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dc.contributor.author
Bothe, Michael
dc.contributor.author
Orrillo, Alfredo Gastón
dc.contributor.author
Furlan, Ricardo Luis Eugenio
dc.contributor.author
von Delius, Max
dc.date.available
2022-02-22T16:04:08Z
dc.date.issued
2019-09
dc.identifier.citation
Bothe, Michael; Orrillo, Alfredo Gastón; Furlan, Ricardo Luis Eugenio; von Delius, Max; Trithioorthoester Exchange and Metathesis: New Tools for Dynamic Covalent Chemistry; Georg Thieme Verlag Kg; Synlett; 30; 17; 9-2019; 1988-1994
dc.identifier.issn
0936-5214
dc.identifier.uri
http://hdl.handle.net/11336/152490
dc.description.abstract
To expand the toolbox of dynamic covalent and systems chemistry, we investigated the acid-catalyzed exchange reaction of trithioorthoesters with thiols. We found that trithioorthoester exchange occurs readily in various solvents in the presence of stoichiometric amounts of strong Bronsted acids or catalytic amounts of certain Lewis acids. The scope of the exchange reaction was explored with various substrates, and conditions were identified that permit clean metathesis reactions between two different trithioorthoesters. One distinct advantage of S, S, S-orthoester exchange over O, O, O-orthoester exchange is that the exchange reaction can kinetically outcompete hydrolysis, thereby making the process less sensitive to residual moisture. We expect that the relatively high stability of the products might be beneficial in future supramolecular receptors or porous materials.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Georg Thieme Verlag Kg
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
DYNAMIC COVALENT CHEMISTRY
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EXCHANGE A REACTION
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METATHESIS
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THIOLS
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TRANSESTERIFICATION
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TRITHIOORTHOESTERS
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Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Trithioorthoester Exchange and Metathesis: New Tools for Dynamic Covalent Chemistry
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-11-25T17:45:37Z
dc.journal.volume
30
dc.journal.number
17
dc.journal.pagination
1988-1994
dc.journal.pais
Alemania
dc.journal.ciudad
Stuttgart
dc.description.fil
Fil: Bothe, Michael. Universitat Ulm; Alemania
dc.description.fil
Fil: Orrillo, Alfredo Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Química Orgánica. Área Farmacognosia; Argentina
dc.description.fil
Fil: Furlan, Ricardo Luis Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Departamento de Química Orgánica. Área Farmacognosia; Argentina
dc.description.fil
Fil: von Delius, Max. Universitat Ulm; Alemania
dc.journal.title
Synlett
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0039-1690992
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1055/s-0039-1690992
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