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Ligand-Free Copper-Catalyzed 1,6-Conjugate Reaction of para-Quinone Methides with gem-Diborylalkanes

Authors
He, J.[He, J.]Meng, D.[Meng, D.]Lee, D.Y.[Lee, D.Y.]Yun, J.[Yun, J.]
Issue Date
Dec-2022
Publisher
John Wiley and Sons Inc
Keywords
Conjugate addition; Copper; Diborylalkanes; Ligand-free system; Quinone methides
Citation
European Journal of Organic Chemistry, v.2022, no.47
Indexed
SCIE
SCOPUS
Journal Title
European Journal of Organic Chemistry
Volume
2022
Number
47
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/105537
DOI
10.1002/ejoc.202201241
ISSN
1434-193X
Abstract
We report a ligand-free copper-catalyzed 1,6-addition of α-borylalkyl copper species, catalytically generated from gem-diborylalkanes to para-quinone methides. The reaction proceeds with good yield for a variety of para-quinone methides and substituted gem-diborylalkanes with a catalytic amount of CuI as catalyst. This catalytic system provides a cost-effective process with good functional group tolerance under mild conditions. © 2022 Wiley-VCH GmbH.
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