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Volumn , Issue 23, 1995, Pages 2391-2392

Periselective and enantioselective carbonyl-ene reaction of isoprene with fluoroalkyl glyoxylate catalysed by modified binaphthol-titanium complex: Asymmetric catalytic synthesis of enantiomerically pure ipsdienol

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EID: 37049067513     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39950002391     Document Type: Article
Times cited : (41)

References (26)
  • 2
  • 5
    • 0016224888 scopus 로고
    • Acrylate derivatives of fluoroalkyl or fluorophenyl esters as activated dienophiles in Diels–Alder reactions:, see also:, Whereas the steric size of the CF3 group is estimated to be as bulky as the isopropyl group by dynamic NMR measurements of 2, 2′-disubstituted biphenyls, the CF3 group tends to act as a more bulky group such as tert-butyl group in reactions such as asymmetric borane reductions:, 6-Br-BINOL-TiX2 2b as an asymmetric catalyst of carbonyl-ene reactions:, Asymmetric hetero-Diels–Alder reactions catalysed by 2a:, Asymmetric glyoxylate-ene reactions catalysed by 2a:, 91% ee:, 92% ee:, 96% ee:, > 96% ee:, Asymmetric syntheses of enantiomerically enriched ipsdienol:, also see
    • J.P. Vite, A. Bakke and P.R. Highes, Naturwissenschaften, 1974, 61, 365, Acrylate derivatives of fluoroalkyl or fluorophenyl esters as activated dienophiles in Diels–Alder reactions:, see also:, Whereas the steric size of the CF3 group is estimated to be as bulky as the isopropyl group by dynamic NMR measurements of 2, 2′-disubstituted biphenyls, the CF3 group tends to act as a more bulky group such as tert-butyl group in reactions such as asymmetric borane reductions:, 6-Br-BINOL-TiX2 2b as an asymmetric catalyst of carbonyl-ene reactions:, Asymmetric hetero-Diels–Alder reactions catalysed by 2a:, Asymmetric glyoxylate-ene reactions catalysed by 2a:, 91% ee:, 92% ee:, 96% ee:, > 96% ee:, Asymmetric syntheses of enantiomerically enriched ipsdienol:, also see
    • (1974) Naturwissenschaften , vol.61 , pp. 365
    • Vite, J.P.1    Bakke, A.2    Highes, P.R.3
  • 8
    • 0001385922 scopus 로고
    • Review: ed. A. Hassner, JAI, London and references cited therein;
    • K. Mori, Advances in Asymmetric Synthesis, 1995, 1, 211, Review: ed. A. Hassner, JAI, London and references cited therein;
    • (1995) Advances in Asymmetric Synthesis , vol.1 , pp. 211
    • Mori, K.1
  • 13
    • 0001856207 scopus 로고
    • Reviews on ene reactions: ed. A. Hassner, JAI, London
    • K. Mikami, Advances in Asymmetric Synthesis, 1994, 1, Reviews on ene reactions: ed. A. Hassner, JAI, London
    • (1994) Advances in Asymmetric Synthesis , pp. 1
    • Mikami, K.1
  • 15
    • 0001899585 scopus 로고
    • ed. B. M. Trost, I. Fleming, Pergamon, Oxford, vol. 2, p. 527;
    • B.B. Snider, Comprehensive Organic Synthesis, 1991, 5, 1, ed. B. M. Trost, I. Fleming, Pergamon, Oxford, vol. 2, p. 527;
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 1
    • Snider, B.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.