Asymmetric Neber Reaction in the Synthesis of Chiral 2-(Tetrazol-5-yl)-2H-Azirines
| dc.contributor.author | Alves, Cláudia | |
| dc.contributor.author | Grosso, Carla | |
| dc.contributor.author | Barrulas, Pedro | |
| dc.contributor.author | Paixão, José | |
| dc.contributor.author | Cardoso, Ana | |
| dc.contributor.author | Burke, Anthony | |
| dc.contributor.author | Lemos, Américo | |
| dc.contributor.author | Pinho e Melo, Teresa | |
| dc.date.accessioned | 2021-12-07T15:57:29Z | |
| dc.date.available | 2021-12-07T15:57:29Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | A successful one-pot methodology for the synthesis of chiral 2-tetrazolyl-2H-azirines has been established, resorting to organocatalysis. The protocol involves the in situ tosylation of β-ketoxime-1H-tetrazoles followed by the Neber reaction, in the presence of chiral organocatalysts. Among the organocatalysts studied a novel thiourea catalyst derived from 6β-aminopenicillanic acid afforded excellent enantioselectivities. | por |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | pbarrulas@uevora.pt | |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | nd | |
| dc.identifier.authoremail | nd | |
| dc.identifier.doi | 10.1055/s-0039-1691533 | por |
| dc.identifier.uri | https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0039-1691533 | |
| dc.identifier.uri | http://hdl.handle.net/10174/30451 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.publisher | Synlett | por |
| dc.rights | restrictedAccess | por |
| dc.subject | Organocatalysis | por |
| dc.title | Asymmetric Neber Reaction in the Synthesis of Chiral 2-(Tetrazol-5-yl)-2H-Azirines | por |
| dc.type | article |
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