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Volumn 38, Issue 6, 2009, Pages 594-595

Diastereoselective coupling of 1,3-diene, ketone, and organometallic reagents by nickel catalyst: stereoselective construction of tetrasubstituted carbon centers

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EID: 67650502351     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.2009.594     Document Type: Article
Times cited : (14)

References (34)
  • 1
    • 84890597202 scopus 로고    scopus 로고
    • ed. by J. Zhu, H. Bienaymé, Wiley-VCH Verlag Gmbh and Co, KGaA, Weinheim, Germany
    • a) Multicomponent Reactions, ed. by J. Zhu, H. Bienaymé, Wiley-VCH Verlag Gmbh and Co, KGaA, Weinheim, Germany, 2005
    • (2005) Multicomponent Reactions
  • 9
    • 0033855773 scopus 로고    scopus 로고
    • For reviews of Ni-catalyzed multicomponent coupling, see: a
    • For reviews of Ni-catalyzed multicomponent coupling, see: a) S. Ikeda, Acc. Chem. Res. 2000, 33, 511.
    • (2000) Acc. Chem. Res , vol.33 , pp. 511
    • Ikeda, S.1
  • 12
    • 1642354777 scopus 로고    scopus 로고
    • For recent examples of Ni-catalyzed multicomponent coupling, see: a
    • For recent examples of Ni-catalyzed multicomponent coupling, see: a) G. M. Mahandru, G. Liu, J. Montgomery, J. Am. Chem. Soc. 2004, 126, 3698.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 3698
    • Mahandru, G.M.1    Liu, G.2    Montgomery, J.3
  • 25
    • 0032577043 scopus 로고    scopus 로고
    • For reductive or alkylative coupling of 1, 3-diene and aldehyde via transmetallation of nickelacycle with Organometallics reagent, see: a M. Kimura, A. Ezoe, K. Shibata, Y. Tamaru, J. Am. Chem. Soc. 1998, 120, 4033.
    • For reductive or alkylative coupling of 1, 3-diene and aldehyde via transmetallation of nickelacycle with Organometallics reagent, see: a) M. Kimura, A. Ezoe, K. Shibata, Y. Tamaru, J. Am. Chem. Soc. 1998, 120, 4033.
  • 28
    • 0037039891 scopus 로고    scopus 로고
    • For an alkylative cyclization of 1, 3-diene and aldehyde via nickelacycle see
    • Y. Sato, R. Sawaki, N. Saito, M. Mori, J. Org. Chem. 2002, 67, 656. For an alkylative cyclization of 1, 3-diene and aldehyde via nickelacycle see:
    • (2002) J. Org. Chem , vol.67 , pp. 656
    • Sato, Y.1    Sawaki, R.2    Saito, N.3    Mori, M.4
  • 31
    • 67650458104 scopus 로고    scopus 로고
    • Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
    • Supporting Information is available electronically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
  • 32
    • 67650483292 scopus 로고    scopus 로고
    • In the case of coupling with aldehyde, the use of that bearing an electrondonating group on the aromatic ring gave good results see, ref 5, Although the reason is unclear yet, it is interesting that the contrary results with respect to the effect of substituents on the aromatic ring were obtained in the reaction using ketones
    • In the case of coupling with aldehyde, the use of that bearing an electrondonating group on the aromatic ring gave good results (see, ref 5). Although the reason is unclear yet, it is interesting that the contrary results with respect to the effect of substituents on the aromatic ring were obtained in the reaction using ketones.
  • 34
    • 33744795735 scopus 로고    scopus 로고
    • 3-allylalkoxynickel complex from 1, 3-diene and aldehyde was isolated: S. Ogoshi, K. Tonomori, M. Oka, H. Kurosawa, J. Am. Chem. Soc. 2006, 128, 7077.
    • 3-allylalkoxynickel complex from 1, 3-diene and aldehyde was isolated: S. Ogoshi, K. Tonomori, M. Oka, H. Kurosawa, J. Am. Chem. Soc. 2006, 128, 7077.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.