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Volumn 35, Issue 2, 1994, Pages 203-206

Cerium(III) chloride remarkably increases the rates of formation and yields of ketones in the reaction of lithium carboxylates with organolithiums

Author keywords

[No Author keywords available]

Indexed keywords

KETONE;

EID: 0028078680     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)76511-7     Document Type: Article
Times cited : (45)

References (54)
  • 1
    • 0002233116 scopus 로고
    • For a review on the reactions of carboxylic acids with organolithium reagents, see
    • (1970) Org. React. , vol.18 , pp. 1
    • Jorgenson1
  • 29
    • 33845377388 scopus 로고
    • Relative reactivity of bridgehead adamantyl and homoadamantyl substrates from solvolyses with heptafluorobutyrate as a highly reactive carboxylate leaving group. Absence of SN2 character of solvolysis of tert-butyl derivatives
    • (1985) Journal of the American Chemical Society , vol.107 , pp. 5717
    • Farcasiu1    Jähme2    Rüchardt3
  • 33
    • 0041614891 scopus 로고
    • Synthesis of isomeric methyl benzoylbenzoates and substituted o-, m-, and p-benzoylbenzoic acids
    • (1974) The Journal of Organic Chemistry , vol.39 , pp. 2053


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.