Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions

Mingzong Li; Cong Wang; Ping Fang; Haibo Ge

doi:10.1039/c1cc11635e

Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions

Mingzong Li, Cong Wang, Ping Fang, Haibo Ge

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

43 Scopus citations

Abstract

A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.

Original language	English
Pages (from-to)	6587-6589
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	23
DOIs	https://doi.org/10.1039/c1cc11635e
State	Published - Jun 21 2011

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title = "Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions",

abstract = "A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.",

author = "Mingzong Li and Cong Wang and Ping Fang and Haibo Ge",

year = "2011",

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T1 - Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions

AU - Li, Mingzong

AU - Wang, Cong

AU - Fang, Ping

AU - Ge, Haibo

PY - 2011/6/21

Y1 - 2011/6/21

N2 - A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.

AB - A novel Pd-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates has been realized under mild reaction conditions. This method provides an efficient access to N-mono- or N,N-disubstituted benzamides and benzoates.

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U2 - 10.1039/c1cc11635e

DO - 10.1039/c1cc11635e

M3 - Article

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AN - SCOPUS:79958006600

SN - 1359-7345

VL - 47

SP - 6587

EP - 6589

JO - Chemical Communications

JF - Chemical Communications

IS - 23

ER -

Pd(ii)-catalyzed decarboxylative cross-coupling of oxamic acids with potassium phenyltrifluoroborates under mild conditions

Abstract

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