New development in amide bond formation reaction via oxidation process

Taniyuki Furuyama

doi:10.5059/yukigoseikyokaishi.66.1005

New development in amide bond formation reaction via oxidation process

Taniyuki Furuyama

SCI - Chemistry

Research output: Contribution to journal › Review article › peer-review

2 Citations (Scopus)

Abstract

Oxidation of hemiaminal prepared from aldehydes and amines is an alternative method for creating amide bond. In this mini review, recent developments of versatile amide bond formation reactions via oxidation process from aldehydes (or alcohols) and amines are described.

Original language	English
Pages (from-to)	1005-1006
Number of pages	2
Journal	Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Volume	66
Issue number	10
DOIs	https://doi.org/10.5059/yukigoseikyokaishi.66.1005
Publication status	Published - 2008 Oct

ASJC Scopus subject areas

Organic Chemistry

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title = "New development in amide bond formation reaction via oxidation process",

abstract = "Oxidation of hemiaminal prepared from aldehydes and amines is an alternative method for creating amide bond. In this mini review, recent developments of versatile amide bond formation reactions via oxidation process from aldehydes (or alcohols) and amines are described.",

author = "Taniyuki Furuyama",

year = "2008",

month = oct,

doi = "10.5059/yukigoseikyokaishi.66.1005",

language = "English",

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pages = "1005--1006",

journal = "Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry",

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AU - Furuyama, Taniyuki

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AB - Oxidation of hemiaminal prepared from aldehydes and amines is an alternative method for creating amide bond. In this mini review, recent developments of versatile amide bond formation reactions via oxidation process from aldehydes (or alcohols) and amines are described.

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DO - 10.5059/yukigoseikyokaishi.66.1005

M3 - Review article

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SP - 1005

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JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry

JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry

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