Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay
Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with different arenes using eco-friendly FeCl3 and K-10 clay under thermal heating was accomplished, in good to excellent yields (66–79%). The methodology was extended to benzaldehyde derived simple MBH adducts als...
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Elsevier
2022-01-01
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Series: | Results in Chemistry |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2211715622003964 |
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author | Sivaprakasam Sivaraman Selvaraj Aruljothi Vadivel Vaithiyanathan |
author_facet | Sivaprakasam Sivaraman Selvaraj Aruljothi Vadivel Vaithiyanathan |
author_sort | Sivaprakasam Sivaraman |
collection | DOAJ |
description | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with different arenes using eco-friendly FeCl3 and K-10 clay under thermal heating was accomplished, in good to excellent yields (66–79%). The methodology was extended to benzaldehyde derived simple MBH adducts also. The details of the work are elaborately discussed in this letter. |
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format | Article |
id | doaj.art-10fa155112484f29a5634210729c6bfb |
institution | Directory Open Access Journal |
issn | 2211-7156 |
language | English |
last_indexed | 2024-04-12T01:40:15Z |
publishDate | 2022-01-01 |
publisher | Elsevier |
record_format | Article |
series | Results in Chemistry |
spelling | doaj.art-10fa155112484f29a5634210729c6bfb2022-12-22T03:53:13ZengElsevierResults in Chemistry2211-71562022-01-014100677Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 claySivaprakasam Sivaraman0Selvaraj Aruljothi1Vadivel Vaithiyanathan2Department of Chemistry, Arignar Anna Govt. Arts College, Villupuram (Re-accredited by the NAAC with “B+” and Affiliated to Annamalai University, Chidambaram), Tamilnadu 605 602, IndiaDepartment of Chemistry, Arignar Anna Govt. Arts College, Villupuram (Re-accredited by the NAAC with “B+” and Affiliated to Annamalai University, Chidambaram), Tamilnadu 605 602, IndiaCorresponding author.; Department of Chemistry, Arignar Anna Govt. Arts College, Villupuram (Re-accredited by the NAAC with “B+” and Affiliated to Annamalai University, Chidambaram), Tamilnadu 605 602, IndiaAllylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with different arenes using eco-friendly FeCl3 and K-10 clay under thermal heating was accomplished, in good to excellent yields (66–79%). The methodology was extended to benzaldehyde derived simple MBH adducts also. The details of the work are elaborately discussed in this letter.http://www.sciencedirect.com/science/article/pii/S2211715622003964Isomerisation_1MBH adduct_2Allylation_3Arylation_4C–C bond formation_5 |
spellingShingle | Sivaprakasam Sivaraman Selvaraj Aruljothi Vadivel Vaithiyanathan Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay Results in Chemistry Isomerisation_1 MBH adduct_2 Allylation_3 Arylation_4 C–C bond formation_5 |
title | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay |
title_full | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay |
title_fullStr | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay |
title_full_unstemmed | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay |
title_short | Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay |
title_sort | allylic arylative isomerisation of morita baylis hillman adduct of isatin derivatives with arenes using fecl3 and k 10 clay |
topic | Isomerisation_1 MBH adduct_2 Allylation_3 Arylation_4 C–C bond formation_5 |
url | http://www.sciencedirect.com/science/article/pii/S2211715622003964 |
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