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Volumn 7, Issue 8, 2009, Pages 1573-1582

An appraisal of oxoketene cycloaddition methodology for the synthesis of 2,6-dideoxysugars and fluorinated 2,6-dideoxysugars

Author keywords

[No Author keywords available]

Indexed keywords

ACYLKETENES; CYCLOADDITION REACTIONS; CYCLOADDUCT; ELECTRONIC STRUCTURE CALCULATIONS; FLUORINE ATOMS; GOOD YIELDS; LITHIUM ENOLATE; METHYL ETHERS; REACTIVE INTERMEDIATES; VINYL ETHERS;

EID: 64149094607     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b817672h     Document Type: Article
Times cited : (9)

References (36)
  • 12
    • 34748872807 scopus 로고    scopus 로고
    • describes syntheses of various 6-deoxy 6-fluorinated sugars and their glycosylation reactions For syntheses of related C-arylglycosides, see: -11765
    • D. Crich O. Vinogradova J. Am. Chem. Soc. 2007 129 11756 11765
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 11756
    • Crich, D.1    Vinogradova, O.2
  • 15
    • 33845184134 scopus 로고
    • shows that acetoacetylations carried via dioxinone fragmentation have oxoketene formation as the rate determining step For a recent application of oxoketene methodology, see: -2193
    • R. J. Clemens J. S. Witzeman J. Am. Chem. Soc. 1989 111 2186 2193
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 2186
    • Clemens, R.J.1    Witzeman, J.S.2
  • 22
    • 33947094130 scopus 로고
    • O'Doherty has shown that dichloromethane can be used as an effective organic co-solvent for Luche reductions; see: -2227
    • J. L. Luche J. Am. Chem. Soc. 1978 100 2226 2227
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 2226
    • Luche, J.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.