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| Articolul precedent |
| Articolul urmator |
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 809 3 |
| Ultima descărcare din IBN: 2017-04-12 22:04 |
| Căutarea după subiecte similare conform CZU |
| 547.466:542.95 (1) |
| Chimie organică (484) |
| Reacţii chimice. Procese chimice speciale (67) |
 SM ISO690:2012FOURNIER, Diane, CIOBANU, Liviu, POIRIER, Donald. A sequential dual cleavage of the arylsulfamate linker to provide both sulfamate and phenol derivatives. In: Chemistry Journal of Moldova, 2015, nr. 2(10), pp. 68-76. ISSN 1857-1727. DOI: https://doi.org/10.19261/cjm.2015.10(2).09 |
| EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
 Chemistry Journal of Moldova |
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| Numărul 2(10) / 2015 / ISSN 1857-1727 /ISSNe 2345-1688 | ||||||
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| DOI:https://doi.org/10.19261/cjm.2015.10(2).09 | ||||||
| CZU: 547.466:542.95 | ||||||
| Pag. 68-76 | ||||||
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Tyramine sulfamate was linked to the trityl chloride resin and this polymeric solid support used to introduce two levels of molecular diversity by formation of peptide bonds. A dual cleavage strategy next generated in a sequential way (without resin split) two different types of compounds (phenol and arylsulfamate derivatives), which are therapeutically attractive types of compounds. Here, we used tyramine as a general scaffold, but other arylsulfamate derivatives could be judiciously used to extend the nature of synthesized compounds. |
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| Cuvinte-cheie solid-phase synthesis, linker, sulfamate, phenol, library |
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Dublin Core Export
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc='http://purl.org/dc/elements/1.1/' xmlns:oai_dc='http://www.openarchives.org/OAI/2.0/oai_dc/' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' xsi:schemaLocation='http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd'> <dc:creator>Fournier, D.</dc:creator> <dc:creator>Ciobanu, L.</dc:creator> <dc:creator>Poirier, D.</dc:creator> <dc:date>2015-12-14</dc:date> <dc:description xml:lang='en'>Tyramine sulfamate was linked to the trityl chloride resin and this polymeric solid support used to introduce two levels of molecular diversity by formation of peptide bonds. A dual cleavage strategy next generated in a sequential way (without resin split) two different types of compounds (phenol and arylsulfamate derivatives), which are therapeutically attractive types of compounds. Here, we used tyramine as a general scaffold, but other arylsulfamate derivatives could be judiciously used to extend the nature of synthesized compounds. </dc:description> <dc:identifier>10.19261/cjm.2015.10(2).09</dc:identifier> <dc:source>Chemistry Journal of Moldova 10 (2) 68-76</dc:source> <dc:subject>solid-phase synthesis</dc:subject> <dc:subject>linker</dc:subject> <dc:subject>sulfamate</dc:subject> <dc:subject>phenol</dc:subject> <dc:subject>library</dc:subject> <dc:title>A sequential dual cleavage of the arylsulfamate linker to provide both sulfamate and phenol derivatives</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> </oai_dc:dc>
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