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Volumn 17, Issue 15, 2006, Pages 2195-2198

Lipase-catalyzed kinetic resolution of tetronic acid derivatives bearing a chiral quaternary carbon: total synthesis of (S)-(-)-vertinolide

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; CARBON; MYCOTOXIN; TETRONIC ACID DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; VETRINOLIDE;

EID: 33748689298     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.07.044     Document Type: Article
Times cited : (12)

References (40)
  • 29
    • 0021021393 scopus 로고
    • Synthesis of chiral (S)-(-)-vertinolide:
    • Synthesis of chiral (S)-(-)-vertinolide:. Wrobel J.E., and Ganem B. J. Org. Chem. 48 (1983) 3761-3764
    • (1983) J. Org. Chem. , vol.48 , pp. 3761-3764
    • Wrobel, J.E.1    Ganem, B.2
  • 39
    • 33748711469 scopus 로고    scopus 로고
    • note
    • Typical procedure: To a solution of the alcohol 6 (0.5 mmol) in vinyl acetate (3 mL), lipase (50 mg) was added, and stirred at 25 °C for an appropriate time. Lipase was removed through filtration and washed with ethyl acetate, and the combined organic filtrates were concentrated to give a crude oil, which was purified by column chromatography (silica gel, eluent: hexane-AcOEt) to give the acetate 9 and the recovered alcohol 6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.