Reactions of Difunctional Electrophiles with Functionalized Aryllithium Compounds: Remarkable Chemoselectivity by Flash Chemistry

Flash chemistry using flow microreactors enables highly chemoselective reactions of difunctional electrophiles with functionalized aryllithium compounds by virtue of extremely fast micromixing. The approach serves as a powerful method for protecting‐group‐free synthesis using organolithium compounds...

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Published inAngewandte Chemie International Edition Vol. 54; no. 6; pp. 1914 - 1918
Main Authors Nagaki, Aiichiro, Imai, Keita, Ishiuchi, Satoshi, Yoshida, Jun-ichi
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 02.02.2015
WILEY‐VCH Verlag
Wiley
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Summary:Flash chemistry using flow microreactors enables highly chemoselective reactions of difunctional electrophiles with functionalized aryllithium compounds by virtue of extremely fast micromixing. The approach serves as a powerful method for protecting‐group‐free synthesis using organolithium compounds and opens a new possibility in the synthesis of polyfunctional organic molecules. Microreactors: Flash chemistry using flow microreactors enables highly chemoselective reactions of difunctional electrophiles with functionalized aryllithium compounds by virtue of extremely fast micromixing. The approach serves as a powerful method for protecting‐group‐free synthesis using organolithium compounds.
Bibliography:ark:/67375/WNG-1Q9P5MZ7-4
istex:E8349F965D5506652052B00E2EEB3EDD233614CD
ArticleID:ANIE201410717
This work was partially supported by the Grant-in-Aid for Scientific Research (S) (no. 26220804) and Scientific Research (B) (no. 26288049)
This work was partially supported by the Grant‐in‐Aid for Scientific Research (S) (no. 26220804) and Scientific Research (B) (no. 26288049)
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201410717