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Volumn 37, Issue 36, 1996, Pages 6583-6586

Rearrangements and cyclizations in vinyl radicals. Unusual example of 1,4-radical translocation

Author keywords

[No Author keywords available]

Indexed keywords

RADICAL; VINYL DERIVATIVE;

EID: 0029680650     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01405-0     Document Type: Article
Times cited : (19)

References (26)
  • 1
    • 0001216647 scopus 로고
    • Radical Addition Reactions
    • Pergamon Press: Oxford, U. K., Chapter 4.1 and 4.2
    • a) Curran, D. P. "Radical Addition Reactions" in Comprehensive Organic Synthesis; Pergamon Press: Oxford, U. K., 1991; Vol. 4, Chapter 4.1 and 4.2;
    • (1991) Comprehensive Organic Synthesis , vol.4
    • Curran, D.P.1
  • 3
    • 0343174026 scopus 로고
    • Radical Addition involving CC Triple Bonds
    • Patai, S., Ed.; J. Wiley: New York, Chapter 16
    • Chatgilialoglu, C.; Ferreri, C. "Radical Addition involving CC Triple Bonds" in The Chemistry of Triple-bonded Functional Groups, Patai, S., Ed.; J. Wiley: New York, 1994; Suppl. C2, Vol. 2, Chapter 16.
    • (1994) The Chemistry of Triple-bonded Functional Groups , vol.2 , Issue.SUPPL. C2
    • Chatgilialoglu, C.1    Ferreri, C.2
  • 16
    • 85033064935 scopus 로고    scopus 로고
    • note
    • Method A: a benzene solution (20 mL) containing thiol (2 mmol), AIBN (0.2 mmol) and the appropriate alkyne (5 mmol) was refluxed for 3h. Method B: a benzene solution (5 mL) of thiol (2 mmol) was added within 3 h with a syringe pump to a boiling benzene solution of AIBN (1 mmol) and the appropriate alkyne 5 mmol). An additional amounts of AIBN (0.5 mmol) was added after 2 h. The resulting solution was refluxed for further 60 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.