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Chemical Communications

Volumn , Issue 45, 2007, Pages 4755-4757

Intramolecular Stetter cyclisation of Morita-Baylis-Hillman adducts: A versatile approach towards bicycloenediones

(3) Wasnaire, Pierre a De Merode, Thierry a Markó, István E a

a UNIVERSITÉ CATHOLIQUE DE LOUVAIN (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ENEDIONE DERIVATIVE; INORGANIC COMPOUND; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PARTICLE SIZE;

EID: 36148992522 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b710492h Document Type: Article

Times cited : (19)

References (43)

1
- 0006644387
- A. Ichihara K. Shiraishi H. Sato S. Sakamura K. Nishiyama R. Sakai A. Furusaki T. Matsumoto J. Am. Chem. Soc. 1979 99 636
- (1979) J. Am. Chem. Soc. , vol.99 , pp. 636
- Ichihara, A.¹ Shiraishi, K.² Sato, H.³ Sakamura, S.⁴ Nishiyama, K.⁵ Sakai, R.⁶ Furusaki, A.⁷ Matsumoto, T.⁸

2
- 36148983097
- For general reviews, see:
- H. Minato Tetrahedron Lett. 1961 2 280
- (1961) Tetrahedron Lett. , vol.2 , pp. 280
- Minato, H.¹

3
- 23944525533
- V. Singh S. R. Iyer S. Pal Tetrahedron 2005 61 9197
- (2005) Tetrahedron , vol.61 , pp. 9197
- Singh, V.¹ Iyer, S.R.² Pal, S.³

4
- 0032192409
- P. Jankowski S. Marczak J. Wicha Tetrahedron 1998 54 12071
- (1998) Tetrahedron , vol.54 , pp. 12071
- Jankowski, P.¹ Marczak, S.² Wicha, J.³

5
- 30344457889
- P. Wasnaire M. Wiaux R. Touillaux I. E. Markó Tetrahedron Lett. 2006 47 985
- (2006) Tetrahedron Lett. , vol.47 , pp. 985
- Wasnaire, P.¹ Wiaux, M.² Touillaux, R.³ Markó, I.E.⁴

6
- 0001461985
- K. Morita Z. Suzuki H. Hirose Bull. Chem. Soc. Jpn. 1968 41 2815
- (1968) Bull. Chem. Soc. Jpn. , vol.41 , pp. 2815
- Morita, K.¹ Suzuki, Z.² Hirose, H.³

7
- 36148957178
- German Patent 2155113 For a general review, see:
- A. B. Baylis and M. E. D. Hillman, German Patent 2155113, 1972
- (1972)
- Baylis, A.B.¹ Hillman, M.E.D.²

8
- 0037366617
- For selected examples, see reference 4 and those cited therein For some leading references, see:
- D. Basavaiah A. J. Rao T. Satyanarayana Chem. Rev. 2003 103 811
- (2003) Chem. Rev. , vol.103 , pp. 811
- Basavaiah, D.¹ Rao, A.J.² Satyanarayana, T.³

9
- 35948961858
- Q. Liu T. Rovis Org. Process Res. Dev. 2007 11 598
- (2007) Org. Process Res. Dev. , vol.11 , pp. 598
- Liu, Q.¹ Rovis, T.²

10
- 33846925017
- W. Schrader P. P. Handayani C. Burstein F. Glorius Chem. Commun. 2007 716
- (2007) Chem. Commun. , pp. 716
- Schrader, W.¹ Handayani, P.P.² Burstein, C.³ Glorius, F.⁴

11
- 34547219364
- T. E. Reynolds C. A. Stern K. A. Scheidt Org. Lett. 2007 9 2581
- (2007) Org. Lett. , vol.9 , pp. 2581
- Reynolds, T.E.¹ Stern, C.A.² Scheidt, K.A.³

12
- 36148996194
- O. L. Epstein T. Rovis Tetrahedron 2006 62 11477
- (2006) Tetrahedron , vol.62 , pp. 11477
- Epstein, O.L.¹ Rovis, T.²

13
- 18244367138
- J. R. de Alaniz T. Rovis J. Am. Chem. Soc. 2005 127 6284
- (2005) J. Am. Chem. Soc. , vol.127 , pp. 6284
- De Alaniz, J.R.¹ Rovis, T.²

14
- 18844424752
- M. Christmann Angew. Chem., Int. Ed. 2005 44 2632
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 2632
- Christmann, M.¹

15
- 1542375011
- A. E. Mattson A. R. Bharadwaj K. A. Scheidt J. Am. Chem. Soc. 2004 126 2314
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 2314
- Mattson, A.E.¹ Bharadwaj, A.R.² Scheidt, K.A.³

16
- 4143051292
- D. Enders T. Balensiefer Acc. Chem. Res. 2004 37 534
- (2004) Acc. Chem. Res. , vol.37 , pp. 534
- Enders, D.¹ Balensiefer, T.²

17
- 5644302516
- For early references, see:
- D. Enders O. Niemeier Synlett 2004 2111
- (2004) Synlett , pp. 2111
- Enders, D.¹ Niemeier, O.²

18
- 84981906064
- H. Stetter M. Schreckenberg Angew. Chem., Int. Ed. Engl. 1973 12 81
- (1973) Angew. Chem., Int. Ed. Engl. , vol.12 , pp. 81
- Stetter, H.¹ Schreckenberg, M.²

19
- 84982417601
- For general reviews, see:
- H. Stetter Angew. Chem., Int. Ed. Engl. 1976 15 639
- (1976) Angew. Chem., Int. Ed. Engl. , vol.15 , pp. 639
- Stetter, H.¹

20
- 0001070365
- H. Stetter H. Kuhlmann Org. React. 1991 40 407
- (1991) Org. React. , vol.40 , pp. 407
- Stetter, H.¹ Kuhlmann, H.²

21
- 0034719742
- Y. M. A. Yamada S. Ikegami Tetrahedron Lett. 2000 41 2165
- (2000) Tetrahedron Lett. , vol.41 , pp. 2165
- Yamada, Y.M.A.¹ Ikegami, S.²

22
- 0001359326
- A. Itoh S. Ozawa K. Oshima H. Nozaki Bull. Chem. Soc. Jpn. 1981 54 274
- (1981) Bull. Chem. Soc. Jpn. , vol.54 , pp. 274
- Itoh, A.¹ Ozawa, S.² Oshima, K.³ Nozaki, H.⁴

23
- 0036404905
- W. Pei H. Wei G. Li Chem. Commun. 2002 2412
- (2002) Chem. Commun. , pp. 2412
- Pei, W.¹ Wei, H.² Li, G.³

24
- 0012615648
- K. Ishihara M. Kubota H. Kurihara H. Yamamoto J. Org. Chem. 1996 61 4560
- (1996) J. Org. Chem. , vol.61 , pp. 4560
- Ishihara, K.¹ Kubota, M.² Kurihara, H.³ Yamamoto, H.⁴

25
- 84987464056
- T. Veysoglu L. A. Mitscher J. K. Swayze Synthesis 1980 807
- (1980) Synthesis , pp. 807
- Veysoglu, T.¹ Mitscher, L.A.² Swayze, J.K.³

26
- 0018454939
- For general reviews, see:
- D. Seebach Angew. Chem., Int. Ed. Engl. 1979 18 239
- (1979) Angew. Chem., Int. Ed. Engl. , vol.18 , pp. 239
- Seebach, D.¹

27
- 18844424752
- M. Christmann Angew. Chem., Int. Ed. 2005 44 2632
- (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 2632
- Christmann, M.¹

28
- 4143051292
- D. Enders T. Balensiefer Acc. Chem. Res. 2004 37 534
- (2004) Acc. Chem. Res. , vol.37 , pp. 534
- Enders, D.¹ Balensiefer, T.²

29
- 36148984990
- For selected recent examples, see:
- J. S. Johnson Angew. Chem., Int. Ed. 2004 44 2632
- (2004) Angew. Chem., Int. Ed. , vol.44 , pp. 2632
- Johnson, J.S.¹

30
- 36148989987
- and references cited therein;
- J. L. Moore M. S. Kerr T. Rovis Tetrahedron 2006 62 11478
- (2006) Tetrahedron , vol.62 , pp. 11478
- Moore, J.L.¹ Kerr, M.S.² Rovis, T.³

31
- 33749348908
- Z. Zhou F. Ji M. Cao G. Yang Adv. Synth. Catal. 2006 348 1826
- (2006) Adv. Synth. Catal. , vol.348 , pp. 1826
- Zhou, Z.¹ Ji, F.² Cao, M.³ Yang, G.⁴

32
- 11844266606
- T. Nakamura O. Hara T. Tamura K. Makino Y. Hamada Synlett 2005 155
- (2005) Synlett , pp. 155
- Nakamura, T.¹ Hara, O.² Tamura, T.³ Makino, K.⁴ Hamada, Y.⁵

33
- 0001710837
- For applications to total synthesis, see:
- D. Enders K. Breuer J. H. Teles Helv. Chim. Acta 1996 79 1899
- (1996) Helv. Chim. Acta , vol.79 , pp. 1899
- Enders, D.¹ Breuer, K.² Teles, J.H.³

34
- 0035812407
- P. E. Harrington M. A. Tius J. Am. Chem. Soc. 2001 123 8509
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 8509
- Harrington, P.E.¹ Tius, M.A.²

35
- 0018422536
- For 11a, increasing the reaction time resulted in decreased yield See for examples:
- B. M. Trost C. D. Shuey F. DiNinno S. S. McElvain J. Am. Chem. Soc. 1979 101 1284
- (1979) J. Am. Chem. Soc. , vol.101 , pp. 1284
- Trost, B.M.¹ Shuey, C.D.² Dininno, F.³ McElvain, S.S.⁴

36
- 33744740159
- B. A. Pearlman A. G. Padilla J. T. Hach J. L. Havens M. D. Pillai Org. Lett. 2006 8 2111
- (2006) Org. Lett. , vol.8 , pp. 2111
- Pearlman, B.A.¹ Padilla, A.G.² Hach, J.T.³ Havens, J.L.⁴ Pillai, M.D.⁵

37
- 33745698046
- S. El Sheikh N. Kausch J. Lex J.-M. Neudoerfl H.-G. Schmaltz Synlett 2006 1527
- (2006) Synlett , pp. 1527
- El Sheikh, S.¹ Kausch, N.² Lex, J.³ Neudoerfl, J.-M.⁴ Schmaltz, H.-G.⁵

38
- 33749246531
- H. Asahara E. Mochizuki T. Oschima Tetrahedron Lett. 2006 47 7881
- (2006) Tetrahedron Lett. , vol.47 , pp. 7881
- Asahara, H.¹ Mochizuki, E.² Oschima, T.³

39
- 0041846476
- K. Yamamoto M. F. Hentemann J. G. Allen S. J. Danishefsky Chem.-Eur. J. 2003 9 3242
- (2003) Chem.-Eur. J. , vol.9 , pp. 3242
- Yamamoto, K.¹ Hentemann, M.F.² Allen, J.G.³ Danishefsky, S.J.⁴

40
- 0037454309
- and references cited therein;
- J. Yu E. J. Corey J. Am. Chem. Soc. 2003 125 3232
- (2003) J. Am. Chem. Soc. , vol.125 , pp. 3232
- Yu, J.¹ Corey, E.J.²

41
- 0001248781
- C. Liu D. J. Burnell J. Org. Chem. 1997 62 3683
- (1997) J. Org. Chem. , vol.62 , pp. 3683
- Liu, C.¹ Burnell, D.J.²

42
- 33748961141
- W. Kroutil M. E. Lasterra-Sánchez S. J. Maddrell P. Mayon P. Morgan S. M. Roberts S. R. Thornton C. J. Todd M. Tüter J. Chem. Soc., Perkin Trans. 1 1996 2837
- (1996) J. Chem. Soc., Perkin Trans. 1 , pp. 2837
- Kroutil, W.¹ Lasterra-Sánchez, M.E.² Maddrell, S.J.³ Mayon, P.⁴ Morgan, P.⁵ Roberts, S.M.⁶ Thornton, S.R.⁷ Todd, C.J.⁸ Tüter, M.⁹

43
- 0000178230
- A 24 h reaction time is necessary to complete the conversion of 11a into the desired diketone 16a due to the formation of a transient and unexpected 5-hydroxyenone intermediate
- L. C. Blaszczak J. E. McMurry J. Org. Chem. 1974 39 258
- (1974) J. Org. Chem. , vol.39 , pp. 258
- Blaszczak, L.C.¹ McMurry, J.E.²

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