M. Litvić

发表

Use of enantioselective liquid chromatography for preparation of pure atenolol enantiomers.

V. Vinković, H. Mikuldaš, I. Cepanec, 2005, Journal of separation science.

Scope and Limitations of Sodium and Potassium Trimethylsilanolate as Reagents for Conversion of Esters to Carboxylic Acids

M. Lovrić, V. Vinković, I. Cepanec, 2007 .

First application of hexaaquaaluminium(III) tetrafluoroborate as a mild, recyclable, non-hygroscopic acid catalyst in organic synthesis: a simple and efficient protocol for the multigram scale synthesis of 3,4-dihydropyrimidinones by Biginelli reaction

M. Lovrić, V. Vinković, M. Litvić, 2010 .

A study of photodegradation of drug rosuvastatin calcium in solid state and solution under UV and visible light irradiation: The influence of certain dyes as efficient stabilizers

V. Vinković, M. Litvić, Mirela Filipan-Litvić, 2013 .

Simple and Efficient Large-scale Metal-free Synthesis of o-(5-Formyl-2-thienyl)benzonitrile and o-(5-Formyl-2-furyl)benzonitrile

M. Lovrić, I. Cepanec, M. Litvić, 2018 .

Remarkably fast and selective aromatization of Hantzsch esters with MoOCl4 and MoCl5: a chemical model for possible biologically relevant properties of molybdenum-containing enzymes.

M. Lovrić, M. Litvić, Mirela Filipan-Litvić, 2012, Bioorganic & medicinal chemistry letters.

Antimony(III) chloride-catalysed Biginelli reaction : a versatile method for the synthesis of dihydropyrimidinones through a different reaction mechanism

I. Cepanec, M. Litvić, Mirela Filipan-Litvić, 2007 .

Rapid, efficient and selective reduction of aromatic nitro compounds with sodium borohydride and Raney nickel

I. Cepanec, M. Litvić, Sonja Merkaš, 2007 .

Ferric chloride/tetraethyl orthosilicate as an efficient system for synthesis of dihydropyrimidinones by Biginelli reaction

M. Lovrić, I. Cepanec, M. Litvić, 2005 .

Calcium trifluoromethanesulfonate-catalysed aminolysis of epoxides

V. Vinković, H. Mikuldaš, I. Cepanec, 2003 .

An efficient, metal-free, room temperature aromatization of Hantzsch-1,4-dihydropyridines with urea–hydrogen peroxide adduct, catalyzed by molecular iodine

V. Vinković, M. Litvić, Mirela Filipan-Litvić, 2008 .

Rapid, efficient, room temperature aromatization of Hantzsch-1,4-dihydropyridines with vanadium(V) salts: superiority of classical technique versus microwave promoted reaction

V. Vinković, M. Litvić, Mirela Filipan-Litvić, 2008 .

First Application of Hexaaquaaluminium(III) Tetrafluoroborate as a Mild, Recyclable, Non-hygroscopic Acid Catalyst in Organic Synthesis: A Simple and Efficient Protocol for the Multigram Scale Synthesis of 3,4-Dihydropyrimidinones by Biginelli Reaction.

M. Lovrić, V. Vinković, M. Litvić, 2010 .

Hantzsch Synthesis of 2,6-Dimethyl-3,5-dimethoxycarbonyl-4-(o-methoxyphenyl)-1,4-dihydropyridine; a Novel Cyclisation Leading to an Unusual Formation of 1-Amino-2-methoxy-carbonyl-3,5-bis(o-methoxyphenyl)-4-oxa-cyclohexan-1-ene

V. Vinković, I. Cepanec, M. Litvić, 2007, Molecules.

A CONVENIENT HANTZSCH SYNTHESIS OF 1,4-DIHYDROPYRIDINES USING TETRAETHYL ORTHOSILICATE

V. Vinković, I. Cepanec, M. Litvić, 2003 .

A highly efficient biomimetic aromatization of Hantzsch-1,4-dihydropyridines with t-butylhydroperoxide, catalysed by iron(III) phthalocyanine chloride.

V. Vinković, M. Litvić, Mirela Filipan-Litvić, 2008, Bioorganic & medicinal chemistry.

Ammonium carbamate; mild, selective and efficient ammonia source for preparation of β-amino-α,β-unsaturated esters at room temperature

I. Cepanec, M. Litvić, Mirela Filipan, 2005 .

Mild, Selective, and High-Yield Oxidation of Hantzsch 1,4-Dihydropyridines with Lead(IV) Acetate.

V. Vinković, I. Cepanec, M. Litvić, 2005 .

Mild, selective, and high-yield oxidation of hantzsch 1,4-dihydropyridines with lead(IV) acetate

V. Vinković, I. Cepanec, M. Litvić, 2005 .

Copper(I)-catalysed homo-coupling of aryldiazonium salts: synthesis of symmetrical biaryls

M. Lovrić, I. Cepanec, M. Litvić, 2007 .

Antimony(V) chloride-promoted room temperature aromatization of 1,4-dihydropyridines in non-acidic solvent

V. Vinković, I. Cepanec, M. Litvić, 2008 .

Simple and efficient synthesis of arbutin

I. Cepanec, M. Litvić, 2007 .

Efficient Synthesis of 3-Hydroxy-1,4-benzodiazepines Oxazepam and Lorazepam by New Acetoxylation Reaction of 3-Position of 1,4-Benzodiazepine Ring

I. Cepanec, M. Litvić, Ivan Pogorelić, 2006 .

Synthesis of Novel, Potentially Biologically Active Dibenzosuberone Derivatives

V. Vinković, I. Cepanec, M. Litvić, 2005, Molecules.

Synthesis of New Substituted Dibenzosuberones

G. Karminski-Zamola,, I. Cepanec, M. Litvić, 1998 .

Synthesis of New Substituted Dibenzosuberones.

G. Karminski-Zamola,, I. Cepanec, M. Litvić, 1998 .