SCOPUS 정보 검색 플랫폼

European Journal of Organic Chemistry

Volumn , Issue 35, 2013, Pages 7979-7988

Enantioselective organocatalytic synthesis of sulfur-containing spirocyclic compounds

(5) Géant, Pierre Yves a Urban, Michal a Remeš, Marek a Císařová, Ivana a Veselý, Jan a

a CHARLES UNIVERSITY (Czech Republic)

Author keywords

Domino reactions; Organocatalysis; Spiro compounds; Sulfur heterocycles

Indexed keywords

EID: 84889084575 PISSN: 1434193X EISSN: 10990690 Source Type: Journal
DOI: 10.1002/ejoc.201300931 Document Type: Article

Times cited : (34)

References (53)

1
- 84876492985
- L. Hong, R. Wang, Adv. Synth. Catal. 2013, 355, 1023-1052.
- (2013) Adv. Synth. Catal. , vol.355 , pp. 1023-1052
- Hong, L.¹ Wang, R.²

2
- 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

3
- 84855913892
- R. Rios, Chem. Soc. Rev. 2012, 41, 1060-1074.
- (2012) Chem. Soc. Rev. , vol.41 , pp. 1060-1074
- Rios, R.¹

4
- 79953065098
- A. Bartoli, F. Rodier, L. Commeiras, J.-L. Parrain, G. Chouraqui, Nat. Prod. Rep. 2011, 28, 763-782.
- (2011) Nat. Prod. Rep. , vol.28 , pp. 763-782
- Bartoli, A.¹ Rodier, F.² Commeiras, L.³ Parrain, J.-L.⁴ Chouraqui, G.⁵

5
- 70449382104
- B. M. Trost, M. K. Brennan, Synthesis 2009, 3003-3025.
- (2009) Synthesis , pp. 3003-3025
- Trost, B.M.¹ Brennan, M.K.²

6
- 29144488083
- R. Pradhan, M. Patra, A. K. Behera, B. K. Mishra, R. K. Behera, Tetrahedron 2006, 62, 779-828.
- (2006) Tetrahedron , vol.62 , pp. 779-828
- Pradhan, R.¹ Patra, M.² Behera, A.K.³ Mishra, B.K.⁴ Behera, R.K.⁵

7
- 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

8
- 0031060189
- C. B. Cui, H. Kakeya, H. Osada, Tetrahedron 1997, 53, 59-72.
- (1997) Tetrahedron , vol.53 , pp. 59-72
- Cui, C.B.¹ Kakeya, H.² Osada, H.³

9
- 0029820050
- C. B. Cui, H. Kakeya, H. Osada, J. Antibiot. 1996, 49, 832-835.
- (1996) J. Antibiot. , vol.49 , pp. 832-835
- Cui, C.B.¹ Kakeya, H.² Osada, H.³

10
- 0015101797
- J. W. Daly, I. Karle, C. Myers, T. Tokuyama, J. A. Waters, B. Witkop, Proc. Natl. Acad. Sci. USA 1971, 68, 1870-1875.
- (1971) Proc. Natl. Acad. Sci. USA , vol.68 , pp. 1870-1875
- Daly, J.W.¹ Karle, I.² Myers, C.³ Tokuyama, T.⁴ Waters, J.A.⁵ Witkop, B.⁶

11
- 37049136444
- K. J. Okabe, K. Yamada, S. Yamamura, S. J. Takasa, J. Chem. Soc. C 1967, 21, 2201-2206.
- (1967) J. Chem. Soc. C , vol.21 , pp. 2201-2206
- Okabe, K.J.¹ Yamada, K.² Yamamura, S.³ Takasa, S.J.⁴

12
- 37049125295
- N. Sakabe, S. Takada, K. J. Okabe, J. Chem. Soc., Chem. Commun. 1967, 6, 259-261.
- (1967) J. Chem. Soc., Chem. Commun. , vol.6 , pp. 259-261
- Sakabe, N.¹ Takada, S.² Okabe, K.J.³

13
- 0001856425
- H. Conroy, J. K. Chakrabarti, Tetrahedron 1959, 4, 6-13.
- (1959) Tetrahedron , vol.4 , pp. 6-13
- Conroy, H.¹ Chakrabarti, J.K.²

14
- 0035823392
- T. Takahashi, H. Tsutsui, M. Tamura, S. Kitagaki, M. Nakajima, S. Hashimoto, Chem. Commun. 2001, 1604-1605.
- (2001) Chem. Commun. , pp. 1604-1605
- Takahashi, T.¹ Tsutsui, H.² Tamura, M.³ Kitagaki, S.⁴ Nakajima, M.⁵ Hashimoto, S.⁶

15
- 0035825133
- Angew. Chem. Int. Ed. 2001, 40, 249 - 253
- M. Hatano, M. Terada, K. Mikami, Angew. Chem. 2001, 113, 255; Angew. Chem. Int. Ed. 2001, 40, 249-253.
- (2001) Angew. Chem. , vol.113 , pp. 255
- Hatano, M.¹ Terada, M.² Mikami, K.³

16
- 77955804883
- Q.-F. Wu, H. He, W.-B. Liu, S.-L. You, J. Am. Chem. Soc. 2010, 132, 11418-11419.
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 11418-11419
- Wu, Q.-F.¹ He, H.² Liu, W.-B.³ You, S.-L.⁴

17
- 33947273987
- B. K. Corkey, F. D. Toste, J. Am. Chem. Soc. 2007, 129, 2764-2765.
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 2764-2765
- Corkey, B.K.¹ Toste, F.D.²

18
- 35348943329
- B. M. Trost, N. Cramer, S. M. Silverman, J. Am. Chem. Soc. 2007, 129, 12396-12397.
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 12396-12397
- Trost, B.M.¹ Cramer, N.² Silverman, S.M.³

19
- 28244472828
- D. Romo, Z. Moussa, K. Kong, Org. Lett. 2005, 7, 5127-5130.
- (2005) Org. Lett. , vol.7 , pp. 5127-5130
- Romo, D.¹ Moussa, Z.² Kong, K.³

20
- 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; Angew. Chem. Int. Ed. 2009, 48, 7200-7203.
- (2009) Angew. Chem. , vol.121 , pp. 7336
- 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

21
- 34248192461
- Angew. Chem. Int. Ed. 2007, 46, 1101 - 1104
- A. Carlone, S. Cabrera, M. Marigo, K. A. Jørgensen, Angew. Chem. 2007, 119, 1119; Angew. Chem. Int. Ed. 2007, 46, 1101-1104.
- (2007) Angew. Chem. , vol.119 , pp. 1119
- Carlone, A.¹ Cabrera, S.² Marigo, M.³ Jørgensen, K.A.⁴

22
- 79955156401
- L.-L. Wang, L. Peng, J.-F. Bai, L.-N. Jia, X.-Y. Luo, Q.-C. Huang, X.-Y. Xu, L.-X. Wang, Chem. Commun. 2011, 47, 5593-5595.
- (2011) Chem. Commun. , vol.47 , pp. 5593-5595
- Wang, L.-L.¹ Peng, L.² Bai, J.-F.³ Jia, L.-N.⁴ Luo, X.-Y.⁵ Huang, Q.-C.⁶ Xu, X.-Y.⁷ Wang, L.-X.⁸

23
- 84876901755
- X. Li, C. Yang, J.-L. Jin, X.-S. Xue, J.-P. Cheng, Chem. Asian J. 2013, 8, 997-1003.
- (2013) Chem. Asian J. , vol.8 , pp. 997-1003
- Li, X.¹ Yang, C.² Jin, J.-L.³ Xue, X.-S.⁴ Cheng, J.-P.⁵

24
- 84874730138
- J.-X. Zhang, N.-K. Li, Z.-M. Liu, X.-F. Huang, Z.-C. Geng, X.-W. Wang, Adv. Synth. Catal. 2013, 355, 797-808.
- (2013) Adv. Synth. Catal. , vol.355 , pp. 797-808
- Zhang, J.-X.¹ Li, N.-K.² Liu, Z.-M.³ Huang, X.-F.⁴ Geng, Z.-C.⁵ Wang, X.-W.⁶

25
- 84869431746
- L. Xiya, W. Liangliang, P. Lin, B. Jianfei, J. Lina, T. Fang, X. Xiaoying, W. Lixin, Chin. J. Chem. 2012, 30, 2703-2706.
- (2012) Chin. J. Chem. , vol.30 , pp. 2703-2706
- Xiya, L.¹ Liangliang, W.² Lin, P.³ Jianfei, B.⁴ Lina, J.⁵ Fang, T.⁶ Xiaoying, X.⁷ Lixin, W.⁸

26
- 84861384792
- L. Xiya, W. Liangliang, P. Lin, B. Jianfei, J. Lina, H. Guangyun, T. Fang, X. Xiaoying, W. Lixin, Chin. J. Chem. 2012, 30, 1185-1188.
- (2012) Chin. J. Chem. , vol.30 , pp. 1185-1188
- Xiya, L.¹ Liangliang, W.² Lin, P.³ Jianfei, B.⁴ Lina, J.⁵ Guangyun, H.⁶ Fang, T.⁷ Xiaoying, X.⁸ Lixin, W.⁹

27
- 84863171044
- B. Wu, J. Chen, M.-Q. Li, J.-X. Zhang, X.-P. Xu, S.-J. Ji, X.-W. Wang, Eur. J. Org. Chem. 2012, 1318-1327.
- (2012) Eur. J. Org. Chem. , pp. 1318-1327
- Wu, B.¹ Chen, J.² Li, M.-Q.³ Zhang, J.-X.⁴ Xu, X.-P.⁵ Ji, S.-J.⁶ Wang, X.-W.⁷

28
- 78049516353
- A. C. Silvanus, B. J. Groombridge, B. I. Andrews, G. Kociok-Koehn, D. R. Carbery, J. Org. Chem. 2010, 75, 7491-7493.
- (2010) J. Org. Chem. , vol.75 , pp. 7491-7493
- Silvanus, A.C.¹ Groombridge, B.J.² Andrews, B.I.³ Kociok-Koehn, G.⁴ Carbery, D.R.⁵

29
- 33947198541
- Angew. Chem. Int. Ed. 2007, 46, 1570 - 1581
- D. Enders, C. Grondal, R. M. Matthias, Angew. Chem. 2007, 119, 1590; Angew. Chem. Int. Ed. 2007, 46, 1570-1581.
- (2007) Angew. Chem. , vol.119 , pp. 1590
- Enders, D.¹ Grondal, C.² Matthias, R.M.³

30
- 73049106494
- A.-N. Alba, X. Companyo, M. Viciano, R. Rios, Curr. Org. Chem. 2009, 13, 1432-1474.
- (2009) Curr. Org. Chem. , vol.13 , pp. 1432-1474
- Alba, A.-N.¹ Companyo, X.² Viciano, M.³ Rios, R.⁴

31
- 84874092918
- M. J. Wanner, S. Ingemann, J. H. van Maarseveen, H. Hiemstra, Eur. J. Org. Chem. 2013, 1100-1106.
- (2013) Eur. J. Org. Chem. , pp. 1100-1106
- Wanner, M.J.¹ Ingemann, S.² Van Maarseveen, J.H.³ Hiemstra, H.⁴

32
- 84870517823
- U. Das, Y.-L. Tsai, W. Lin, Org. Biomol. Chem. 2013, 11, 44-47.
- (2013) Org. Biomol. Chem. , vol.11 , pp. 44-47
- Das, U.¹ Tsai, Y.-L.² Lin, W.³

33
- 84862547343
- D. B. Ramachary, R. Madhavachary, M. S. Prasad, Org. Biomol. Chem. 2012, 10, 5825-5829.
- (2012) Org. Biomol. Chem. , vol.10 , pp. 5825-5829
- Ramachary, D.B.¹ Madhavachary, R.² Prasad, M.S.³

34
- 84867297838
- X. Wu, Q. Liu, H. Fang, J. Chen, W. Cao, G. Zhao, Chem. Eur. J. 2012, 18, 12196-12201.
- (2012) Chem. Eur. J. , vol.18 , pp. 12196-12201
- Wu, X.¹ Liu, Q.² Fang, H.³ Chen, J.⁴ Cao, W.⁵ Zhao, G.⁶

35
- 78649846478
- C. Cassani, X. Tian, E. C. Escudero-Adan, P. Melchiorre, Chem. Commun. 2011, 47, 233-235.
- (2011) Chem. Commun. , vol.47 , pp. 233-235
- Cassani, C.¹ Tian, X.² Escudero-Adan, E.C.³ Melchiorre, P.⁴

36
- 80052743131
- A.-N. R. Alba
- A. Zea, A.-N. R. Alba, A. Mazzanti, A. Moyano, R. Rios, Org. Biomol. Chem. 2011, 9, 6519-6523.
- (2011) Org. Biomol. Chem. , vol.9 , pp. 6519-6523
- Zea, A.¹ Mazzanti, A.² Moyano, A.³ Rios, R.⁴

37
- 80052833054
- 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; Angew. Chem. Int. Ed. 2011, 50, 9124-9127.
- (2011) Angew. Chem. , vol.123 , pp. 9290
- Cao, Y.-M.¹ Jiang, X.-X.² Liu, L.-P.³ Shen, F.-F.⁴ Zhang, F.-T.⁵ Wang, R.⁶

38
- 77956458174
- A.-N. R. Alba
- X. Companyo, 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
- Companyo, X.¹ Zea, A.² Mazzanti, A.³ Moyano, A.⁴ Rios, R.⁵

39
- 84878847929
- During the preparation of this manuscript, W. Wang et al. reported the formation of sulfur-containing heterocycles by a Michael/Michael/Aldol cascade sequence, see
- During the preparation of this manuscript, W. Wang et al. reported the formation of sulfur-containing heterocycles by a Michael/Michael/Aldol cascade sequence, see:, Y. Zhang, S. Wang, S. Wu, S. Zhu, G. Dong, Z. Miao, J. Yao, W. Zhang, C. Sheng, W. Wang, ACS Comb. Sci. 2013, 15, 298-308.
- (2013) ACS Comb. Sci. , vol.15 , pp. 298-308
- Zhang, Y.¹ Wang, S.² Wu, S.³ Zhu, S.⁴ Dong, G.⁵ Miao, Z.⁶ Yao, J.⁷ Zhang, W.⁸ Sheng, C.⁹ Wang, W.¹⁰

40
- 84865133795
- H. Song, Y. S. Lee, E. J. Roh, J. H. Seo, K.-S. Oh, B. H. Lee, H. Han, K. J. Shin, Bioorg. Med. Chem. Lett. 2012, 22, 5668-5674.
- (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 5668-5674
- Song, H.¹ Lee, Y.S.² Roh, E.J.³ Seo, J.H.⁴ Oh, K.-S.⁵ Lee, B.H.⁶ Han, H.⁷ Shin, K.J.⁸

41
- 78751657690
- S. Jiang, S. R. Tala, H. Lu, N. E. Abo-Dya, I. Avan, K. Gyanda, L. Lu, A. R. Katritzky, A. K. Debnath, J. Med. Chem. 2011, 54, 572-579.
- (2011) J. Med. Chem. , vol.54 , pp. 572-579
- Jiang, S.¹ Tala, S.R.² Lu, H.³ Abo-Dya, N.E.⁴ Avan, I.⁵ Gyanda, K.⁶ Lu, L.⁷ Katritzky, A.R.⁸ Debnath, A.K.⁹

42
- 34250189143
- G. Kumar, P. Parasuraman, S. K. Sharma, T. Banerjee, K. Karmodiya, N. Surolia, A. Surolia, J. Med. Chem. 2007, 50, 2665-2675.
- (2007) J. Med. Chem. , vol.50 , pp. 2665-2675
- Kumar, G.¹ Parasuraman, P.² Sharma, S.K.³ Banerjee, T.⁴ Karmodiya, K.⁵ Surolia, N.⁶ Surolia, A.⁷

43
- 20644458125
- N. S. Cutshall, C. O'Day, M. Prezhdo, Bioorg. Med. Chem. Lett. 2005, 15, 3374-3379.
- (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 3374-3379
- Cutshall, N.S.¹ O'Day, C.² Prezhdo, M.³

44
- 0030847779
- N. S. Habib, S. M. Rida, E. A. M. Badawey, H. T. Y. Fahmy, H. A. Ghozlan, Eur. J. Med. Chem. 1997, 32, 759-762.
- (1997) Eur. J. Med. Chem. , vol.32 , pp. 759-762
- Habib, N.S.¹ Rida, S.M.² Badawey, E.A.M.³ Fahmy, H.T.Y.⁴ Ghozlan, H.A.⁵

45
- 0014264889
- Selected examples of benzothiophen-2,3-dione derivatives
- L. M. Werbel, N. Headen, E. F. Elslager, J. Med. Chem. 1968, 11, 364-365. Selected examples of benzothiophen-2,3-dione derivatives
- (1968) J. Med. Chem. , vol.11 , pp. 364-365
- Werbel, L.M.¹ Headen, N.² Elslager, E.F.³

46
- 33645811117
- A. Londhe, B. Gupta, P. Khatri, P. Pardasani, R. T. Pardasani, Indian J. Heterocycl. Chem. 2005, 15, 137-140.
- (2005) Indian J. Heterocycl. Chem. , vol.15 , pp. 137-140
- Londhe, A.¹ Gupta, B.² Khatri, P.³ Pardasani, P.⁴ Pardasani, R.T.⁵

47
- 4444286145
- M. Rajopadhye, F. D. Popp, Heterocycles 1988, 27, 1489-1502.
- (1988) Heterocycles , vol.27 , pp. 1489-1502
- Rajopadhye, M.¹ Popp, F.D.²

48
- 0015881404
- K. Kikugawa, M. Ichino, Chem. Pharm. Bull. 1973, 21, 1151-1155.
- (1973) Chem. Pharm. Bull. , vol.21 , pp. 1151-1155
- Kikugawa, K.¹ Ichino, M.²

49
- 84863649768
- M. Remeš, J. Veselý, Eur. J. Org. Chem. 2012, 20, 3747-3752.
- (2012) Eur. J. Org. Chem. , vol.20 , pp. 3747-3752
- Remeš, M.¹ Veselý, J.²

50
- 79955903587
- S. Číhalová, P. Dziedzic, A. Cõrdova, J. Veselý, Adv. Synth. Catal. 2011, 7, 1096-1108.
- (2011) Adv. Synth. Catal. , vol.7 , pp. 1096-1108
- Číhalová, S.¹ Dziedzic, P.² Cõrdova, A.³ Veselý, J.⁴

51
- 80054006801
- S. Číhalová, G. Valero, J. Schimer, M. Humpl, M. Dračínský, A. Moyano, R. Rios, Tetrahedron 2011, 67, 8942-8950.
- (2011) Tetrahedron , vol.67 , pp. 8942-8950
- Číhalová, S.¹ Valero, G.² Schimer, J.³ Humpl, M.⁴ Dračínský, M.⁵ Moyano, A.⁶ Rios, R.⁷

52
- 77952579545
- For the preparation of 1, see
- For the preparation of 1, see:, S. Chen, X. Zhao, J. Chen, J. Chen, L. Kuznetsova, S. S. Wong, I. Ojima, Bioconjugate Chem. 2010, 21, 979-987.
- (2010) Bioconjugate Chem. , vol.21 , pp. 979-987
- Chen, S.¹ Zhao, X.² Chen, J.³ Chen, J.⁴ Kuznetsova, L.⁵ Wong, S.S.⁶ Ojima, I.⁷

53
- 84876796259
- CCDC-941981 (for 4e), -CCDC-952729 (or 5e), -CCDC-944669 (for 7a), and -CCDC-952728 (for 8a) contain the supplementary crystallographic data for this paper
- CCDC-941981 (for 4e), -CCDC-952729 (or 5e), -CCDC-944669 (for 7a), and -CCDC-952728 (for 8a) contain 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.
- These Data Can Be Obtained Free of Charge from the Cambridge Crystallographic Data Centre

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.