SCOPUS 정보 검색 플랫폼

Chemistry - An Asian Journal

Volumn 2, Issue 2, 2007, Pages 273-283

Diels-alder reactions of novel (1′-arylallylidene)cyclopropanes with heterodienophiles

(5) Ligang, Zhao a Yucel, Baris a Scheurich, René Peter a Frank, Daniel a De Meijere, Armin a

a UNIVERSITY OF GÖTTINGEN (Germany)

Author keywords

Allylic compounds; Bicyclopropylidene; Cycloaddition; Sequential reactions; Spiro compounds

Indexed keywords

EID: 34250867389 PISSN: 18614728 EISSN: 1861471X Source Type: Journal
DOI: 10.1002/asia.200600361 Document Type: Article

Times cited : (12)

References (51)

1
- 7044235263
- For reviews, see: a
- For reviews, see: a) L. F. Tietze, Chem. Rev. 1996, 96, 115-136;
- (1996) Chem. Rev , vol.96 , pp. 115-136
- Tietze, L.F.¹

2
- 0033947531
- b) L. F. Tietze, A. Modi, Med. Res. Rev. 2000, 20, 304-322;
- (2000) Med. Res. Rev , vol.20 , pp. 304-322
- Tietze, L.F.¹ Modi, A.²

3
- 33845375114
- c) G. H. Posner, Chem. Rev. 1986, 86, 831-844;
- (1986) Chem. Rev , vol.86 , pp. 831-844
- Posner, G.H.¹

4
- 0004198491
- Wiley, New York
- d) T.-L. Ho, Tandem Organic Reactions, Wiley, New York, 1992;
- (1992) Tandem Organic Reactions
- Ho, T.-L.¹

5
- 0001146788
- e) P. J. Parsons, C. S. Penkett, A. J. Shell, Chem. Rev. 1996, 96, 195-206.
- (1996) Chem. Rev , vol.96 , pp. 195-206
- Parsons, P.J.¹ Penkett, C.S.² Shell, A.J.³

6
- 84941832018
- For reviews, see: a
- For reviews, see: a) B. M. Trost, Pure Appl. Chem. 1994, 66, 2007-2014;
- (1994) Pure Appl. Chem , vol.66 , pp. 2007-2014
- Trost, B.M.¹

7
- 0000791854
- b) B. M. Trost, Angew. Chem. 1995, 107, 285-307;
- (1995) Angew. Chem , vol.107 , pp. 285-307
- Trost, B.M.¹

8
- 33750309194
- Angew. Chem. Int. Ed. Engl. 1995, 34, 259-281;
- (1995) Angew. Chem. Int. Ed. Engl , vol.34 , pp. 259-281

9
- 0001238512
- c) R. Grigg, V. Sridharan. Pure Appl. Chem. 1998, 70, 1047-1057;
- (1998) Pure Appl. Chem , vol.70 , pp. 1047-1057
- Grigg, R.¹ Sridharan, V.²

10
- 0030575418
- d) A. Heumann, M. Réglier, Tetrahedron 1996, 52, 9289-9346;
- (1996) Tetrahedron , vol.52 , pp. 9289-9346
- Heumann, A.¹ Réglier, M.²

11
- 0036643469
- e) A. de Meijere, P. von Zezschwitz, H. Nüske, B. Stulgies, J. Organomet. Chem. 2002, 653, 129-140.
- (2002) J. Organomet. Chem , vol.653 , pp. 129-140
- de Meijere, A.¹ von Zezschwitz, P.² Nüske, H.³ Stulgies, B.⁴

12
- 0344875138
- a) A. de Meijere. M. Schelper, M. Knoke, B. Yucel, H. W. Sünnemann, R. P. Scheurich, L. Arve, J. Organomet. Chem. 2003, 687, 249-255;
- (2003) J. Organomet. Chem , vol.687 , pp. 249-255
- de Meijere, A.¹ Schelper, M.² Knoke, M.³ Yucel, B.⁴ Sünnemann, H.W.⁵ Scheurich, R.P.⁶ Arve, L.⁷

13
- 0037281894
- b) M. Knoke, A. de Meijere, Synlett 2003, 195-198;
- (2003) Synlett , pp. 195-198
- Knoke, M.¹ de Meijere, A.²

14
- 0037123792
- c) H. Nüske, S. Bräse, S. I. Kozhushkov, M. Noltemeyer, M. Es-Sayed, A. de Meijere, Chem. Eur. J. 2002, 8, 2350-2369;
- (2002) Chem. Eur. J , vol.8 , pp. 2350-2369
- Nüske, H.¹ Bräse, S.² Kozhushkov, S.I.³ Noltemeyer, M.⁴ Es-Sayed, M.⁵ de Meijere, A.⁶

15
- 0036796052
- d) M. von Seebach, R. Grigg, A. de Meijere, Eur. J. Org. Chem. 2002, 3268-3275;
- (2002) Eur. J. Org. Chem , pp. 3268-3275
- von Seebach, M.¹ Grigg, R.² de Meijere, A.³

16
- 0001534474
- e) A. de Meijere, H. Nüske, M. Es-Sayed, T. Labahn, M. Schroen, S. Bräse, Angew. Chem. 1999, 111, 3881-3884;
- (1999) Angew. Chem , vol.111 , pp. 3881-3884
- de Meijere, A.¹ Nüske, H.² Es-Sayed, M.³ Labahn, T.⁴ Schroen, M.⁵ Bräse, S.⁶

17
- 0005572996
- Angew. Chem. Int. Ed. 1999, 38, 3669-3672;
- (1999) Chem. Int. Ed , vol.38 , pp. 3669-3672
- Angew¹

18
- 0030603097
- f) K. H. Ang, S. Bräse, A. G. Steinig, F. E. Meyer, A. Llebaria, K. Voigt, A. de Meijere, Tetrahedron 1996, 52, 11503-11528;
- (1996) Tetrahedron , vol.52 , pp. 11503-11528
- Ang, K.H.¹ Bräse, S.² Steinig, A.G.³ Meyer, F.E.⁴ Llebaria, A.⁵ Voigt, K.⁶ de Meijere, A.⁷

19
- 84985599336
- g) F. E. Meyer, K. H. Ang, A. G. Steinig, A. de Meijere, Synlett 1994, 191-193.
- (1994) Synlett , pp. 191-193
- Meyer, F.E.¹ Ang, K.H.² Steinig, A.G.³ de Meijere, A.⁴

20
- 33751386018
- Bicyclopropylidene (1) is readily available in three simple steps: a) A. de Meijere, S. I. Kozhushkov, T. Späth, N. S. Zefirov, J. Org. Chem. 1993, 55, 502-505;
- Bicyclopropylidene (1) is readily available in three simple steps: a) A. de Meijere, S. I. Kozhushkov, T. Späth, N. S. Zefirov, J. Org. Chem. 1993, 55, 502-505;

21
- 85027835480
- b) A. de Meijere, S. I. Kozhushkov, T. Späth, Org. Synth. 2000, 78, 142-151.
- (2000) Org. Synth , vol.78 , pp. 142-151
- de Meijere, A.¹ Kozhushkov, S.I.² Späth, T.³

22
- 0000847293
- a) S. Bräse, A. deMeijere, Angew. Chem. 1995, 107, 2741-2743;
- (1995) Angew. Chem , vol.107 , pp. 2741-2743
- Bräse, S.¹ deMeijere, A.²

23
- 33748241772
- Angew. Chem. Int. Ed. Engl. 1995, 34, 2545-2547.
- (1995) Angew. Chem. Int. Ed. Engl , vol.34 , pp. 2545-2547

24
- 34250831261
- Doctoral dissertation. Universität Göttingen, Göttingen Germany
- H. Nüske, Doctoral dissertation. Universität Göttingen, Göttingen (Germany), 2000.
- (2000)
- Nüske, H.¹

25
- 85082557276
- a) T. Jeffery, Synthesis 1987, 70-71;
- (1987) Synthesis , pp. 70-71
- Jeffery, T.¹

26
- 46549101525
- b) T. Jeffery, Tetrahedron Lett. 1985, 26, 2667-2670;
- (1985) Tetrahedron Lett , vol.26 , pp. 2667-2670
- Jeffery, T.¹

27
- 37049111808
- c) T. Jeffery, J. Chem. Soc. Chem. Commun. 1984, 1287-1289.
- (1984) J. Chem. Soc. Chem. Commun , pp. 1287-1289
- Jeffery, T.¹

28
- 85024741038
- For the acceleration of Diels-Alder reactions with heterodienophiles under high pressure, see: a
- For the acceleration of Diels-Alder reactions with heterodienophiles under high pressure, see: a) J. Jurczak, M. Chmielewski, S. Filipek, Synthesis 1979, 41-42;
- (1979) Synthesis , pp. 41-42
- Jurczak, J.¹ Chmielewski, M.² Filipek, S.³

29
- 34250794804
- b) J. Jurczak, M. Tkosz, Synthesis 1979, 42-44.
- (1979) Synthesis , pp. 42-44
- Jurczak, J.¹ Tkosz, M.²

30
- 0001546043
- For reviews on Diels-Alder reactions with carbonyl compounds as heterodienophiles, see: a
- For reviews on Diels-Alder reactions with carbonyl compounds as heterodienophiles, see: a) K. A. Jørgensen, Angew. Chem. 2000, 112, 3702-3733;
- (2000) Angew. Chem , vol.112 , pp. 3702-3733
- Jørgensen, K.A.¹

31
- 0034675619
- Angew. Chem. Int. Ed. 2000, 39, 3558-3588;
- (2000) Chem. Int. Ed , vol.39 , pp. 3558-3588
- Angew¹

32
- 4544247886
- b) K. A. Jørgensen, Eur. J. Org. Chem. 2004, 2093-2102;
- (2004) Eur. J. Org. Chem , pp. 2093-2102
- Jørgensen, K.A.¹

33
- 0001184378
- c) S. M. Weinreb, R. R. Staib, Tetrahedron 1982, 38, 3087-3128.
- (1982) Tetrahedron , vol.38 , pp. 3087-3128
- Weinreb, S.M.¹ Staib, R.R.²

34
- 84986394892
- For the combination of a Lewis acid catalyst and high pressure to promote a Diels-Alder reaction with a heterodienophile, see: J. Jurczak, A. Golebiowski, T. Bauer, Synthesis 1985, 928-929
- For the combination of a Lewis acid catalyst and high pressure to promote a Diels-Alder reaction with a heterodienophile, see: J. Jurczak, A. Golebiowski, T. Bauer, Synthesis 1985, 928-929.

35
- 3543110157
- For reviews on nitroso compounds, see: a
- For reviews on nitroso compounds, see: a) B. G. Gowenlock, G. B. Richter-Addo, Chem. Rev. 2004, 104, 3315-3340;
- (2004) Chem. Rev , vol.104 , pp. 3315-3340
- Gowenlock, B.G.¹ Richter-Addo, G.B.²

36
- 0142169492
- b) W. Adam, O. Krebs, Chem. Rev. 2003, 103, 4131-4146.
- (2003) Chem. Rev , vol.103 , pp. 4131-4146
- Adam, W.¹ Krebs, O.²

37
- 0001971115
- For Diels-Alder reactions employing nitroso compounds as dienophiles, see: a, Ed, P. Metz, Springer, Berlin
- For Diels-Alder reactions employing nitroso compounds as dienophiles, see: a) L. F. Tietze, G. Kettschau in Topics in Current Chemistry, Vol. 189, (Ed.: P. Metz), Springer, Berlin, 1997, pp. 1-120;
- (1997) Topics in Current Chemistry , vol.189 , pp. 1-120
- Tietze, L.F.¹ Kettschau, G.²

38
- 0000730407
- Ed, B. M. Trost, Pergamon, Oxford
- b) S. M. Weinreb in Comprehesive Organic Synthesis Vol. 5 (Ed.: B. M. Trost), Pergamon, Oxford, 1991, pp. 401-449;
- (1991) Comprehesive Organic Synthesis , vol.5 , pp. 401-449
- Weinreb, S.M.¹

39
- 0000884707
- Ed, B. M. Trost, Pergamon, Oxford
- c) D. L. Boger in Comprehensive Organic Synthesis, Vol. 5 (Ed.: B. M. Trost), Pergamon, Oxford, 1991, pp. 451-512;
- (1991) Comprehensive Organic Synthesis , vol.5 , pp. 451-512
- Boger, D.L.¹

40
- 0001184378
- d) S. M. Weinreb, R. P. Staib, Tetrahedron 1982, 38, 3087-3128;
- (1982) Tetrahedron , vol.38 , pp. 3087-3128
- Weinreb, S.M.¹ Staib, R.P.²

41
- 0010745317
- e) G. W. Kirby, Chem. Soc. Rev. 1977, 6, 1-24.
- (1977) Chem. Soc. Rev , vol.6 , pp. 1-24
- Kirby, G.W.¹

42
- 34250840933
- C19H19NO (277.35, crystal size 0.30 × 0.20 × 0.20 mm3, triclinic, a, 995.10(9, b, 1076.39(11, c, 1495.42(14) pm, α, 100.884(8, β, 96.444(8, γ, 106.121(8)°, V, 1.4879(2) nm3; Z, 4, space group P1, T, 133(2) K. ρ, 1.238 Mgm3, absorption coefficient, 0.076 mm -1. F0, 592, θ range for data collection, 2.02-24.61°, reflections collected, 20297, Rint, 4996 (0.1158, data/restraints/paramaters, 4996/0/380, GOF on F2, 0.825, final R indices [I > 2σa(I, R1, 0.0520, wR2, 0.0754, R indices (all data, R1, 0.1313. wR2, 0.0910, largest diff. peak and hole, 0.192 and -0.203 eÅ-3. CCDC-286026 (23c) contains the supplementary cristallographie data (excluding structure factors) for this paper. These data can be obtained free of charge from the Cambridge Cristallographie Data Centre, 12 Union Road. Cambrid
- -3. CCDC-286026 (23c) contains the supplementary cristallographie data (excluding structure factors) for this paper. These data can be obtained free of charge from the Cambridge Cristallographie Data Centre, 12 Union Road. Cambridge CB2 1EZ. UK (fax: (+44) 1223-336-033; e-mail: deposit@ccdc.cam.ac.uk) or at www.ccdc.cam.ac.uk/data_request.ci f.

43
- 0038882536
- Nitroso compounds are known to inhibit the carbopalladation step in Heck reactions: R. Skoda-Földes, K. Vándor. L. Kollár, J. Horváth, Z. Tuba, J. Org. Chem. 1999, 64, 5921-5925.
- Nitroso compounds are known to inhibit the carbopalladation step in Heck reactions: R. Skoda-Földes, K. Vándor. L. Kollár, J. Horváth, Z. Tuba, J. Org. Chem. 1999, 64, 5921-5925.

44
- 0027181772
- A. de Meijere, S. I. Kozhushkov, N. S. Zefirov, Synthesis 1993, 681-683.
- (1993) Synthesis , pp. 681-683
- de Meijere, A.¹ Kozhushkov, S.I.² Zefirov, N.S.³

45
- 34250878743
- For regioselective palladium-catalyzed reactions involving coordination of palladium species with heteroatoms. see: J. Tsuji, Palladium Reagents and Catalysts: New Perspectives for the 21st Century, John Wiley, Chichester, 2004, pp. 79-86, and references therein
- For regioselective palladium-catalyzed reactions involving coordination of palladium species with heteroatoms. see: J. Tsuji, Palladium Reagents and Catalysts: New Perspectives for the 21st Century, John Wiley, Chichester, 2004, pp. 79-86, and references therein.

46
- 1942425027
- A. Defoin, Synthesis 2004, 5, 706-710.
- (2004) Synthesis , vol.5 , pp. 706-710
- Defoin, A.¹

47
- 37049069755
- K. L. Platt, F. Setiabudi, J. Chem. Soc. Perkin Trans. 1 1992, 2005-2009.
- (1992) J. Chem. Soc. Perkin Trans. 1 , pp. 2005-2009
- Platt, K.L.¹ Setiabudi, F.²

48
- 0022358611
- a) S. Danishefsky, M. Barbachyn, J. Am. Chem. Soc. 1985, 107, 7761-7762;
- (1985) J. Am. Chem. Soc , vol.107 , pp. 7761-7762
- Danishefsky, S.¹ Barbachyn, M.²

49
- 0022408443
- b) S. Danishefsky, C. Maring, J. Am. Chem. Soc. 1985, 107, 7762-7764.
- (1985) J. Am. Chem. Soc , vol.107 , pp. 7762-7764
- Danishefsky, S.¹ Maring, C.²

50
- 0642309881
- a) V. Panteleon, P. Marakos, N. Pouli, E. Mikros, I. Andreadou, Chem. Pharm. Bull. 2003, 51, 522-529;
- (2003) Chem. Pharm. Bull , vol.51 , pp. 522-529
- Panteleon, V.¹ Marakos, P.² Pouli, N.³ Mikros, E.⁴ Andreadou, I.⁵

51
- 0042666860
- b) V. Panteleon, P. Marakos, N. Pouli, E. Mikros, I. Andreadou, J. Pharm. Pharmacol. 2003, 55, 1029-1039.
- (2003) J. Pharm. Pharmacol , vol.55 , pp. 1029-1039
- Panteleon, V.¹ Marakos, P.² Pouli, N.³ Mikros, E.⁴ Andreadou, I.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.