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首页> 外文期刊>Angewandte Chemie >Scalable Negishi Coupling between Organozinc Compounds and (Hetero)Aryl Bromides under Aerobic Conditions when using Bulk Water or Deep Eutectic Solvents with no Additional Ligands
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Scalable Negishi Coupling between Organozinc Compounds and (Hetero)Aryl Bromides under Aerobic Conditions when using Bulk Water or Deep Eutectic Solvents with no Additional Ligands

机译:在无氧条件下使用大量水或深的共晶溶剂,无需额外配体时有机锌化合物和(杂)芳基溴之间的可缩放的粘合剂

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摘要

Pd-catalyzed Negishi cross-coupling reactions between organozinc compounds and (hetero)aryl bromides have been reported when using bulk water as the reaction medium in the presence of NaCl or the biodegradable choline chloride/urea eutectic mixture. Both C(sp(3))-C(sp(2)) and C(sp(2))-C(sp(2)) couplings have been found to proceed smoothly, with high chemoselectivity, under mild conditions (room temperature or 60 degrees C) in air, and in competition with protonolysis. Additional benefits include very short reaction times (20 s), good to excellent yields (up to 98 %), wide substrate scope, and the tolerance of a variety of functional groups. The proposed novel protocol is scalable, and the practicability of the method is further highlighted by an easy recycling of both the catalyst and the eutectic mixture or water.
机译:在NaCl或可生物降解氯化胆碱/尿素共晶混合物存在下,以大量水为反应介质,报道了钯催化的有机锌化合物与(杂)芳基溴化物之间的Negishi交叉偶联反应。研究发现,C(sp(3))-C(sp(2))和C(sp(2))-C(sp(2))偶联反应在温和条件下(室温或60℃)在空气中进行,并且与质子解反应竞争,进行得很顺利,具有很高的化学选择性。额外的好处包括反应时间很短(20秒),良到优产率(高达98%),底物范围宽,以及对各种官能团的耐受性。所提出的新方案是可扩展的,并且该方法的实用性通过催化剂和共晶混合物或水的容易回收而进一步突出。

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