Facile access to α-acyloxyamides via epoxide rearrangement/three-component domino reaction catalyzed by indium(III) chloride. Issue 15 (2nd August 2016)
- Record Type:
- Journal Article
- Title:
- Facile access to α-acyloxyamides via epoxide rearrangement/three-component domino reaction catalyzed by indium(III) chloride. Issue 15 (2nd August 2016)
- Main Title:
- Facile access to α-acyloxyamides via epoxide rearrangement/three-component domino reaction catalyzed by indium(III) chloride
- Authors:
- Lingaswamy, Kadari
Krishna, Palakodety Radha
Prapurna, Y. Lakshmi - Abstract:
- ABSTRACT: A simple and efficient Passerini reaction of epoxides involving highly regioselective rearrangement of epoxide to aldehyde/three-component Passerini reaction catalyzed by indium(III) chloride is described. In the present protocol, epoxides served as wonderful substrates to furnish a library ofα -acyloxyamides under mild reaction conditions in shorter reaction times and in good yields. GRAPHICAL ABSTRACT:
- Is Part Of:
- Synthetic communications. Volume 46:Issue 15(2016)
- Journal:
- Synthetic communications
- Issue:
- Volume 46:Issue 15(2016)
- Issue Display:
- Volume 46, Issue 15 (2016)
- Year:
- 2016
- Volume:
- 46
- Issue:
- 15
- Issue Sort Value:
- 2016-0046-0015-0000
- Page Start:
- 1275
- Page End:
- 1282
- Publication Date:
- 2016-08-02
- Subjects:
- Epoxides -- highly regioselective -- indium(III) chloride -- tandem rearrangement/Passerini condensation -- TosMIC
Organic compounds -- Synthesis -- Periodicals
Chemistry, Organic
Synthesis
547.205 - Journal URLs:
- http://www.tandfonline.com/toc/lsyc20/current ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/00397911.2016.1201511 ↗
- Languages:
- English
- ISSNs:
- 0039-7911
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8586.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 399.xml