SCOPUS 정보 검색 플랫폼

Organic and Biomolecular Chemistry

Volumn 10, Issue 11, 2012, Pages 2209-2213

Highly efficient asymmetric aldol reaction in brine using a fluorous sulfonamide organocatalyst

(7) Miura, Tsuyoshi a Kasuga, Hikaru a Imai, Kie a Ina, Mariko a Tada, Norihiro a Imai, Nobuyuki b Itoh, Akichika a

a GIFU PHARMACEUTICAL UNIVERSITY (Japan)

b CHIBA INSTITUTE OF SCIENCE (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC ALDEHYDE; ASYMMETRIC ALDOL REACTIONS; FLUOROUS; FLUOROUS SILICA GEL; HIGH YIELD; ORGANOCATALYSTS; SOLID-PHASE EXTRACTION;

ALDEHYDES; KETONES; ORGANIC COMPOUNDS; SILICA GEL; SULFUR COMPOUNDS;

CONDENSATION REACTIONS;

3-HYDROXYBUTANAL; ALDEHYDE; ALDOL; BRINE; FLUORINE DERIVATIVE; INORGANIC SALT; SULFONAMIDE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

ALDEHYDES; CATALYSIS; FLUORINE COMPOUNDS; MOLECULAR STRUCTURE; SALTS; STEREOISOMERISM; SULFONAMIDES;

EID: 84857584176 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c2ob06955e Document Type: Article

Times cited : (27)

References (96)

1
- 6044269452
- P. I. Dalko L. Moisan Angew. Chem., Int. Ed. 2004 43 5138
- (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5138
- Dalko, P.I.¹ Moisan, L.²

2
- 34547623607
- H. Pellisier Tetrahedron 2007 63 9267
- (2007) Tetrahedron , vol.63 , pp. 9267
- Pellisier, H.¹

3
- 38349100690
- S. Mukherjee J. W. Yang S. Hoffmann B. List Chem. Rev. 2007 107 5471
- (2007) Chem. Rev. , vol.107 , pp. 5471
- Mukherjee, S.¹ Yang, J.W.² Hoffmann, S.³ List, B.⁴

4
- 48849094479
- A. Dondoni A. Massi Angew. Chem., Int. Ed. 2008 47 4638
- (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4638
- Dondoni, A.¹ Massi, A.²

5
- 61849117439
- A. Lattanzi Chem. Commun. 2009 1452
- (2009) Chem. Commun. , pp. 1452
- Lattanzi, A.¹

6
- 70349904154
- X. Liu L. Lin X. Feng Chem. Commun. 2009 6145
- (2009) Chem. Commun. , pp. 6145
- Liu, X.¹ Lin, L.² Feng, X.³

7
- 77956043021
- X.-H. Chen J. Yu L.-Z. Gong Chem. Commun. 2010 46 6437
- (2010) Chem. Commun. , vol.46 , pp. 6437
- Chen, X.-H.¹ Yu, J.² Gong, L.-Z.³

8
- 79958094929
- For examples of organocatalyzed aldol reactions in water using organocatalysts with primary amino group, see
- M. Bhanushali C.-G. Zhao Synthesis 2011 1815
- (2011) Synthesis , pp. 1815
- Bhanushali, M.¹ Zhao, C.-G.²

9
- 33745500082
- Z. Jiang Z. Liang X. Wu Y. Lu Chem. Commun. 2006 2801
- (2006) Chem. Commun. , pp. 2801
- Jiang, Z.¹ Liang, Z.² Wu, X.³ Lu, Y.⁴

10
- 34547236177
- X. Wu Z. Jiang H.-M. Shen Y. Lu Adv. Synth. Catal. 2007 349 812
- (2007) Adv. Synth. Catal. , vol.349 , pp. 812
- Wu, X.¹ Jiang, Z.² Shen, H.-M.³ Lu, Y.⁴

11
- 53849091309
- M.-K. Zhu X.-Y. Xu L.-Z. Gong Adv. Synth. Catal. 2008 350 1390
- (2008) Adv. Synth. Catal. , vol.350 , pp. 1390
- Zhu, M.-K.¹ Xu, X.-Y.² Gong, L.-Z.³

12
- 44449111898
- S. S. V. Ramasastry K. Albertshofer N. Utsumi C. F. Barbas Org. Lett. 2008 10 1621
- (2008) Org. Lett. , vol.10 , pp. 1621
- Ramasastry, S.S.V.¹ Albertshofer, K.² Utsumi, N.³ Barbas, C.F.⁴

13
- 68749100830
- Y.-C. Tea P. P. Lee Synth. Commun. 2009 39 3081
- (2009) Synth. Commun. , vol.39 , pp. 3081
- Tea, Y.-C.¹ Lee, P.P.²

14
- 55049126678
- F.-Z. Peng Z.-H. Shao X.-W. Pu H.-B. Zhang Adv. Synth. Catal. 2008 350 2199
- (2008) Adv. Synth. Catal. , vol.350 , pp. 2199
- Peng, F.-Z.¹ Shao, Z.-H.² Pu, X.-W.³ Zhang, H.-B.⁴

15
- 67649831572
- X. Ma C.-S. Da L. Yi Y.-N. Jia Q.-P. Guo L.-P. Che F.-C. Wu J.-R. Wang W.-P. Li Tetrahedron: Asymmetry 2009 20 1419
- (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1419
- Ma, X.¹ Da, C.-S.² Yi, L.³ Jia, Y.-N.⁴ Guo, Q.-P.⁵ Che, L.-P.⁶ Wu, F.-C.⁷ Wang, J.-R.⁸ Li, W.-P.⁹

16
- 67649105969
- H. Zhou Y. Xie L. Ren K. Wang Adv. Synth. Catal. 2009 351 1284
- (2009) Adv. Synth. Catal. , vol.351 , pp. 1284
- Zhou, H.¹ Xie, Y.² Ren, L.³ Wang, K.⁴

17
- 77954135235
- J. Li N. Fu X. Li S. Luo J.-P. Cheng J. Org. Chem. 2010 75 4501
- (2010) J. Org. Chem. , vol.75 , pp. 4501
- Li, J.¹ Fu, N.² Li, X.³ Luo, S.⁴ Cheng, J.-P.⁵

18
- 77955797795
- For examples of organocatalyzed aldol reactions in organic solvents using organocatalysts with primary amino groups, see
- A. Ricci L. Bernardi C. Gioia S. Vierucci M. Robitzer F. Quignard Chem. Commun. 2010 46 6288
- (2010) Chem. Commun. , vol.46 , pp. 6288
- Ricci, A.¹ Bernardi, L.² Gioia, C.³ Vierucci, S.⁴ Robitzer, M.⁵ Quignard, F.⁶

19
- 23944447473
- A. Córdova W. Zou I. Ibrahem E. Reyes M. Engqvist W.-W. Liao Chem. Commun. 2005 3586
- (2005) Chem. Commun. , pp. 3586
- Córdova, A.¹ Zou, W.² Ibrahem, I.³ Reyes, E.⁴ Engqvist, M.⁵ Liao, W.-W.⁶

20
- 27444433708
- W. Zou I. Ibrahem P. Dziedzic H. Sundén A. Córdova Chem. Commun. 2005 4946
- (2005) Chem. Commun. , pp. 4946
- Zou, W.¹ Ibrahem, I.² Dziedzic, P.³ Sundén, H.⁴ Córdova, A.⁵

21
- 33645457905
- P. Dziedzic W. Zou J. Háfren A. Córdova Org. Biomol. Chem. 2006 4 38
- (2006) Org. Biomol. Chem. , vol.4 , pp. 38
- Dziedzic, P.¹ Zou, W.² Háfren, J.³ Córdova, A.⁴

22
- 33745893522
- A. Córdova W. Zou P. Dziedzic I. Ibrahem E. Reyes Y. Xu Chem.-Eur. J. 2006 12 5383
- (2006) Chem.-Eur. J. , vol.12 , pp. 5383
- Córdova, A.¹ Zou, W.² Dziedzic, P.³ Ibrahem, I.⁴ Reyes, E.⁵ Xu, Y.⁶

23
- 33846198424
- S. S. V. Ramasastry H. Zhang F. Tanaka C. F. Barbas J. Am. Chem. Soc. 2007 129 288
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 288
- Ramasastry, S.S.V.¹ Zhang, H.² Tanaka, F.³ Barbas, C.F.⁴

24
- 33947389167
- S. Luo H. Xu J. Li L. Zhang J.-P. Cheng J. Am. Chem. Soc. 2007 129 3074
- (2007) J. Am. Chem. Soc. , vol.129 , pp. 3074
- Luo, S.¹ Xu, H.² Li, J.³ Zhang, L.⁴ Cheng, J.-P.⁵

25
- 34548192245
- N. Utsumi M. Imai F. Tanaka S. S. V. Ramasastry C. F. Barbas Org. Lett. 2007 9 3445
- (2007) Org. Lett. , vol.9 , pp. 3445
- Utsumi, N.¹ Imai, M.² Tanaka, F.³ Ramasastry, S.S.V.⁴ Barbas, C.F.⁵

26
- 35548984503
- X.-Y. Xu Y.-Z. Wang L.-Z. Gong Org. Lett. 2007 9 4247
- (2007) Org. Lett. , vol.9 , pp. 4247
- Xu, X.-Y.¹ Wang, Y.-Z.² Gong, L.-Z.³

27
- 39749164990
- S. Luo H. Xu L. Zhang J. Li J.-P. Cheng Org. Lett. 2008 10 653
- (2008) Org. Lett. , vol.10 , pp. 653
- Luo, S.¹ Xu, H.² Zhang, L.³ Li, J.⁴ Cheng, J.-P.⁵

28
- 38849124986
- S. Luo J. Li L. Zhang H. Xu J.-P. Cheng Chem.-Eur. J. 2008 14 1273
- (2008) Chem.-Eur. J. , vol.14 , pp. 1273
- Luo, S.¹ Li, J.² Zhang, L.³ Xu, H.⁴ Cheng, J.-P.⁵

29
- 48849100191
- S. Luo H. Xu L. Chen J.-P. Cheng Org. Lett. 2008 10 1775
- (2008) Org. Lett. , vol.10 , pp. 1775
- Luo, S.¹ Xu, H.² Chen, L.³ Cheng, J.-P.⁴

30
- 58549105929
- X. Wu Z. Ma Z. Ye S. Qian G. Zhao Adv. Synth. Catal. 2009 351 158
- (2009) Adv. Synth. Catal. , vol.351 , pp. 158
- Wu, X.¹ Ma, Z.² Ye, Z.³ Qian, S.⁴ Zhao, G.⁵

31
- 64349094223
- J. Li S. Luo J.-P. Cheng J. Org. Chem. 2009 74 1747
- (2009) J. Org. Chem. , vol.74 , pp. 1747
- Li, J.¹ Luo, S.² Cheng, J.-P.³

32
- 73149084448
- S. Luo Y. Qiao L. Zhang J. Li X. Li J.-P. Cheng J. Org. Chem. 2009 74 9521
- (2009) J. Org. Chem. , vol.74 , pp. 9521
- Luo, S.¹ Qiao, Y.² Zhang, L.³ Li, J.⁴ Li, X.⁵ Cheng, J.-P.⁶

33
- 77950799490
- S. Luo P. Zhou J. Li J.-P. Cheng Chem.-Eur. J. 2010 16 4457
- (2010) Chem.-Eur. J. , vol.16 , pp. 4457
- Luo, S.¹ Zhou, P.² Li, J.³ Cheng, J.-P.⁴

34
- 77954135235
- J. Li N. Fu X. Li S. Luo J.-P. Cheng J. Org. Chem. 2010 75 4501
- (2010) J. Org. Chem. , vol.75 , pp. 4501
- Li, J.¹ Fu, N.² Li, X.³ Luo, S.⁴ Cheng, J.-P.⁵

35
- 79952124240
- For reviews on organic synthesis in water, see
- P. Zhou S. Luo J.-P. Cheng Org. Biomol. Chem. 2011 9 1784
- (2011) Org. Biomol. Chem. , vol.9 , pp. 1784
- Zhou, P.¹ Luo, S.² Cheng, J.-P.³

36
- 0004252595
- ed., Blackie A & P, London
- Organic Synthesis in Water, ed., P. A. Grieco, Blackie A & P, London, 1998
- (1998) Organic Synthesis in Water
- Grieco, P.A.¹

37
- 0036105107
- S. Kobayashi K. Manabe Acc. Chem. Res. 2002 35 209
- (2002) Acc. Chem. Res. , vol.35 , pp. 209
- Kobayashi, S.¹ Manabe, K.²

38
- 0036703508
- U. M. Lindstrom Chem. Rev. 2002 102 2751
- (2002) Chem. Rev. , vol.102 , pp. 2751
- Lindstrom, U.M.¹

39
- 24044470646
- C. J. Li Chem. Rev. 2005 105 3095
- (2005) Chem. Rev. , vol.105 , pp. 3095
- Li, C.J.¹

40
- 70449345895
- M. Raj V. K. Singh Chem. Commun. 2009 6687
- (2009) Chem. Commun. , pp. 6687
- Raj, M.¹ Singh, V.K.²

41
- 70349786439
- J. Paradowska M. Stodulski J. Mlynarski Angew. Chem., Int. Ed. 2009 48 4288
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 4288
- Paradowska, J.¹ Stodulski, M.² Mlynarski, J.³

42
- 58549093369
- M. Gruttadauria F. Giacalone R. Noto Adv. Synth. Catal. 2009 351 33
- (2009) Adv. Synth. Catal. , vol.351 , pp. 33
- Gruttadauria, M.¹ Giacalone, F.² Noto, R.³

43
- 77955953727
- For examples of organocatalyzed aldol reactions in water without any organic solvent using pyrrolidine derivatives, see
- N. Mase C. F. Barbas Org. Biomol. Chem. 2010 8 4043
- (2010) Org. Biomol. Chem. , vol.8 , pp. 4043
- Mase, N.¹ Barbas, C.F.²

44
- 22544448382
- S. S. Chimni D. Mahajan V. V. S. Babu Tetrahedron Lett. 2005 46 5617
- (2005) Tetrahedron Lett. , vol.46 , pp. 5617
- Chimni, S.S.¹ Mahajan, D.² Babu, V.V.S.³

45
- 31444456557
- N. Mase Y. Nakai N. Ohara H. Yoda K. Takabe F. Tanaka C. F. Barbas J. Am. Chem. Soc. 2006 128 734
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 734
- Mase, N.¹ Nakai, Y.² Ohara, N.³ Yoda, H.⁴ Takabe, K.⁵ Tanaka, F.⁶ Barbas, C.F.⁷

46
- 32044463187
- Y. Hayashi T. Sumiya J. Takahashi H. Gotoh T. Urushima M. Shoji Angew. Chem., Int. Ed. 2006 45 958
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 958
- Hayashi, Y.¹ Sumiya, T.² Takahashi, J.³ Gotoh, H.⁴ Urushima, T.⁵ Shoji, M.⁶

47
- 33748655418
- Y. Hayashi S. Aratake T. Okano J. Takahashi T. Sumiya M. Shoji Angew. Chem., Int. Ed. 2006 45 5527
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5527
- Hayashi, Y.¹ Aratake, S.² Okano, T.³ Takahashi, J.⁴ Sumiya, T.⁵ Shoji, M.⁶

48
- 33750070045
- D. Font C. Jimeno M. A. Pericàs Org. Lett. 2006 8 4653
- (2006) Org. Lett. , vol.8 , pp. 4653
- Font, D.¹ Jimeno, C.² Pericàs, M.A.³

49
- 33750041086
- Y. Wu Y. Zhang M. Yu G. Zhao S. Wang Org. Lett. 2006 8 4417
- (2006) Org. Lett. , vol.8 , pp. 4417
- Wu, Y.¹ Zhang, Y.² Yu, M.³ Zhao, G.⁴ Wang, S.⁵

50
- 34250332250
- W.-P. Huang J.-R. Chen X.-Y. Li Y.-J. Cao W.-J. Xiao Can. J. Chem. 2007 85 208
- (2007) Can. J. Chem. , vol.85 , pp. 208
- Huang, W.-P.¹ Chen, J.-R.² Li, X.-Y.³ Cao, Y.-J.⁴ Xiao, W.-J.⁵

51
- 33845336873
- F. Giacalone M. Gruttadauria A. M. Marculescu R. Noto Tetrahedron Lett. 2007 48 255
- (2007) Tetrahedron Lett. , vol.48 , pp. 255
- Giacalone, F.¹ Gruttadauria, M.² Marculescu, A.M.³ Noto, R.⁴

52
- 34250189569
- S. Aratake T. Itoh T. Okano T. Usui M. Shoji Y. Hayashi Chem. Commun. 2007 2524
- (2007) Chem. Commun. , pp. 2524
- Aratake, S.¹ Itoh, T.² Okano, T.³ Usui, T.⁴ Shoji, M.⁵ Hayashi, Y.⁶

53
- 34547144181
- V. Maya M. Raj V. K. Singh Org. Lett. 2007 9 2593
- (2007) Org. Lett. , vol.9 , pp. 2593
- Maya, V.¹ Raj, M.² Singh, V.K.³

54
- 35348857641
- M. Gruttadauria F. Giacalone A. M. Marculescu P. L. Meo S. Riela R. Noto Eur. J. Org. Chem. 2007 4688
- (2007) Eur. J. Org. Chem. , pp. 4688
- Gruttadauria, M.¹ Giacalone, F.² Marculescu, A.M.³ Meo, P.L.⁴ Riela, S.⁵ Noto, R.⁶

55
- 38749143339
- D. Font S. Sayalero A. Bastero C. Jimeno M. A. Pericàs Org. Lett. 2008 10 337
- (2008) Org. Lett. , vol.10 , pp. 337
- Font, D.¹ Sayalero, S.² Bastero, A.³ Jimeno, C.⁴ Pericàs, M.A.⁵

56
- 49549107813
- L. Zu H. Xie H. Li J. Wang W. Wang Org. Lett. 2008 10 1211
- (2008) Org. Lett. , vol.10 , pp. 1211
- Zu, L.¹ Xie, H.² Li, H.³ Wang, J.⁴ Wang, W.⁵

57
- 54149117629
- M. Lombardo F. Pasi S. Easwar C. Trombini Synlett 2008 2471
- (2008) Synlett , pp. 2471
- Lombardo, M.¹ Pasi, F.² Easwar, S.³ Trombini, C.⁴

58
- 85019513357
- S. S. Chimni S. Singh D. Mahajan Tetrahedron: Asymmetry 2008 19 2276
- (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2276
- Chimni, S.S.¹ Singh, S.² Mahajan, D.³

59
- 69149083759
- S. S. Chimni S. Singh A. Kumar Tetrahedron: Asymmetry 2009 20 1722
- (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1722
- Chimni, S.S.¹ Singh, S.² Kumar, A.³

60
- 59149103572
- S.-P. Zhang X.-K. Fu S.-D. Fu Tetrahedron Lett. 2009 50 1173
- (2009) Tetrahedron Lett. , vol.50 , pp. 1173
- Zhang, S.-P.¹ Fu, X.-K.² Fu, S.-D.³

61
- 72149126893
- S.-D. Fu X.-K. Fu S.-P. Zhang X.-C. Zou X.-J. Wu Tetrahedron: Asymmetry 2009 20 2390
- (2009) Tetrahedron: Asymmetry , vol.20 , pp. 2390
- Fu, S.-D.¹ Fu, X.-K.² Zhang, S.-P.³ Zou, X.-C.⁴ Wu, X.-J.⁵

62
- 73149113747
- M. D. Nisco S. Pedatella H. Ullah J. H. Zaidi D. Naviglio O. Ozdamar R. Caputo J. Org. Chem. 2009 74 9562
- (2009) J. Org. Chem. , vol.74 , pp. 9562
- Nisco, M.D.¹ Pedatella, S.² Ullah, H.³ Zaidi, J.H.⁴ Naviglio, D.⁵ Ozdamar, O.⁶ Caputo, R.⁷

63
- 66249084153
- M. R. Vishnumaya V. K. Singh J. Org. Chem. 2009 74 4289
- (2009) J. Org. Chem. , vol.74 , pp. 4289
- Vishnumaya, M.R.¹ Singh, V.K.²

64
- 72149095111
- N. Mase N. Noshiro A. Mokuya K. Takabe Adv. Synth. Catal. 2009 351 2791
- (2009) Adv. Synth. Catal. , vol.351 , pp. 2791
- Mase, N.¹ Noshiro, N.² Mokuya, A.³ Takabe, K.⁴

65
- 65449160459
- Y.-N. Jia F.-C. Wu X. Ma G.-J. Zhu C.-S. Da Tetrahedron Lett. 2009 50 3059
- (2009) Tetrahedron Lett. , vol.50 , pp. 3059
- Jia, Y.-N.¹ Wu, F.-C.² Ma, X.³ Zhu, G.-J.⁴ Da, C.-S.⁵

66
- 77953130840
- Y.-J. An Y.-X. Zhang Y. Wu Z.-M. Liu C. Pi J.-C. Tao Tetrahedron: Asymmetry 2010 21 688
- (2010) Tetrahedron: Asymmetry , vol.21 , pp. 688
- An, Y.-J.¹ Zhang, Y.-X.² Wu, Y.³ Liu, Z.-M.⁴ Pi, C.⁵ Tao, J.-C.⁶

67
- 79251529216
- R. Pedrosa J. M. Andrés R. Manzano D. Román S. Téllez Org. Biomol. Chem. 2011 9 935
- (2011) Org. Biomol. Chem. , vol.9 , pp. 935
- Pedrosa, R.¹ Andrés, J.M.² Manzano, R.³ Román, D.⁴ Téllez, S.⁵

68
- 33746620447
- L. Zu J. Wang H. Li W. Wang Org. Lett. 2006 8 3077
- (2006) Org. Lett. , vol.8 , pp. 3077
- Zu, L.¹ Wang, J.² Li, H.³ Wang, W.⁴

69
- 77950233672
- T. Miura K. Imai M. Ina N. Tada N. Imai A. Itoh Org. Lett. 2010 12 1620
- (2010) Org. Lett. , vol.12 , pp. 1620
- Miura, T.¹ Imai, K.² Ina, M.³ Tada, N.⁴ Imai, N.⁵ Itoh, A.⁶

70
- 79960585752
- For a review on fluorous tag techniques, see
- T. Miura K. Imai H. Kasuga M. Ina N. Tada N. Imai A. Itoh Tetrahedron 2011 67 6340
- (2011) Tetrahedron , vol.67 , pp. 6340
- Miura, T.¹ Imai, K.² Kasuga, H.³ Ina, M.⁴ Tada, N.⁵ Imai, N.⁶ Itoh, A.⁷

71
- 0034840718
- D. P. Curran Synlett 2001 1488
- (2001) Synlett , pp. 1488
- Curran, D.P.¹

72
- 0348072278
- in, ed. J. A. Gladysz, I. T. Horváth, D. Curran, Wiley-VCH, Weinheim
- D. P. Curran, in The Handbook of Fluorous Chemistry, ed., J. A. Gladysz, I. T. Horváth, D. P. Curran, Wiley-VCH, Weinheim, 2004
- (2004) The Handbook of Fluorous Chemistry
- Curran, D.P.¹

73
- 33750910189
- For a review on fluorous organocatalysts, see
- W. Thang D. P. Curran Tetrahedron 2006 62 11837
- (2006) Tetrahedron , vol.62 , pp. 11837
- Thang, W.¹ Curran, D.P.²

74
- 56349163815
- For examples of fluorous organocatalysts, see
- W. Zhang C. Cai Chem. Commun. 2008 5686
- (2008) Chem. Commun. , pp. 5686
- Zhang, W.¹ Cai, C.²

75
- 0035855262
- F. Fache O. Piva Tetrahedron Lett. 2001 42 5655
- (2001) Tetrahedron Lett. , vol.42 , pp. 5655
- Fache, F.¹ Piva, O.²

76
- 0037421273
- F. Fache O. Piva Tetrahedron: Asymmetry 2003 14 139
- (2003) Tetrahedron: Asymmetry , vol.14 , pp. 139
- Fache, F.¹ Piva, O.²

77
- 23044509130
- Z. Dalicsek F. Pollreisz A. Gomory T. Soós Org. Lett. 2005 7 3243
- (2005) Org. Lett. , vol.7 , pp. 3243
- Dalicsek, Z.¹ Pollreisz, F.² Gomory, A.³ Soós, T.⁴

78
- 33746620447
- L. Zu J. Wang H. Li W. Wang Org. Lett. 2006 8 3077
- (2006) Org. Lett. , vol.8 , pp. 3077
- Zu, L.¹ Wang, J.² Li, H.³ Wang, W.⁴

79
- 33744979311
- L. Zu J. Wang H. Li X.-H. Yu W. Wang Tetrahedron Lett. 2006 47 5131
- (2006) Tetrahedron Lett. , vol.47 , pp. 5131
- Zu, L.¹ Wang, J.² Li, H.³ Yu, X.-H.⁴ Wang, W.⁵

80
- 33751194087
- Q. Chu W. Zhang D. P. Curran Tetrahedron Lett. 2006 47 9287
- (2006) Tetrahedron Lett. , vol.47 , pp. 9287
- Chu, Q.¹ Zhang, W.² Curran, D.P.³

81
- 33847051249
- A. V. Malkov M. Figlus S. Stonius P. Koovský J. Org. Chem. 2007 72 1315
- (2007) J. Org. Chem. , vol.72 , pp. 1315
- Malkov, A.V.¹ Figlus, M.² Stonius, S.³ Koovský, P.⁴

82
- 34047106648
- S. Goushi K. Funabiki M. Ohta K. Hatano M. Matsui Tetrahedron 2007 63 4061
- (2007) Tetrahedron , vol.63 , pp. 4061
- Goushi, S.¹ Funabiki, K.² Ohta, M.³ Hatano, K.⁴ Matsui, M.⁵

83
- 37249045164
- H. Cui Y. Li C. Zheng G. Zhao S. Zhu J. Fluorine Chem. 2008 129 45
- (2008) J. Fluorine Chem. , vol.129 , pp. 45
- Cui, H.¹ Li, Y.² Zheng, C.³ Zhao, G.⁴ Zhu, S.⁵

84
- 43549118736
- Q. Chu M. S. Yu D. P. Curran Org. Lett. 2008 10 749
- (2008) Org. Lett. , vol.10 , pp. 749
- Chu, Q.¹ Yu, M.S.² Curran, D.P.³

85
- 55049098255
- F. O. Seidel J. A. Gladysz Adv. Synth. Catal. 2008 350 2443
- (2008) Adv. Synth. Catal. , vol.350 , pp. 2443
- Seidel, F.O.¹ Gladysz, J.A.²

86
- 61349167055
- A. Gheorghe T. Chinnusamy E. C. Yanez P. Hilgers O. Reiser Org. Lett. 2008 10 4171
- (2008) Org. Lett. , vol.10 , pp. 4171
- Gheorghe, A.¹ Chinnusamy, T.² Yanez, E.C.³ Hilgers, P.⁴ Reiser, O.⁵

87
- 75749090354
- D. Vuluga J. Legros B. Crousse D. B. Delpon Chem.-Eur. J. 2010 16 1776
- (2010) Chem.-Eur. J. , vol.16 , pp. 1776
- Vuluga, D.¹ Legros, J.² Crousse, B.³ Delpon, D.B.⁴

88
- 76249085117
- L. Wang C. Cai D. P. Curran W. Zhang Synlett 2010 433
- (2010) Synlett , pp. 433
- Wang, L.¹ Cai, C.² Curran, D.P.³ Zhang, W.⁴

89
- 79955574301
- S. Dordonne B. Crousse D. B. Delpon J. Legros Chem. Commun. 2011 47 5855
- (2011) Chem. Commun. , vol.47 , pp. 5855
- Dordonne, S.¹ Crousse, B.² Delpon, D.B.³ Legros, J.⁴

90
- 79960437210
- T. Miura S. Nishida A. Masuda N. Tada A. Itoh Tetrahedron Lett. 2011 52 4158
- (2011) Tetrahedron Lett. , vol.52 , pp. 4158
- Miura, T.¹ Nishida, S.² Masuda, A.³ Tada, N.⁴ Itoh, A.⁵

91
- 79251521007
- T. Miura K. Nakashima N. Tada A. Itoh Chem. Commun. 2011 47 1875
- (2011) Chem. Commun. , vol.47 , pp. 1875
- Miura, T.¹ Nakashima, K.² Tada, N.³ Itoh, A.⁴

92
- 64249158222
- T. Miura Y. Yasaku N. Koyata Y. Murakami N. Imai Tetrahedron Lett. 2009 50 2632
- (2009) Tetrahedron Lett. , vol.50 , pp. 2632
- Miura, T.¹ Yasaku, Y.² Koyata, N.³ Murakami, Y.⁴ Imai, N.⁵

93
- 79960959357
- T. Miura M. Ina K. Imai K. Nakashima Y. Yasaku N. Koyata Y. Murakami N. Imai N. Tada A. Itoh Tetrahedron: Asymmetry 2011 22 1028
- (2011) Tetrahedron: Asymmetry , vol.22 , pp. 1028
- Miura, T.¹ Ina, M.² Imai, K.³ Nakashima, K.⁴ Yasaku, Y.⁵ Koyata, N.⁶ Murakami, Y.⁷ Imai, N.⁸ Tada, N.⁹ Itoh, A.¹⁰

94
- 79551686994
- The first example of the synthesis of both enantiomeric products using two different organocatalysts that were prepared from common chiral source
- T. Miura M. Ina K. Imai K. Nakashima A. Masuda N. Imai N. Tada A. Itoh Synlett 2011 410
- (2011) Synlett , pp. 410
- Miura, T.¹ Ina, M.² Imai, K.³ Nakashima, K.⁴ Masuda, A.⁵ Imai, N.⁶ Tada, N.⁷ Itoh, A.⁸

95
- 67749137436
- We have reported fluorous chiral ligand 3 for enantioselective Simmons-Smith cyclopropanation
- K. Nakayama K. Maruoka J. Am. Chem. Soc. 2008 130 17666
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 17666
- Nakayama, K.¹ Maruoka, K.²

96
- 49549083485
- T. Miura K. Itoh Y. Yasaku N. Koyata Y. Murakami N. Imai Tetrahedron Lett. 2008 49 5813
- (2008) Tetrahedron Lett. , vol.49 , pp. 5813
- Miura, T.¹ Itoh, K.² Yasaku, Y.³ Koyata, N.⁴ Murakami, Y.⁵ Imai, N.⁶

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