![DSpace logo](/jspui/image/logo.gif)
Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3338
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sakhuja, Rajeev | - |
dc.date.accessioned | 2021-11-11T10:57:40Z | - |
dc.date.available | 2021-11-11T10:57:40Z | - |
dc.date.issued | 2021-08 | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/abs/10.1002/ajoc.202100384 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3338 | - |
dc.description.abstract | A one-pot spirocyclization of 2-aryl-2,3-dihydrophthalazine-1,4-diones with maleimides was achieved via RhIII-catalyzed sequential ortho-alkenylation followed by intramolecular aza-Michael-type addition/protonation process. The featured strategy furnishes a series of diversely decorated spiro[indazolo[1,2-b]phthalazine-13,3′-pyrrolidine]-2′,5′,6,11-tetraones in high yields from a variety of 2-aryl-2,3-dihydrophthalazine-1,4-diones and N-aryl/alkyl maleimides, which can be scaled-up easily. Isolation and characterization of a maleimide-coordinated five-membered rhodacyclic intermediate provided a strong evidence for the proposed mechanism of the reaction. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Rhodium-Catalyzed | en_US |
dc.subject | Spirocyclization of Maleimide | en_US |
dc.subject | Pentacyclic Spiro-Succinimides | en_US |
dc.title | Rhodium-Catalyzed Spirocyclization of Maleimide with N-Aryl-2,3-dihydrophthalazine-1,4-dione to Access Pentacyclic Spiro-Succinimides | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.