Metal free synthesis of α-keto amides from 2-hydroxy acetophenones through domino alcohol oxidation–oxidative amidation reaction. Issue 46 (18th November 2015)
- Record Type:
- Journal Article
- Title:
- Metal free synthesis of α-keto amides from 2-hydroxy acetophenones through domino alcohol oxidation–oxidative amidation reaction. Issue 46 (18th November 2015)
- Main Title:
- Metal free synthesis of α-keto amides from 2-hydroxy acetophenones through domino alcohol oxidation–oxidative amidation reaction
- Authors:
- Kotha, Surya Srinivas
Sekar, Govindasamy - Abstract:
- Graphical abstract: Abstract: An efficient method for the synthesis of α-keto amides using 2-iodoxybenzoic acid (IBX) promoted domino alcohol oxidation and oxidative amidation reaction sequence between 2-oxoalcohols and amines under metal-free conditions is developed. In this protocol, IBX is used as an oxidizing agent to synthesize the α-keto amides, which makes this methodology highly efficient, practical, and environmentally benign.
- Is Part Of:
- Tetrahedron letters. Volume 56:Issue 46(2015)
- Journal:
- Tetrahedron letters
- Issue:
- Volume 56:Issue 46(2015)
- Issue Display:
- Volume 56, Issue 46 (2015)
- Year:
- 2015
- Volume:
- 56
- Issue:
- 46
- Issue Sort Value:
- 2015-0056-0046-0000
- Page Start:
- 6323
- Page End:
- 6326
- Publication Date:
- 2015-11-18
- Subjects:
- Metal free synthesis -- α-Keto amide -- 2-Hydroxy acetophenone -- Oxidative amidation -- 2-Iodoxybenzoic acid
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tetlet.2015.09.053 ↗
- Languages:
- English
- ISSNs:
- 0040-4039
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.860000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2016.xml