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Generation of mono- and bis-dioxiranes from 2,3-butanedione

机译:由2,3-丁二酮生成单-和双-二恶烷

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摘要

Biacetyl reacts with oxone to give bis-dioxirane [3,3'-dimethyl-3,3'-bidioxirane, 3B] and mono-dioxirane [1-(3-methyl- dioxiran-3-yl)ethanone, 3A)]. Bis-dioxirane 3B is formed when two oxygens are incorporated into biacetyl, while mono- dioxirane 3A incorporated only one. A greater stability is observed in 3B compared to 3A, which is attributed to an alpha-dioxiranyl (anomeric) effect in the former. In contrast, 3A suffers from a destabilizing pi-electron withdrawing effect from the adjacent carbonyl group.
机译:联乙酰与氧杂环戊烷反应生成双二环氧乙烷[3,3'-二甲基-3,3'-二碘环氧乙烷,3B]和单二环氧乙烷[1-(3-甲基-二氧杂锡-3-基)乙酮,3A)。当将两个氧结合到联乙酰中时,会形成双二环氧乙烷3B,而单二环氧乙烷3A仅结合一个氧。与3A相比,在3B中观察到更大的稳定性,这归因于前者中的α-二氧杂环戊烷基(异头)效应。相反,3A遭受从相邻羰基的不稳定的π电子抽出作用。

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