In the thesis I tested in detail the reactivity of some classical synthesis reactions for the conversion of carbonyl compounds and used them to prepare 37 products with high added value. With the classical and modern synthesis of Friedel–Crafts acylation, I prepared aryl ketones with good to excellent yields. I analyzed the influence of the aromatic ring activation of the substrate on the acylation of the aromatic compounds. With a catalytic reaction and without the use of a solvent, I synthesized methyl esters from acid chlorides and methanol. Methyl esters served as precursors for the Kulinkovich synthesis reaction of cyclopropanols. I first conducted the reactions on a smaller scale and only carried out the successful ones on a larger scale. Scale played a significant role on the reactivity of the reactions.
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