SCOPUS 정보 검색 플랫폼

Volumn , Issue 11, 2013, Pages 2071-2075

Highly enantioselective organocatalytic michael addition/cyclization cascade reaction of ylideneoxindoles with isothiocyanato oxindoles: A formal [3+2] cycloaddition approach to optically active bispirooxindole derivatives

(7) Tan, Fen a Cheng, Hong Gang a Feng, Bin a Zou, You Quan a Duan, Shu Wen a Chen, Jia Rong a Xiao, Wen Jing a

a CENTRAL CHINA NORMAL UNIVERSITY (China)

Author keywords

Asymmetric synthesis; Cascade reaction; Cyclization; Domino reactions; Michael addition; Organocatalysis; Spiro compounds

Indexed keywords

EID: 84875850546 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201300081 Document Type: Article

Times cited : (81)

References (70)

1
- 0042437190
- Angew. Chem. Int. Ed. 2003, 42, 36 -51
- H. Lin, S. J. Danishefsky, Angew. Chem. 2003, 115, 38-53; Angew. Chem. Int. Ed. 2003, 42, 36 -51.
- (2003) Angew. Chem. , vol.115 , pp. 38-53
- Lin, H.¹ Danishefsky, S.J.²

2
- 0038392407
- C. Marti, E. M. Carreira, Eur. J. Org. Chem. 2003, 2209-2219.
- (2003) Eur. J. Org. Chem. , pp. 2209-2219
- Marti, C.¹ Carreira, E.M.²

3
- 60749118899
- Angew. Chem. Int. Ed. 2007, 46, 8748 -8758
- C. V. Galliford, K. A. Scheidt, Angew. Chem. 2007, 119, 8902-8912; Angew. Chem. Int. Ed. 2007, 46, 8748 -8758.
- (2007) Angew. Chem. , vol.119 , pp. 8902-8912
- Galliford, C.V.¹ Scheidt, K.A.²

4
- 70449382104
- B. M. Trost, M. K. Brennan, Synthesis 2009, 3003-3025.
- (2009) Synthesis , pp. 3003-3025
- Trost, B.M.¹ Brennan, M.K.²

5
- 78650142189
- J. J. Badillo, N. V. Hanhan, A. K. Franz, Curr. Opin. Drug Discov. Devel. 2010, 13, 758-776.
- (2010) Curr. Opin. Drug Discov. Devel. , vol.13 , pp. 758-776
- Badillo, J.J.¹ Hanhan, N.V.² Franz, A.K.³

6
- 77954271846
- F. Zhou, Y.-L. Liu, J. Zhou, Adv. Synth. Catal. 2010, 352, 1381-1407.
- (2010) Adv. Synth. Catal. , vol.352 , pp. 1381-1407
- Zhou, F.¹ Liu, Y.-L.² Zhou, J.³

7
- 81255211335
- J. Yu, F. Shi, L.-Z. Gong, Acc. Chem. Res. 2011, 44, 1156-1171.
- (2011) Acc. Chem. Res. , vol.44 , pp. 1156-1171
- Yu, J.¹ Shi, F.² Gong, L.-Z.³

8
- 84869188848
- G. S. Singh, Z. Y. Desta, Chem. Rev. 2012, 112, 6104-6155.
- (2012) Chem. Rev. , vol.112 , pp. 6104-6155
- Singh, G.S.¹ Desta, Z.Y.²

9
- 84862864632
- N. R. Ball-Jones, J. J. Badillo, A. K. Franz, Org. Biomol. Chem. 2012, 10, 5165-5181 for recent examples of the asymmetric construction of spirooxindoles fused with three-membered rings, see
- (2012) Org. Biomol. Chem. , vol.10 , pp. 5165-5181
- Ball-Jones, N.R.¹ Badillo, J.J.² Franz, A.K.³

10
- 82355168631
- C. Palumbo, G. Mazzeo, A. Mazziotta, A. Gambacorta, M. A. Loreto, A. Migliorini, S. Superchi, D. Tofani, T. Gasperi, Org. Lett. 2011, 13, 6248-6251.
- (2011) Org. Lett. , vol.13 , pp. 6248-6251
- Palumbo, C.¹ Mazzeo, G.² Mazziotta, A.³ Gambacorta, A.⁴ Loreto, M.A.⁵ Migliorini, A.⁶ Superchi, S.⁷ Tofani, D.⁸ Gasperi, T.⁹

11
- 78650917570
- T. Gasperi, M. A. Loreto, A. Migliorini, C. Ventura, Eur. J. Org. Chem. 2011, 385-391.
- (2011) Eur. J. Org. Chem. , pp. 385-391
- Gasperi, T.¹ Loreto, M.A.² Migliorini, A.³ Ventura, C.⁴

12
- 79951971249
- F. Pesciaioli, P. Righi, A. Mazzanti, G. Bartoli, G. Bencivenni, Chem. Eur. J. 2011, 17, 2842-2845.
- (2011) Chem. Eur. J. , vol.17 , pp. 2842-2845
- Pesciaioli, F.¹ Righi, P.² Mazzanti, A.³ Bartoli, G.⁴ Bencivenni, G.⁵

13
- 84869115073
- A. Noole, N. S. Sucman, M. A. Kabeshov, T. Kanger, F. Z. Macaev, A. V. Malkov, Chem. Eur. J. 2012, 18, 14929-14933.
- (2012) Chem. Eur. J. , vol.18 , pp. 14929-14933
- Noole, A.¹ Sucman, N.S.² Kabeshov, M.A.³ Kanger, T.⁴ Macaev, F.Z.⁵ Malkov, A.V.⁶

14
- 84862729667
- X.-W. Dou, Y.-X. Lu, Chem. Eur. J. 2012, 18, 8315-8319.
- (2012) Chem. Eur. J. , vol.18 , pp. 8315-8319
- Dou, X.-W.¹ Lu, Y.-X.²

15
- 77956381671
- An example of the enantioselective synthesis of a spirooxindole-fused four-membered ring
- An example of the enantioselective synthesis of a spirooxindole-fused four-membered ring:, X.-N. Wang, Y.-Y. Zhang, S. Ye, Adv. Synth. Catal. 2010, 352, 1892-1895.
- (2010) Adv. Synth. Catal. , vol.352 , pp. 1892-1895
- Wang, X.-N.¹ Zhang, Y.-Y.² Ye, S.³

16
- 35348943329
- B. M. Trost, N. Cramer, S. M. Silverman, J. Am. Chem. Soc. 2007, 129, 12396-12937.
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 12396-12937
- Trost, B.M.¹ Cramer, N.² Silverman, S.M.³

17
- 77956042533
- A. P. Antonchick, C. Gerding-Reimers, M. Catarinella, M. Schürmann, H. Preut, S. Ziegler, D. Rauh, H. Waldmann, Nat. Chem. 2010, 2, 735-740.
- (2010) Nat. Chem. , vol.2 , pp. 735-740
- Antonchick, A.P.¹ Gerding-Reimers, C.² Catarinella, M.³ Schürmann, M.⁴ Preut, H.⁵ Ziegler, S.⁶ Rauh, D.⁷ Waldmann, H.⁸

18
- 79952182033
- T.-L. Liu, Z.-Y. Xue, H.-Y. Tao, C.-J. Wang, Org. Biomol. Chem. 2011, 9, 1980-1986.
- (2011) Org. Biomol. Chem. , vol.9 , pp. 1980-1986
- Liu, T.-L.¹ Xue, Z.-Y.² Tao, H.-Y.³ Wang, C.-J.⁴

19
- 79953843860
- B. Tan, N. R. Candeias, C. F. Barbas III, J. Am. Chem. Soc. 2011, 133, 4672-4675 for selected examples of the enantioselective synthesis of spirooxindoles fused with five-membered rings from isatin, see
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 4672-4675
- Tan, B.¹ Candeias, N.R.² Barbas Iii, C.F.³

20
- 80052310709
- L.-H. Sun, L.-T. Shen, S. Ye, Chem. Commun. 2011, 47, 10136-10138.
- (2011) Chem. Commun. , vol.47 , pp. 10136-10138
- Sun, L.-H.¹ Shen, L.-T.² Ye, S.³

21
- 81555224306
- Angew. Chem. Int. Ed. 2011, 50, 7837 -7841
- F. Zhong, X. Han, Y. Wang, Y. Lu, Angew. Chem. 2011, 123, 7983-7987; Angew. Chem. Int. Ed. 2011, 50, 7837 -7841.
- (2011) Angew. Chem. , vol.123 , pp. 7983-7987
- Zhong, F.¹ Han, X.² Wang, Y.³ Lu, Y.⁴

22
- 84860844949
- Angew. Chem. Int. Ed. 2012, 51, 989 -992
- N. V. Hanhan, N. R. Ball-Jones, N. T. Tran, A. K. Franz, Angew. Chem. 2012, 124, 1013-1016; Angew. Chem. Int. Ed. 2012, 51, 989 -992.
- (2012) Angew. Chem. , vol.124 , pp. 1013-1016
- Hanhan, N.V.¹ Ball-Jones, N.R.² Tran, N.T.³ Franz, A.K.⁴

23
- 70349784950
- Angew. Chem. Int. Ed. 2009, 48, 7200 -7203
- G. Bencivenni, L.-Y. Wu, A. Mazzanti, B. Giannichi, F. Pesciaioli, M.-P. Song, G. Bartoli, P. Melchiorre, Angew. Chem. 2009, 121, 7336-7339; Angew. Chem. Int. Ed. 2009, 48, 7200 -7203.
- (2009) Angew. Chem. , vol.121 , pp. 7336-7339
- Bencivenni, G.¹ Wu, L.-Y.² Mazzanti, A.³ Giannichi, B.⁴ Pesciaioli, F.⁵ Song, M.-P.⁶ Bartoli, G.⁷ Melchiorre, P.⁸

24
- 77749298301
- Q. Wei, L.-Z. Gong, Org. Lett. 2010, 12, 1008-1011.
- (2010) Org. Lett. , vol.12 , pp. 1008-1011
- Wei, Q.¹ Gong, L.-Z.²

25
- 80053089739
- Y. Liu, M. Nappi, E. Arceo, S. Vera, P. Melchiorre, J. Am. Chem. Soc. 2011, 133, 15212-15218 for selected examples of the enantioselective synthesis of spirooxindoles fused with six-membered rings from isatin, see
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 15212-15218
- Liu, Y.¹ Nappi, M.² Arceo, E.³ Vera, S.⁴ Melchiorre, P.⁵

26
- 70349952069
- Angew. Chem. Int. Ed. 2008, 47, 5820 -5822
- D. Hojo, K. Noguchi, M. Hirano, K. Tanaka, Angew. Chem. 2008, 120, 5904-5906; Angew. Chem. Int. Ed. 2008, 47, 5820 -5822.
- (2008) Angew. Chem. , vol.120 , pp. 5904-5906
- Hojo, D.¹ Noguchi, K.² Hirano, M.³ Tanaka, K.⁴

27
- 80052008516
- L.-T. Shen, P.-L. Shao, S. Ye, Adv. Synth. Catal. 2011, 353, 1943-1948.
- (2011) Adv. Synth. Catal. , vol.353 , pp. 1943-1948
- Shen, L.-T.¹ Shao, P.-L.² Ye, S.³

28
- 79955443470
- S. Duce, F. Pesciaioli, L. Gramigna, L. Bernardi, A. Mazzanti, A. Ricci, G. Bartoli, G. Bencivenni, Adv. Synth. Catal. 2011, 353, 860-864.
- (2011) Adv. Synth. Catal. , vol.353 , pp. 860-864
- Duce, S.¹ Pesciaioli, F.² Gramigna, L.³ Bernardi, L.⁴ Mazzanti, A.⁵ Ricci, A.⁶ Bartoli, G.⁷ Bencivenni, G.⁸

29
- 80053181266
- J. J. Badillo, A. Silva-Garcia, B. H. Shupe, J. C. Fettinger, A. K. Franz, Tetrahedron Lett. 2011, 52, 5550-5553.
- (2011) Tetrahedron Lett. , vol.52 , pp. 5550-5553
- Badillo, J.J.¹ Silva-Garcia, A.² Shupe, B.H.³ Fettinger, J.C.⁴ Franz, A.K.⁵

30
- 70349742473
- X.-H. Chen, Q. Wei, S.-W. Luo, H. Xiao, L.-Z. Gong, J. Am. Chem. Soc. 2009, 131, 13819-13825.
- (2009) J. Am. Chem. Soc. , vol.131 , pp. 13819-13825
- Chen, X.-H.¹ Wei, Q.² Luo, S.-W.³ Xiao, H.⁴ Gong, L.-Z.⁵

31
- 78249241499
- A. Voituriez, N. Pinto, M. Neel, P. Retailleau, A. Marinetti, Chem. Eur. J. 2010, 16, 12541-12544.
- (2010) Chem. Eur. J. , vol.16 , pp. 12541-12544
- Voituriez, A.¹ Pinto, N.² Neel, M.³ Retailleau, P.⁴ Marinetti, A.⁵

32
- 77149127044
- K. Jiang, Z.-J. Jia, S. Chen, L. Wu, Y.-C. Chen, Chem. Eur. J. 2010, 16, 2852-2856.
- (2010) Chem. Eur. J. , vol.16 , pp. 2852-2856
- Jiang, K.¹ Jia, Z.-J.² Chen, S.³ Wu, L.⁴ Chen, Y.-C.⁵

33
- 77956458174
- A.-N. R. Alba
- X. Companyõ, A. Zea, A.-N. R. Alba, A. Mazzanti, A. Moyano, R. Rios, Chem. Commun. 2010, 46, 6953-6955.
- (2010) Chem. Commun. , vol.46 , pp. 6953-6955
- Companyõ, X.¹ Zea, A.² Mazzanti, A.³ Moyano, A.⁴ Rios, R.⁵

34
- 77954560523
- W.-B. Chen, Z.-J. Wu, Q.-L. Pei, L.-F. Cun, X.-M. Zhang, W.-C. Yuan, Org. Lett. 2010, 12, 3132-3135.
- (2010) Org. Lett. , vol.12 , pp. 3132-3135
- Chen, W.-B.¹ Wu, Z.-J.² Pei, Q.-L.³ Cun, L.-F.⁴ Zhang, X.-M.⁵ Yuan, W.-C.⁶

35
- 78049400296
- X.-X. Jiang, Y.-M. Cao, Y.-Q. Wang, L.-P. Liu, F.-F. Shen, R. Wang, J. Am. Chem. Soc. 2010, 132, 15328-15333.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 15328-15333
- Jiang, X.-X.¹ Cao, Y.-M.² Wang, Y.-Q.³ Liu, L.-P.⁴ Shen, F.-F.⁵ Wang, R.⁶

36
- 84555211692
- Angew. Chem. Int. Ed. 2011, 50, 9124 -9127
- Y.-M. Cao, X.-X. Jiang, L.-P. Liu, F.-F. Shen, F.-T. Zhang, R. Wang, Angew. Chem. 2011, 123, 9290-9293; Angew. Chem. Int. Ed. 2011, 50, 9124 -9127.
- (2011) Angew. Chem. , vol.123 , pp. 9290-9293
- Cao, Y.-M.¹ Jiang, X.-X.² Liu, L.-P.³ Shen, F.-F.⁴ Zhang, F.-T.⁵ Wang, R.⁶

37
- 79955595508
- W.-B. Chen, Z.-J. Wu, J. Hu, L.-F. Cun, X.-M. Zhang, W.-C. Yuan, Org. Lett. 2011, 13, 2472-2475.
- (2011) Org. Lett. , vol.13 , pp. 2472-2475
- Chen, W.-B.¹ Wu, Z.-J.² Hu, J.³ Cun, L.-F.⁴ Zhang, X.-M.⁵ Yuan, W.-C.⁶

38
- 80052780706
- Y.-B. Lan, H. Zhao, Z.-M. Liu, G.-G. Liu, J.-C. Tao, X.-W. Wang, Org. Lett. 2011, 13, 4866-4869.
- (2011) Org. Lett. , vol.13 , pp. 4866-4869
- Lan, Y.-B.¹ Zhao, H.² Liu, Z.-M.³ Liu, G.-G.⁴ Tao, J.-C.⁵ Wang, X.-W.⁶

39
- 80051594488
- B. Tan, G. Hernández-Torres, C. F. Barbas III, J. Am. Chem. Soc. 2011, 133, 12354-12357.
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 12354-12357
- Tan, B.¹ Hernández-Torres, G.² Barbas Iii, C.F.³

40
- 79957462689
- B. Tan, N. R. Candeias, C. F. Barabs III, Nat. Chem. 2011, 3, 473-477.
- (2011) Nat. Chem. , vol.3 , pp. 473-477
- Tan, B.¹ Candeias, N.R.² Barabs Iii, C.F.³

41
- 84859560876
- K. Albertshofer, B. Tan, C. F. Barbas III, Org. Lett. 2012, 14, 1834-1837.
- (2012) Org. Lett. , vol.14 , pp. 1834-1837
- Albertshofer, K.¹ Tan, B.² Barbas Iii, C.F.³

42
- 84555191597
- B. Tan, X.-F. Zeng, W. W. Y. Leong, Z.-G. Shi, C. F. Barbas III, G. Zhong, Chem. Eur. J. 2012, 18, 63-67.
- (2012) Chem. Eur. J. , vol.18 , pp. 63-67
- Tan, B.¹ Zeng, X.-F.² Leong, W.W.Y.³ Shi, Z.-G.⁴ Barbas Iii, C.F.⁵ Zhong, G.⁶

43
- 84867298005
- X. Xie, C. Peng, G. He, H.-J. Leng, B. Wang, W. Huang, B. Han, Chem. Commun. 2012, 48, 10487-10489.
- (2012) Chem. Commun. , vol.48 , pp. 10487-10489
- Xie, X.¹ Peng, C.² He, G.³ Leng, H.-J.⁴ Wang, B.⁵ Huang, W.⁶ Han, B.⁷

44
- 84863230138
- D. Du, Z.-H. Hu, J.-L. Jin, Y.-Y. Lu, W.-F. Tang, B. Wang, T. Lu, Org. Lett. 2012, 14, 1274-1277.
- (2012) Org. Lett. , vol.14 , pp. 1274-1277
- Du, D.¹ Hu, Z.-H.² Jin, J.-L.³ Lu, Y.-Y.⁴ Tang, W.-F.⁵ Wang, B.⁶ Lu, T.⁷

45
- 84869192360
- L.-P. Liu, Y. Zhong, P.-P. Zhang, X.-X. Zhang, R. Wang, J. Org. Chem. 2012, 77, 10228-10234.
- (2012) J. Org. Chem. , vol.77 , pp. 10228-10234
- Liu, L.-P.¹ Zhong, Y.² Zhang, P.-P.³ Zhang, X.-X.⁴ Wang, R.⁵

46
- 84861553129
- W.-S. Sun, G.-M. Zhu, C.-Y. Wu, L. Hong, R. Wang, Chem. Eur. J. 2012, 18, 6737-6741.
- (2012) Chem. Eur. J. , vol.18 , pp. 6737-6741
- Sun, W.-S.¹ Zhu, G.-M.² Wu, C.-Y.³ Hong, L.⁴ Wang, R.⁵

47
- 84868223494
- A. Noole, I. Järving, F. Werner, M. Lopp, A. Malkov, T. Kanger, Org. Lett. 2012, 14, 4922-4925.
- (2012) Org. Lett. , vol.14 , pp. 4922-4925
- Noole, A.¹ Järving, I.² Werner, F.³ Lopp, M.⁴ Malkov, A.⁵ Kanger, T.⁶

48
- 84875869101
- Angew. Chem. Int. Ed. 2013, 52, 585 -588
- L.-T. Shen, W.-Q. Jia, S. Ye, Angew. Chem. 2013, 125, 613-616; Angew. Chem. Int. Ed. 2013, 52, 585 -588.
- (2013) Angew. Chem. , vol.125 , pp. 613-616
- Shen, L.-T.¹ Jia, W.-Q.² Ye, S.³

49
- 84872452603
- Angew. Chem. Int. Ed. 2012, 51, 7007 -7010
- S. Kato, T. Yoshino, M. Shibasaki, M. Kanai, S. Matsunaga, Angew. Chem. 2012, 124, 7113-7116; Angew. Chem. Int. Ed. 2012, 51, 7007 -7010.
- (2012) Angew. Chem. , vol.124 , pp. 7113-7116
- Kato, S.¹ Yoshino, T.² Shibasaki, M.³ Kanai, M.⁴ Matsunaga, S.⁵

50
- 84862908937
- Y.-Y. Han, W.-B. Chen, W.-Y. Han, Z.-J. Wu, X.-M. Zhang, W.-C. Yuan, Org. Lett. 2012, 14, 490-493.
- (2012) Org. Lett. , vol.14 , pp. 490-493
- Han, Y.-Y.¹ Chen, W.-B.² Han, W.-Y.³ Wu, Z.-J.⁴ Zhang, X.-M.⁵ Yuan, W.-C.⁶

51
- 79551475188
- Angew. Chem. Int. Ed. 2010, 49, 4495 -4498
- L.-Q. Lu, J.-J. Zhang, F. Li, Y. Cheng, J. An, J.-R. Chen, W.-J. Xiao, Angew. Chem. 2010, 122, 4597-4600; Angew. Chem. Int. Ed. 2010, 49, 4495 -4498.
- (2010) Angew. Chem. , vol.122 , pp. 4597-4600
- Lu, L.-Q.¹ Zhang, J.-J.² Li, F.³ Cheng, Y.⁴ An, J.⁵ Chen, J.-R.⁶ Xiao, W.-J.⁷

52
- 79952541524
- Angew. Chem. Int. Ed. 2010, 49, 8379 -8383
- X.-F. Wang, Q.-L. Hua, Y. Cheng, X.-L. An, Q.-Q. Yang, J.-R. Chen, W.-J. Xiao, Angew. Chem. 2010, 122, 8557-8561; Angew. Chem. Int. Ed. 2010, 49, 8379 -8383.
- (2010) Angew. Chem. , vol.122 , pp. 8557-8561
- Wang, X.-F.¹ Hua, Q.-L.² Cheng, Y.³ An, X.-L.⁴ Yang, Q.-Q.⁵ Chen, J.-R.⁶ Xiao, W.-J.⁷

53
- 84863011216
- L. Wang, W. Guo, X.-X. Zhang, X.-D. Xia, W.-J. Xiao, Org. Lett. 2012, 14, 740-743.
- (2012) Org. Lett. , vol.14 , pp. 740-743
- Wang, L.¹ Guo, W.² Zhang, X.-X.³ Xia, X.-D.⁴ Xiao, W.-J.⁵

54
- 84860382282
- S.-W. Duan, Y. Li, Y.-Y. Liu, Y.-Q. Zou, D.-Q. Shi, W.-J. Xiao, Chem. Commun. 2012, 48, 5160-5162.
- (2012) Chem. Commun. , vol.48 , pp. 5160-5162
- Duan, S.-W.¹ Li, Y.² Liu, Y.-Y.³ Zou, Y.-Q.⁴ Shi, D.-Q.⁵ Xiao, W.-J.⁶

55
- 84865343822
- L.-Q. Lu, J.-R. Chen, W.-J. Xiao, Acc. Chem. Res. 2012, 45, 1278-1293.
- (2012) Acc. Chem. Res. , vol.45 , pp. 1278-1293
- Lu, L.-Q.¹ Chen, J.-R.² Xiao, W.-J.³

56
- 84863623639
- Y.-Q. Zou, S.-W. Duan, X.-G. Meng, X.-Q. Hu, S. Gao, J.-R. Chen, W.-J. Xiao, Tetrahedron 2012, 68, 6914-6919.
- (2012) Tetrahedron , vol.68 , pp. 6914-6919
- Zou, Y.-Q.¹ Duan, S.-W.² Meng, X.-G.³ Hu, X.-Q.⁴ Gao, S.⁵ Chen, J.-R.⁶ Xiao, W.-J.⁷

57
- 84872454361
- Y.-M. Cao, F.-F. Shen, F.-T. Zhang, R. Wang, Chem. Eur. J. 2013, 19, 1184-1188.
- (2013) Chem. Eur. J. , vol.19 , pp. 1184-1188
- Cao, Y.-M.¹ Shen, F.-F.² Zhang, F.-T.³ Wang, R.⁴

58
- 84872736889
- H. Wu, L.-L. Zhang, Z.-Q. Tian, Y.-D. Huang, Y.-M. Wang, Chem. Eur. J. 2013, 19, 1747-1753.
- (2013) Chem. Eur. J. , vol.19 , pp. 1747-1753
- Wu, H.¹ Zhang, L.-L.² Tian, Z.-Q.³ Huang, Y.-D.⁴ Wang, Y.-M.⁵

59
- 79958185446
- J. Alemán, A. Parra, H. Jiang, K. A. Jørgensen, Chem. Eur. J. 2011, 17, 6890-6899 for selected examples, see
- (2011) Chem. Eur. J. , vol.17 , pp. 6890-6899
- Alemán, J.¹ Parra, A.² Jiang, H.³ Jørgensen, K.A.⁴

60
- 77956361896
- Angew. Chem. Int. Ed. 2010, 49, 153 -156
- Y. Zhu, J. P. Malerich, V. H. Rawal, Angew. Chem. 2010, 122, 157-160; Angew. Chem. Int. Ed. 2010, 49, 153 -156.
- (2010) Angew. Chem. , vol.122 , pp. 157-160
- Zhu, Y.¹ Malerich, J.P.² Rawal, V.H.³

61
- 77950829460
- D.-Q. Xu, Y.-F. Wang, W. Zhang, S.-P. Luo, A.-G. Zhong, A.-B. Xia, Z.-Y. Xu, Chem. Eur. J. 2010, 16, 4177-4180.
- (2010) Chem. Eur. J. , vol.16 , pp. 4177-4180
- Xu, D.-Q.¹ Wang, Y.-F.² Zhang, W.³ Luo, S.-P.⁴ Zhong, A.-G.⁵ Xia, A.-B.⁶ Xu, Z.-Y.⁷

62
- 77956384260
- Y.-F. Wang, W. Zhang, S.-P. Luo, G.-C. Zhang, A.-B. Xia, X.-S. Xu, D.-Q. Xu, Eur. J. Org. Chem. 2010, 4981-4985.
- (2010) Eur. J. Org. Chem. , pp. 4981-4985
- Wang, Y.-F.¹ Zhang, W.² Luo, S.-P.³ Zhang, G.-C.⁴ Xia, A.-B.⁵ Xu, X.-S.⁶ Xu, D.-Q.⁷

63
- 77950856715
- V. Amendola, G. Bergamaschi, M. Boiocchi, L. Fabbrizzi, M. Milani, Chem. Eur. J. 2010, 16, 4368-4380.
- (2010) Chem. Eur. J. , vol.16 , pp. 4368-4380
- Amendola, V.¹ Bergamaschi, G.² Boiocchi, M.³ Fabbrizzi, L.⁴ Milani, M.⁵

64
- 78650333733
- W. Yang, D.-M. Du, Org. Lett. 2010, 12, 5450-5453.
- (2010) Org. Lett. , vol.12 , pp. 5450-5453
- Yang, W.¹ Du, D.-M.²

65
- 80052220803
- L. Dai, H.-J. Yang, F. Chen, Eur. J. Org. Chem. 2011, 5071-5076.
- (2011) Eur. J. Org. Chem. , pp. 5071-5076
- Dai, L.¹ Yang, H.-J.² Chen, F.³

66
- 19544393388
- B. Vakulya, S. Varga, A. Csámpai, T. Soõs, Org. Lett. 2005, 7, 1967-1969.
- (2005) Org. Lett. , vol.7 , pp. 1967-1969
- Vakulya, B.¹ Varga, S.² Csámpai, A.³ Soõs, T.⁴

67
- 77649329258
- H. Jiang, M. W. Paixão, D. Monge, K. A. Jørgensen, J. Am. Chem. Soc. 2010, 132, 2775-2783.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 2775-2783
- Jiang, H.¹ Paixão, M.W.² Monge, D.³ Jørgensen, K.A.⁴

68
- 79958846486
- V. Marcos, J. Alemán, J. L. G. Ruano, F. Marini, M. Tiecco, Org. Lett. 2011, 13, 3052-3055.
- (2011) Org. Lett. , vol.13 , pp. 3052-3055
- Marcos, V.¹ Alemán, J.² Ruano, J.L.G.³ Marini, F.⁴ Tiecco, M.⁵

69
- 84860713010
- Angew. Chem. Int. Ed. 2011, 50, 6893 -6895
- M. Moccia, F. Fini, M. Scagnetti, M. F. A. Adamo, Angew. Chem. 2011, 123, 7025-7027; Angew. Chem. Int. Ed. 2011, 50, 6893 -6895.
- (2011) Angew. Chem. , vol.123 , pp. 7025-7027
- Moccia, M.¹ Fini, F.² Scagnetti, M.³ Adamo, M.F.A.⁴

70
- 84875859310
- The structure of compound 3aa was determined by X-ray analysis. CCDC-908920 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
- The structure of compound 3aa was determined by X-ray analysis. CCDC-908920 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.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.