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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  
dc.subject
EXCHANGE A REACTION  
dc.subject
METATHESIS  
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THIOLS  
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TRANSESTERIFICATION  
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TRITHIOORTHOESTERS  
dc.subject.classification
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