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Volumn , Issue SPEC. ISS., 1997, Pages 432-434

Regiocontrolled and stereocontrolled Diels-Alder cycloadditions of 2-pyrones and unactivated, unbranched 1-alkenes

Author keywords

[No Author keywords available]

Indexed keywords


EID: 1542429712     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-6126     Document Type: Article
Times cited : (14)

References (29)
  • 6
    • 29344469160 scopus 로고
    • Bateson, J. H., Mitchell, M. B., Eds.; Academic Press: New York, Ch. 2
    • Markó, I. E. In Organometallic Reagents in Organic Synthesis; Bateson, J. H., Mitchell, M. B., Eds.; Academic Press: New York, 1994, Ch. 2. One example is cited of an 18.5 Kbar cycloaddition between unsubstituted 2-pyrone and an unactivated 1-alkene, forming a syn-endo cycloadduct in 33% yield.
    • (1994) Organometallic Reagents in Organic Synthesis
    • Markó, I.E.1
  • 8
    • 0025726963 scopus 로고
    • Swarbrick, T. M.; Markó, I. E.; Kennard, L. Tetrahedron Lett. 1991, 32, 2549; in two cases at 19 Kbar a mixture of endo and exo cycloadducts was formed in 45-46% yields from 2-pyrone and unactivated alkenes.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2549
    • Swarbrick, T.M.1    Markó, I.E.2    Kennard, L.3
  • 18
    • 29344456488 scopus 로고    scopus 로고
    • note
    • 3, relative intensity) 344 (M+18, 80), 327(M+1, 100), 225(80); HRMS calculated for M+H = 327.1628, found 327.1624.
  • 26
    • 29344442403 scopus 로고
    • Ph.D. thesis, Johns Hopkins University
    • H. Dai, Ph.D. thesis, Johns Hopkins University, 1994;
    • (1994)
    • Dai, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.