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Volumn 51, Issue 6, 2003, Pages 640-645

Synthesis and anti-tumor activity of new steroidal nuclear analogues of aragusterol A

Author keywords

Analogue; Anti tumor; Aragusterol A; Steroid; Synthesis

Indexed keywords

3ALPHA,7ALPHA DIHYDROXY 5 EPIARAGUSTEROL A; 5 EPIARAGUSTEROL A; 7ALPHA HYDROXYARAGUSTEROL A; ARAGUSTEROL A; CHOLIC ACID; STEROID; UNCLASSIFIED DRUG; XESTOKEROL B;

EID: 14844306670     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.51.640     Document Type: Article
Times cited : (5)

References (25)
  • 11
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    • Charette A. B., C&EN, 73, February 6, 2 (1995).
    • (1995) C&EN , vol.73 , Issue.FEBRUARY 6 , pp. 2
    • Charette, A.B.1
  • 16
    • 27944440280 scopus 로고    scopus 로고
    • note
    • In this reaction, 7β-isomer was not obtained.
  • 19
    • 27944480614 scopus 로고    scopus 로고
    • note
    • 13C-NMR spectrum.
  • 21
    • 27944436338 scopus 로고    scopus 로고
    • note
    • Diastereoselectivity in the epoxidation of 14 and 17 can be explained based on the transition state in which vanadium metal is coordinated with hydroxy group at C-12. See ref. 8.
  • 23
    • 27944456260 scopus 로고    scopus 로고
    • note
    • The stereoselectivity of epoxidation with mCPBA is explained by preferential attack of the reagent from the less hindered side. See ref. 8.
  • 24
    • 27944458596 scopus 로고    scopus 로고
    • note
    • On a larger scale, this procedure will sometimes lead to violent explosions. See ref. 12 and 13.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.