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Projects source: E-CRIS

The development of new synthetic methods and their application in the synthesis of natural products and biologically active molecules

Research activity

Code Science Field
P003  Natural sciences and mathematics  Chemistry 
P390  Natural sciences and mathematics  Organic chemistry 
P395  Natural sciences and mathematics  Organometallic chemistry 
Keywords
Organocatalysis; catalytic asymmetric reactions; total synthesis; Oseltamivir (Tamiflu); Paclitaxel
Organisations (3) , Researchers (1)
0011  University of Belgrade, Faculty of Chemistry
no. Code Name and surname Research area Role Period No. of publicationsNo. of publications
1.  02051  Radomir Saičić  Organic chemistry  Head  2011 - 2019  47 
0095  University of Belgrade, Institute of Chemistry, Technology and Metallurgy - National Institute of the Republic of Serbia
0257  Innovation Center, Faculty of Chemistry in Belgrade Ltd (IC)
Abstract
The planned research encompasses several topics, which can be classified into two main groups: A) The development of new synthetic methods, and B) Total syntheses of natural products and biologically active compounds. Methodological studies, within the first group (A), will include: 1) Organocatalyzed aldol reactions of structurally complex substrates (additions of functionalized proenolates to aldehyde acceptors possessing stereocenters and heteroatom substituents in the alpha-position); 2) Formation of carbon-carbon bonds using dual catalysis (a combination of organocatalysis and organotransition metal catalysis); 3) Allylation in aqueous conditions with highly functionalized allylic halides, and 4) Intramolecular Fischer indole synthesis. Within the second group (B), total syntheses of the following molecules are planned: 1) Oseltamivir phosphate (Tamiflu); 2) Structurally modified, water soluble Paclitaxel analogues; 3) Structural analogues of Abyssomicin; 4) Otteliones and their structural analogues, and 5) (+)-Allokainic acid and its derivatives. All synthesized compounds will be tested for biological activity.
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