메뉴 건너뛰기




Volumn 54, Issue 21, 2013, Pages 2619-2622

Dearomative radical spirocyclization from N-ce: Raghubenzyltrichloroacetamides revisited using a copper(I)-mediated atom transfer reaction leading to 2-azaspiro[4.5]decanes

Author keywords

Atom transfer radical cyclization; Azaspirodecanes; Copper; Dearomatization; Heterocycles

Indexed keywords

2 AZASPIRO[4.5]DECADIENE; 2 AZASPIRO[4.5]DECANE; ALKADIENE; ALLYLAMINE; CHLORINE; CHLOROACETAMIDE; COPPER; COPPER CHLORIDE; DECANE; HYDROXYL GROUP; METHANOL; N BENZYLTRICHLOROACETAMIDE; UNCLASSIFIED DRUG;

EID: 84876413398     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2013.03.019     Document Type: Article
Times cited : (10)

References (49)
  • 22
    • 0001144669 scopus 로고    scopus 로고
    • For other synthetic approaches, see
    • For other synthetic approaches, see: J. Cossy, A. Bouzide, and M. Pfau J. Org. Chem. 62 1997 7106 7113
    • (1997) J. Org. Chem. , vol.62 , pp. 7106-7113
    • Cossy, J.1    Bouzide, A.2    Pfau, M.3
  • 42
    • 0001219196 scopus 로고
    • The formation of 1,4-dienes reflects the known propensity of cyclohexanedienyl radicals for kinetic trapping at the internal position
    • The formation of 1,4-dienes reflects the known propensity of cyclohexanedienyl radicals for kinetic trapping at the internal position: A.L.J. Beckwith, D.M. O'Shea, and D.H. Roberts J. Am. Chem. Soc. 108 1986 6408 6409
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6408-6409
    • Beckwith, A.L.J.1    O'Shea, D.M.2    Roberts, D.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.