1972
DOI: 10.1002/chin.197230190
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ChemInform Abstract: METHODE ZUR KONDENSATION VON DIACETYLEN MIT CARBONYLVERBINDUNGEN

Abstract: Beim Einleiten von Diacetylen (II) in eine Suspension des Anionenaustauschharzes AB‐17 in einem Keton (I) entstehen die tert. Carbinole (III) sowie die Glykole (IV).

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“…224 It was shown that the anion-exchange resin AB-17-8P (OH) catalyses the condensation of diacetylene with carbonyl compounds. 226 Tetramethylammonium hydroxide also catalyses the reaction of diacetylene with formaldehyde. 227 The reaction with formaldehyde occurs smoothly at 20 ± 40 8C and yields, in addition to hexa-2,4diyne-1,6-diol (96), 1,3-dioxolanes 97 and 98 which are the products of subsequent reaction of formaldehyde with the diol 96 and 2,4-pentadiynol.…”
Section: Reactions With Carbonyl Compoundsmentioning
confidence: 99%
“…224 It was shown that the anion-exchange resin AB-17-8P (OH) catalyses the condensation of diacetylene with carbonyl compounds. 226 Tetramethylammonium hydroxide also catalyses the reaction of diacetylene with formaldehyde. 227 The reaction with formaldehyde occurs smoothly at 20 ± 40 8C and yields, in addition to hexa-2,4diyne-1,6-diol (96), 1,3-dioxolanes 97 and 98 which are the products of subsequent reaction of formaldehyde with the diol 96 and 2,4-pentadiynol.…”
Section: Reactions With Carbonyl Compoundsmentioning
confidence: 99%