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Cited by 239

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond

Open access
García-Álvarez, Rocío, Crochet, Pascale, Cadierno, Victorio·2013·Green Chem.

Abstract

Amides are versatile building blocks in synthetic organic chemistry, presenting a wide range of pharmacological applications, and are used as raw materials in industry for the large-scale production of engineering plastics, detergents and lubricants. The development of green procedures for the synthesis of this relevant class of compounds from various starting materials, which replace antiquated methods using carboxylic acid derivatives and amines, is therefore of prime interest in modern chemistry. In this review article, a survey of metal-catalyzed synthetic approaches of amides conducted in an environmentally friendly aqueous medium is given.

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Crossref · 10.1039/c2gc36534k

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Metadata

Authors
García-Álvarez, R., Crochet, P., & Cadierno, V.
Venue
Green Chem.
Published
2013
Volume
15
Issue
1
Pages
46-66
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
OpenAlex
W2101381885
Cited by
239
References
1
FWCI
12.10
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond. https://app.cochat.ai/papers/10.1039/c2gc36534k
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García-Álvarez, R., Crochet, P., & Cadierno, V. (2013). Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: nitrile hydrations and beyond. Green Chem. https://doi.org/10.1039/c2gc36534k

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.