http://10.10.120.238:8080/xmlui/handle/123456789/869| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Tamanna N. | en_US |
| dc.contributor.author | Sharma D. | en_US |
| dc.contributor.author | Chauhan P. | en_US |
| dc.date.accessioned | 2023-11-30T08:52:15Z | - |
| dc.date.available | 2023-11-30T08:52:15Z | - |
| dc.date.issued | 2023 | - |
| dc.identifier.issn | 1477-0520 | - |
| dc.identifier.other | EID(2-s2.0-85150212162) | - |
| dc.identifier.uri | https://dx.doi.org/10.1039/d3ob00126a | - |
| dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/869 | - |
| dc.description.abstract | Enantioselective synthesis of spirocyclohexenone isobenzofuranones has been achieved through an organocatalysed sulfa-Michael desymmetrisation reaction. A cinchona-derived squaramide effectively promotes the desymmetrisation of spirocyclic 2,5-cyclohexadienone isobenzofuranones via the controlled addition of various aryl thiols to generate two vicinal stereocenters with perfect diastereoselectivities and up to very good enantioselectivities. © 2023 The Royal Society of Chemistry. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.source | Organic and Biomolecular Chemistry | en_US |
| dc.title | Asymmetric synthesis of spirocyclic isobenzofuranones via a squaramide-catalysed sulfa-Michael desymmetrisation reaction | en_US |
| dc.type | Journal Article | en_US |
| Appears in Collections: | Journal Article | |
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