메뉴 건너뛰기




Volumn , Issue 11, 2003, Pages 2062-2070

Enantioselective synthesis of clavepictine analogues and evaluation of their cytotoxic activity

Author keywords

Cytotoxic compounds; Human cancer cell lines; Iminium ions; Quinolizidines

Indexed keywords

3 HYDROXY 4 METHYL 6 PHENYLETHYNYLOCTAHYDROQUINOLIZIDINE; 6 (DEC 1 ENYL) 3 HYDROXY 4 METHYLOCTAHYDROQUINOLIZIDINE; 6 (DEC 3 EN 1 YNYL) 3 HYDROXY 4 METHYLOCTAHYDROQUINOLIZIDINE; 6 DECYL 3 HYDROXY 4 METHYLOCTAHYDROQUINOLIZIDINE; 6 ETHYNYL 3 HYDROXY 6 METHYLOCTAHYDROQUINOLIZIDINE; 7 HYDROXY 6 METHYLOCTAHYDROQUINOLIZIDINE 4 CARBONITRILE; ALKALOID DERIVATIVE; AMINONITRILE; CLAVEPICTINE DERIVATIVE; CYTOTOXIC AGENT; DOXORUBICIN; ETOPOSIDE; IRINOTECAN; NITRILE; OXAZOLIDINE DERIVATIVE; QUINOLIZIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037934623     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300057     Document Type: Article
Times cited : (31)

References (18)
  • 13
    • 0038659609 scopus 로고    scopus 로고
    • note
    • A first approach involving formation of aminonitrile 19 through a more-classical Strecker reaction was unsuccessful. The high stereoselectivity of this step results from thermodynamic control (axial position of the nitrile moity results from the anomeric effect).
  • 16
    • 0038659610 scopus 로고    scopus 로고
    • note
    • For clarity, only the major isomer at C-2 is depicted in Figure 5, but the same explanation accounts for the production of 14 from the minor stereoisomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.