SCOPUS 정보 검색 플랫폼 - 논문 보기

메뉴 건너뛰기

Chemical Communications

Volumn 46, Issue 43, 2010, Pages 8246-8248

Auto-tandem catalysis: Facile synthesis of substituted alkylidenecyclohexanones by domino (4+2) cycloaddition-elimination reaction

(4) Takasu, Kiyosei a Tanaka, Toru a Azuma, Takumi a Takemoto, Yoshiji a

a KYOTO UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANONE DERIVATIVE;

ARTICLE; BAYLIS HILLMAN REACTION; CATALYSIS; CYCLOADDITION; ELIMINATION REACTION; SYNTHESIS;

EID: 77958508531 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/c0cc03336g Document Type: Article

Times cited : (12)

References (21)

1
- 84890766709
- Wiley-VCH, Weinheim
- L. F. Tietze, G. Brasche and K. M. Gericke, Domino Reactions in Organic Chemistry, Wiley-VCH, Weinheim, 2007
- (2007) Domino Reactions in Organic Chemistry
- Tietze, L.F.¹ Brasche, G.² Gericke, K.M.³

2
- 77950795829
- For recent reviews, see:
- S. Suga D. Yamada J. Yoshida Chem. Lett. 2010 404
- (2010) Chem. Lett. , pp. 404
- Suga, S.¹ Yamada, D.² Yoshida, J.³

3
- 9744257740
- D. E. Fogg E. N. dos Santos Coord. Chem. Rev. 2004 248 2365
- (2004) Coord. Chem. Rev. , vol.248 , pp. 2365
- Fogg, D.E.¹ Dos Santos, E.N.²

4
- 17444401687
- J.-C. Wasilke S. J. Obrey R. T. Baler G. C. Bazan Chem. Rev. 2005 105 1001
- (2005) Chem. Rev. , vol.105 , pp. 1001
- Wasilke, J.-C.¹ Obrey, S.J.² Baler, R.T.³ Bazan, G.C.⁴

5
- 70849124098
- N. Shindoh Y. Takemoto K. Takasu Chem.-Eur. J. 2009 15 12168
- (2009) Chem.-Eur. J. , vol.15 , pp. 12168
- Shindoh, N.¹ Takemoto, Y.² Takasu, K.³

6
- 1042265091
- K. Inanaga K. Takasu M. Ihara J. Am. Chem. Soc. 2004 126 1352
- (2004) J. Am. Chem. Soc. , vol.126 , pp. 1352
- Inanaga, K.¹ Takasu, K.² Ihara, M.³

7
- 44249097983
- Reviews, see:
- K. Takasu K. Inanaga M. Ihara Tetrahedron Lett. 2007 49 4220
- (2007) Tetrahedron Lett. , vol.49 , pp. 4220
- Takasu, K.¹ Inanaga, K.² Ihara, M.³

8
- 50949111780
- K. Takasu J. Synth. Org. Chem. Jpn. 2008 66 554
- (2008) J. Synth. Org. Chem. Jpn. , vol.66 , pp. 554
- Takasu, K.¹

9
- 67651241741
- K. Takasu Synlett 2009 1905
- (2009) Synlett , pp. 1905
- Takasu, K.¹

10
- 0030755603
- B. Mathieu L. Ghosez Tetrahedron Lett. 1997 38 5497
- (1997) Tetrahedron Lett. , vol.38 , pp. 5497
- Mathieu, B.¹ Ghosez, L.²

11
- 0037037846
- B. Mathieu L. Ghosez Tetrahedron 2002 58 8219
- (2002) Tetrahedron , vol.58 , pp. 8219
- Mathieu, B.¹ Ghosez, L.²

12
- 77950371598
- O. Mendoza G. Rossey L. Ghosez Tetrahedron Lett. 2010 51 2571
- (2010) Tetrahedron Lett. , vol.51 , pp. 2571
- Mendoza, O.¹ Rossey, G.² Ghosez, L.³

13
- 37049074937
- D. Batty D. Crich J. Chem. Soc., Perkin Trans. 1 1992 3205
- (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 3205
- Batty, D.¹ Crich, D.²

14
- 77958507006
- Y. Du X. Lu J. Org. Chem. 2003 68 6462
- (2003) J. Org. Chem. , vol.68 , pp. 6462
- Du, Y.¹ Lu, X.²

15
- 77958458983
- D. J. Wallace R. L. Sidda R. L. Reamer J. Org. Chem. 2007 48 4749
- (2007) J. Org. Chem. , vol.48 , pp. 4749
- Wallace, D.J.¹ Sidda, R.L.² Reamer, R.L.³

16
- 0037099747
- E. A. Oho-Amaize E. J. Nchekwube H. B. Cottam R. Bai P. Verdier-Pinard V. N. Kakkanaiah J. I. Okogun A. A. Adesomoju O. A. Oyemade E. Hamel Cancer Res. 2002 62 4007
- (2002) Cancer Res. , vol.62 , pp. 4007
- Oho-Amaize, E.A.¹ Nchekwube, E.J.² Cottam, H.B.³ Bai, R.⁴ Verdier-Pinard, P.⁵ Kakkanaiah, V.N.⁶ Okogun, J.I.⁷ Adesomoju, A.A.⁸ Oyemade, O.A.⁹ Hamel, E.¹⁰

17
- 3843105997
- R. Sancho M. Medarde S. S. Palomino B. M. Madrigal J. Alcami E. Munoz A. S. Feliciano Bioorg. Med. Chem. Lett. 2004 14 4483
- (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 4483
- Sancho, R.¹ Medarde, M.² Palomino, S.S.³ Madrigal, B.M.⁴ Alcami, J.⁵ Munoz, E.⁶ Feliciano, A.S.⁷

18
- 77958450429
- Z. He X. Tang Y. Cheng Z. He Adv. Synth. Catal. 2006 348 4173
- (2006) Adv. Synth. Catal. , vol.348 , pp. 4173
- He, Z.¹ Tang, X.² Cheng, Y.³ He, Z.⁴

19
- 0025804638
- 3 (approximately 0.1 mmol) at the same temperature. Concentration of the resulting mixture, followed by column chromatography on silica gel (AcOEthexane = 1090), furnished 5b (42 mg, 78% yield) as colorless solids. Spectral data for 5b; mp 78-79°C, IR (neat)
- S. Kim Y. G. Kim J. H. Park Tetrahedron Lett. 1991 32 2043
- (1991) Tetrahedron Lett. , vol.32 , pp. 2043
- Kim, S.¹ Kim, Y.G.² Park, J.H.³

20
- 33846610058
- 2NH (Table 2, entry 1), Mukaiyama-Michael adduct was obtained in 12% yield (see ESI)
- M. E. Jung D. G. Ho Org. Lett. 2007 9 375
- (2007) Org. Lett. , vol.9 , pp. 375
- Jung, M.E.¹ Ho, D.G.²

21
- 33847805195
- S. Danishefsky T. Kitahara J. Am. Chem. Soc. 1974 96 7807
- (1974) J. Am. Chem. Soc. , vol.96 , pp. 7807
- Danishefsky, S.¹ Kitahara, T.²

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.