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Volumn , Issue 2, 1996, Pages 223-234

Pronounced electronic effect of allylic amino groups on the π-facial stereoselectivity and reactivity of the iodoetherification of N-substituted 3-amino-4-penten-1-ols

Author keywords

3 Amino 2 (iodomethyl)tetrahydrofuran, cis and trans ; Diastereoselectivity; Iodoetherification; Taft * constant

Indexed keywords


EID: 33748907567     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199619960212     Document Type: Article
Times cited : (7)

References (63)
  • 2
    • 0000046858 scopus 로고
    • (Ed.: J. D. Morrison), Academic
    • E. L. Eliel in Asymmetric Synthesis (Ed.: J. D. Morrison), Academic, 1983, vol. 2, part A, p. 125.
    • (1983) Asymmetric Synthesis , vol.2 , Issue.PART A , pp. 125
    • Eliel, E.L.1
  • 55
    • 0010313691 scopus 로고
    • (Ed.: H. B. Kagan), Georg Thieme, Stuttgart, chapter 2
    • A. Gaudemer in Stereochemistry (Ed.: H. B. Kagan), Georg Thieme, Stuttgart, 1977; vol. 1, chapter 2;
    • (1977) Stereochemistry , vol.1
    • Gaudemer, A.1
  • 58
    • 85088544919 scopus 로고    scopus 로고
    • note
    • [9b].
  • 59
    • 33748909081 scopus 로고    scopus 로고
    • note
    • 2 at 0°C for additional 10 h) proceeded relatively straightforwardly and provided the expected tetrahydrofuran derivatives cis- and trans-15k, though iodinated in the para-position of the phenyl ring. (Chemical Equation Presented)
  • 61
    • 85088544179 scopus 로고    scopus 로고
    • note
    • 5 skeleton involving NH and OH groups. The steric effects involving the substituents of C-1, C-2 and nitrogen atom are discussed later.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.