Naučni savetnik

 

 

 

 

 

Adresa:

Centar za hemiju,
Institut za hemiju, tehnologiju i metalurgiju, Univerzitet u Beogradu,
Njegoševa 12, 11000 Beograd, Srbij
Telefon: +381 11 3336778
Fax: +381 11 3640227
E-mail: rmatovic@chem.bg.ac.rs

Lični podaci: Rođen 1956 u Beloj Crkvi, Srbija.

Obrazovanje:

1996 Doktorat hemijskih nauka, Univerzitet u Beogradu – Hemijski fakultet u Beogradu, Srbija.

Zvanje:

2006 Naučni savetnik - Centar za hemiju, Institut za hemiju, tehnologiju i metalurgiju, Univerzitet u Beogradu.

Članstvo u drustvima:

1982 Srpsko hemijsko drustvo – Sekcija za organsku hemiju, medicinsku hemiju

Profesionalno iskustvo:

1982 Centar za hemiju, Institut za hemiju, tehnologiju i metalurgiju, Univerzitet u Beogradu.

Oblast istraživanja: 

• Organska hemija
• Organske sinteze
• Medicinska hemija

Naučna dostignuća:

Razvijene i primenjene nove sintetičke metode u sintezi prirodnih proizvoda i bioloških aktivnih jedinjenja.

Znanje jezika: Engleski

Projekat:

2011 – 2016 Razvoj novih sintetičkih metoda i njihova primena u sintezi prirodnih proizvoda i biološki aktivnih jedinjenja, Projekat 172027 Ministarstvo za nauku i tehnološki razvoj Republike Srbije.

Izabrane publikacije:

1. Novkovic, L.; Trmcic, M.; Rodic, M.; Bihelovic, F.; Zlatar, M.; Matovic, R.; Saicic, R. N., Synthesis of endoperoxides by domino reactions of ketones and molecular oxygen, RSC Advances (2015), 5(120), 99577-99584.
2. Matovic, R.; Bihelovic, F.; Gruden-Pavlovic, M.; Saicic, R. N.:Total synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin C, Organic & Biomolecular Chemistry (2014), 12(39), 7682-7685.
3. Vulovic, Bojan; Gruden-Pavlovic, Maja; Matovic, Radomir; Saicic, Radomir N.,Substrate Stereocontrol in the Intramolecular Organocatalyzed Tsuji-Trost Reaction: Enantioselective Synthesis of Allokainates, Organic Letters (2014), 16(1), 34-37.
4. Bihelovic, Filip; Karadzic, Ivanka; Matovic, Radomir; Saicic, Radomir N.,Total synthesis and biological evaluation of (-)-atrop-abyssomicin C, Organic & Biomolecular Chemistry (2013), 11(33), 5413-5424.
5. Marjanovic, Jasna; Divjakovic, Vladimir; Matovic, Radomir; Ferjancic, Zorana; Saicic, Radomir N., Double Asymmetric Induction in Organo-catalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A2 and (-)-3-epi-Hyacinthacine A1, European Journal of Organic Chemistry (2013), 2013(25), 5555-5560.
6. Trmcic, Milena V.; Matovic, Radomir V.; Tovilovic, Gordana I.; Ristic, Biljana Z.; Trajkovic, Vladimir S.; Ferjancic, Zorana B.; Saicic, Radomir N., C,D-spirolactone analogue of paclitaxel: autophagy instead of apoptosis as a previously unknown mechanism of cytotoxic action for taxoids, Organic & Biomolecular Chemistry (2012), 10(25), 4933-4942
7. Vulovic, Bojan; Bihelovic, Filip; Matovic, Radomir; Saicic, Radomir N.,Organocatalyzed Tsuji-Trost reaction: a new method for the closure of five- and six-membered rings, Tetrahedron (2009), 65(50), 10485-10494.
8. Bihelovic, Filip; Matovic, Radomir; Vulovic, Bojan; Saicic, Radomir N., Organocatalyzed Cyclizations of π-Allylpalladium Complexes: A New Method for the Construction of Five- and Six-Membered Rings, Organic Letters (2007), 9(24), 5063-5066.
9. Matovic, Radomir; Ivkovic, Aleksandar; Manojlovic, Marija; Tokic-Vujosevic, Zorana; Saicic, Radomir N.,Ring Closing Metathesis/Fragmentation Route to (Z)-Configured Medium Ring Cycloalkenes. Total Synthesis of (±)-Periplanone C, Journal of Organic Chemistry (2006), 71(25), 9411-9419.
10. Ferjancic, Zorana; Matovic, Radomir; Cekovic, Zivorad; Jiang, Yi; Snyder, James P.; Trajkovic, Vladimir; Saicic, Radomir N., Synthesis, biology, and modeling of a C-4 carbonyl C,D-seco-taxoid, Tetrahedron (2006), 62(36), 8503-8514.
11. Ferjancic, Zorana; Matovic, Radomir; Cekovic, Zivorad; Snyder, James P.; Saicic, Radomir N., Synthesis, biological evaluation, and modeling of a C,D-seco-taxoid, Tetrahedron Letters (2005), 46(30), 5049-5052.
12. Tokic-Vujosevic, Zorana; Petrovic, Goran; Rakic, Bojana; Matovic, Radomir; Saicic, Radomir N.,Synthesis of (-)-cytoxazone and (+)-epi-cytoxazone: the chiral pool approach, Synthetic Communications (2005), 35(3), 435-447.