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Volumn 1, Issue 2, 1999, Pages 269-271

Inhibition of stannane-mediated radical rearrangements by a recoverable, minimally fluorous selenol

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EID: 0001485558     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990590+     Document Type: Article
Times cited : (26)

References (32)
  • 18
    • 0043078389 scopus 로고    scopus 로고
    • note
    • In each of these experiments 1 was recovered in a minimum of 85% yield by continuous fluorous extraction with the modified continuous extractor.
  • 22
    • 0041575470 scopus 로고    scopus 로고
    • note
    • The selenol does not catalyze the reduction of the initial vinyl or aryl radical owing to the already very high rate constants for trapping of these types of radical by the stannane. For discussions of this point, see refs 1c and 1f.
  • 27
    • 0001608244 scopus 로고
    • Preparation and stannane-mediated opening of a related phenyl selenide: Clive, D. L. J.; Daigneault, S. J. Org. Chem. 1991, 56, 3801.
    • (1991) J. Org. Chem. , vol.56 , pp. 3801
    • Clive, D.L.J.1    Daigneault, S.2
  • 32
    • 0009514092 scopus 로고
    • Wiley: New York, Collect.
    • (b) Muchmore, D. C. Organic Syntheses; Wiley: New York, 1988; Collect. Vol. 6, p 762.
    • (1988) Organic Syntheses , vol.6 , pp. 762
    • Muchmore, D.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.