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Volumn 44, Issue 31, 2005, Pages 4914-4917

Stable reagents for the generation of N-centered radicals: Hydroamination of norbornene

Author keywords

Hydroaminations; Radical chemistry; Synthetic methods

Indexed keywords

BORON COMPOUNDS; COMPLEXATION; SYNTHESIS (CHEMICAL);

EID: 23744503053     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200463032     Document Type: Article
Times cited : (88)

References (35)
  • 3
    • 4143082679 scopus 로고    scopus 로고
    • For a review in hydroaminations of alkynes, see: S. Doye, Synlett 2004, 1653.
    • (2004) Synlett , pp. 1653
    • Doye, S.1
  • 8
    • 0001253023 scopus 로고    scopus 로고
    • (Eds.: P. Renaud, M. P. Sibi), Wiley-VCH, Weinheim
    • L. Stella in Radicals in Organic Synthesis, Vol. 2 (Eds.: P. Renaud, M. P. Sibi), Wiley-VCH, Weinheim, 2001, p. 407.
    • (2001) Radicals in Organic Synthesis, Vol. 2 , vol.2 , pp. 407
    • Stella, L.1
  • 29
    • 33645201157 scopus 로고    scopus 로고
    • note
    • In the presence of 30 % thiol catalyst the yield decreased (28 %) and thiyl radical addition to vinyl pivalate was observed as a side reaction.
  • 30
    • 33645199413 scopus 로고    scopus 로고
    • note
    • The regioisomeric hydroamination product, the cyclic N,O acetal, was formed in 5 % yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.