Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
| dc.contributor.author | Ramachary, D. B. | |
| dc.contributor.author | Venkaiah, Chintalapudi | |
| dc.contributor.author | Madhavachary, R. | |
| dc.date.accessioned | 2022-03-27T09:39:56Z | |
| dc.date.available | 2022-03-27T09:39:56Z | |
| dc.date.issued | 2013-06-21 | |
| dc.description.abstract | An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis. © 2013 American Chemical Society. | |
| dc.identifier.citation | Organic Letters. v.15(12) | |
| dc.identifier.issn | 15237060 | |
| dc.identifier.uri | 10.1021/ol401227q | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol401227q | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/13173 | |
| dc.title | Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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