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Volumn , Issue 22, 1992, Pages 1680-1681

First examples of seleno-Claisen rearrangements of allyl vinyl selenides

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EID: 37049077859     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/C39920001680     Document Type: Article
Times cited : (16)

References (24)
  • 13
    • 0004112606 scopus 로고
    • D. Liotta, Wiley, New York
    • T. G. Back, in Organoselenium Chemistry, ed. D. Liotta, Wiley, New York, 1987, pp. 325–364.
    • (1987) Organoselenium Chemistry , pp. 325-364
    • Back, T.G.1
  • 17
    • 33845278370 scopus 로고
    • Selenoaldehydes are known to be good dienophiles giving mainly the endo adduct when reacted with cyclopentadiene:
    • Selenoaldehydes are known to be good dienophiles giving mainly the endo adduct when reacted with cyclopentadiene: P. T. Meinke and G. A. Krafft, J. Am. Chem. Soc., 1988, 110, 8671.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8671
    • Meinke, P.T.1    Krafft, G.A.2
  • 21
    • 33947087636 scopus 로고
    • These conditions were previously used to trap thioaldehydes generated by thio-Claisen rearrangements:
    • These conditions were previously used to trap thioaldehydes generated by thio-Claisen rearrangements: K. Oshima, H. Yamamoto and H. Nozaki, J. Am. Chem. Soc., 1973, 95, 4446.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4446
    • Oshima, K.1    Yamamoto, H.2    Nozaki, H.3
  • 23
    • 33645975315 scopus 로고
    • Reviews on selenocarbonyl compounds: ed. D. L. Klayman and H. H. Günther, Wiley, New York
    • Reviews on selenocarbonyl compounds: R. B. Silverman, in Organic Selenium Compounds: Their Chemistry and Biology, ed. D. L. Klayman and H. H. Günther, Wiley, New York, 1973, pp. 245–262;.
    • (1973) Organic Selenium Compounds: Their Chemistry and Biology , pp. 245-262
    • Silverman, R.B.1
  • 24
    • 84943848267 scopus 로고    scopus 로고
    • ref. 5
    • F. S. Guziec in ref. 5, pp. 277–324.
    • Guziec, F.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.