SCOPUS 정보 검색 플랫폼

Organic and Biomolecular Chemistry

Volumn 9, Issue 14, 2011, Pages 5297-5302

Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael-enolation-cyclization reaction

(3) Ren, Qiao a Gao, Yaojun a Wang, Jian a

a NATIONAL UNIVERSITY OF SINGAPORE (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

BIFUNCTIONAL; CASCADE REACTIONS; ONE POT; STEREO-SELECTIVE; STEREOGENIC CENTERS;

CATALYSIS; STEREOSELECTIVITY; THIOUREAS; UREA;

CYCLIZATION;

AMINE; PYRAN DERIVATIVE; THIOUREA;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

AMINES; CATALYSIS; CYCLIZATION; MOLECULAR STRUCTURE; PYRANS; STEREOISOMERISM; THIOUREA;

EID: 79959797938 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c1ob05477e Document Type: Article

Times cited : (27)

References (34)

1
- 33947198541
- D. Enders C. Grondal M. R. M. Hüttl Angew. Chem., Int. Ed. 2007 119 1570
- (2007) Angew. Chem., Int. Ed. , vol.119 , pp. 1570
- Enders, D.¹ Grondal, C.² Hüttl, M.R.M.³

2
- 34347335758
- A. M. Walji D. W. C. MacMillan Synlett. 2007 1477
- (2007) Synlett. , pp. 1477
- Walji, A.M.¹ MacMillan, D.W.C.²

3
- 77649087999
- For recent selected examples of cascade reactions, see:
- C. Grondal M. Jeanty D. Enders Nat. Chem. 2010 2 167
- (2010) Nat. Chem. , vol.2 , pp. 167
- Grondal, C.¹ Jeanty, M.² Enders, D.³

4
- 2442435852
- Y. Yamamoto N. Momiyama H. Yamamoto J. Am. Chem. Soc. 2004 126 5962
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 5962
- Yamamoto, Y.¹ Momiyama, N.² Yamamoto, H.³

5
- 27544485685
- Y. Huang A. M. Walji C. H. Larsen D. W. C. MacMillan J. Am. Chem. Soc. 2005 127 15051
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 15051
- Huang, Y.¹ Walji, A.M.² Larsen, C.H.³ MacMillan, D.W.C.⁴

6
- 27544489337
- J. W. Yang M. T. H. Fonseca B. List J. Am. Chem. Soc. 2005 127 15036
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 15036
- Yang, J.W.¹ Fonseca, M.T.H.² List, B.³

7
- 27844440320
- M. Marigo T. Schulte J. Franzen K. A. Jørgensen J. Am. Chem. Soc. 2005 127 15710
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 15710
- Marigo, M.¹ Schulte, T.² Franzen, J.³ Jørgensen, K.A.⁴

8
- 33745211429
- D. Enders M. R. M. Huttl C. Grondal G. Raabe Nature 2006 441 861
- (2006) Nature , vol.441 , pp. 861
- Enders, D.¹ Huttl, M.R.M.² Grondal, C.³ Raabe, G.⁴

9
- 33747594792
- W. Wang H. Li J. Wang L. Zu J. Am. Chem. Soc. 2006 128 10354
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 10354
- Wang, W.¹ Li, H.² Wang, J.³ Zu, L.⁴

10
- 33750307526
- R. Rios H. Sunden I. Ibrahem G.-L. Zhao L. Eriksson A. Córdova Tetrahedron Lett. 2006 47 8547
- (2006) Tetrahedron Lett. , vol.47 , pp. 8547
- Rios, R.¹ Sunden, H.² Ibrahem, I.³ Zhao, G.-L.⁴ Eriksson, L.⁵ Córdova, A.⁶

11
- 33846250463
- H. Sunden I. Ibrahem G.-L. Zhao L. Eriksson A. Córdova Chem.-Eur. J. 2007 12 574
- (2007) Chem.-Eur. J. , vol.12 , pp. 574
- Sunden, H.¹ Ibrahem, I.² Zhao, G.-L.³ Eriksson, L.⁴ Córdova, A.⁵

12
- 34250849026
- H. Li L. Zu H. Xie J. Wang W. Jiang W. Wang Angew. Chem., Int. Ed. 2007 46 3732
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 3732
- Li, H.¹ Zu, L.² Xie, H.³ Wang, J.⁴ Jiang, W.⁵ Wang, W.⁶

13
- 34447294558
- Y. Hayashi T. Okano S. Aratake D. Hazelard Angew. Chem., Int. Ed. 2007 46 4922
- (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4922
- Hayashi, Y.¹ Okano, T.² Aratake, S.³ Hazelard, D.⁴

14
- 35048854739
- For selected examples of the application of 1,2-diones in organic synthesis, see:
- J. L. Vicario S. Reboredo D. BadNa L. Carrillo Angew. Chem. Int. Ed. 2007 119 5260
- (2007) Angew. Chem. Int. Ed. , vol.119 , pp. 5260
- Vicario, J.L.¹ Reboredo, S.² Badna, D.³ Carrillo, L.⁴

15
- 0034622915
- A. F. Parsons D. Williams Tetrahedron Lett. 2000 56 7217
- (2000) Tetrahedron Lett. , vol.56 , pp. 7217
- Parsons, A.F.¹ Williams, D.²

16
- 33748058878
- C. Wolf S. Liu J. Am. Chem. Soc. 2006 128 10996
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 10996
- Wolf, C.¹ Liu, S.²

17
- 33644989711
- X. Li R. Vince Bioorg. Med. Chem. Lett. 2006 14 2942
- (2006) Bioorg. Med. Chem. Lett. , vol.14 , pp. 2942
- Li, X.¹ Vince, R.²

18
- 26444502597
- H. Maruoka N. Kashige F. Miake T. Yamaguchi Chem. Pharm. Bull. 2005 53 1359
- (2005) Chem. Pharm. Bull. , vol.53 , pp. 1359
- Maruoka, H.¹ Kashige, N.² Miake, F.³ Yamaguchi, T.⁴

19
- 2942519827
- Z. Zhao D. D. Wisnoski S. E. Wolkenberg W. H. Leister Y. Wang C. W. Lindsley Tetrahedron Lett. 2004 45 4873
- (2004) Tetrahedron Lett. , vol.45 , pp. 4873
- Zhao, Z.¹ Wisnoski, D.D.² Wolkenberg, S.E.³ Leister, W.H.⁴ Wang, Y.⁵ Lindsley, C.W.⁶

20
- 12744259937
- D. Curiel A. Cowley P. D. Beer Chem. Commun. 2005 2 236
- (2005) Chem. Commun. , vol.2 , pp. 236
- Curiel, D.¹ Cowley, A.² Beer, P.D.³

21
- 12444313914
- Y. Ding J. Girardet K. L. Smith G. Larson B. Prigaro V. C. H. Lai W. Zhong J. Z. Wu Bioorg. Med. Chem. Lett. 2005 15 675
- (2005) Bioorg. Med. Chem. Lett. , vol.15 , pp. 675
- Ding, Y.¹ Girardet, J.² Smith, K.L.³ Larson, G.⁴ Prigaro, B.⁵ Lai, V.C.H.⁶ Zhong, W.⁷ Wu, J.Z.⁸

22
- 33749238378
- S. Wu A. Fluxe J. M. Janusz J. B. Sheffer G. Browning B. B. K. Cobum R. Hedges M. Murawsky B. Fang G. M. Fadayel M. Hare L. Djandjighian Bioorg. Med. Chem. Lett. 2006 16 5859
- (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 5859
- Wu, S.¹ Fluxe, A.² Janusz, J.M.³ Sheffer, J.B.⁴ Browning, G.⁵ Cobum, B.B.K.⁶ Hedges, R.⁷ Murawsky, M.⁸ Fang, B.⁹ Fadayel, G.M.¹⁰ Hare, M.¹¹ Djandjighian, L.¹²

23
- 34247641363
- I. Held S. Xu H. Zipse Synthesis 2007 1185
- (2007) Synthesis , pp. 1185
- Held, I.¹ Xu, S.² Zipse, H.³

24
- 34547938550
- S. Liu C. Wolf Org. Lett. 2007 9 2965
- (2007) Org. Lett. , vol.9 , pp. 2965
- Liu, S.¹ Wolf, C.²

25
- 70349777755
- M. Rueping A. Kuenkel F. Tato J. W. Bats Angew. Chem., Int. Ed. 2009 48 3699
- (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 3699
- Rueping, M.¹ Kuenkel, A.² Tato, F.³ Bats, J.W.⁴

26
- 77950790406
- M. Rueping A. Kuenkel R. Fröhlich Chem.-Eur. J. 2010 16 4173
- (2010) Chem.-Eur. J. , vol.16 , pp. 4173
- Rueping, M.¹ Kuenkel, A.² Fröhlich, R.³

27
- 79959773496
- D. Ding C.-G. Zhao Q. S. Guo H. Arman Tetrahedron 2010 66 4424
- (2010) Tetrahedron , vol.66 , pp. 4424
- Ding, D.¹ Zhao, C.-G.² Guo, Q.S.³ Arman, H.⁴

28
- 19544393388
- B. Vakulya S. Varga A. Csampai T. Soós Org. Lett. 2005 7 1967
- (2005) Org. Lett. , vol.7 , pp. 1967
- Vakulya, B.¹ Varga, S.² Csampai, A.³ Soós, T.⁴

29
- 25444473664
- J. Ye D. J. Dixon P. S. Hynes Chem. Commun. 2005 4481
- (2005) Chem. Commun. , pp. 4481
- Ye, J.¹ Dixon, D.J.² Hynes, P.S.³

30
- 26844450640
- For some examples of our group's developed bifunctional indane thiourea catalyzed reactions, see:
- S. H. McCooey S. J. Connon Angew. Chem., Int. Ed. 2005 44 6367
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6367
- McCooey, S.H.¹ Connon, S.J.²

31
- 78649685991
- Y. J. Gao Q. Ren H. Wu M. G. Li J. Wang Chem. Commun. 2010 46 9232
- (2010) Chem. Commun. , vol.46 , pp. 9232
- Gao, Y.J.¹ Ren, Q.² Wu, H.³ Li, M.G.⁴ Wang, J.⁵

32
- 78649959108
- Q. Ren Y. J. Gao J. Wang Chem.-Eur. J. 2010 16 13594
- (2010) Chem.-Eur. J. , vol.16 , pp. 13594
- Ren, Q.¹ Gao, Y.J.² Wang, J.³

33
- 79955587686
- Y. J. Gao Q. Ren W.-Y. Siau J. Wang Chem. Commun. 2011 47 5819
- (2011) Chem. Commun. , vol.47 , pp. 5819
- Gao, Y.J.¹ Ren, Q.² Siau, W.-Y.³ Wang, J.⁴

34
- 79955409865
- CCDC 800064
- Y. J. Gao Q. Ren S.-M. Ang J. Wang Org. Biomol. Chem. 2011 9 3691
- (2011) Org. Biomol. Chem. , vol.9 , pp. 3691
- Gao, Y.J.¹ Ren, Q.² Ang, S.-M.³ Wang, J.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.