General and greener route to ketones by palladium-catalyzed direct conversion of carboxylic acids with organoboronic acids

Ryuki Kakino; Hirohisa Narahashi; Isao Shimizu; Akio Yamamoto

General and greener route to ketones by palladium-catalyzed direct conversion of carboxylic acids with organoboronic acids

Ryuki Kakino, Hirohisa Narahashi, Isao Shimizu, Akio Yamamoto

研究成果: Article › 査読

抄録

Cross-coupling reaction of carboxylic acids with organoboron compounds catalyzed by palladium complexes in the presence of an activator such as dimethyl dicarbonate under mild conditions gives ketones in excellent yields except for certain substrates.

本文言語	English
ページ（範囲）	1242-1243
ページ数	2
ジャーナル	Chemistry Letters
号	12
出版ステータス	Published - 2001

ASJC Scopus subject areas

化学 (全般)

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title = "General and greener route to ketones by palladium-catalyzed direct conversion of carboxylic acids with organoboronic acids",

abstract = "Cross-coupling reaction of carboxylic acids with organoboron compounds catalyzed by palladium complexes in the presence of an activator such as dimethyl dicarbonate under mild conditions gives ketones in excellent yields except for certain substrates.",

author = "Ryuki Kakino and Hirohisa Narahashi and Isao Shimizu and Akio Yamamoto",

year = "2001",

language = "English",

pages = "1242--1243",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "12",

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TY - JOUR

T1 - General and greener route to ketones by palladium-catalyzed direct conversion of carboxylic acids with organoboronic acids

AU - Kakino, Ryuki

AU - Narahashi, Hirohisa

AU - Shimizu, Isao

AU - Yamamoto, Akio

PY - 2001

Y1 - 2001

N2 - Cross-coupling reaction of carboxylic acids with organoboron compounds catalyzed by palladium complexes in the presence of an activator such as dimethyl dicarbonate under mild conditions gives ketones in excellent yields except for certain substrates.

AB - Cross-coupling reaction of carboxylic acids with organoboron compounds catalyzed by palladium complexes in the presence of an activator such as dimethyl dicarbonate under mild conditions gives ketones in excellent yields except for certain substrates.

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M3 - Article

AN - SCOPUS:0035528511

SN - 0366-7022

SP - 1242

EP - 1243

JO - Chemistry Letters

JF - Chemistry Letters

IS - 12

ER -

General and greener route to ketones by palladium-catalyzed direct conversion of carboxylic acids with organoboronic acids

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