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Volumn 45, Issue 46, 2004, Pages 8549-8552

C1-C2 cleavage of C1-functionalized 8-oxabicyclo-[3.2.1]-oct-6-en-3-one. Stereoselective preparation of 4-substituted butenolides

Author keywords

1,3 Dicarbonyl systems; 8 Oxabicyclo 3.2.1 oct 6 en 3 one; 4 + 3 Cycloaddition; Butenolides; C C bond cleavage; Hydrolysis

Indexed keywords

1 METHOXY 8 OXABICYCLO[3.2.1]OCT 6 EN 3 ONE; 4 (1 METHYL 2 OXOBUTYL) 2 BUTENOLIDE; BUTENOLIDE; GAMMA LACTONE DERIVATIVE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 5644267856     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.111     Document Type: Article
Times cited : (16)

References (56)
  • 47
    • 5644225393 scopus 로고    scopus 로고
    • note
    • 4, filtered and concentrated to dryness using a rotary evaporator, to obtain a crude product that was purified by flash column chromatography eluting with hexane/AcOEt mixtures of increasing polarity, to isolate 63 mg of pure 5 (69% yield)
  • 56
    • 5644268789 scopus 로고    scopus 로고
    • note
    • 13C NMR correlations


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.