双(pinacoloto)diboran/4-苯基吡啶体系的一锅光催化硼化和醛还原:在流动反应器中合成tavaborole

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC Synthesis-Stuttgart Pub Date : 2023-09-06 DOI:10.1055/a-2169-6200
Kankanala Naveen Kumar, Mouzma Mhate, Velayutham Ravichandiran, S. Swain
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引用次数: 0

摘要

报道了双(pinacoloto)diboran/4-苯基吡啶共催化卤化芳烃的一锅硼化反应和醛还原反应。在流动反应器中进行反应,在410nm处照射反应,停留时间为10min。该方法成功地用于一步合成他瓦波罗,收率为81%。
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Bis(pinacoloto)diboran/4-phenyl pyridine system for one-pot photocatalyzed borylation and reduction of aldehyde: synthesis of tavaborole in a flow reactor
A photocatalyzed one-pot borylation of haloarene and reduction of aldehyde by cocatalysis of bis(pinacoloto)diboran/4-phenyl pyridine is reported. The reaction was carried out in a flow reactor by irradiating the reaction at 410nm, with residence time of 10 min. The method was successfully applied for the synthesis of tavaborole in a single step with 81% yield.
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来源期刊
Synthesis-Stuttgart
Synthesis-Stuttgart 化学-有机化学
CiteScore
4.50
自引率
7.70%
发文量
435
审稿时长
1 months
期刊介绍: SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.
期刊最新文献
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