SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 18, 2015, Pages 3835-3837

Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(iii)-complex catalyzed inverse-electron-demand hetero-Diels-Alder reaction

(7) Hu, Haipeng a Liu, Yangbin a Guo, Jing a Lin, Lili a Xu, Yali a Liu, Xiaohua a Feng, Xiaoming a,b

a Sichuan University (China)

b SynBio Research Platform (China)

Author keywords

[No Author keywords available]

Indexed keywords

COUMARIN DERIVATIVE; DIHYDROCOUMARIN DERIVATIVE; SCANDIUM; UNCLASSIFIED DRUG; COORDINATION COMPOUND; LACTONE; QUINONE DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; CONTROLLED STUDY; DIELS ALDER REACTION; ENANTIOSELECTIVITY; MICHAEL ADDITION; REACTION ANALYSIS; STEREOSPECIFICITY; SYNTHESIS; CHEMISTRY; CYCLOADDITION; ELECTRON; STEREOISOMERISM;

CATALYSIS; COORDINATION COMPLEXES; COUMARINS; CYCLOADDITION REACTION; ELECTRONS; LACTONES; QUINONES; SCANDIUM; STEREOISOMERISM;

EID: 84923212034 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c4cc10343b Document Type: Article

Times cited : (111)

References (44)

1
- 0004102743
- Wiley, New York
- R. D. H. Murray, J. Mendez and S. A. Brown, The Natural Coumarin: Occurrence, Chemistry, and Biochemistry, Wiley, New York, 1982
- (1982) The Natural Coumarin: Occurrence, Chemistry, and Biochemistry
- Murray, R.D.H.¹ Mendez, J.² Brown, S.A.³

2
- 0003765137
- Wiley, Chichester, UK, 1st edn
- R. O'Kennedy and R. D. Thornes, Coumarins: Biology, Applications, and Mode of Action, Wiley, Chichester, UK, 1st edn, 1997
- (1997) Coumarins: Biology, Applications, and Mode of Action
- O'Kennedy, R.¹ Thornes, R.D.²

3
- 26444461246
- C. A. Kontogiorgis D. J. Hadjipavlou-Litina J. Med. Chem. 2005 48 6400
- (2005) J. Med. Chem. , vol.48 , pp. 6400
- Kontogiorgis, C.A.¹ Hadjipavlou-Litina, D.J.²

4
- 79961098788
- Y. L. Kuang X. H. Liu L. Chang M. Wang L. L. Lin X. M. Feng Org. Lett. 2011 13 3814
- (2011) Org. Lett. , vol.13 , pp. 3814
- Kuang, Y.L.¹ Liu, X.H.² Chang, L.³ Wang, M.⁴ Lin, L.L.⁵ Feng, X.M.⁶

5
- 84902118158
- P. Niharika B. V. Ramulu G. Satyanarayana Org. Biomol. Chem. 2014 12 4347
- (2014) Org. Biomol. Chem. , vol.12 , pp. 4347
- Niharika, P.¹ Ramulu, B.V.² Satyanarayana, G.³

6
- 77950350920
- J. L. Li S. L. Zhou B. Han L. Wu Y. C. Chen Chem. Commun. 2010 46 2665
- (2010) Chem. Commun. , vol.46 , pp. 2665
- Li, J.L.¹ Zhou, S.L.² Han, B.³ Wu, L.⁴ Chen, Y.C.⁵

7
- 34547645249
- M. Marchetti O. Piccolo F. Ulgheri J. Org. Chem. 2007 72 6056
- (2007) J. Org. Chem. , vol.72 , pp. 6056
- Marchetti, M.¹ Piccolo, O.² Ulgheri, F.³

8
- 23944522515
- S. Aoki K. Yamamoto J. Yamada T. Kitamura Tetrahedron 2005 61 9291
- (2005) Tetrahedron , vol.61 , pp. 9291
- Aoki, S.¹ Yamamoto, K.² Yamada, J.³ Kitamura, T.⁴

9
- 0033597255
- M. A. Mcguire S. C. Shilcrat E. Sorenson Tetrahedron Letters 1999 40 3293
- (1999) Tetrahedron Letters , vol.40 , pp. 3293
- McGuire, M.A.¹ Shilcrat, S.C.² Sorenson, E.³

10
- 84908066004
- O. D. Engl S. P. Fritz A. Käslin H. Wennemers Org. Lett. 2014 16 5454
- (2014) Org. Lett. , vol.16 , pp. 5454
- Engl, O.D.¹ Fritz, S.P.² Käslin, A.³ Wennemers, H.⁴

11
- 77957929482
- D. F. Lu Y. J. Li Y. F. Gong J. Org. Chem. 2010 75 6900
- (2010) J. Org. Chem. , vol.75 , pp. 6900
- Lu, D.F.¹ Li, Y.J.² Gong, Y.F.³

12
- 84868355594
- C. B. Jacobsen Ł. Albrecht J. Udmark K. A. Jørgensen Org. Lett. 2012 14 5526
- (2012) Org. Lett. , vol.14 , pp. 5526
- Jacobsen, C.B.¹ Albrecht Ł.² Udmark, J.³ Jørgensen, K.A.⁴

13
- 33746170307
- J. Barluenga F. Andina F. Aznar Org. Lett. 2006 8 2703
- (2006) Org. Lett. , vol.8 , pp. 2703
- Barluenga, J.¹ Andina, F.² Aznar, F.³

14
- 80055085165
- B. C. Hong P. Kotame G. H. Lee Org. Lett. 2011 13 5758
- (2011) Org. Lett. , vol.13 , pp. 5758
- Hong, B.C.¹ Kotame, P.² Lee, G.H.³

15
- 84923129379
- X. H. Li P. Fang D. Chen X. L. Hou Org. Chem. Front. 2014 1 969
- (2014) Org. Chem. Front. , vol.1 , pp. 969
- Li, X.H.¹ Fang, P.² Chen, D.³ Hou, X.L.⁴

16
- 58149175558
- E. Alden-Danforth M. T. Scerba T. Lectka Org. Lett. 2008 10 4951
- (2008) Org. Lett. , vol.10 , pp. 4951
- Alden-Danforth, E.¹ Scerba, M.T.² Lectka, T.³

17
- 72149087428
- For the cycloaddition reactions of azlactones, see
- H. Lv L. You S. Ye Adv. Synth. Catal. 2009 351 2822
- (2009) Adv. Synth. Catal. , vol.351 , pp. 2822
- Lv, H.¹ You, L.² Ye, S.³

18
- 84880015183
- S. X. Dong X. H. Liu Y. Zhu P. He L. L. Lin X. M. Feng J. Am. Chem. Soc. 2013 135 10026
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 10026
- Dong, S.X.¹ Liu, X.H.² Zhu, Y.³ He, P.⁴ Lin, L.L.⁵ Feng, X.M.⁶

19
- 84882411324
- W. S. Sun G. M. Zhu C. Y. Wu G. F. Li L. Hong R. Wang Angew. Chem. Int. Ed. 2013 52 8633
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 8633
- Sun, W.S.¹ Zhu, G.M.² Wu, C.Y.³ Li, G.F.⁴ Hong, L.⁵ Wang, R.⁶

20
- 84875752965
- X. X. Jiang H. Zhu X. M. Shi Y. Zhong Y. F. Li R. Wang Adv. Synth. Catal. 2013 355 308
- (2013) Adv. Synth. Catal. , vol.355 , pp. 308
- Jiang, X.X.¹ Zhu, H.² Shi, X.M.³ Zhong, Y.⁴ Li, Y.F.⁵ Wang, R.⁶

21
- 84894426840
- For examples of inverse-electron-demand hetero-Diels-Alder reactions, see
- F. Esteban R. Alfaro F. Yuste A. Parra J. L. J. Ruano J. Alemán Eur. J. Org. Chem. 2014 1395
- (2014) Eur. J. Org. Chem. , pp. 1395
- Esteban, F.¹ Alfaro, R.² Yuste, F.³ Parra, A.⁴ Ruano, J.L.J.⁵ Alemán, J.⁶

22
- 0013059152
- K. Gademann D. E. Chavez E. N. Jacobsen Angew. Chem. 2002 114 3185
- (2002) Angew. Chem. , vol.114 , pp. 3185
- Gademann, K.¹ Chavez, D.E.² Jacobsen, E.N.³

23
- 84871995353
- Ł. Albrecht G. Dickmeiss C. F. Weise C. Rodrguez-Escrich K. A. Jørgensen Angew. Chem. Int. Ed. 2012 51 13109
- (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 13109
- Albrecht Ł.¹ Dickmeiss, G.² Weise, C.F.³ Rodrguez-Escrich, C.⁴ Jørgensen, K.A.⁵

24
- 33750071714
- C. J. Abraham D. H. Paull M. T. Scerba J. W. Grebinski T. Lectka J. Am. Chem. Soc. 2006 128 13370
- (2006) J. Am. Chem. Soc. , vol.128 , pp. 13370
- Abraham, C.J.¹ Paull, D.H.² Scerba, M.T.³ Grebinski, J.W.⁴ Lectka, T.⁵

25
- 84870531420
- R. A. A. Foster M. C. Willis Chem. Soc. Rev. 2013 42 63
- (2013) Chem. Soc. Rev. , vol.42 , pp. 63
- Foster, R.A.A.¹ Willis, M.C.²

26
- 84878640125
- A. C. Knall C. Slugovc Chem. Soc. Rev. 2013 42 5131
- (2013) Chem. Soc. Rev. , vol.42 , pp. 5131
- Knall, A.C.¹ Slugovc, C.²

27
- 84880100773
- X. X. Jiang R. Wang Chem. Rev. 2013 113 5515
- (2013) Chem. Rev. , vol.113 , pp. 5515
- Jiang, X.X.¹ Wang, R.²

28
- 85081861833
- 3161655
- D. F. Reinhold, N. J. North Plainfield, J. H. Markillie, K. Mich and M. Sletzinger, US Pat., 3161655, 1964
- (1964) US Pat.
- Reinhold, D.F.¹ North Plainfield, N.J.² Markillie, J.H.³ Mich, K.⁴ Sletzinger, M.⁵

29
- 0027936714
- J. G. Rico Tetrahedron Letter 1994 35 6599
- (1994) Tetrahedron Letter , vol.35 , pp. 6599
- Rico, J.G.¹

30
- 0033524886
- D. Cabaret S. A. Adediran M. J. Garcia Gonzalez R. F. Pratt M. Wakselman J. Org. Chem. 1999 64 713
- (1999) J. Org. Chem. , vol.64 , pp. 713
- Cabaret, D.¹ Adediran, S.A.² Garcia Gonzalez, M.J.³ Pratt, R.F.⁴ Wakselman, M.⁵

31
- 0011196019
- 9312103
- P. R. Bovy, M. Miyano, J. G. Rico and T. E. Rogers, PCT Int. Appl., 9312103, 1993
- (1993) PCT Int. Appl.
- Bovy, P.R.¹ Miyano, M.² Rico, J.G.³ Rogers, T.E.⁴

32
- 80054721905
- For selected examples using chiral N,N′-dioxide ligands, see
- S. X. Dong X. H. Liu Y. L. Zhang L. L. Lin X. M. Feng Org. Lett. 2011 13 5060
- (2011) Org. Lett. , vol.13 , pp. 5060
- Dong, S.X.¹ Liu, X.H.² Zhang, Y.L.³ Lin, L.L.⁴ Feng, X.M.⁵

33
- 80051741339
- X. H. Liu L. L. Lin X. M. Feng Acc. Chem. Res. 2011 44 574
- (2011) Acc. Chem. Res. , vol.44 , pp. 574
- Liu, X.H.¹ Lin, L.L.² Feng, X.M.³

34
- 0003458658
- Elsevier, Oxford, 3th edn
- A. Hassner and I. Namboothiri, Organic Syntheses Based on Name Reactions, Elsevier, Oxford, 3th edn, 2011, p. 408
- (2011) Organic Syntheses Based on Name Reactions , pp. 408
- Hassner, A.¹ Namboothiri, I.²

35
- 84863280512
- ed. V. A. Greene, Nova Science, New York
- X. M. Feng and X. H. Liu, Scandium Compounds, Productions and Applications, ed., V. A. Greene, Nova Science, New York, 2011, pp. 1-48
- (2011) Scandium Compounds, Productions and Applications , pp. 1-48
- Feng, X.M.¹ Liu, X.H.²

36
- 84867727646
- K. Zheng L. L. Lin X. M. Feng Acta Chim. Sinica. 2012 70 1785
- (2012) Acta Chim. Sinica. , vol.70 , pp. 1785
- Zheng, K.¹ Lin, L.L.² Feng, X.M.³

37
- 84895172220
- J. Ji L. L. Lin Y. H. Zhang Y. B. Liu X. H. Liu X. M. Feng Adv. Synth. Catal. 2013 355 2764
- (2013) Adv. Synth. Catal. , vol.355 , pp. 2764
- Ji, J.¹ Lin, L.L.² Zhang, Y.H.³ Liu, Y.B.⁴ Liu, X.H.⁵ Feng, X.M.⁶

38
- 84901586222
- X. H. Liu L. L. Lin X. M. Feng Org. Chem. Front. 2014 1 298
- (2014) Org. Chem. Front. , vol.1 , pp. 298
- Liu, X.H.¹ Lin, L.L.² Feng, X.M.³

39
- 84904857282
- M. S. Xie X. X. Wu G. Wang L. L. Lin X. M. Feng Acta Chim. Sinica. 2014 72 856
- (2014) Acta Chim. Sinica. , vol.72 , pp. 856
- Xie, M.S.¹ Wu, X.X.² Wang, G.³ Lin, L.L.⁴ Feng, X.M.⁵

40
- 0010867053
- For the selected examples of QMs, see
- L. Jurd Tetrahedron 1977 33 163
- (1977) Tetrahedron , vol.33 , pp. 163
- Jurd, L.¹

41
- 84889266778
- ed., Wiley, New York
- Quinone Methides, ed., S. E. Rokita, Wiley, New York, 2009
- (2009) Quinone Methides
- Rokita, S.E.¹

42
- 0003719612
- Academic Press, San Diego
- D. L. Boger and S. M. Weinreb, Hetero Diels-Alder Methodology in Organic Synthesis, Academic Press, San Diego, 1987
- (1987) Hetero Diels-Alder Methodology in Organic Synthesis
- Boger, D.L.¹ Weinreb, S.M.²

43
- 84870868655
- Y. Luan S. E. Schaus J. Am. Chem. Soc. 2012 134 19965
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 19965
- Luan, Y.¹ Schaus, S.E.²

44
- 84880835415
- CCDC (3d) for more data see ESI
- H. Lv W. Q. Jia L. H. Sun S. Ye Angew. Chem. Int. Ed. 2013 52 8607
- (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 8607
- Lv, H.¹ Jia, W.Q.² Sun, L.H.³ Ye, S.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.