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Oxidative oxygen-nucleophilic bromo-cyclization of alkenyl carbonyl compounds without organic wastes using alkali metal reagents in green solvent

机译:在绿色溶剂中使用碱金属试剂对烯基羰基化合物进行氧化性氧亲核溴化,而无需有机废物

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摘要

A bromo-lactonization of alkenyl carboxylic acids and a bromo-cyclization of N-allyl amides as oxygen-nucleophilic bromo-cyclization reactions were developed via the oxidative umpolung of bromide using alkali metal bromide and inorganic oxidant to provide the corresponding cyclization products in high yields. In particular, the use of AcOEt, the solvent of choice for green sustainable reactions, led to the high reactivities of the present reactions. This methodology is highly recommended for green sustainable chemistry because it uses stable and non-hazardous reagents instead of other bromo reagents and oxidants, and does not produce organic wastes that pollute the environment.
机译:通过使用碱金属溴化物和无机氧化剂,通过溴化物的氧化反应,开发了烯基羧酸的溴内酯化和作为氧亲核性溴环化反应的N-烯丙基酰胺的溴环化反应,从而高产率地提供了相应的环化产物。特别地,使用AcOEt,绿色可持续反应的首选溶剂,导致了本反应的高反应性。强烈建议将此方法用于绿色可持续化学,因为它使用稳定且无害的试剂代替其他溴试剂和氧化剂,并且不会产生污染环境的有机废物。

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