No trace of acetylated pyrrolidine was observed where acylated morpholine was isolated Key Words in good yields when morpholine enamines were reacted.
📌 3 Key Takeaways
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Objective & Hypothesis:Acylation reaction of a variety of cyclic ketones via acylation of the corresponding enamines is well-defined in the literature.
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Key Findings & Data:Enamine acylation of carbonyl compounds is a significant synthetic method because of its mildness and the ease of preparing various β- diketones.The pyrrolidine and morpholine enamines of cyclic ketones such as cyclohexanone and cyclopentanone were successfully reacted with phenylacetyl chloride and chloroacetyl chloride respectively, to yield various acetylated or diacetylated enamines.
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Conclusion & Impact:No trace of acetylated pyrrolidine was observed where acylated morpholine was isolated Key Words in good yields when morpholine enamines were reacted.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Acylation reaction of a variety of cyclic ketones via acylation of the corresponding enamines is well-defined in the literature. Enamine acylation of carbonyl compounds is a significant synthetic method because of its mildness and the ease of preparing various β- diketones.The pyrrolidine and morpholine enamines of cyclic ketones such as cyclohexanone and cyclopentanone were successfully reacted with phenylacetyl chloride and chloroacetyl chloride respectively, to yield various acetylated or diacetylated enamines. No trace of acetylated pyrrolidine was observed where acylated morpholine was isolated Key Words in good yields when morpholine enamines were reacted.
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Cite This Article
ŞENÖZ, H., TUNOĞLU, N. (2022). Acetylation of some cyclic enamines with substituted acetyl chlorides. Hacettepe Journal of Biology and Chemistry, Cilt: 38 - Sayı: 2, 95–106. https://ajindex.com/articles/529281
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