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Switchable Chemoselectivity of Reactive Intermediates Formation and Their Direct Use in A Flow Microreactor.

Yosuke AshikariTakashi TamakiTomoko KawaguchiMai FurusawaYuya YonekuraSusumu IshikawaYusuke TakahashiYoko AizawaAiichiro Nagaki
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2021)
A chemoselectivity switchable microflow reaction was developed to generate reactive and unstable intermediates. The switchable chemoselectivity of this reaction enables a selection for one of two different intermediates, an aryllithium or a benzyl lithium, at will from the same starting material. Starting from bromo-substituted styrenes, the aryllithium intermediates were converted to the substituted styrenes, whereas the benzyl lithium intermediates were engaged in an anionic polymerization. These chemoselectivity-switchable reactions can be integrated to produce polymers that cannot be formed during typical polymerization reactions.
Keyphrases
  • molecular docking
  • solid state