Pairing Suzuki–Miyaura cross-coupling and catalyst transfer polymerization
نویسندگان
چکیده
Borylation strategies to make AB Suzuki–Miyaura monomers for use in catalyst-transfer polymerization with nickel or palladium catalysts.
منابع مشابه
An air stable and efficient palladium catalyst for Suzuki-Miyaura cross coupling reaction at room temperature
The cross-coupling reaction between phenylboronic acid and various types of aryl halides (Suzuki reaction) was carried out using a catalytic amount of a new palladium catalyst (1-benzyl-3-(1-benzyl-1-methylpyrrolidin-1-ium-2-yl) pyridin-1-ium palladium chloride [DBNT][PdCl4]) in poly (ethylene glycol) (PEG-200) in the presence of KOH as the base. This new catalyst was synthesized and...
متن کاملAn air stable and efficient palladium catalyst for Suzuki-Miyaura cross coupling reaction at room temperature
The cross-coupling reaction between phenylboronic acid and various types of aryl halides (Suzuki reaction) was carried out using a catalytic amount of a new palladium catalyst (1-benzyl-3-(1-benzyl-1-methylpyrrolidin-1-ium-2-yl) pyridin-1-ium palladium chloride [DBNT][PdCl4]) in poly (ethylene glycol) (PEG-200) in the presence of KOH as the base. This new catalyst was synthesized and...
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متن کاملan air stable and efficient palladium catalyst for suzuki-miyaura cross coupling reaction at room temperature
the cross-coupling reaction between phenylboronic acid and various types of aryl halides (suzuki reaction) was carried out using a catalytic amount of a new palladium catalyst (1-benzyl-3-(1-benzyl-1-methylpyrrolidin-1-ium-2-yl) pyridin-1-ium palladium chloride [dbnt][pdcl4]) in poly (ethylene glycol) (peg-200) in the presence of koh as the base. this new catalyst was synthesized and characteri...
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ژورنال
عنوان ژورنال: Polymer Chemistry
سال: 2021
ISSN: ['1759-9962', '1759-9954']
DOI: https://doi.org/10.1039/d0py01507e