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Volumn 43, Issue 8, 2000, Pages 1586-1603

Structure-activity studies for a novel series of tricyclic substituted hexahydrobenz[e]isoindole α(1A) adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia (BPH)

Author keywords

[No Author keywords available]

Indexed keywords

3 [2 (6 METHOXY 2,3,3A,4,5,9B HEXAHYDRO[1H] BENZ[E]ISOINDOL 2 YL)ETHYL] 8 CHLORO PYRAZINOL[2'3':4,5]THIENOL[3,2 DEXTRO]PYRIMIDINE 2,4(1H,3H) DIONE; ALPHA 1 ADRENERGIC RECEPTOR BLOCKING AGENT; INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034692176     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm990567u     Document Type: Article
Times cited : (55)

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    • note
    • Dinitriles epimerize under the reaction conditions. It seems likely that the trans dinitrile is converted to trans benzoisoindole at a greater rate than the cis dinitrile, leading to predominant formation of trans benzoisoindole in accordance with Curtin-Hammett principle.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.