A scalable homogeneous metal‐catalyzed protocol for direct amidation of carboxylic acids is presented. The use of 2–10 mol% of the commercially available Zr(Cp)2(OTf)2·THF results in high yields of amides at moderate temperature, using an operationally convenient reaction protocol that circumvents the use of water scavenging techniques
The amide functionality is found in a wide variety of biological and synthetic structures such as pr...
Abstract A general procedure for the synthesis of amides via the direct condensation of carboxylic a...
The ZrCl4-catalyzed direct amide bond formation between non-activated carboxylic acids and amines ha...
A scalable homogeneous metal‐catalyzed protocol for direct amidation of carboxylic acids is presente...
The mechanism of the zirconium-catalyzed condensation of carboxylic acids and amines for direct form...
The amide unit constitutes the backbone of proteins, and it is present in a large number of pharmace...
A simple, safe and inexpensive amide bond formation directly from non-activated carboxylic acids and...
Herein, the first example of a metal-catalyzed protocol for direct amidation of nonactivated carboxy...
International audienceThe partial reduction of amides is a challenging transformation that must over...
Despite the amide formation reaction being a key reaction in organic chemistry, the direct amide for...
International audienceThe partial reduction of amides is a challenging transformation that must over...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
[EN]In this work, zirconium-based metal–organic framework Zr-MOF-808-P has been found to be an effic...
A general method for the synthesis of amides involving the direct coupling of alkali metal carboxyla...
The amide functionality is found in a wide variety of biological and synthetic structures such as pr...
Abstract A general procedure for the synthesis of amides via the direct condensation of carboxylic a...
The ZrCl4-catalyzed direct amide bond formation between non-activated carboxylic acids and amines ha...
A scalable homogeneous metal‐catalyzed protocol for direct amidation of carboxylic acids is presente...
The mechanism of the zirconium-catalyzed condensation of carboxylic acids and amines for direct form...
The amide unit constitutes the backbone of proteins, and it is present in a large number of pharmace...
A simple, safe and inexpensive amide bond formation directly from non-activated carboxylic acids and...
Herein, the first example of a metal-catalyzed protocol for direct amidation of nonactivated carboxy...
International audienceThe partial reduction of amides is a challenging transformation that must over...
Despite the amide formation reaction being a key reaction in organic chemistry, the direct amide for...
International audienceThe partial reduction of amides is a challenging transformation that must over...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
[EN]In this work, zirconium-based metal–organic framework Zr-MOF-808-P has been found to be an effic...
A general method for the synthesis of amides involving the direct coupling of alkali metal carboxyla...
The amide functionality is found in a wide variety of biological and synthetic structures such as pr...
Abstract A general procedure for the synthesis of amides via the direct condensation of carboxylic a...
The ZrCl4-catalyzed direct amide bond formation between non-activated carboxylic acids and amines ha...
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