Abstract
AbstractDie Ringöffnung der Epoxide (I) mit den Alkoholen (II) zu den Glykolmonoalkylethern (III) und (IV) unter Katalyse durch Heteropolysäuren wird untersucht; die Katalyse ist selektiver und effizienter als durch H2SO4, HClO4 oder p‐Toluolsulfonsäure (V).
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