dc.contributor.author | Olaizola Alvarez, Yurre | |
dc.contributor.author | Abdine, R. A. A. | |
dc.contributor.author | Dhimane, Hamid | |
dc.contributor.author | Dalko, Peter I. | |
dc.date.accessioned | 2024-01-29T18:10:22Z | |
dc.date.available | 2024-01-29T18:10:22Z | |
dc.date.issued | 2016-12-01 | |
dc.identifier.citation | Synthesis 49(2) : 391-396 (2017) | es_ES |
dc.identifier.issn | 0039-7881 | |
dc.identifier.issn | 1437-210X | |
dc.identifier.uri | http://hdl.handle.net/10810/64447 | |
dc.description.abstract | The desymmetrized meso-chimonantine core of leptosin C was prepared in a short stereoselective convergent sequence in 5 steps as the longest linear path from methyl l-tryptophan hydrochloride as starting material. The key step of this approach was a diastereoselective [4+2] cycloaddition between the bromooxindole and tryptophan derivatives allowing to define the adjacent quaternary benzylic centers in a high chemical yield. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Georg Thieme | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.title | Cyclotryptophan Mycotoxins: Short Synthesis of the Desymmetrized meso-Chimonantine Core of Leptosin C | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | © 2017 Georg Thieme Verlag Stuttgart | es_ES |
dc.relation.publisherversion | https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1588355 | es_ES |
dc.identifier.doi | 10.1055/s-0036-1588355 | |
dc.departamentoes | Química orgánica I | es_ES |
dc.departamentoeu | Kimika organikoa I | es_ES |