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- W2321478129 abstract "Die durch Grignardierung endständiger Acetylene mit Äthyl-MgBr und nachfolgende Reaktion mit Orthoameisensäuretriäthylester leicht erhältlichen Acetylenacetale (II) (Ausbeute über 80%) reagieren mit überschüssigem Disiamylboran zu entsprechenden 0rganoborverbindungen, die durch alkalische H,O,-Oxidation die β-Ketoäther (I) bzw. durch saure Hydrolyse die cis-Alkenyläther (III) ergeben." @default.
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- W2321478129 date "1974-03-26" @default.
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- W2321478129 title "ChemInform Abstract: NOVEL SYNTHESES OF ALPHA-KETO ETHERS AND CIS-ALLYLIC ETHERS VIA THE HYDROBORATION OF ACETYLENIC ACETALS" @default.
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- W2321478129 doi "https://doi.org/10.1002/chin.197412204" @default.
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