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Volumn 13, Issue 8, 2015, Pages 2260-2263

A novel enantioselective synthesis of 6H-dibenzopyran derivatives by combined palladium/norbornene and cinchona alkaloid catalysis

(6) Xu, Di a Dai, Li a Catellani, Marta b Motti, Elena b Della Ca', Nicola b Zhou, Zhiming a

a BEIJING INSTITUTE OF TECHNOLOGY (China)

b UNIVERSITY OF PARMA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; METABOLITES; NITROGEN COMPOUNDS; ORGANOMETALLICS; SYNTHESIS (CHEMICAL);

CINCHONA ALKALOID; ENANTIOSELECTIVE SYNTHESIS; ONE-POT REACTION;

ENANTIOSELECTIVITY;

CINCHONA;

6H-DIBENZOPYRAN; BENZOPYRAN DERIVATIVE; CINCHONA ALKALOID; NORBORNANE DERIVATIVE; ORGANOMETALLIC COMPOUND; PALLADIUM;

CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

BENZOPYRANS; CATALYSIS; CINCHONA ALKALOIDS; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; NORBORNANES; ORGANOMETALLIC COMPOUNDS; PALLADIUM; STEREOISOMERISM;

EID: 84922831506 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c4ob02551b Document Type: Article

Times cited : (27)

References (43)

1
- 84874110939
- A. Ahmed S. Dhara J. K. Ray Tetrahedron Lett. 2013 54 1673
- (2013) Tetrahedron Lett. , vol.54 , pp. 1673
- Ahmed, A.¹ Dhara, S.² Ray, J.K.³

2
- 12144286283
- S. W. Elmore J. K. Pratt M. J. Coghlan Y. Mao B. E. Green D. D. Anderson M. A. Stashko C. W. Lin D. Falls M. Nakane L. Miller C. M. Tyree J. N. Miner B. Lane Bioorg. Med. Chem. Lett. 2004 14 1721
- (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 1721
- Elmore, S.W.¹ Pratt, J.K.² Coghlan, M.J.³ Mao, Y.⁴ Green, B.E.⁵ Anderson, D.D.⁶ Stashko, M.A.⁷ Lin, C.W.⁸ Falls, D.⁹ Nakane, M.¹⁰ Miller, L.¹¹ Tyree, C.M.¹² Miner, J.N.¹³ Lane, B.¹⁴

3
- 84997401634
- P. Melloni, P. Salvatori and P. P. Lovisolo, U.S. Patent, 4463001, 1984
- (1984) U.S. Patent , pp. 4463001
- Melloni, P.¹ Salvatori, P.² Lovisolo, P.P.³

4
- 84872193414
- M. G. Ahmed D. Slade W. Gul T. E. A. Alfy D. Ferreira M. A. Elsohly Recent Pat. CNS Drug Discov. 2009 4 118
- (2009) Recent Pat. CNS Drug Discov. , vol.4 , pp. 118
- Ahmed, M.G.¹ Slade, D.² Gul, W.³ Alfy, T.E.A.⁴ Ferreira, D.⁵ Elsohly, M.A.⁶

5
- 0029941536
- R. E. TenBrink C. L. Bergh J. N. Duncan D. W. Harris R. M. Huff R. A. Lahti C. F. Lawson B. S. Lutzke I. J. Martin S. A. Rees S. K. Schlachter J. C. Sih M. W. Smith J. Med. Chem. 1996 39 2435
- (1996) J. Med. Chem. , vol.39 , pp. 2435
- Tenbrink, R.E.¹ Bergh, C.L.² Duncan, J.N.³ Harris, D.W.⁴ Huff, R.M.⁵ Lahti, R.A.⁶ Lawson, C.F.⁷ Lutzke, B.S.⁸ Martin, I.J.⁹ Rees, S.A.¹⁰ Schlachter, S.K.¹¹ Sih, J.C.¹² Smith, M.W.¹³

6
- 85043038344
- 6506766 B1 20030114
- M. J. Coghlan, J. P. Edwards, S. W. Elmore, T. K. Jones, M. E. Kort, P. R. Kym, J. L. Moore, J. K. Pratt and A. X. Wang, U.S. Patent, US 6506766 B1 20030114, 2003
- (2003) U.S. Patent , pp. US
- Coghlan, M.J.¹ Edwards, J.P.² Elmore, S.W.³ Jones, T.K.⁴ Kort, M.E.⁵ Kym, P.R.⁶ Moore, J.L.⁷ Pratt, J.K.⁸ Wang, A.X.⁹

7
- 84899785142
- K. Groom S. M. S. Hussain J. Morin C. Nilewski T. Rantanenand V. Snieckus Org. Lett. 2014 16 2378
- (2014) Org. Lett. , vol.16 , pp. 2378
- Groom, K.¹ Hussain, S.M.S.² Morin, J.³ Nilewski, C.⁴ Rantanenand, T.⁵ Snieckus, V.⁶

8
- 53749089571
- N. Saito A. Ryoda W. Nakanishi T. Kumamoto T. Ishikawa Eur. J. Org. Chem. 2008 2759
- (2008) Eur. J. Org. Chem. , pp. 2759
- Saito, N.¹ Ryoda, A.² Nakanishi, W.³ Kumamoto, T.⁴ Ishikawa, T.⁵

9
- 84869490990
- For reviews and examples of organocatalyzed cascade reactions, see
- J. Zhou L. Z. Huang Y. Q. Li Z. T. Du Tetrahedron Lett. 2012 53 7036
- (2012) Tetrahedron Lett. , vol.53 , pp. 7036
- Zhou, J.¹ Huang, L.Z.² Li, Y.Q.³ Du, Z.T.⁴

10
- 84899788924
- Y. Zhao Y. Wang J. Cao Y. Liang P. Xu Org. Lett. 2014 16 2438
- (2014) Org. Lett. , vol.16 , pp. 2438
- Zhao, Y.¹ Wang, Y.² Cao, J.³ Liang, Y.⁴ Xu, P.⁵

11
- 84880009151
- Z. X. Jia Y. C. Luo X. N. Cheng P. F. Xu Y. C. Gu J. Org. Chem. 2013 78 6488
- (2013) J. Org. Chem. , vol.78 , pp. 6488
- Jia, Z.X.¹ Luo, Y.C.² Cheng, X.N.³ Xu, P.F.⁴ Gu, Y.C.⁵

12
- 84887083597
- Y. Su J. B. Ling S. Zhang P. F. Xu J. Org. Chem. 2013 78 11053
- (2013) J. Org. Chem. , vol.78 , pp. 11053
- Su, Y.¹ Ling, J.B.² Zhang, S.³ Xu, P.F.⁴

13
- 84855432965
- A. Grossmann D. Enders Angew. Chem., Int. Ed. 2012 51 314
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 314
- Grossmann, A.¹ Enders, D.²

14
- 84867049980
- Z. X. Jia Y. C. Luo Y. Wang L. Chen P. F. Xu B. H. Wang Chem.-Eur. J. 2012 18 12958
- (2012) Chem.-Eur. J. , vol.18 , pp. 12958
- Jia, Z.X.¹ Luo, Y.C.² Wang, Y.³ Chen, L.⁴ Xu, P.F.⁵ Wang, B.H.⁶

15
- 84863115170
- J. B. Ling Y. Su H. L. Zhu G. Y. Wang P. F. Xu Org. Lett. 2012 14 1090
- (2012) Org. Lett. , vol.14 , pp. 1090
- Ling, J.B.¹ Su, Y.² Zhu, H.L.³ Wang, G.Y.⁴ Xu, P.F.⁵

16
- 77950257271
- Y. Wang D. F. Yu Y. Z. Liu H. Wei Y. C. Luo D. J. Dixon P. F. Xu Chem.-Eur. J. 2010 16 3922
- (2010) Chem.-Eur. J. , vol.16 , pp. 3922
- Wang, Y.¹ Yu, D.F.² Liu, Y.Z.³ Wei, H.⁴ Luo, Y.C.⁵ Dixon, D.J.⁶ Xu, P.F.⁷

17
- 84907841790
- For a recent review of metal catalysis combined with asymmetric organocatalysis, see
- J. Qi G. T. Fan J. Chen M. H. Sun Y. T. Dong L. Zhou Chem. Commun. 2014 50 12367
- (2014) Chem. Commun. , vol.50 , pp. 12367
- Qi, J.¹ Fan, G.T.² Chen, J.³ Sun, M.H.⁴ Dong, Y.T.⁵ Zhou, L.⁶

18
- 84906266327
- For examples of organocatalysts used in asymmetric Michael addition, see
- D. Chen Z. Han X. Zhou L. Gong Acc. Chem. Res. 2014 47 2365
- (2014) Acc. Chem. Res. , vol.47 , pp. 2365
- Chen, D.¹ Han, Z.² Zhou, X.³ Gong, L.⁴

19
- 84904725081
- J. Kwiatkowski Y. Lu Chem. Commun. 2014 50 9313
- (2014) Chem. Commun. , vol.50 , pp. 9313
- Kwiatkowski, J.¹ Lu, Y.²

20
- 84898904271
- J. Chen Y. Cai G. Zhao Adv. Synth. Catal. 2014 356 359
- (2014) Adv. Synth. Catal. , vol.356 , pp. 359
- Chen, J.¹ Cai, Y.² Zhao, G.³

21
- 84902148773
- A. S. Kucherenko V. G. Lisnyak A. O. Chizhov S. G. Zlotin Eur. J. Org. Chem. 2014 3808
- (2014) Eur. J. Org. Chem. , pp. 3808
- Kucherenko, A.S.¹ Lisnyak, V.G.² Chizhov, A.O.³ Zlotin, S.G.⁴

22
- 84880557087
- R. Miyaji K. Asano S. Matsubara Org. Lett. 2013 15 3658
- (2013) Org. Lett. , vol.15 , pp. 3658
- Miyaji, R.¹ Asano, K.² Matsubara, S.³

23
- 84865020581
- W. Yang D. Du Org. Biomol. Chem. 2012 10 6876
- (2012) Org. Biomol. Chem. , vol.10 , pp. 6876
- Yang, W.¹ Du, D.²

24
- 47749134165
- For selected examples of organocatalysts used in oxa-Michael addition, see
- T. R. Kang J. W. Xie W. Du X. Feng Y. C. Chen Org. Biomol. Chem. 2008 6 2673
- (2008) Org. Biomol. Chem. , vol.6 , pp. 2673
- Kang, T.R.¹ Xie, J.W.² Du, W.³ Feng, X.⁴ Chen, Y.C.⁵

25
- 80055064449
- C. F. Nising S. Bräse Chem. Soc. Rev. 2012 41 988
- (2012) Chem. Soc. Rev. , vol.41 , pp. 988
- Nising, C.F.¹ Bräse, S.²

26
- 84873354566
- L. Hintermann J. Ackerstaff F. Boeck Chem.-Eur. J. 2013 19 2311
- (2013) Chem.-Eur. J. , vol.19 , pp. 2311
- Hintermann, L.¹ Ackerstaff, J.² Boeck, F.³

27
- 84869018775
- C. Wang X. Yang C. Raabe D. Enders Adv. Synth. Catal. 2012 354 2629
- (2012) Adv. Synth. Catal. , vol.354 , pp. 2629
- Wang, C.¹ Yang, X.² Raabe, C.³ Enders, D.⁴

28
- 84873361721
- W. Wu X. Li H. Huang X. Yuan J. Lu K. Zhu J. Ye Angew. Chem., Int. Ed. 2013 52 1743
- (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 1743
- Wu, W.¹ Li, X.² Huang, H.³ Yuan, X.⁴ Lu, J.⁵ Zhu, K.⁶ Ye, J.⁷

29
- 33749003211
- For condition optimization and scope screening details, see ESI
- E. Motti F. Faccini I. Ferrari M. Catellani R. Ferraccioli Org. Lett. 2006 8 3967
- (2006) Org. Lett. , vol.8 , pp. 3967
- Motti, E.¹ Faccini, F.² Ferrari, I.³ Catellani, M.⁴ Ferraccioli, R.⁵

30
- 84864984658
- F. Morana A. Basso M. Bella R. Riva L. Banfi Adv. Synth. Catal. 2012 354 2199
- (2012) Adv. Synth. Catal. , vol.354 , pp. 2199
- Morana, F.¹ Basso, A.² Bella, M.³ Riva, R.⁴ Banfi, L.⁵

31
- 19544393388
- B. Vakulya S. Varga A. Csámpai T. Soós Org. Lett. 2005 7 1967
- (2005) Org. Lett. , vol.7 , pp. 1967
- Vakulya, B.¹ Varga, S.² Csámpai, A.³ Soós, T.⁴

32
- 84880557087
- R. K. Asano S. Matsubara Org. Lett. 2013 15 3658
- (2013) Org. Lett. , vol.15 , pp. 3658
- Asano, R.K.¹ Matsubara, S.²

33
- 84997377334
- E. V. Dehnlow S. Düttmann B. Neumann H. G. Stammler Eur. J. Org. Chem. 2002 2087
- (2002) Eur. J. Org. Chem. , pp. 2087
- Dehnlow, E.V.¹ Düttmann, S.² Neumann, B.³ Stammler, H.G.⁴

34
- 2442661261
- A. Merschaert P. Delbeke D. Daloze G. Dive Tetrahedron Lett. 2004 45 4697
- (2004) Tetrahedron Lett. , vol.45 , pp. 4697
- Merschaert, A.¹ Delbeke, P.² Daloze, D.³ Dive, G.⁴

35
- 0000879572
- M. Catellani E. Motti New J. Chem. 1998 22 759
- (1998) New J. Chem. , vol.22 , pp. 759
- Catellani, M.¹ Motti, E.²

36
- 84985534954
- A. Bhattacharta U. H. Dolling Angew. Chem., Int. Ed. 1986 25 476
- (1986) Angew. Chem., Int. Ed. , vol.25 , pp. 476
- Bhattacharta, A.¹ Dolling, U.H.²

37
- 84864218590
- D. C. Powers E. Lee A. Ariafard M. S. Sanford B. F. Yates A. J. Canty T. Ritter J. Am. Chem. Soc. 2012 134 12002
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 12002
- Powers, D.C.¹ Lee, E.² Ariafard, A.³ Sanford, M.S.⁴ Yates, B.F.⁵ Canty, A.J.⁶ Ritter, T.⁷

38
- 84859616806
- A. J. Hickman M. S. Sanford Nature 2012 484 177
- (2012) Nature , vol.484 , pp. 177
- Hickman, A.J.¹ Sanford, M.S.²

39
- 79960250277
- J. Vicente A. Arcas F. Juliá-Hernández D. Bautista Angew. Chem., Int. Ed. 2011 50 6896
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6896
- Vicente, J.¹ Arcas, A.² Juliá-Hernández, F.³ Bautista, D.⁴

40
- 57549092674
- M. Catellani E. Motti N. Della Ca' Acc. Chem. Res. 2008 41 1512
- (2008) Acc. Chem. Res. , vol.41 , pp. 1512
- Catellani, M.¹ Motti, E.² Della Ca, N.³

41
- 53849125035
- C. Amatore M. Catellani S. Deledda A. Jutand E. Motti Organometallics 2008 27 4549
- (2008) Organometallics , vol.27 , pp. 4549
- Amatore, C.¹ Catellani, M.² Deledda, S.³ Jutand, A.⁴ Motti, E.⁵

42
- 84869167873
- E. Motti N. Della Ca' D. Xu A. Piersimoni E. Bedogni Z. M. Zhou M. Catellani Org. Lett. 2012 14 5792
- (2012) Org. Lett. , vol.14 , pp. 5792
- Motti, E.¹ Della Ca² Xu, D.³ Piersimoni, A.⁴ Bedogni, E.⁵ Zhou, Z.M.⁶ Catellani, M.⁷

43
- 84876685985
- E. Motti N. Della Ca' D. Xu S. Armani B. M. Aresta M. Catellani Tetrahedron 2013 69 4421
- (2013) Tetrahedron , vol.69 , pp. 4421
- Motti, E.¹ Della Ca, N.² Xu, D.³ Armani, S.⁴ Aresta, B.M.⁵ Catellani, M.⁶

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