Please use this identifier to cite or link to this item:
https://dspace.iiti.ac.in/handle/123456789/72
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | Samanta, Sampak | - |
dc.contributor.author | Khadsang, Namrata | - |
dc.date.accessioned | 2016-09-29T07:22:03Z | - |
dc.date.available | 2016-09-29T07:22:03Z | - |
dc.date.issued | 2016-07-06 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/72 | - |
dc.description.abstract | A green, convenient and efficient procedure has been developed for the synthesis of hydroxyindole derivatives. Magnetically separable and recyclable nanoparticles are used as a heterogeneous catalyst for the synthesis of indoles via the one-pot Friedel– Crafts reaction with isoquinoline -1,3,4-trione . Interestingly, indole derivatives are regioselectively acylated in the 3-position under mild conditions, short reaction times high yields with the green aspects by avoiding toxic catalysts. The catalyst could be easily separated from the reaction mixture by using an external magnet and recycled. These operational simple procedures furnish good to high yields of corresponding synthetically as well as biologically interesting functionalized 4-hydroxy-4- indolylisoquinoline-1,3(2H,4H)- diones. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Department of Chemistry, IIT Indore | en_US |
dc.relation.ispartofseries | MS027 | - |
dc.subject | Chemistry | en_US |
dc.title | Fe3O4 nanoparticle : an efficient recyclable catalyst for the friedel-crafts reaction of indoles with isoquinoline-1,3,4-trione in water | en_US |
dc.type | Thesis_M.Sc | en_US |
Appears in Collections: | Department of Chemistry_ETD |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
MS27_Khadsang, Namrata.pdf | 1.83 MB | Adobe PDF | ![]() View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Altmetric Badge: