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Advanced Synthesis & Catalysis

Advanced Synthesis & Catalysis

IF: 4.4
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Bench‐Stable Sulfoxide‐Based Boronates: Preparation and Application in a Tandem Suzuki Reaction

Published:1 December 2018 DOI: 10.1002/adsc.201801000
Marek ?ubiňák , Václav Eigner , Tomá? Tobrman

Abstract

A set of novel aromatic and heteroaromatic bench‐stable sulfoxide‐based boronates was prepared. The structure of the boronates was established by means of X‐ray crystallography, and the prepared boronates were successively used in Suzuki cross‐coupling reactions under different conditions. We also developed a tandem Suzuki reaction so that a base is generated during the nucleophilic addition of Grignard reagents to 4‐bromobenzaldehyde. The formed intermediates were smoothly coupled with the prepared boronates and the boronic acids under external base‐free conditions.

Synthesis

Bromobenzene
Triisopropyl borate
N-Methyliminodiacetic acid
2-Phenyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione

Substances (3)

Related products
Procduct Name CAS Molecular Formula Supplier Price
4-Bromobenzaldehyde 1122-91-4 C7H5BrO 815 suppliers $9.00-$810.65
3 5-DIMETHYOXYPHENYLMAGNESIUM CHLORIDE 89981-17-9 C8H9ClMgO2 17 suppliers $55.00-$227.00
3-Bromo-5-fluorophenylboronic acid MIDA ester 1257650-61-5 C11H10BBrFNO4 5 suppliers $38.30-$897.44

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