ Dai, L.-X.² You, S.-L.³

24
- 84856997714
- Angew. Chem. 2012, 124, 1712.
- Q.-F. Wu, C. Zheng, S.-L. You, Angew. Chem. Int. Ed. 2012, 51, 1680; Angew. Chem. 2012, 124, 1712.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 1680
- Wu, Q.-F.¹ Zheng, C.² You, S.-L.³

25
- 84855272527
- C. C. J. Loh, Angew. Chem. 2012, 124, 46.
- C. C. J. Loh, D. Enders, Angew. Chem. Int. Ed. 2012, 51, 46; Angew. Chem. 2012, 124, 46.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 46
- Enders, D.¹

26
- 84864146844
- K.-J. Wu, L.-X. Dai, S.-L. You, Org. Lett. 2012, 14, 3772.
- (2012) Org. Lett. , vol.14 , pp. 3772
- Wu, K.-J.¹ Dai, L.-X.² You, S.-L.³

27
- 82455186175
- C.-X. Zhuo, W.-B. Liu, Q.-F. Wu, S.-L. You, Chem. Sci. 2012, 3, 205.
- (2012) Chem. Sci. , vol.3 , pp. 205
- Zhuo, C.-X.¹ Liu, W.-B.² Wu, Q.-F.³ You, S.-L.⁴

28
- 80052498685
- Angew. Chem. 2011, 123, 8824.
- Q. Cai, C. Zheng, J.-W. Zhang, S.-L. You, Angew. Chem. Int. Ed. 2011, 50, 8665; Angew. Chem. 2011, 123, 8824.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 8665
- Cai, Q.¹ Zheng, C.² Zhang, J.-W.³ You, S.-L.⁴

29
- 77955804883
- Q.-F. Wu, H. He, W.-B. Liu, S.-L. You, J. Am. Chem. Soc. 2010, 132, 11418.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 11418
- Wu, Q.-F.¹ He, H.² Liu, W.-B.³ You, S.-L.⁴

30
- 33646557360
- B. M. Trost, J. Quancard, J. Am. Chem. Soc. 2006, 128, 6314.
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 6314
- Trost, B.M.¹ Quancard, J.²

31
- 85028207227
- For the chiral hypervalent iodine-mediated asymmetric oxidative dearomatization of phenols and naphthols, see
- For the chiral hypervalent iodine-mediated asymmetric oxidative dearomatization of phenols and naphthols, see

32
- 45549094716
- Angew. Chem. 2008, 120, 3847.
- T. Dohi, A. Maruyama, N. Takenaga, K. Senami, Y. Minamitsuji, H. Fujioka, S. B. Caemmerer, Y. Kita, Angew. Chem. Int. Ed. 2008, 47, 3787; Angew. Chem. 2008, 120, 3847.
- (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3787
- Dohi, T.¹ Maruyama, A.² Takenaga, N.³ Senami, K.⁴ Minamitsuji, Y.⁵ Fujioka, H.⁶ Caemmerer, S.B.⁷ Kita, Y.⁸

33
- 70349941087
- Angew. Chem. 2009, 121, 4675.
- S. Quideau, G. Lyvinec, M. Marguerit, K. Bathany, A. Ozanne-Beaudenon, T. Buffeteau, D. Cavagnat, A. Chénedé, Angew. Chem. Int. Ed. 2009, 48, 4605; Angew. Chem. 2009, 121, 4675.
- (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4605
- Quideau, S.¹ Lyvinec, G.² Marguerit, M.³ Bathany, K.⁴ Ozanne-Beaudenon, A.⁵ Buffeteau, T.⁶ Cavagnat, D.⁷ Chénedé, A.⁸

34
- 64049119391
- J. K. Boppisetti, V. B. Birman, Org. Lett. 2009, 11, 1221.
- (2009) Org. Lett. , vol.11 , pp. 1221
- Boppisetti, J.K.¹ Birman, V.B.²

35
- 77949413500
- Angew. Chem. 2010, 122, 2221.
- M. Uyanik, T. Yasui, K. Ishihara, Angew. Chem. Int. Ed. 2010, 49, 2175; Angew. Chem. 2010, 122, 2221.
- (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2175
- Uyanik, M.¹ Yasui, T.² Ishihara, K.³

36
- 77955470411
- M. Uyanik, T. Yasui, K. Ishihara, Tetrahedron 2010, 66, 5841.
- (2010) Tetrahedron , vol.66 , pp. 5841
- Uyanik, M.¹ Yasui, T.² Ishihara, K.³

37
- 84875801681
- K. A. Volp, A. M. Harned, Chem. Commun. 2013, 49, 3001.
- (2013) Chem. Commun. , vol.49 , pp. 3001
- Volp, K.A.¹ Harned, A.M.²

38
- 84875449090
- T. Dohi, N. Takenaga, T. Nakae, Y. Toyoda, M. Yamasaki, M. Shiro, H. Fujioka, A. Maruyama, Y. Kita, J. Am. Chem. Soc. 2013, 135, 4558.
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 4558
- Dohi, T.¹ Takenaga, N.² Nakae, T.³ Toyoda, Y.⁴ Yamasaki, M.⁵ Shiro, M.⁶ Fujioka, H.⁷ Maruyama, A.⁸ Kita, Y.⁹

39
- 84882951205
- Angew. Chem. 2013, 125, 9385.
- M. Uyanik, T. Yasui, K. Ishihara, Angew. Chem. Int. Ed. 2013, 52, 9215; Angew. Chem. 2013, 125, 9385.
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9215
- Uyanik, M.¹ Yasui, T.² Ishihara, K.³

40
- 84906946497
- Angew. Chem. 2014, 126, 10018.
- C. Bosset, R. Coffinier, P. A. Peixoto, M. E. Assal, K. Miqueu, J.-M. Sotiropoulos, L. Pouységu, S. Quideau, Angew. Chem. Int. Ed. 2014, 53, 9860; Angew. Chem. 2014, 126, 10018.
- (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 9860
- Bosset, C.¹ Coffinier, R.² Peixoto, P.A.³ Assal, M.E.⁴ Miqueu, K.⁵ Sotiropoulos, J.-M.⁶ Pouységu, L.⁷ Quideau, S.⁸

41
- 84906081685
- A. M. Harned, Tetrahedron Lett. 2014, 55, 4681.
- (2014) Tetrahedron Lett. , vol.55 , pp. 4681
- Harned, A.M.¹

42
- 85028225136
- For noncatalytic dearomatizations by double C-C bond formation, see
- For noncatalytic dearomatizations by double C-C bond formation, see

43
- 84866638161
- D. A. Evans, A. H. Cowley, J. Am. Chem. Soc. 2012, 134, 15672.
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 15672
- Evans, D.A.¹ Cowley, A.H.²

44
- 84862626039
- D. Liu, Y. Zhou, J. Pu, L. Li, Chem. Eur. J. 2012, 18, 7823.
- (2012) Chem. Eur. J. , vol.18 , pp. 7823
- Liu, D.¹ Zhou, Y.² Pu, J.³ Li, L.⁴

45
- 84870048979
- L. Severa, M. Ončák, D. Koval, R. Pohl, D. Šaman, I. Císařová, P. E. Reyes-Gutiěrrez, P. Sázelová, V. Kašička, F. Teplý, P. Slavíček, Angew. Chem. Int. Ed. 2012, 51, 11972.
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 11972
- Severa, L.¹ Ončák, M.² Koval, D.³ Pohl, R.⁴ Šaman, D.⁵ Císařová, I.⁶ Reyes-Gutiěrrez, P.E.⁷ Sázelová, P.⁸ Kašička, V.⁹ Teplý, F.¹⁰ Slavíček, P.¹¹

46
- 77956894522
- A. Bramborga, T. Linkera, Adv. Synth. Catal. 2010, 352, 2195.
- (2010) Adv. Synth. Catal. , vol.352 , pp. 2195
- Bramborga, A.¹ Linkera, T.²

47
- 70449880098
- H. Pérez, C. Melero, A. Guijarro, M. Yus, Tetrahedron 2009, 65, 10769.
- (2009) Tetrahedron , vol.65 , pp. 10769
- Pérez, H.¹ Melero, C.² Guijarro, A.³ Yus, M.⁴

48
- 36349021382
- Á. J. Pérez-Jiménez.
- C. Melero, A. Guijarro, V. Baumann, Á. J. Pérez-Jiménez, M. Yus, Eur. J. Org. Chem. 2007, 5514.
- (2007) Eur. J. Org. Chem. , pp. 5514
- Melero, C.¹ Guijarro, A.² Baumann, V.³ Yus, M.⁴

49
- 34047098339
- M. Matsunami, N. Sakai, T. Morimoto, H. Maekawa, I. Nishiguchi, Synlett 2007, 769.
- (2007) Synlett , pp. 769
- Matsunami, M.¹ Sakai, N.² Morimoto, T.³ Maekawa, H.⁴ Nishiguchi, I.⁵

50
- 33644940110
- P. Monje, P. Graña, M. R. Paleo, F. J. Sardina, Org. Lett. 2006, 8, 951.
- (2006) Org. Lett. , vol.8 , pp. 951
- Monje, P.¹ Graña, P.² Paleo, M.R.³ Sardina, F.J.⁴

51
- 0141519437
- Y. He, C. P. Junk, D. M. Lemal, Org. Lett. 2003, 5, 2135.
- (2003) Org. Lett. , vol.5 , pp. 2135
- He, Y.¹ Junk, C.P.² Lemal, D.M.³

52
- 0036399185
- J. Clayden, Y. J. Y. Foricher, H. K. Lam, Chem. Commun. 2002, 2138.
- (2002) Chem. Commun. , pp. 2138
- Clayden, J.¹ Foricher, Y.J.Y.² Lam, H.K.³

53
- 0037032302
- F. Ding, M. E. Kopach, M. Sabat, W. D. Harman, J. Am. Chem. Soc. 2002, 124, 13080.
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 13080
- Ding, F.¹ Kopach, M.E.² Sabat, M.³ Harman, W.D.⁴

54
- 0001254025
- Y. L. Chow, X. Ouyang, Can. J. Chem. 1991, 69, 423.
- (1991) Can. J. Chem. , vol.69 , pp. 423
- Chow, Y.L.¹ Ouyang, X.²

55
- 0001125312
- K. Tomioka, M. Shindo, K. Koga, J. Org. Chem. 1990, 55, 2276.
- (1990) J. Org. Chem. , vol.55 , pp. 2276
- Tomioka, K.¹ Shindo, M.² Koga, K.³

56
- 78650903117
- The trifluoroacetic acid catalyzed dearomatization of nitroarenes with N-benzyl-substituted azomethine ylide has been reported; for details, see:, Angew. Chem. 2011, 123, 492.
- The trifluoroacetic acid catalyzed dearomatization of nitroarenes with N-benzyl-substituted azomethine ylide has been reported; for details, see:, S. Lee, I. Chataigner, S. R. Piettre, Angew. Chem. Int. Ed. 2011, 50, 472; Angew. Chem. 2011, 123, 492.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 472
- Lee, S.¹ Chataigner, I.² Piettre, S.R.³

57
- 85028194900
- For recent examples of the transition-metal-catalyzed dearomatization of arenes by cyclopropanation, see
- For recent examples of the transition-metal-catalyzed dearomatization of arenes by cyclopropanation, see

58
- 84892985968
- A. Seoane, N. Casanova, N. Quiñones, J. L. Mascareñas, M. Guilías, J. Am. Chem. Soc. 2014, 136, 7607.
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 7607
- Seoane, A.¹ Casanova, N.² Quiñones, N.³ Mascareñas, J.L.⁴ Guilías, M.⁵

59
- 84903689374
- S. Kujawa, D. Best, D. J. Burns, H. W. Lam, Chem. Eur. J. 2014, 20, 8599.
- (2014) Chem. Eur. J. , vol.20 , pp. 8599
- Kujawa, S.¹ Best, D.² Burns, D.J.³ Lam, H.W.⁴

60
- 84888372785
- J. Nan, Z. Zuo, L. Luo, L. Bai, H. Zheng, Y. Yuan, J. Liu, X. Luan, Y. Wang, J. Am. Chem. Soc. 2013, 135, 17306.
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 17306
- Nan, J.¹ Zuo, Z.² Luo, L.³ Bai, L.⁴ Zheng, H.⁵ Yuan, Y.⁶ Liu, J.⁷ Luan, X.⁸ Wang, Y.⁹

61
- 85028214648
- For the intramolecular C-C bond-forming ipso-iodocyclization of N-arylpropiolamides, see
- For the intramolecular C-C bond-forming ipso-iodocyclization of N-arylpropiolamides, see

62
- 24644449080
- X. Zhang, R. C. Larock, J. Am. Chem. Soc. 2005, 127, 12230.
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 12230
- Zhang, X.¹ Larock, R.C.²

63
- 45549090574
- B.-X. Tang, D.-J. Tang, S. Tang, Q.-F. Yu, Y.-H. Zhang, Y. Liang, P. Zhong, J.-H. Li, Org. Lett. 2008, 10, 1063.
- (2008) Org. Lett. , vol.10 , pp. 1063
- Tang, B.-X.¹ Tang, D.-J.² Tang, S.³ Yu, Q.-F.⁴ Zhang, Y.-H.⁵ Liang, Y.⁶ Zhong, P.⁷ Li, J.-H.⁸

64
- 43449133004
- Q.-F. Yu, Y.-H. Zhang, Q. Yin, B.-X. Tang, R.-Y. Tang, P. Zhong, J.-H. Li, J. Org. Chem. 2008, 73, 3658.
- (2008) J. Org. Chem. , vol.73 , pp. 3658
- Yu, Q.-F.¹ Zhang, Y.-H.² Yin, Q.³ Tang, B.-X.⁴ Tang, R.-Y.⁵ Zhong, P.⁶ Li, J.-H.⁷

65
- 56449119902
- B.-X. Tang, Q. Yin, R.-Y. Tang, J.-H. Li, J. Org. Chem. 2008, 73, 9008.
- (2008) J. Org. Chem. , vol.73 , pp. 9008
- Tang, B.-X.¹ Yin, Q.² Tang, R.-Y.³ Li, J.-H.⁴

66
- 67649448971
- Z.-Q. Wang, B.-X. Tang, H.-P. Zhang, F. Wang, J.-H. Li, Synthesis 2009, 6, 891.
- (2009) Synthesis , vol.6 , pp. 891
- Wang, Z.-Q.¹ Tang, B.-X.² Zhang, H.-P.³ Wang, F.⁴ Li, J.-H.⁵

67
- 79953692993
- Angew. Chem. 2011, 123, 3868.
- T. Dohi, D. Kato, R. Hyodo, D. Yamashita, M. Shiro, Y. Kita, Angew. Chem. Int. Ed. 2011, 50, 3784; Angew. Chem. 2011, 123, 3868.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 3784
- Dohi, T.¹ Kato, D.² Hyodo, R.³ Yamashita, D.⁴ Shiro, M.⁵ Kita, Y.⁶

68
- 79960847189
- P. R. Likhar, S. S. Racharlawar, M. V. Karkhelikar, M. S. Subhas, B. Sridhar, Synthesis 2011, 15, 2407.
- (2011) Synthesis , vol.15 , pp. 2407
- Likhar, P.R.¹ Racharlawar, S.S.² Karkhelikar, M.V.³ Subhas, M.S.⁴ Sridhar, B.⁵

69
- 80054772707
- R. Leon, A. Jawalekar, T. Redert, M. J. Gaunt, Chem. Sci. 2011, 2, 1487.
- (2011) Chem. Sci. , vol.2 , pp. 1487
- Leon, R.¹ Jawalekar, A.² Redert, T.³ Gaunt, M.J.⁴

70
- 80053320764
- T. Dohi, T. Nakae, Y. Ishikado, D. Kato, Y. Kita, Org. Biomol. Chem. 2011, 9, 6899.
- (2011) Org. Biomol. Chem. , vol.9 , pp. 6899
- Dohi, T.¹ Nakae, T.² Ishikado, Y.³ Kato, D.⁴ Kita, Y.⁵

71
- 84863337623
- B.-X. Tang, Y.-H. Zhang, R.-J. Song, D.-J. Tang, G.-B. Deng, Z.-Q. Wang, Y.-X. Xie, Y.-Z. Xia, J.-H. Li, J. Org. Chem. 2012, 77, 2837.
- (2012) J. Org. Chem. , vol.77 , pp. 2837
- Tang, B.-X.¹ Zhang, Y.-H.² Song, R.-J.³ Tang, D.-J.⁴ Deng, G.-B.⁵ Wang, Z.-Q.⁶ Xie, Y.-X.⁷ Xia, Y.-Z.⁸ Li, J.-H.⁹

72
- 84862232526
- M.-Q. Jia, S.-L. You, Chem. Commun. 2012, 48, 6363.
- (2012) Chem. Commun. , vol.48 , pp. 6363
- Jia, M.-Q.¹ You, S.-L.²

73
- 84922612364
- J. Oka, R. Okamoto, K. Noguchi, K. Tanaka, Org. Lett. 2015, 17, 676.
- (2015) Org. Lett. , vol.17 , pp. 676
- Oka, J.¹ Okamoto, R.² Noguchi, K.³ Tanaka, K.⁴

74
- 84862662830
- Angew. Chem. 2012, 124, 6323. for the closely related iodocyclization that has very recently been reported, see
- T. Shibuya, K. Noguchi, K. Tanaka, Angew. Chem. Int. Ed. 2012, 51, 6219; Angew. Chem. 2012, 124, 6323. for the closely related iodocyclization that has very recently been reported, see
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 6219
- Shibuya, T.¹ Noguchi, K.² Tanaka, K.³

75
- 84890841033
- L.-J. Wang, H.-T. Zhu, Y.-F. Qiu, X.-Y. Liu, Y.-M. Liang, Org. Biomol. Chem. 2014, 12, 643.
- (2014) Org. Biomol. Chem. , vol.12 , pp. 643
- Wang, L.-J.¹ Zhu, H.-T.² Qiu, Y.-F.³ Liu, X.-Y.⁴ Liang, Y.-M.⁵

76
- 85028217866
- For our reports of the palladium(II)- or gold(I)-catalyzed asymmetric hydroarylations of N-arylpropiolamides, see
- For our reports of the palladium(II)- or gold(I)-catalyzed asymmetric hydroarylations of N-arylpropiolamides, see

77
- 79954587374
- Angew. Chem. 2011, 123, 4049.
- T. Shibuya, Y. Shibata, K. Noguchi, K. Tanaka, Angew. Chem. Int. Ed. 2011, 50, 3963; Angew. Chem. 2011, 123, 4049.
- (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 3963
- Shibuya, T.¹ Shibata, Y.² Noguchi, K.³ Tanaka, K.⁴

78
- 79960416863
- for our report of the palladium(II)-catalyzed asymmetric hydroalkenylation of N-arylpropiolamides, see
- T. Shibuya, K. Nakamura, K. Tanaka, Beilstein J. Org. Chem. 2011, 7, 944. for our report of the palladium(II)-catalyzed asymmetric hydroalkenylation of N-arylpropiolamides, see
- (2011) Beilstein J. Org. Chem. , vol.7 , pp. 944
- Shibuya, T.¹ Nakamura, K.² Tanaka, K.³

79
- 65249122083
- for our initial discovery, see
- H. Imase, T. Suda, Y. Shibata, K. Noguchi, M. Hirano, K. Tanaka, Org. Lett. 2009, 11, 1805. for our initial discovery, see
- (2009) Org. Lett. , vol.11 , pp. 1805
- Imase, H.¹ Suda, T.² Shibata, Y.³ Noguchi, K.⁴ Hirano, M.⁵ Tanaka, K.⁶

80
- 54049143342
- H. Imase, K. Noguchi, M. Hirano, K. Tanaka, Org. Lett. 2008, 10, 3563.
- (2008) Org. Lett. , vol.10 , pp. 3563
- Imase, H.¹ Noguchi, K.² Hirano, M.³ Tanaka, K.⁴

81
- 85028206087
- Pyrrole derivative 1h was also tested, but instead of the dearomatization product, the hydroarylation product 6 was generated exclusively.
- Pyrrole derivative 1h was also tested, but instead of the dearomatization product, the hydroarylation product 6 was generated exclusively.

82
- 85028210837
- CCDC-1059900 [for (±)- 2f ] contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
- CCDC-1059900 [for (±)- 2f ] contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.

83
- 78649563239
- L. J. Goossen, N. Rodriguez, F. Manjolinho, P. P. Lange, Adv. Synth. Catal. 2010, 352, 2913.
- (2010) Adv. Synth. Catal. , vol.352 , pp. 2913
- Goossen, L.J.¹ Rodriguez, N.² Manjolinho, F.³ Lange, P.P.⁴

84
- 77955338337
- S. Vangveravonga, M. Taylorb, J. Xua, J. Cuia, W. Calvinb, S. Babicb, R. R. Luedtkeb, R. H. Macha, Bioorg. Med. Chem. 2010, 18, 5291.
- (2010) Bioorg. Med. Chem. , vol.18 , pp. 5291
- Vangveravonga, S.¹ Taylorb, M.² Xua, J.³ Cuia, J.⁴ Calvinb, W.⁵ Babicb, S.⁶ Luedtkeb, R.R.⁷ Macha, R.H.⁸

85
- 84903977425
- T. C. Atack, R. M. Lecker, S. P. Cook, J. Am. Chem. Soc. 2014, 136, 9521.
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 9521
- Atack, T.C.¹ Lecker, R.M.² Cook, S.P.³

86
- 78649854008
- K. M. Joseph, I. Larraza-Sanchez, Tetrahedron Lett. 2011, 52, 13.
- (2011) Tetrahedron Lett. , vol.52 , pp. 13
- Joseph, K.M.¹ Larraza-Sanchez, I.²

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