Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process.
نویسندگان
چکیده
Stable enols were synthesized from the reaction of (1Z,3Z)-1,4-dilithio-1,3-dienes with acid chlorides and structurally characterized by single-crystal X-ray analysis. These stable enols were formed by a novel de-aromatization/Michael addition/re-aromatization domino process.
منابع مشابه
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ورودعنوان ژورنال:
- Organic & biomolecular chemistry
دوره 5 13 شماره
صفحات -
تاریخ انتشار 2007