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Volumn 44, Issue 3, 2003, Pages 503-506

Sulfur-mediated radical cyclisation reactions on solid support

Author keywords

[No Author keywords available]

Indexed keywords

4 TOLYLBENZENESELENOSULFONATE; ALKADIENE; CYCLOPENTANE DERIVATIVE; SULFONIC ACID DERIVATIVE; SULFUR; THIOPHENOL; UNCLASSIFIED DRUG;

EID: 0037433941     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02594-7     Document Type: Article
Times cited : (24)

References (35)
  • 2
    • 0000315424 scopus 로고
    • Trost, B. M., Ed. Pergamon: Oxford
    • For recent overviews of radical cyclisation reactions, see: (b) Curran, D. P. In Comprehensive Organic Synthesis, Trost, B. M., Ed. Pergamon: Oxford, 1991; Vol. 4, pp. 779-831;
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 779-831
    • Curran, D.P.1
  • 5
    • 0004317627 scopus 로고
    • US Department of Health, Education and Welfare, Washington, Nov.
    • For a detailed report on the toxicity of tin reagents, see Occupational Exposure to Organotin Compounds, US Department of Health, Education and Welfare, Washington, Nov. 1976.
    • (1976) Occupational Exposure to Organotin Compounds
  • 12
    • 0033214241 scopus 로고    scopus 로고
    • For further examples of intermolecular radical reactions involving solid supported substrates, see: (a) Caddick, S.; Hamza, D.; Wadman, S. N. Tetrahedron Lett. 1999, 40, 7285-7588;
    • (1999) Tetrahedron Lett. , vol.40 , pp. 7285-7588
    • Caddick, S.1    Hamza, D.2    Wadman, S.N.3
  • 13
    • 0035102971 scopus 로고    scopus 로고
    • For further examples of intermolecular radical reactions involving solid supported substrates, see: (b) Plourde, R., Jr.; Johnson, L. L., Jr.; Longo, R. K. Synlett 2001, 439-441;
    • (2001) Synlett , pp. 439-441
    • Plourde R., Jr.1    Johnson L.L., Jr.2    Longo, R.K.3
  • 14
    • 0035858760 scopus 로고    scopus 로고
    • For further examples of intermolecular radical reactions involving solid supported substrates, see: (c) Taddei, M.; Attardi, M. E. Tetrahedron Lett. 2001, 42, 3519-3522;
    • (2001) Tetrahedron Lett. , vol.42 , pp. 3519-3522
    • Taddei, M.1    Attardi, M.E.2
  • 15
    • 0033607738 scopus 로고    scopus 로고
    • For further examples of intermolecular radical reactions involving solid supported substrates, see: (d) Miyabe, H.; Tanaka, H.; Naito, T. Tetrahedron Lett. 1999, 40, 8387-8390;
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8387-8390
    • Miyabe, H.1    Tanaka, H.2    Naito, T.3
  • 19
    • 0033597973 scopus 로고    scopus 로고
    • For examples of thiyl radical induced cyclisation reactions, see: (c) Harrowven, D. C.; Hannam, J. C. Tetrahedron 1999, 55, 9341-9346;
    • (1999) Tetrahedron , vol.55 , pp. 9341-9346
    • Harrowven, D.C.1    Hannam, J.C.2
  • 25
    • 0001304521 scopus 로고
    • For examples of thiyl radical induced cyclisation reactions, see: (h) Kuehne, M. E.; Damon, R. E. J. Org. Chem. 1977, 42, 1825-1832;
    • (1977) J. Org. Chem. , vol.42 , pp. 1825-1832
    • Kuehne, M.E.1    Damon, R.E.2
  • 26
    • 26444563031 scopus 로고    scopus 로고
    • Kharasch, N.; Meyers, C. Y., Eds. Pergamon: Oxford, Chapter 9
    • For examples of thiyl radical induced cyclisation reactions, see: (i) Oswald, A. A.; Griesbaum K. In The Chemistry of Organic Sulfur Compound; Kharasch, N.; Meyers, C. Y., Eds. Pergamon: Oxford, 1966; Vol. 2, Chapter 9, pp. 233-256.
    • (1996) The Chemistry of Organic Sulfur Compound , vol.2 , pp. 233-256
    • Oswald, A.A.1    Griesbaum, K.2
  • 30
    • 0012121711 scopus 로고    scopus 로고
    • note
    • AIBN was added hourly from the commencement of each reaction in nine equal portions.
  • 35
    • 0012197293 scopus 로고    scopus 로고
    • note
    • Solution phase analogues of all the solid supported radical reactions outlined in this paper were conducted using the appropriate dimethyl diallylmalonate derivative. The products derived from both the solid and solution phase experiments gave near identical stereochemical outcomes.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.