Conţinutul numărului revistei |
Articolul precedent |
Articolul urmator |
807 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 ISO690:2012 FOURNIER, 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 | ||||||
Numărul 2(10) / 2015 / ISSN 1857-1727 /ISSNe 2345-1688 | ||||||
|
||||||
DOI:https://doi.org/10.19261/cjm.2015.10(2).09 | ||||||
CZU: 547.466:542.95 | ||||||
Pag. 68-76 | ||||||
|
||||||
Descarcă PDF | ||||||
Rezumat | ||||||
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. |
||||||
Cuvinte-cheie solid-phase synthesis, linker, sulfamate, phenol, library |
||||||
|