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Volumn 40, Issue 34, 1999, Pages 6293-6296

Catalytic use of organostannyl radical: The reaction of 1,2,3- selenadiazole with olefins in the presence of a catalytic amount of tributyltin hydride

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3 SELENADIAZOLE; ALKENE; CYCLOHEXANONE; TRIBUTYLTIN; TRIBUTYLTIN HYDRIDE; UNCLASSIFIED DRUG;

EID: 0033588282     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01286-1     Document Type: Article
Times cited : (19)

References (25)
  • 1
    • 0001562822 scopus 로고
    • For examples, see; a) Fart, D. J. Science, 1984, 223, 883.
    • (1984) Science , vol.223 , pp. 883
    • Fart, D.J.1
  • 7
    • 4944230527 scopus 로고
    • For reviews of the chemistry of organotin compounds, see: a) Neumann, W. P. Synthesis, 1987, 665.
    • (1987) Synthesis , pp. 665
    • Neumann, W.P.1
  • 10
    • 0000315424 scopus 로고
    • Trost, B, M.; Fleming, I. Eds. Pergamon, Oxford
    • d) Curran, D. P. In Comprehensive Organic Synthesis, Trost, B, M.; Fleming, I. Eds. Pergamon, Oxford, 1991, Vol. 4, p. 779.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 779
    • Curran, D.P.1
  • 14
    • 0026059062 scopus 로고
    • As another example of catalytic use of tributyltin hydride, intermolecular cyclization of organotin compounds has been shown. See; Kim, S.; Lee, S. Tetrahedron Lett. 1991, 32, 6575.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6575
    • Kim, S.1    Lee, S.2
  • 22
    • 0033593393 scopus 로고    scopus 로고
    • More recently, R. E. Maleczka, Jr. showed a new approach for the catalytic use of organotin compounds. See: Terstiege, I.; Maleczka, Jr. R. E. J. Org. Chem. 1999, 64, 342.
    • (1999) J. Org. Chem. , vol.64 , pp. 342
    • Terstiege, I.1    Maleczka R.E., Jr.2
  • 23
    • 0009577441 scopus 로고
    • and references cited therein
    • For reviews of the chemistry of hindered ,2,3-selenadiazoles, see: Ando, W.; Tokitoh, N. Heteroatom Chem. 1989, 2, 1 and references cited therein.
    • (1989) Heteroatom Chem. , vol.2 , pp. 1
    • Ando, W.1    Tokitoh, N.2
  • 24
    • 0009577309 scopus 로고    scopus 로고
    • In the absence of benzene, the yield of 5a was slightly decreased (55 %)
    • In the absence of benzene, the yield of 5a was slightly decreased (55 %).
  • 25
    • 0009577737 scopus 로고    scopus 로고
    • note
    • 3Sn radical to 1,2,3-selenadiazole, the addition of the vinyl radical to the carbon-carbon double bond and the intramolecular cyclization were faster than that of the reaction of the tributylstannyl radical with hydroquinone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.