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Volumn 65, Issue 9, 2000, Pages 2830-2833

A simple, efficient and general method for the conversion of alcohols into alkyl iodides by a CeCl3·7H2O/NaI system acetonitrile

Author keywords

[No Author keywords available]

Indexed keywords

ACETONITRILE; ALCOHOL; CESIUM CHLORIDE; IODINE DERIVATIVE; SODIUM IODIDE;

EID: 0034608005     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo991894c     Document Type: Article
Times cited : (76)

References (35)
  • 1
    • 0000817472 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • (a) Bohlmann, R. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 6, pp 203-223.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 203-223
    • Bohlmann, R.1
  • 2
    • 0009673976 scopus 로고
    • Supplement D; Patai, S., Rappoport, Z., Eds.; Wiley: New York
    • (b) Hudlicky, M., Hudlicky, T. In The Chemistry of Functional Groups, Supplement D; Patai, S., Rappoport, Z., Eds.; Wiley: New York, 1983; p 1021.
    • (1983) The Chemistry of Functional Groups , pp. 1021
    • Hudlicky, M.1    Hudlicky, T.2
  • 3
    • 0000302107 scopus 로고
    • Barton, D., Ollis, W. D., Eds.; Pergamon Press: Oxford
    • (c) Chambers, R. D.; James, S. R. In Comprehensive Organic Chemistry; Barton, D., Ollis, W. D., Eds.; Pergamon Press: Oxford, 1979; vol. 1, pp 493-575.
    • (1979) Comprehensive Organic Chemistry , vol.1 , pp. 493-575
    • Chambers, R.D.1    James, S.R.2
  • 35
    • 0342745088 scopus 로고    scopus 로고
    • note
    • Preparation of 2-methyl-1,8-octanediol (8): The DIBAL-H reduction of ε-caprolactone followed by Wittig reaction with triethyl 2-phosphono propionate afforded ethyl 8-hydroxy-2-methyl-2-octenoate in 90% yield (two steps). The ester was hydrogenated (Pd/C) and reduced by DIBAL-H to give 8 in 78% yield (two steps).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.