Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Bojan P. Bondzic"'
Autor:
Dunja Jovanović, Ana Filipović, Goran Janjić, Tamara Lazarević-Pašti, Zdravko Džambaski, Bojan P. Bondžić, Aleksandra M. Bondžić
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 2, p 1033 (2024)
We have synthesized 22 C-1 functionalized-N-aryl-1,2,3,4-tetrahydroisoquinoline derivatives showing biological activities towards cholinergic enzymes. Synthesis was performed using visible-light-promoted photo-redox chemistry, starting from a common
Externí odkaz:
https://doaj.org/article/decbd3a7ee5343b5a4dcfbe739d29505
Autor:
Aleksandra M. Bondžić, Dunja Jovanović, Nevena Arsenijević, Bojana Laban, Tamara Lazarević Pašti, Urszula Klekotka, Bojan P. Bondžić
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 16, p 8985 (2022)
The study of the interactions between nanoparticles (NPs) and proteins has had a pivotal role in facilitating the understanding of biological effects and safe application of NPs after exposure to the physiological environment. Herein, for the first t
Externí odkaz:
https://doaj.org/article/63683fc1f2f044a59e1f37b28fd8fa78
Autor:
Bojan P. Bondzic, Zdravko Džambaski, Christoforos G. Kokotos, Dimitrios‐Ioannis Tzaras, Sunggi Lee
Publikováno v:
Advanced Synthesis & Catalysis
α,β‐unsaturated aldehydes have been traditionally used in LUMO lowering asymmetric aminocatalysis (iminium catalysis), while the use of saturated aldehydes as substrates in this type of catalysis has been elusive, until recently. Herein, we demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23ffacd0529010ed88eb6c39e5eb3720
https://cer.ihtm.bg.ac.rs/handle/123456789/2954
https://cer.ihtm.bg.ac.rs/handle/123456789/2954
Autor:
Yujiro Hayashi, Tohru Taniguchi, Tatsuya Yamazaki, Shin Ogasawara, Bojan P. Bondzic, Kenji Monde, Yogesh Gupta
Publikováno v:
Chemistry - A European Journal. 22:15874-15880
The asymmetric Diels-Alder reaction of α-substituted acrolein proceeds in the presence of the trifluoroacetic acid salt of trifluoromethyl-substituted diarylprolinol silyl ether to afford the exo-isomer with both excellent diastereoselectivity and h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df7082fef462b21fae4431bcd7d6ce88
https://doi.org/10.1002/chem.201602345
https://doi.org/10.1002/chem.201602345
Publikováno v:
European Journal of Organic Chemistry. 2011:6020-6031
A microflow reaction of the Curtius rearrangement by using trimethylsilyl azide as an azide source, followed by trapping of the generated isocyanate with a nucleophile was established, which is safe, inexpensive, and suitable for large-scale synthesi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a478095a23d2d434e6bd9edadeb63480
https://doi.org/10.1002/ejoc.201100074
https://doi.org/10.1002/ejoc.201100074
Autor:
Ivo Starý, David Šaman, Petr Sehnal, Serghei Chercheja, Peter Eilbracht, Zuzana Krausová, Bojan P. Bondzic, Irena G. Stará
Publikováno v:
European Journal of Organic Chemistry. 2011:3849-3857
Starting from the optically pure [6]helicene-like alcohol(P,3S)-3-methyl-4-(4-methylphenyl)-1,3,6,7-tetrahydrobenzo[c]benzo[5,6]phenanthro[4,3-e]oxepin-14-ol, four helical phosphites were prepared from the corresponding chlorophosphites. These ligand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::115b08ae9244509e245079a982cb46f0
https://doi.org/10.1002/ejoc.201100259
https://doi.org/10.1002/ejoc.201100259
Publikováno v:
Organic Letters. 12:5434-5437
Asymmetric epoxidation of α-substituted acroleins with hydrogen peroxide has been catalyzed by diphenylprolinol diphenylmethylsilyl ether to afford α-substituted-β,β-unsubstituted-α,β-epoxy aldehyde with excellent enantioselectivity and the gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::847584e73bee0307e700a1eaf4cd6ff8
https://doi.org/10.1021/ol102269s
https://doi.org/10.1021/ol102269s
Autor:
Peter Eilbracht, Bojan P. Bondzic
Publikováno v:
Organic Letters. 10:3433-3436
The two component one-pot hydroformylation/Fischer indole synthesis sequence of 2,5 dihydropyrroles and phenyl hydrazines allows a facile and convenient access to tetrahydro-beta-carbolines in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c49f2babe57980fd5e665d151c41372
https://doi.org/10.1021/ol801071y
https://doi.org/10.1021/ol801071y
Autor:
Milovan Stojanovic, Bojan P. Bondzic, Zdravko Dzambaski, Jovana Aleksić, Marija Baranac-Stojanović
Publikováno v:
ChemInform. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1eb8ec08a1ac15161a057db37a5eb6d6
https://doi.org/10.1002/chin.201502264
https://doi.org/10.1002/chin.201502264