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Tetrahedron Letters
Volumn 19, Issue 5, 1978, Pages 419-420
One-step conversion of protected lactols into lactones
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[No Author keywords available]
Indexed keywords

EID: 49349140549     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)91443-1     Document Type: Article
Times cited : (136)
References (4)
  • 1
    • 84917989882 scopus 로고    scopus 로고
    • The protected lactols were prepared in 〉90% yield from the corresponding lactones via reduction with diisobutylaluminum hydride in toluene at −78° followed by treatment (0°) with methanol in the presence of a catalytic amount of boron trifluoride etherate.
  • 2
    • 84917989881 scopus 로고    scopus 로고
    • The yields for the conversion of cyclic methyl acetals into their respective γ-butyrolactones are given in the parentheses under the structures 3-7.
  • 3
    • 0001612231 scopus 로고
    • The oxidation of noncyclic acetals to esters in moderate yield employing peracetic acid—sulfuric acid at 40–60°C has been reported
    • (1960) J. Org. Chem. , vol.25 , pp. 1699
    • Heywood1    Phillips2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.