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Akademický článek
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Autor:
Zubčić, Gabrijel, Kolympadi Marković, Maria, Marković, Dean, Portada, Tomislav, Bešić, Erim, Šakić, Davor
A wide variety of systems are being researched with the goal of functionalizing distant unfunctionalized (alkane) carbons using updated versions of the Hoffmann-Löffler-Freytag (HLF) reaction. [1] The induced cleavage of sulfonamides with iodine and
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https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::b201829e7f79f744b8653a9abaabf86b
https://www.bib.irb.hr/1266580
https://www.bib.irb.hr/1266580
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Proline is an unusual proteinogenic alfa amino acid, where the side chain is connected to the amino group, forming a pyrrolidine ring and secondary amine. Due to its unique internal bonding it has different structural properties compared to other ami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::f9fbbcbd4b43a6834c1de63032929bb4
https://www.bib.irb.hr/1219381
https://www.bib.irb.hr/1219381
Autor:
Zubčić, Gabrijel, Šakić, Davor
Moderne inačice Hoffmann-Löffler-Freytag (HLF) reakcije proučavaju se na velikom broju sustava kako bi se funkcionalizirali udaljeni nefunkcionalizirani (alkanski) ugljici [1]. Naročitu primjenu pronalaze u farmaceutskoj industriji prilikom funkc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::98305d7ba742a81c0425fa8b27b0f3c5
https://www.bib.irb.hr/1182450
https://www.bib.irb.hr/1182450
Hofmann-Löffler-Freytag (HLF) is a well-established reaction used for late-stage functionalization for producing pyrrolidine rings, and more rarely piperidine rings, via C-H activation. However, according to Šakić and Zipse, [1] the driving force
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::5d2fe29d3e66f32dbd23bc6af370d3bd
https://www.bib.irb.hr/1199640
https://www.bib.irb.hr/1199640
A series of N6-substituted adenine-ferrocene conjugates were prepared and the reaction mechanism underlying the synthesis was explored. The SN2-like reaction between ferrocenoyl chloride and adenine anions is a regioselective process in which the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::ec0a5a545a9856f29e6658555638eef7
https://www.bib.irb.hr/1216864
https://www.bib.irb.hr/1216864
Autor:
Zubčić, Gabrijel, Vrček, Valerije
U ovoj radionici bit će obrađen work-flow za izračun fizikalno- kemijskih svojstava organskih reakcija. Radionica će imati sljedeće dijelove: 1) upoznavanje s dostupnim programskim paketima instaliranim na klasteru sw.pharma.hr, 2) upoznavanje s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::d19c0661266eec132b3396ef6263fbc5
https://www.bib.irb.hr/1229490
https://www.bib.irb.hr/1229490
Autor:
Zubčić, Gabrijel, Šakić, Davor
The Hofmann-Löffler-Freytag (HLF) reaction represents a distinctive radical-based procedure for the synthesis of nitrogen-containing heterocycles. Although the formation of piperidine and pyrrolidine rings is equally likely [1], due to the driving f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::12434abf991ad6ccc5958a360cf15659
https://www.bib.irb.hr/1219388
https://www.bib.irb.hr/1219388
Modern synthetic approaches try to incorporate already known chemical entities and then modify them using late-stage functionalization (LSF) procedures. Hofmann–Löffler–Freytag (HLF) reaction was originally discovered by Hofmann [1–3] in synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7741a0161f096443978d38ecb4db980d
https://www.bib.irb.hr/1161087
https://www.bib.irb.hr/1161087