4.5 Article

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

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2022, 期 47, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202201241

关键词

Conjugate addition; Copper; Diborylalkanes; Ligand-free system; Quinone methides

资金

  1. National Research Foundation of Korea [2022R1A2C2092161]
  2. Korea Basic Science Institute (National Research Facilities and Equipment Center) - Ministry of Education [2022R1A6C101A751]
  3. National Research Foundation of Korea [2022R1A2C2092161, 2022R1A6C101A751] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

We report a ligand-free copper-catalyzed 1,6-addition reaction of alpha-borylalkyl copper species with para-quinone methides. The reaction, catalytically generated from gem-diborylalkanes, shows good yield for various para-quinone methides and substituted gem-diborylalkanes with a catalytic amount of CuI. This catalytic system provides a cost-effective process with good functional group tolerance under mild conditions.
We report a ligand-free copper-catalyzed 1,6-addition of alpha-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.

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