Oxidative N‐Formylation of Amines to Formamides.
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| Title: | Oxidative N‐Formylation of Amines to Formamides. |
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| Authors: | Dai, Xingchao1 (AUTHOR) daixingchao@licp.cas.cn, Rabeah, Jabor1,2 (AUTHOR) Jabor.Rabeah@licp.cas.cn |
| Source: | ChemCatChem. 7/22/2025, Vol. 17 Issue 14, p1-10. 10p. |
| Subjects: | Formamide, Amines, Chemical synthesis, Amine oxidase, Methanol, Oxidizing agents, Chemical products manufacturing |
| Abstract: | Formamides are an important class of amine chemicals with a wide range of applications in industry, synthetic chemistry, and materials, and their synthesis has gained increasing attention. Among the various methods developed, oxidative N‐formylation of amines with methanol, formaldehyde, and non‐C1 feedstocks constitutes an attractive one, especially using green oxidants, such as air, O2, and H2O2, due to satisfied production efficiency, mild reaction conditions, and effective cost. Although great progress has been made in this direction, a review focusing on this aspect remains scarce. This review summarizes the recent development on the oxidative N‐formylation of amines to formamides according to the kinds of formyl sources and oxidants. [ABSTRACT FROM AUTHOR] |
| Copyright of ChemCatChem is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
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| Header | DbId: egs DbLabel: Engineering Source An: 186991157 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Oxidative N‐Formylation of Amines to Formamides. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Dai%2C+Xingchao%22">Dai, Xingchao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> daixingchao@licp.cas.cn</i><br /><searchLink fieldCode="AR" term="%22Rabeah%2C+Jabor%22">Rabeah, Jabor</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> Jabor.Rabeah@licp.cas.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22ChemCatChem%22">ChemCatChem</searchLink>. 7/22/2025, Vol. 17 Issue 14, p1-10. 10p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Formamide%22">Formamide</searchLink><br /><searchLink fieldCode="DE" term="%22Amines%22">Amines</searchLink><br /><searchLink fieldCode="DE" term="%22Chemical+synthesis%22">Chemical synthesis</searchLink><br /><searchLink fieldCode="DE" term="%22Amine+oxidase%22">Amine oxidase</searchLink><br /><searchLink fieldCode="DE" term="%22Methanol%22">Methanol</searchLink><br /><searchLink fieldCode="DE" term="%22Oxidizing+agents%22">Oxidizing agents</searchLink><br /><searchLink fieldCode="DE" term="%22Chemical+products+manufacturing%22">Chemical products manufacturing</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Formamides are an important class of amine chemicals with a wide range of applications in industry, synthetic chemistry, and materials, and their synthesis has gained increasing attention. Among the various methods developed, oxidative N‐formylation of amines with methanol, formaldehyde, and non‐C1 feedstocks constitutes an attractive one, especially using green oxidants, such as air, O2, and H2O2, due to satisfied production efficiency, mild reaction conditions, and effective cost. Although great progress has been made in this direction, a review focusing on this aspect remains scarce. This review summarizes the recent development on the oxidative N‐formylation of amines to formamides according to the kinds of formyl sources and oxidants. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of ChemCatChem is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/cctc.202500359 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 10 StartPage: 1 Subjects: – SubjectFull: Formamide Type: general – SubjectFull: Amines Type: general – SubjectFull: Chemical synthesis Type: general – SubjectFull: Amine oxidase Type: general – SubjectFull: Methanol Type: general – SubjectFull: Oxidizing agents Type: general – SubjectFull: Chemical products manufacturing Type: general Titles: – TitleFull: Oxidative N‐Formylation of Amines to Formamides. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dai, Xingchao – PersonEntity: Name: NameFull: Rabeah, Jabor IsPartOfRelationships: – BibEntity: Dates: – D: 22 M: 07 Text: 7/22/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 18673880 Numbering: – Type: volume Value: 17 – Type: issue Value: 14 Titles: – TitleFull: ChemCatChem Type: main |
| ResultId | 1 |
