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Volumn 45, Issue 4, 2004, Pages 765-768

Recent developments in the synthesis of 11β-aryl-estrone derivatives

Author keywords

11 Aryl estrogen; Aromatization; Estrone derivatives; Industrial synthesis

Indexed keywords

ACETONE; EPOXIDE; ESTRONE DERIVATIVE; HEXACHLOROACETONE; SELECTIVE ESTROGEN RECEPTOR MODULATOR; UNCLASSIFIED DRUG;

EID: 0346157346     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.11.028     Document Type: Article
Times cited : (14)

References (27)
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    • note
    • The Grignard reagent was prepared in two steps from 4-bromo-phenol, 2-chloroethyl diethylamine hydrochloride, and magnesium turnings, as described in Ref. 2 with the parent piperidine derivative.
  • 18
    • 85030928822 scopus 로고    scopus 로고
    • note
    • This type of dienone has been described by F. Nique, Ref. [1b].
  • 19
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    • note
    • +).
  • 20
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    • note
    • +), 100.
  • 21
    • 85030923199 scopus 로고    scopus 로고
    • note
    • +).
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    • FR 81840, 1962 (Roussel Uclaf);
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  • 25
    • 85030933756 scopus 로고    scopus 로고
    • note
    • +), 446, 362, 86, 38, and 36 (HCl).
  • 26
    • 85030915195 scopus 로고    scopus 로고
    • note
    • Variable amounts of 8b (as base) were formed during the aqueous work-up after aromatization. Isolation of 7b would thus have resulted in some loss of this intermediate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.