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Volumn , Issue 21, 2010, Pages 4098-4105

Asymmetric aza-Morita-Baylis-Hillman reactions of alkyl vinyl ketones with N-protected imines or in situ generated N-protected imines

Author keywords

Asymmetric synthesis; Enantioselectivity; Lewis bases; Nucleophilic addition; Phosphanes; Sulfur

Indexed keywords


EID: 77954710559     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000496     Document Type: Article
Times cited : (25)

References (53)
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    • d) P. Langer, Angew. Chem. 2000, 112, 3177-3180;
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  • 8
    • 34347262098 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 4614-4628;
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    • 0037011306 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 4507-4510;
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    • 29144448796 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 7975-7978;
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  • 49
    • 77954702397 scopus 로고    scopus 로고
    • note
    • 2 = 0.1148. Diffractometer: Rigaku AFC7R.
  • 50
    • 0025170563 scopus 로고
    • Aiken et al. demonstrated that protonated cinchona alkaloids could be catalytically active for asymmetric anhydride opening but the enantioselectivities were rather low; a) R. A. Aitken, J. Gopal, Tetrahedron: Asymmetry 1990, 1, 517;
    • (1990) Tetrahedron: Asymmetry , vol.1 , pp. 517
    • Aitken, R.A.1    Gopal, J.2
  • 52
    • 77954727382 scopus 로고    scopus 로고
    • note
    • 2 = 0.1055. Diffractometer: Rigaku AFC7R.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.