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Chemical Communications

Volumn 51, Issue 22, 2015, Pages 4576-4578

Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline

(6) Huang, Pei Qiang a,b Huang, Su Yu a Gao, Long Hui a Mao, Zhong Yi a Chang, Zong a Wang, Ai E a

a XIAMEN UNIVERSITY (China)

b LANZHOU UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINESTERASE; ALKALOID DERIVATIVE; BUTENOLIDE; DESS MARTIN PERIODINANE; ALKALOID; FUSED HETEROCYCLIC RINGS; METHOXYSTEMOFOLINE;

ARTICLE; CHEMICAL STRUCTURE; DESILYLATION; DIASTEREOISOMER; ENANTIOSELECTIVITY; HYDROGENATION; NUCLEAR OVERHAUSER EFFECT; STEREOCHEMISTRY; SYNTHESIS; X RAY ANALYSIS; CHEMISTRY; STEREOISOMERISM; X RAY CRYSTALLOGRAPHY;

ALKALOIDS; CRYSTALLOGRAPHY, X-RAY; HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84929302675 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c4cc09598g Document Type: Article

Times cited : (42)

References (44)

1
- 37049117452
- H. Irie N. Masaki K. Ohno K. Osaki T. Taga H. Uyeo J. Chem. Soc., Chem. Commun. 1970 1066
- (1970) J. Chem. Soc., Chem. Commun. , pp. 1066
- Irie, H.¹ Masaki, N.² Ohno, K.³ Osaki, K.⁴ Taga, T.⁵ Uyeo, H.⁶

2
- 0000093463
- For reviews on the chemistry and biological activities of Stemona alkaloids, see
- H. W. Lin R. S. Xu Acta Chim. Sin. 1991 49 1034
- (1991) Acta Chim. Sin. , vol.49 , pp. 1034
- Lin, H.W.¹ Xu, R.S.²

3
- 33644537939
- H. Greger Planta Med. 2006 72 99
- (2006) Planta Med. , vol.72 , pp. 99
- Greger, H.¹

4
- 78649247534
- For a review, see
- R. A. Pilli G. B. Rosso M. C. F. De Oliveira Nat. Prod. Rep. 2010 27 1908
- (2010) Nat. Prod. Rep. , vol.27 , pp. 1908
- Pilli, R.A.¹ Rosso, G.B.² De Oliveira, M.C.F.³

5
- 66149101661
- For recent enantioselective total synthesis of Stemona alkaloids, see
- R. Alibés M. Figueredo Eur. J. Org. Chem. 2009 2421
- (2009) Eur. J. Org. Chem. , pp. 2421
- Alibés, R.¹ Figueredo, M.²

6
- 79951634999
- Z.-H. Chen Y.-Q. Tu S.-Y. Zhang F.-M. Zhang Org. Lett. 2011 13 724
- (2011) Org. Lett. , vol.13 , pp. 724
- Chen, Z.-H.¹ Tu, Y.-Q.² Zhang, S.-Y.³ Zhang, F.-M.⁴

7
- 79251485324
- Z.-H. Chen Y.-Q. Zhang Z.-M. Chen Y.-Q. Tu F.-M. Zhang Chem. Commun. 2011 47 1836
- (2011) Chem. Commun. , vol.47 , pp. 1836
- Chen, Z.-H.¹ Zhang, Y.-Q.² Chen, Z.-M.³ Tu, Y.-Q.⁴ Zhang, F.-M.⁵

8
- 79956119071
- A. T. Hoye P. Wipf Org. Lett. 2011 13 2634
- (2011) Org. Lett. , vol.13 , pp. 2634
- Hoye, A.T.¹ Wipf, P.²

9
- 79952522406
- Y. Wang L.-L. Zhu Y.-Y. Zhang R. Hong Angew. Chem., Int. Ed. 2011 50 2787
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 2787
- Wang, Y.¹ Zhu, L.-L.² Zhang, Y.-Y.³ Hong, R.⁴

10
- 84862958665
- J. B. Chen J. C. Chen Y. Xie H. B. Zhang Angew. Chem., Int. Ed. 2012 51 1024
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 1024
- Chen, J.B.¹ Chen, J.C.² Xie, Y.³ Zhang, H.B.⁴

11
- 84866428329
- Z.-H. Chen J.-M. Tian Z.-M. Chen Y.-Q. Tu Chem.-Asian J. 2012 7 2199
- (2012) Chem.-Asian J. , vol.7 , pp. 2199
- Chen, Z.-H.¹ Tian, J.-M.² Chen, Z.-M.³ Tu, Y.-Q.⁴

12
- 84868221207
- N. Bardají F. Sánchez-Izquierdo R. Alibés J. Font F. Busqué M. Figueredo Org. Lett. 2012 14 4854
- (2012) Org. Lett. , vol.14 , pp. 4854
- Bardají, N.¹ Sánchez-Izquierdo, F.² Alibés, R.³ Font, J.⁴ Busqué, F.⁵ Figueredo, M.⁶

13
- 84874041184
- For recent synthetic studies on stemofoline alkaloids, see
- X.-K. Liu J.-L. Ye Y.-P. Ruan Y.-X. Li P.-Q. Huang J. Org. Chem. 2013 78 35
- (2013) J. Org. Chem. , vol.78 , pp. 35
- Liu, X.-K.¹ Ye, J.-L.² Ruan, Y.-P.³ Li, Y.-X.⁴ Huang, P.-Q.⁵

14
- 34548741241
- A. M. Baylis M. P. H. Davies E. J. Thomas Org. Biomol. Chem. 2007 5 3139
- (2007) Org. Biomol. Chem. , vol.5 , pp. 3139
- Baylis, A.M.¹ Davies, M.P.H.² Thomas, E.J.³

15
- 34948860044
- A. M. Baylis E. J. Thomas Tetrahedron 2007 63 11666
- (2007) Tetrahedron , vol.63 , pp. 11666
- Baylis, A.M.¹ Thomas, E.J.²

16
- 40649088525
- R. J. Carra M. T. Epperson D. Y. Gin Tetrahedron 2008 64 3629
- (2008) Tetrahedron , vol.64 , pp. 3629
- Carra, R.J.¹ Epperson, M.T.² Gin, D.Y.³

17
- 65549154705
- E. J. Thomas C. F. Vickers Tetrahedron: Asymmetry 2009 20 970
- (2009) Tetrahedron: Asymmetry , vol.20 , pp. 970
- Thomas, E.J.¹ Vickers, C.F.²

18
- 82955235572
- T. Sastraruji S. G. Pyne A. T. Ung Tetrahedron 2012 68 598
- (2012) Tetrahedron , vol.68 , pp. 598
- Sastraruji, T.¹ Pyne, S.G.² Ung, A.T.³

19
- 84863853821
- K. Sastraruji T. Sastraruji A. T. Ung R. Griffith A. Jatisatienr S. G. Pyne Tetrahedron 2012 68 7103
- (2012) Tetrahedron , vol.68 , pp. 7103
- Sastraruji, K.¹ Sastraruji, T.² Ung, A.T.³ Griffith, R.⁴ Jatisatienr, A.⁵ Pyne, S.G.⁶

20
- 84875260507
- T. Burns M. Helliwell E. J. Thomas Tetrahedron Lett. 2013 54 2120
- (2013) Tetrahedron Lett. , vol.54 , pp. 2120
- Burns, T.¹ Helliwell, M.² Thomas, E.J.³

21
- 0033581207
- A. S. Kende T. L. Smalley Jr H. Huang J. Am. Chem. Soc. 1999 121 7431
- (1999) J. Am. Chem. Soc. , vol.121 , pp. 7431
- Kende, A.S.¹ Smalley, Jr.T.L.² Huang, H.³

22
- 0348109461
- M. Brüggemann A. I. McDonald L. E. Overman M. D. Rosen L. Schwink J. P. Scott J. Am. Chem. Soc. 2003 125 15284
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 15284
- Brüggemann, M.¹ McDonald, A.I.² Overman, L.E.³ Rosen, M.D.⁴ Schwink, L.⁵ Scott, J.P.⁶

23
- 84867566846
- C. Fang C. S. Shanahan D. H. Paull S. F. Martin Angew. Chem., Int. Ed. 2012 51 10596
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 10596
- Fang, C.¹ Shanahan, C.S.² Paull, D.H.³ Martin, S.F.⁴

24
- 84880924956
- C. S. Shanahan C. Fang D. H. Paull S. F. Martin Tetrahedron 2013 69 7592
- (2013) Tetrahedron , vol.69 , pp. 7592
- Shanahan, C.S.¹ Fang, C.² Paull, D.H.³ Martin, S.F.⁴

25
- 77952982010
- K. Sastraruji T. Sastraruji S. G. Pyne A. T. Ung A. Jatisatienr W. Lie J. Nat. Prod. 2010 73 935
- (2010) J. Nat. Prod. , vol.73 , pp. 935
- Sastraruji, K.¹ Sastraruji, T.² Pyne, S.G.³ Ung, A.T.⁴ Jatisatienr, A.⁵ Lie, W.⁶

26
- 65649116635
- M. C. Baird S. G. Pyne A. T. Ung W. Lie T. Sastraruji A. Jatisatienr C. Jatisatienr S. Dheeranupattana J. Lowlam S. Boonchalermkit J. Nat. Prod. 2009 72 679
- (2009) J. Nat. Prod. , vol.72 , pp. 679
- Baird, M.C.¹ Pyne, S.G.² Ung, A.T.³ Lie, W.⁴ Sastraruji, T.⁵ Jatisatienr, A.⁶ Jatisatienr, C.⁷ Dheeranupattana, S.⁸ Lowlam, J.⁹ Boonchalermkit, S.¹⁰

27
- 84863853821
- K. Sastraruji T. Sastraruji A. T. Ung R. Griffith A. Jatisatienr S. G. Pyne Tetrahedron 2012 68 7103
- (2012) Tetrahedron , vol.68 , pp. 7103
- Sastraruji, K.¹ Sastraruji, T.² Ung, A.T.³ Griffith, R.⁴ Jatisatienr, A.⁵ Pyne, S.G.⁶

28
- 84898029092
- C.-P. Xu S.-P. Luo A.-E Wang P.-Q. Huang Org. Biomol. Chem. 2014 12 2859
- (2014) Org. Biomol. Chem. , vol.12 , pp. 2859
- Xu, C.-P.¹ Luo, S.-P.² Wang, A.-E.³ Huang, P.-Q.⁴

29
- 84893216787
- Q.-L. Peng S.-P. Luo X.-E. Xia L.-X. Liu P.-Q. Huang Chem. Commun. 2014 50 1986
- (2014) Chem. Commun. , vol.50 , pp. 1986
- Peng, Q.-L.¹ Luo, S.-P.² Xia, X.-E.³ Liu, L.-X.⁴ Huang, P.-Q.⁵

30
- 84871562525
- S.-P. Luo L.-D. Guo L.-H. Gao S. Li P.-Q. Huang Chem.-Eur. J. 2013 19 87
- (2013) Chem.-Eur. J. , vol.19 , pp. 87
- Luo, S.-P.¹ Guo, L.-D.² Gao, L.-H.³ Li, S.⁴ Huang, P.-Q.⁵

31
- 84872527538
- H.-H. Huo X.-E. Xia H.-K. Zhang P.-Q. Huang J. Org. Chem. 2013 78 455
- (2013) J. Org. Chem. , vol.78 , pp. 455
- Huo, H.-H.¹ Xia, X.-E.² Zhang, H.-K.³ Huang, P.-Q.⁴

32
- 84882277654
- S.-Y. Huang Z. Chang S.-C. Tuo L.-H. Gao A.-E Wang P.-Q. Huang Chem. Commun. 2013 49 7088
- (2013) Chem. Commun. , vol.49 , pp. 7088
- Huang, S.-Y.¹ Chang, Z.² Tuo, S.-C.³ Gao, L.-H.⁴ Wang, A.-E.⁵ Huang, P.-Q.⁶

33
- 84893843308
- Z.-Y. Mao S.-Y. Huang L.-H. Gao A.-E Wang P.-Q. Huang Sci. China: Chem. 2014 57 252
- (2014) Sci. China: Chem. , vol.57 , pp. 252
- Mao, Z.-Y.¹ Huang, S.-Y.² Gao, L.-H.³ Wang, A.-E.⁴ Huang, P.-Q.⁵

34
- 78249281266
- G. C. Fu S. T. Nguyen R. H. Grubbs J. Am. Chem. Soc. 1993 115 9856
- (1993) J. Am. Chem. Soc. , vol.115 , pp. 9856
- Fu, G.C.¹ Nguyen, S.T.² Grubbs, R.H.³

35
- 33644528891
- For recent reviews on α-amidoalkylation via N-acyliminium ions, see
- D. B. Dess J. C. Marin J. Org. Chem. 1983 48 4155
- (1983) J. Org. Chem. , vol.48 , pp. 4155
- Dess, D.B.¹ Marin, J.C.²

36
- 63549142605
- A. Yazici S. G. Pyne Synthesis 2009 339
- (2009) Synthesis , pp. 339
- Yazici, A.¹ Pyne, S.G.²

37
- 63549102143
- A. Yazici S. G. Pyne Synthesis 2009 513
- (2009) Synthesis , pp. 513
- Yazici, A.¹ Pyne, S.G.²

38
- 14544275012
- T. Taniguchi A. Ishita M. Uchiyama O. Tamura O. Muraoka G. Tanabe H. Ishibasi J. Org. Chem. 2005 70 1922
- (2005) J. Org. Chem. , vol.70 , pp. 1922
- Taniguchi, T.¹ Ishita, A.² Uchiyama, M.³ Tamura, O.⁴ Muraoka, O.⁵ Tanabe, G.⁶ Ishibasi, H.⁷

39
- 0027394568
- G. A. Kraus B. Andersh Q. Su J. Shi Tetrahedron Lett. 1993 34 1741
- (1993) Tetrahedron Lett. , vol.34 , pp. 1741
- Kraus, G.A.¹ Andersh, B.² Su, Q.³ Shi, J.⁴

40
- 33845554752
- G. E. Keck J. B. Yates J. Am. Chem. Soc. 1982 104 5829
- (1982) J. Am. Chem. Soc. , vol.104 , pp. 5829
- Keck, G.E.¹ Yates, J.B.²

41
- 0000382297
- CCDC
- G. Büchi H. Wuest J. Org. Chem. 1979 44 546
- (1979) J. Org. Chem. , vol.44 , pp. 546
- Büchi, G.¹ Wuest, H.²

42
- 37049107132
- D. W. Knight G. Pattenden J. Chem. Soc., Perkin Trans. 1 1975 635
- (1975) J. Chem. Soc., Perkin Trans. 1 , pp. 635
- Knight, D.W.¹ Pattenden, G.²

43
- 37049072174
- A. Pelter R. I. H. Al-Bayati M. T. Ayoub W. Lewis P. Pardasani R. Hansel J. Chem. Soc., Perkin Trans. 1 1987 717
- (1987) J. Chem. Soc., Perkin Trans. 1 , pp. 717
- Pelter, A.¹ Al-Bayati, R.I.H.² Ayoub, M.T.³ Lewis, W.⁴ Pardasani, P.⁵ Hansel, R.⁶

44
- 0000215322
- E. J. Corey P. B. Hopkins Tetrahedron Lett. 1982 23 1979
- (1982) Tetrahedron Lett. , vol.23 , pp. 1979
- Corey, E.J.¹ Hopkins, P.B.²

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