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Suzuki Cross-Coupling Reactionof Benzylic Halides with Arylboronic Acids in the Presence of aTetraphosphine/Palladium Catalyst

Ludovic Chahen, +2 more
- 01 Sep 2003 - 
- Vol. 2003, Iss: 11, pp 1668-1672
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This article is published in Synlett.The article was published on 2003-09-01. It has received 4 citations till now. The article focuses on the topics: Palladium & Catalysis.

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Journal ArticleDOI

Palladium/tetraphosphine catalyzed suzuki cross‐coupling of heteroarylboronic acids with aryl halides

TL;DR: In this paper, the Suzuki reaction of hetero-boronic acids with aryl bromides and also the coupling of arylsboronic acid with heteroaryl bromide was studied.
Journal ArticleDOI

Selective Synthesis of (Benzyl)biphenyls by Successive Suzuki–Miyaura Coupling of Phenylboronic Acids with 4-Bromobenzyl Acetate under Air Atmosphere

TL;DR: An efficient Pd-catalyzed cross-coupling reaction of phenylboronic acids and benzyl carbonates was developed, producing diarylmethanes, facilitating the selective synthesis of diverse (benzyl)biphenyls by successive Suzuki–Miyaura coupling reactions.
Journal ArticleDOI

Substrate switchable Suzuki–Miyaura coupling for benzyl ester vs. benzyl halide

TL;DR: In this paper, two reaction conditions were developed to accomplish the substrate switchable Suzuki-Miyaura coupling of benzyl derivatives and arylboronic acid derivatives, in which water was found to play an important role.
Journal ArticleDOI

Palladium-catalyzed substitution of (coumarinyl)methyl acetates with C-, N-, and S-nucleophiles

TL;DR: The palladium-catalyzed nucleophilic substitution of (coumarinyl)methyl acetates is described, which allows for many different types of C, N, and S-nucleophiles to be regioselectively added to the biologically active coumarin motif.
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