This MedLibrary.org supplementary page on Formylation reaction is provided directly from the open source Wikipedia as a service to our readers. Please see the note below on authorship of this content, as well as the Wikipedia usage guidelines. To search for other content from our encyclopedia supplement, please use the form below:
Related Sponsors
A formylation reaction in organic chemistry is the catch-all name for any organic reaction in which an organic compound is functionalized with a formyl group (-CH=O).
Aromatic formylation reactions via electrophilic aromatic substitution include:
- Dimethylformamide and phosphorus oxychloride in the Vilsmeier-Haack reaction
- Hexamine in the Duff reaction and the Sommelet reaction
- Carbon monoxide and hydrochloric acid in the Gattermann-Koch reaction
- Zinc cyanide and hydrochloric acid in the Gatterman aldehyde synthesis
- Chloroform in the Reimer-Tiemann reaction
In biological systems, formylation is one of the processes of posttranslational modification in which a formyl group is added to the N-terminus of a protein.
See also
Wikipedia content modification information:
- This page was last modified on 26 September 2008, at 10:05.
Wikipedia Authorship and Review
Wikipedia content provided here is not reviewed directly by MedLibrary.org. Wikipedia content is authored by an open community of volunteers and is not produced by or in any way affiliated with MedLibrary.org.
Wikipedia Usage Guidelines
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article on "Formylation reaction".
The URL for this specific entry is:
All Wikipedia text is available under the terms of the GNU Free Documentation License. (See Copyrights for details). Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc.