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Volumn , Issue 3, 1981, Pages 115-117

Stereoselective introduction of hydroxy-groups into the 24-, 25-, and 26-positions of the cholesterol side chain

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Indexed keywords


EID: 37049099227     PISSN: 00224936     EISSN: None     Source Type: Journal    
DOI: 10.1039/c39810000115     Document Type: Article
Times cited : (21)

References (20)
  • 9
    • 0017302088 scopus 로고
    • A. stereoselective preparation of 24,25-dihydroxycholesterol was reported by
    • A. stereoselective preparation of 24,25-dihydroxycholesterol was reported by J. J. Partridge, V. Toome, and M. R. Uskokovic, J. Am. Chem. Soc., 1976, 98, 3739
    • (1976) J. Am. Chem. Soc , vol.98 , pp. 3739
    • Partridge, J.J.1    Toome, V.2    Uskokovic, M.R.3
  • 10
    • 0018251407 scopus 로고
    • gives a method for inversion of the configuration of hydroxy-groups on the side chain
    • M. Ishiguro, H. Saito, A. Sakamoto, and N. Ikekawa, Chem. Pharm. Bull., 1978, 26, 3715, gives a method for inversion of the configuration of hydroxy-groups on the side chain.
    • (1978) Chem. Pharm. Bull , vol.26 , pp. 3715
    • Ishiguro, M.1    Saito, H.2    Sakamoto, A.3    Ikekawa, N.4
  • 19
    • 84917806564 scopus 로고
    • 18O]-labelled 24, 25-epoxy-26-ol 26-benzoate (details will be reported elsewhere). Recently, the French group also revised their previous assignment
    • 18O]-labelled 24, 25-epoxy-26-ol 26-benzoate (details will be reported elsewhere). Recently, the French group also revised their previous assignment: M. Cesario, J. Guilhem, C. Pascard, and J. Redel, Tetrahedron Lett., 1980, 1588
    • (1980) Tetrahedron Lett , pp. 1588
    • Cesario, M.1    Guilhem, J.2    Pascard, C.3    Redel, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.