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Tetrahedron Letters
Volumn 31, Issue 32, 1990, Pages 4601-4604
Addition of sulfinylated and sulfonylated carbon centered radicals to alkenes and enolethers
Author keywords

[No Author keywords available]
Indexed keywords

SULFOXIDE;
EID: 0025369894     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97686-X     Document Type: Article
Times cited : (43)
References (15)
  • 2
    • 85064667006 scopus 로고
    • The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2
    • (1988) Synthesis , vol.417 , pp. 489
    • Curran1
  • 3
    • 0000078448 scopus 로고
    • Polar effects in radical addition reactions: Borderline cases
    • Carbon centered radicals substituted with only one electron withdrawing group are generally considered as ambiphilic radicals:
    • (1988) Chemische Berichte , vol.121 , pp. 2063
    • Giese1    He2    Mehl3
  • 11
    • 84918626711 scopus 로고    scopus 로고
    • The chlorides were sufficiently reactive for the generation of the radicals.
  • 13
    • 84918610441 scopus 로고    scopus 로고
    • The cyclization reaction was not diastereoselective with respect to the chiral sulfur center.
  • 15
    • 84918600160 scopus 로고    scopus 로고
    • 4, filtrated and evaporated to give the crude product.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.