SCOPUS 정보 검색 플랫폼

Volumn 51, Issue 58, 2015, Pages 11689-11692

The N,N′-dioxide/Ni(II)-catalyzed asymmetric inverse-electron-demand hetero-Diels-Alder reaction of methyleneindolinones with hetero-substituted alkenes

(6) Zhou, Yuhang a Lin, Lili a Yin, Chengkai a Wang, Zhengmeng a Liu, Xiaohua a Feng, Xiaoming a

a Sichuan University (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; CARBENE; INDOLE DERIVATIVE; NICKEL; OXIDE;

ARTICLE; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; CHEMICAL STRUCTURE; CHIRALITY; CRYSTAL STRUCTURE; DIASTEREOISOMER; DIELS ALDER REACTION; ELECTRON; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SUBSTITUTION REACTION; X RAY CRYSTALLOGRAPHY; X RAY DIFFRACTION;

EID: 84936130404 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c5cc04245c Document Type: Article

Times cited : (28)

References (37)

1
- 0000016331
- S. Danishefsky Acc. Chem. Res. 1981 14 400
- (1981) Acc. Chem. Res. , vol.14 , pp. 400
- Danishefsky, S.¹

2
- 4244033876
- H. B. Kagan O. Riant Chem. Rev. 1992 92 1007
- (1992) Chem. Rev. , vol.92 , pp. 1007
- Kagan, H.B.¹ Riant, O.²

3
- 0033936085
- J. S. Johnson D. A. Evans Acc. Chem. Res. 2000 33 325
- (2000) Acc. Chem. Res. , vol.33 , pp. 325
- Johnson, J.S.¹ Evans, D.A.²

4
- 0036259981
- K. C. Nicolaou S. A. Snyder T. Montagnon G. Vassilikogiannakis Angew. Chem., Int. Ed. 2002 41 1668
- (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1668
- Nicolaou, K.C.¹ Snyder, S.A.² Montagnon, T.³ Vassilikogiannakis, G.⁴

5
- 0036263839
- E. J. Corey Angew. Chem., Int. Ed. 2002 41 1650
- (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1650
- Corey, E.J.¹

6
- 4544247886
- K. A. Jørgensen Eur. J. Org. Chem. 2004 2093
- (2004) Eur. J. Org. Chem. , pp. 2093
- Jørgensen, K.A.¹

7
- 34548807523
- L. L. Lin X. H. Liu X. M. Feng Synlett 2007 2147
- (2007) Synlett , pp. 2147
- Lin, L.L.¹ Liu, X.H.² Feng, X.M.³

8
- 84857046098
- H. Pellissier Tetrahedron 2012 68 2197
- (2012) Tetrahedron , vol.68 , pp. 2197
- Pellissier, H.¹

9
- 84907820575
- For selected examples of enantioselective IED hetero-DA reactions, see
- V. Eschenbrenner-Lux K. Kumar H. Waldmann Angew. Chem., Int. Ed. 2014 53 11146
- (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 11146
- Eschenbrenner-Lux, V.¹ Kumar, K.² Waldmann, H.³

10
- 78249231383
- Y. Zhu X. H. Chen M. S. Xie S. X. Dong Z. Qiao L. L. Lin X. H. Liu X. M. Feng Chem.-Eur. J. 2010 16 11963
- (2010) Chem.-Eur. J. , vol.16 , pp. 11963
- Zhu, Y.¹ Chen, X.H.² Xie, M.S.³ Dong, S.X.⁴ Qiao, Z.⁵ Lin, L.L.⁶ Liu, X.H.⁷ Feng, X.M.⁸

11
- 79959939047
- Y. Zhu M. S. Xie S. X. Dong X. H. Zhao L. L. Lin X. H. Liu X. M. Feng Chem.-Eur. J. 2011 17 8202
- (2011) Chem.-Eur. J. , vol.17 , pp. 8202
- Zhu, Y.¹ Xie, M.S.² Dong, S.X.³ Zhao, X.H.⁴ Lin, L.L.⁵ Liu, X.H.⁶ Feng, X.M.⁷

12
- 84862908238
- J. Lv L. Zhang S. Hu J.-P. Cheng S. Luo Chem.-Eur. J. 2012 18 799
- (2012) Chem.-Eur. J. , vol.18 , pp. 799
- Lv, J.¹ Zhang, L.² Hu, S.³ Cheng, J.-P.⁴ Luo, S.⁵

13
- 84880100773
- X. Jiang R. Wang Chem. Rev. 2013 113 5515
- (2013) Chem. Rev. , vol.113 , pp. 5515
- Jiang, X.¹ Wang, R.²

14
- 84883517822
- J. Lv L. Zhang S. Luo J.-P. Cheng Angew. Chem., Int. Ed. 2013 52 9786
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 9786
- Lv, J.¹ Zhang, L.² Luo, S.³ Cheng, J.-P.⁴

15
- 84902208810
- For selected asymmetric examples of cycloadditions using methyleneindolinones to afford spirooxindoles, see
- Y. Matsumura T. Suzuki A. Sakakura K. Ishihara Angew. Chem., Int. Ed. 2014 53 6131
- (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 6131
- Matsumura, Y.¹ Suzuki, T.² Sakakura, A.³ Ishihara, K.⁴

16
- 79953845548
- Z.-J. Jia H. Jiang J.-L. Li B. Gschwend Q.-Z. Li X. Yin J. Grouleff Y.-C. Chen K. A. Jørgensen J. Am. Chem. Soc. 2011 133 5053
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 5053
- Jia, Z.-J.¹ Jiang, H.² Li, J.-L.³ Gschwend, B.⁴ Li, Q.-Z.⁵ Yin, X.⁶ Grouleff, J.⁷ Chen, Y.-C.⁸ Jørgensen, K.A.⁹

17
- 84876500903
- G. L. Li T. Liang L. Wojtas J. C. Antilla Angew. Chem., Int. Ed. 2013 52 4628
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 4628
- Li, G.L.¹ Liang, T.² Wojtas, L.³ Antilla, J.C.⁴

18
- 55949087431
- T. S. Kam S. J. Tan S. W. Ng K. Komiyama Org. Lett. 2008 10 3749
- (2008) Org. Lett. , vol.10 , pp. 3749
- Kam, T.S.¹ Tan, S.J.² Ng, S.W.³ Komiyama, K.⁴

19
- 84865250065
- The synthesis of dihydropyran-fused indoles, see
- M. A. Beniddir M.-T. Martin M.-E. Tran Huu Dau P. Grellier P. Rasoanaivo F. Guéritte M. Litaudon Org. Lett. 2012 14 4162
- (2012) Org. Lett. , vol.14 , pp. 4162
- Beniddir, M.A.¹ Martin, M.-T.² Tran Huu Dau, M.-E.³ Grellier, P.⁴ Rasoanaivo, P.⁵ Guéritte, F.⁶ Litaudon, M.⁷

20
- 0008207942
- T. Sakakibara S. Karasumaru I. Kawano J. Am. Chem. Soc. 1985 107 6417
- (1985) J. Am. Chem. Soc. , vol.107 , pp. 6417
- Sakakibara, T.¹ Karasumaru, S.² Kawano, I.³

21
- 33746297623
- H. Miyamoto Y. Okawa A. Nakazaki S. Kobayashi Angew. Chem., Int. Ed. 2006 45 2274
- (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 2274
- Miyamoto, H.¹ Okawa, Y.² Nakazaki, A.³ Kobayashi, S.⁴

22
- 68149176713
- B. W. Boal A. W. Schammel N. K. Garg Org. Lett. 2009 11 3458
- (2009) Org. Lett. , vol.11 , pp. 3458
- Boal, B.W.¹ Schammel, A.W.² Garg, N.K.³

23
- 84880009060
- X. Zhang Z.-P. Yang C. Liu S.-L. You Chem. Sci. 2013 4 3239
- (2013) Chem. Sci. , vol.4 , pp. 3239
- Zhang, X.¹ Yang, Z.-P.² Liu, C.³ You, S.-L.⁴

24
- 77957921131
- H. Lv X.-Y. Chen L.-H. Sun S. Ye J. Org. Chem. 2010 75 6973
- (2010) J. Org. Chem. , vol.75 , pp. 6973
- Lv, H.¹ Chen, X.-Y.² Sun, L.-H.³ Ye, S.⁴

25
- 84861820257
- L. M. Yang F. Wang P. J. Chua Y. B. Lv L.-J. Zhong G. Zhong Org. Lett. 2012 14 2894
- (2012) Org. Lett. , vol.14 , pp. 2894
- Yang, L.M.¹ Wang, F.² Chua, P.J.³ Lv, Y.B.⁴ Zhong, L.-J.⁵ Zhong, G.⁶

26
- 84929598167
- F. Wang Z. Li J. Wang X. Li J.-P. Cheng J. Org. Chem. 2015 80 5279
- (2015) J. Org. Chem. , vol.80 , pp. 5279
- Wang, F.¹ Li, Z.² Wang, J.³ Li, X.⁴ Cheng, J.-P.⁵

27
- 84880264709
- For selected asymmetric examples of IED hetero-DA reactions using enecarbamate derivatives, see
- Z. Mao W. Li Y. Shi H. Mao A. Lin C. Zhu Y. Cheng Chem.-Eur. J. 2013 19 9754
- (2013) Chem.-Eur. J. , vol.19 , pp. 9754
- Mao, Z.¹ Li, W.² Shi, Y.³ Mao, H.⁴ Lin, A.⁵ Zhu, C.⁶ Cheng, Y.⁷

28
- 58549106138
- S. Barroso G. Blay M. C. Muñoz J. R. Pedro Adv. Synth. Catal. 2009 351 107
- (2009) Adv. Synth. Catal. , vol.351 , pp. 107
- Barroso, S.¹ Blay, G.² Muñoz, M.C.³ Pedro, J.R.⁴

29
- 79959379896
- A. Barba S. Barroso G. Blay L. Cardona M. Melegari J. R. Pedro Synlett 2011 1592
- (2011) Synlett , pp. 1592
- Barba, A.¹ Barroso, S.² Blay, G.³ Cardona, L.⁴ Melegari, M.⁵ Pedro, J.R.⁶

30
- 84931283680
- For selected asymmetric examples based on chiral N,N′-dioxides, see
- Y. H. Zhou Y. Zhu L. L. Lin Y. L. Zhang J. F. Zheng X. H. Liu X. M. Feng Chem.-Eur. J. 2014 20 16753
- (2014) Chem.-Eur. J. , vol.20 , pp. 16753
- Zhou, Y.H.¹ Zhu, Y.² Lin, L.L.³ Zhang, Y.L.⁴ Zheng, J.F.⁵ Liu, X.H.⁶ Feng, X.M.⁷

31
- 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

32
- 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

33
- 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

34
- 84901586222
- CCDC (3t). The absolute configuration of 3a-3s (2R,4R), 3u-3v (2R,4R), and 3w (2S,4R), was determined by comparison of the CD spectra with that of 3t. The absolute configuration of 3x (4aS,5R,11aR) was predicted by the absolute configuration of 3t and by a NOESY effect. The absolute configuration of 3aa and 5a-5g (2R,4R) were assigned by analogy For more data see ESI
- 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

35
- 84874045843
- G. Wang X. H. Liu T. Y. Huang Y. L. Kuang L. L. Lin X. M. Feng Org. Lett. 2013 15 76
- (2013) Org. Lett. , vol.15 , pp. 76
- Wang, G.¹ Liu, X.H.² Huang, T.Y.³ Kuang, Y.L.⁴ Lin, L.L.⁵ Feng, X.M.⁶

36
- 84906086444
- X. J. Lian S. S. Guo G. Wang L. L. Lin X. H. Liu X. M. Feng J. Org. Chem. 2014 79 7703
- (2014) J. Org. Chem. , vol.79 , pp. 7703
- Lian, X.J.¹ Guo, S.S.² Wang, G.³ Lin, L.L.⁴ Liu, X.H.⁵ Feng, X.M.⁶

37
- 84904162534
- H. F. Zheng P. He Y. B. Liu Y. L. Zhang X. H. Liu L. L. Lin X. M. Feng Chem. Commun. 2014 50 8794
- (2014) Chem. Commun. , vol.50 , pp. 8794
- Zheng, H.F.¹ He, P.² Liu, Y.B.³ Zhang, Y.L.⁴ Liu, X.H.⁵ Lin, L.L.⁶ Feng, X.M.⁷

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.