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Journal ArticleDOI

Palladium-Catalyzed Arylation of Polar Organometallics Mediated by 9-Methoxy-9-Borabicyclo[3.3.1]nonane: Suzuki Reactions of Extended Scope

Alois Fürstner, +1 more
- 09 Oct 1995 - 
- Vol. 51, Iss: 41, pp 11165-11176
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TLDR
In this paper, an alternative way for performing Suzuki reactions is presented, where the necessary borate which is the actual nucleophile in these palladium catalyzed C-C-bond formations is prepared from 9-methoxy-9-bora-bicyclo[3.3]nonane (9-OMe- 9-BBN) and a polar organometallic reagent RM, and not as usually from a borane and a base.
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This article is published in Tetrahedron.The article was published on 1995-10-09. It has received 113 citations till now. The article focuses on the topics: 9-Borabicyclo[3.3.1]nonane & Suzuki reaction.

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Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998

TL;DR: The palladium-catalyzed cross-coupling reaction between organoboron compounds and organic halides or triflates provides a powerful and general methodology for the formation of carbon-carbon bonds as discussed by the authors.
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Selection of boron reagents for Suzuki-Miyaura coupling

TL;DR: This review analyses the seven main classes of boron reagent and evaluates the general physical and chemical properties of each class with special emphasis on the currently understood mechanisms of transmetalation.
References
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Journal ArticleDOI

The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases

TL;DR: The transition metal-catalyzed reactions of organometallics with organic halides have been extensively studied to prove a new approach to selective formation of carbon-carbon bonds as mentioned in this paper.
Journal ArticleDOI

Tetrahedron report number 163

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Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II): an effective catalyst for cross-coupling of secondary and primary alkyl Grignard and alkylzinc reagents with organic halides

TL;DR: Etude d'une trentaine de reactions, avec des complexes de Ni au Pd pour le couplage des bromo-benzene, -styrene, -anisole, -toluene avec le chlorure de butylmagnesium as discussed by the authors.
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