메뉴 건너뛰기




Volumn 60, Issue 20, 2004, Pages 4413-4424

Asymmetric radical cyclization reactions of axially chiral N-allyl-o-iodoanilides to form enantioenriched N-acyl dihydroindoles

Author keywords

Axially chiral N allyl o iodoanilides; Intramolecular reaction; Radical cyclization

Indexed keywords

AMIDE; ANILIDE; INDOLE DERIVATIVE;

EID: 1942436913     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.02.064     Document Type: Article
Times cited : (44)

References (41)
  • 1
    • 1942445210 scopus 로고
    • N.L. Allinger, E. Eliel, Wilen S.H.
    • Oki M. Allinger N.L., Eliel E., Wilen S.H. Topics in stereochemistry. Vol. 14:1986;1-76
    • (1986) Topics in Stereochemistry , vol.14 , pp. 1-76
    • Oki, M.1
  • 31
    • 0027322369 scopus 로고
    • Similar preferences are seen for reactions on the N-acyl side of many anilide radicals. See: (a)
    • Similar preferences are seen for reactions on the N-acyl side of many anilide radicals. See: (a) Curran D.P., Abraham A.C. Tetrahedron. 49:1993;4821-4840
    • (1993) Tetrahedron , vol.49 , pp. 4821-4840
    • Curran, D.P.1    Abraham, A.C.2
  • 39
    • 1942477489 scopus 로고    scopus 로고
    • The sample for crystallography was prepared by the 'amide ketal' route summarized below (see Ref. 2d). These experiments also show that amides and amide ketals give the same sense of asymmetric induction
    • The sample for crystallography was prepared by the 'amide ketal' route summarized below (see Ref. 2d). These experiments also show that amides and amide ketals give the same sense of asymmetric induction


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.