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Volumn , Issue 12, 2004, Pages 2051-2065

Highly diastereoselective syntheses of propargylic acid and homopropargylic systems

Author keywords

Aziridines; Carbenoids; Epoxides; Homopropargylic alcohols; Zinc

Indexed keywords

ACETYLENE DERIVATIVE; ALCOHOL; ALDEHYDE; ALPHA CHLOROHYDRIN; AZIRIDINE DERIVATIVE; CARBENOID; EPOXIDE; ETHYLENE OXIDE; HOMOPROPARGYLIC ALCOHOL; IMINE; LEWIS ACID; PROPARGYLIC ACID; PROPARGYLIC OXIRANE; PROPIONIC ACID DERIVATIVE; UNCLASSIFIED DRUG; ZINC;

EID: 5644289709     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-832816     Document Type: Review
Times cited : (27)

References (126)
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  • 18
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    • The formation and transformations of allenic and α-acetylenic carbanions
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  • 19
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  • 39
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    • Reactivity of oxiranes with organolithium reagents
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    • (2004) The Chemistry of Organolithium Reagents , pp. 1165
    • Chemla, F.1    Vrancken, E.2
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    • note
    • (b) It should be noted that in this case the kinetic ratio of the chlorohydrin, obtained by reaction of an α-chloro lithiocarbenoid with aldehydes, was almost 0% de, the observed ratio after equilibration was attributed to ring-closure into oxiranes and ring opening of these oxiranes.
  • 81
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    • Jones, G.B.1    Chapman, B.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.