Transition-metal-free cross-coupling reaction of benzylic halides with arylboronic acids leading to diarylmethanes
Author:
Funder
MEXT
JSPS
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. A Transition-Metal-Free Cross-Coupling Reaction of Allylic Bromides with Aryl- and Vinylboronic Acids
2. Catalyst-Free Suzuki-Type Coupling of Allylic Bromides with Arylboronic Acids
3. Transition-Metal-Free Suzuki-Miyaura Coupling Reaction of Arylpropargylic Bromides with Aryl- and Alkenylboronic Acids
4. Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)
5. Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
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2. Recent Advance of Transition Metal-Free Catalyzed Suzuki-Type Cross Coupling Reaction;Chinese Journal of Organic Chemistry;2023
3. Visible light-mediated metal-free alkyl Suzuki–Miyaura coupling of alkyl halides and alkenylboronic acids/esters: a green method for the synthesis of allyl difluoride derivatives;Green Chemistry;2023
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