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Volumn , Issue 3, 1997, Pages 339-347

Remote functionalization by tandem radical chain reactions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33748558814     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a600172f     Document Type: Article
Times cited : (9)

References (41)
  • 10
    • 0343869691 scopus 로고
    • E. S. Huyser, ed., Marcel Dekker, New York
    • (a) For a review of free-radical brominations, see reference 4 and: W. A. Thaler, in Methods in Free-Radical Chemistry, E. S. Huyser, ed., Marcel Dekker, New York, 1969, vol. 2, p. 121;
    • (1969) Methods in Free-Radical Chemistry , vol.2 , pp. 121
    • Thaler, W.A.1
  • 16
    • 33748519996 scopus 로고
    • PhD Thesis, Columbia University
    • (a) R. Corocoran, PhD Thesis, Columbia University, 1975;
    • (1975)
    • Corocoran, R.1
  • 17
    • 33748556669 scopus 로고
    • PhD Thesis, Columbia University
    • (b) D. Heyer, PhD Thesis, Columbia University, 1983;
    • (1983)
    • Heyer, D.1
  • 18
    • 33748557916 scopus 로고
    • PhD Thesis, Columbia University
    • (c) U. Maitra, PhD Thesis, Columbia University, 1986;
    • (1986)
    • Maitra, U.1
  • 19
    • 33748582417 scopus 로고
    • PhD Thesis, Columbia University
    • (d) T. Guo, PhD Thesis, Columbia University, 1990;
    • (1990)
    • Guo, T.1
  • 20
    • 33748557591 scopus 로고
    • PhD Thesis, Columbia University
    • (e) R. Batra, PhD Thesis, Columbia University, 1989.
    • (1989)
    • Batra, R.1
  • 21
    • 33748544382 scopus 로고    scopus 로고
    • Thanks to Dr Branco Jursic for a sample of NPID
    • Thanks to Dr Branco Jursic for a sample of NPID.
  • 27
    • 0000817070 scopus 로고
    • R. Adams, ed., Wiley New York
    • J. L. Wood, in Organic Reactions, R. Adams, ed., Wiley New York 1946, vol. 3, pp. 240-266.
    • (1946) Organic Reactions , vol.3 , pp. 240-266
    • Wood, J.L.1
  • 30
    • 85088076357 scopus 로고    scopus 로고
    • note
    • 18 This report seemed to preclude the postulated formation of phenyliodine dithiocyanate.
  • 32
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    • (a) R. Neu, Chem. Ber., 1939, 72, 1505;
    • (1939) Chem. Ber. , vol.72 , pp. 1505
    • Neu, R.1
  • 39
    • 85088076426 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum of the 9-chloride 2, two methine proton peaks are shifted downfield of the steroidal envelope to δ 2.2-2.4 and 2.5-2.7. In the spectrum of the steroid 9-bromide 4, two new peaks shifted downfield of the steroidal envelope, each of which had the same general line shape as those of the two methine proton peaks observed in the spectrum of the 9-chloride 2, were observed at δ 2.3-2.5 and 2.6-2.8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.