First palladium-catalyzed aminations of aryl chlorides

Matthias Beller; Thomas H. Riermeier; Claus Peter Reisinger; Wolfgang A. Herrmann

doi:10.1016/S0040-4039(97)00289-X

First palladium-catalyzed aminations of aryl chlorides

Matthias Beller, Thomas H. Riermeier, Claus Peter Reisinger, Wolfgang A. Herrmann

Technical University of Munich

Technical University of Munich

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

103 Scopus citations

Abstract

The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tert-butoxide as base. Turn over numbers up to 900 and yields up to 80% have been obtained.

Original language	English
Pages (from-to)	2073-2074
Number of pages	2
Journal	Tetrahedron Letters
Volume	38
Issue number	12
DOIs	https://doi.org/10.1016/S0040-4039(97)00289-X
State	Published - 24 Mar 1997

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title = "First palladium-catalyzed aminations of aryl chlorides",

abstract = "The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tert-butoxide as base. Turn over numbers up to 900 and yields up to 80% have been obtained.",

author = "Matthias Beller and Riermeier, {Thomas H.} and Reisinger, {Claus Peter} and Herrmann, {Wolfgang A.}",

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T1 - First palladium-catalyzed aminations of aryl chlorides

AU - Beller, Matthias

AU - Riermeier, Thomas H.

AU - Reisinger, Claus Peter

AU - Herrmann, Wolfgang A.

PY - 1997/3/24

Y1 - 1997/3/24

N2 - The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tert-butoxide as base. Turn over numbers up to 900 and yields up to 80% have been obtained.

AB - The palladium-catalyzed coupling reaction of aryl chlorides with various amines has been studied for the first time. Crucial for the success of this C-N bond forming reaction is the use of potassium tert-butoxide as base. Turn over numbers up to 900 and yields up to 80% have been obtained.

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U2 - 10.1016/S0040-4039(97)00289-X

DO - 10.1016/S0040-4039(97)00289-X

M3 - Article

AN - SCOPUS:0031585038

SN - 0040-4039

VL - 38

SP - 2073

EP - 2074

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

First palladium-catalyzed aminations of aryl chlorides

Abstract

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