Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mateja Đud"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 1313-1320 (2019)
Friedel–Crafts (FC) acylation reactions were exploited in the preparation of ketone-functionalized aromatics. Environmentally more friendly, solvent-free mechanochemical reaction conditions of this industrially important reaction were developed. Re
Externí odkaz:
https://doaj.org/article/388f86874ba74e9096b79c87854cf78c
Publikováno v:
Molecules, Vol 26, Iss 17, p 5160 (2021)
Amine-containing drugs often show poor pharmacological properties, but these disadvantages can be overcome by using a prodrug approach involving self-immolative linkers. Accordingly, we designed l-lactate linkers as ideal candidates for amine deliver
Externí odkaz:
https://doaj.org/article/87e515ac3bbf45af8674cbb73d46f56e
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1745-1752 (2017)
The mechanochemical N-alkylation of imide derivatives was studied. Reactions under solvent-free conditions in a ball mill gave good yields and could be put in place of the classical solution conditions. The method is general and can be applied to var
Externí odkaz:
https://doaj.org/article/2f419bc926bd42a78b0ea52981feab09
A series of aryl-substituted guanidines revealed a pKa of about 10 in aqueous medium, thus positioning themselves between the more basic aliphatic guanidines (pKa > 13) and the acidic guanidinocarbonyl-pyrrole (pKa 6). The study revealed that for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee489bc3bae4e341c6f10167a0e46cc1
https://doi.org/10.1039/d0nj01879a
https://doi.org/10.1039/d0nj01879a
Autor:
Mateja Đud, Davor Margetić
Publikováno v:
International Journal of Organic Chemistry. :140-144
Boc protection group could be readily removed in a very mild mechanochemical conditions. In a short reaction time, ball milling of Boc-protected amines with p-toluenesulfonic acid in solvent-free conditions affords corresponding amine p-TsOH salts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02f11ae59826e0d15033a644ef8d1c62
https://doi.org/10.4236/ijoc.2017.72011
https://doi.org/10.4236/ijoc.2017.72011
Solid state ball milling was used in guanidinylation reactions of aromatic amines with N,N′-Di-Boc-1H-pyrazole-1-carboxamidine reagent. Reaction conditions are advantageous, and in general reactions proceed in significantly shorter reaction times a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::147ac6aaacef27f1591a42ef44e4991f
https://www.bib.irb.hr/989107
https://www.bib.irb.hr/989107
Publikováno v:
Green Chemistry
Thiocarbamoyl benzotriazoles, as safe and easy-to-handle isothiocyanate equivalents, were quantitatively converted to N-monosubstituted thioureas by vapour digestion synthesis under an ammonia atmosphere. This simple, but timely process provided a sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adbfb19764ee47d5fe8011d54b61d1f0
https://doi.org/10.1039/c6gc00089d
https://doi.org/10.1039/c6gc00089d
Publikováno v:
Beilstein Journal of Organic Chemistry
The mechanochemical N-alkylation of imide derivatives was studied. Reactions under solvent-free conditions in a ball mill gave good yields and could be put in place of the classical solution conditions. The method is general and can be applied to var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4310119e98eb947084063a6c8a048f26
https://pubmed.ncbi.nlm.nih.gov/28904618
https://pubmed.ncbi.nlm.nih.gov/28904618
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1745-1752 (2017)
The mechanochemical N-alkylation of imide derivatives was studied. Reactions under solvent-free conditions in a ball mill gave good yields and could be put in place of the classical solution conditions. The method is general and can be applied to var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3fdd4cceab79f07af8c2db11ea035a7
https://www.bib.irb.hr/888837
https://www.bib.irb.hr/888837