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Lundberg, H., Tinnis, F. & Adolfsson, H. (2019). Zirconium catalyzed amide formation without water scavenging. Applied organometallic chemistry, 33(9), Article ID e5062.
Open this publication in new window or tab >>Zirconium catalyzed amide formation without water scavenging
2019 (English)In: Applied organometallic chemistry, ISSN 0268-2605, E-ISSN 1099-0739, Vol. 33, no 9, article id e5062Article in journal (Refereed) Published
Abstract [en]

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)center dot THF results in high yields of amides at moderate temperature, using an operationally convenient reaction protocol that circumvents the use of water scavenging techniques.

Keywords
mides, amines, carboxylic acids, catalysis, direct amidation, trifluoromethanesulfonate, zirconium
National Category
Organic Chemistry
Identifiers
urn:nbn:se:su:diva-171723 (URN)10.1002/aoc.5062 (DOI)000476374900001 ()
Available from: 2019-09-11 Created: 2019-09-11 Last updated: 2022-03-23Bibliographically approved
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Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0002-4704-1892

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