Direct introduction of acetylene moieties into azines by methodology
AM Prokhorov, M Mąkosza, ON Chupakhin
Index: Prokhorov, Anton M.; Makosza, Mieczyslaw; Chupakhin, Oleg N. Tetrahedron Letters, 2009 , vol. 50, # 13 p. 1444 - 1446
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Citation Number: 19
Abstract
The N-oxides of azines 1a–g react with lithium and/or potassium acetylides to give the corresponding ethynylazines 2a–g. Reaction with lithium acetylide requires subsequent acylation of the intermediate anionic adduct for rearomatization whereas in the case of potassium acetylide, auto-aromatization takes place.
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