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Volumn , Issue 21, 1996, Pages 2619-2622

Enantiodivergent synthesis of both enantiomers of the macrocyclic lactone lasiodiplodin

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EID: 33748969701     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/p19960002619     Document Type: Article
Times cited : (40)

References (25)
  • 21
    • 33750283011 scopus 로고
    • A related intramolecular hydroboration/cross coupling sequence starting from bromophenylalkenes was described to give benzo-fused cyclopentenes and cyclohexenes, but failed to give seven-membered rings: N. Miyaura, T. Ishiyama, H. Sasaki, M. Ishikawa, M. Satoh and A. Suzuki, J. Am. Chem. Soc., 1989, 111, 314.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 314
    • Miyaura, N.1    Ishiyama, T.2    Sasaki, H.3    Ishikawa, M.4    Satoh, M.5    Suzuki, A.6
  • 22
    • 33751499427 scopus 로고
    • For the preparation of macrocyclic lactones (e.g. zearalenone) by intramolecular Pd-catalysed coupling of an aryl iodide with a vinyl stannane, see, A. Kalivretenos, J. K. Stille and L. S. Hegedus, J. Org. Chem., 1991, 65, 2883.
    • (1991) J. Org. Chem. , vol.65 , pp. 2883
    • Kalivretenos, A.1    Stille, J.K.2    Hegedus, L.S.3
  • 23
    • 0025907731 scopus 로고
    • For an example of reductive desulfurization without affecting a benzyl ether, see, D. Dobson, A. Todd and J. Gilmore, Synth. Commun., 1991, 21, 611.
    • (1991) Synth. Commun. , vol.21 , pp. 611
    • Dobson, D.1    Todd, A.2    Gilmore, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.