메뉴 건너뛰기




Volumn , Issue 28, 2010, Pages 5471-5481

Vinylogous Mukaiyania-Michael Reactions between 2-SiLyIoxyfurans and cyclic enones or unsaturated oxo esters

Author keywords

Cyclic enones; Diastereoselectivity; Homogeneous catalysis; Michael addition; Mukaiyama reaction

Indexed keywords


EID: 77957120761     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000504     Document Type: Article
Times cited : (22)

References (85)
  • 52
    • 77957155978 scopus 로고    scopus 로고
    • [10] However, our attempts to apply this method to cyclo.hex-2-enone led to extensive polymerization of the enone
    • [10] However, our attempts to apply this method to cyclo.hex-2-enone led to extensive polymerization of the enone.
  • 56
    • 0001490032 scopus 로고
    • For a discussion on the influence of the silyl group on stereoselectivity, see: a) J. Otera, Y. Fujita, T. Sato, H. Nozaki, J. Org. Chem. 1992, 57, 5054-5055;
    • (1992) J. Org. Chem. , vol.57 , pp. 5054-5055
    • Otera, J.1    Fujita, Y.2    Sato, T.3    Nozaki, H.4
  • 58
    • 77957155612 scopus 로고    scopus 로고
    • [10]
    • [10]
  • 78
    • 77957123083 scopus 로고    scopus 로고
    • CCDC-704234 (3a), -704233 (3a′), -704235 (3d), and -771.491 (5″a) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-704234 (3a), -704233 (3a′), -704235 (3d), and -771.491 (5″a) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-requ.est/cif.
  • 84
    • 33845552460 scopus 로고
    • 3, known to catalyze Diels-Alder reactions, did not allowed us to observe any Diels-Alder adduct.
    • 3, known to catalyze Diels-Alder reactions, did not allowed us to observe any Diels-Alder adduct. M. Bednarski, S. Danishefsky, J. Am. Chem. Soc. 1983, 105, 3716-3717.
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 3716-3717
    • Bednarski, M.1    Danishefsky, S.2
  • 85
    • 77957167994 scopus 로고    scopus 로고
    • At this stage, it cannot be excluded that different pathways might be possible with each substrate 2 and 4
    • At this stage, it cannot be excluded that different pathways might be possible with each substrate 2 and 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.