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Volumn 53, Issue 9, 2005, Pages 1088-1091

Synthesis of a capillarisin sulfur-analogue possessing aldose reductase inhibitory activity by selective isopropylation

Author keywords

3,4,5 trimethoxyphenol; Aldose reductase inhibitor; Capillarisin; Selective isopropylation; Substitution reaction

Indexed keywords

2 [(4 HYDROXYPHENYL)THIO] 7 ISOPROPOXY 5,6 DIMETHOXY 4H CHROMEN 4 ONE; ACETIC ACID DERIVATIVE; ALDOSE REDUCTASE INHIBITOR; ANTIOXIDANT; CAPILLARISIN DERIVATIVE; CHROMENE DERIVATIVE; IMIDAZOLE DERIVATIVE; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 24944517917     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.53.1088     Document Type: Article
Times cited : (14)

References (13)
  • 9
    • 24944591977 scopus 로고    scopus 로고
    • note
    • Although the acetophenone 7 was a commercially available material, it was synthesized by the following method. Friedel-Crafts reaction of 3,4,5-trimethoxyphenol and acetic anhydride using zinc choride in nitromethane followed by hydrolysis using sodium hydrogencarbonate to give 7 in 91% yield.
  • 10
    • 70449367182 scopus 로고
    • Gammil R. B., Synthesis, 1979, 901-903 (1979).
    • (1979) Synthesis , vol.1979 , pp. 901-903
    • Gammil, R.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.