A new ketone synthesis by palladium-catalyzed cross-coupling reactions of esters with organoboron compounds

Hiroto Tatamidani; Fumitoshi Kakiuchi; Naoto Chatani

doi:10.1021/ol048513o

A new ketone synthesis by palladium-catalyzed cross-coupling reactions of esters with organoboron compounds

Hiroto Tatamidani, Fumitoshi Kakiuchi, Naoto Chatani

Research output: Contribution to journal › Article

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Abstract

(Chemical Equation Presented) The palladium-catalyzed coupling reaction of 2-pyridyl esters with organoboron compounds is described. The reaction is compatible with various functional groups and proceeds under mild reaction conditions. The coordination of the nitrogen atom to Pd is a key step for efficient reaction.

Original language	English
Pages (from-to)	3597-3599
Number of pages	3
Journal	Organic Letters
Volume	6
Issue number	20
DOIs	https://doi.org/10.1021/ol048513o
Publication status	Published - 2004 Sep 30
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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title = "A new ketone synthesis by palladium-catalyzed cross-coupling reactions of esters with organoboron compounds",

abstract = "(Chemical Equation Presented) The palladium-catalyzed coupling reaction of 2-pyridyl esters with organoboron compounds is described. The reaction is compatible with various functional groups and proceeds under mild reaction conditions. The coordination of the nitrogen atom to Pd is a key step for efficient reaction.",

author = "Hiroto Tatamidani and Fumitoshi Kakiuchi and Naoto Chatani",

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AU - Kakiuchi, Fumitoshi

AU - Chatani, Naoto

PY - 2004/9/30

Y1 - 2004/9/30

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AB - (Chemical Equation Presented) The palladium-catalyzed coupling reaction of 2-pyridyl esters with organoboron compounds is described. The reaction is compatible with various functional groups and proceeds under mild reaction conditions. The coordination of the nitrogen atom to Pd is a key step for efficient reaction.

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