D. Korbonits

发表

Experimental studies on the antitussive properties of the new xanthine derivative 1H-purine-2,6-dione, 3,7-dihydro-3-methyl-7[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]. 1st communication: in vivo demonstration of the effects on animal models of cough and of mucociliary clearance.

M. Pascal, V. Saano, P. Arányi, 1997, Arzneimittel-Forschung.

Influence of Chinoin‐170, a Novel Antitussive, on the Mucociliary Activity in Respiratory Airways of Rats, Rabbits, Guinea‐pigs and Man

J. Nuutinen, V. Saano, P. Virta, 1993, The Journal of pharmacy and pharmacology.

X-ray study of two 1-substituted 3-acylamino-2-pyrazolines

L. Párkányi, K. Simon, K. Horváth, 1981 .

Experimental studies on the antitussive properties of the new xanthine derivative 1H-purine-2,6-dione, 3,7-dihydro-3-methyl-7[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]. 2nd communication: investigations on theophylline-like activities.

M. Pascal, F. Lacheretz, P. Arányi, 1997, Arzneimittel-Forschung.

Mannich-type reactions of an isobasic isoquinoline†

D. Korbonits, KáLmán Iiarsányi, P. Kiss, 1973 .

Synthesis of 4-aminopyrimidines from 1,2,4-oxadiazoles. Part 4. A novel heterocyclic rearrangement: formation of 4-hydroximinohexahydropyrimidines from 3-(2-aminoethyl)-4,5-dihydro-1,2,4-oxadiazoles

K. Simon, P. Kolonits, D. Korbonits, 1992 .

Recent Developments in Ring-Chain Tautomerism II. Intramolecular Reversible Addition Reactions to the C=N, C=N, C=C, and C=C Groups

F. Fülöp, R. Valters, D. Korbonits, 1996 .

Ring – Chain Tautomerism of 4‐Hydroximino‐hexahydropyrimidines Substituted in Position 2

P. Kolonits, D. Korbonits, E. Tobias‐Heja, 1991 .

Ring Transformation of 1,2‐Disubstituted 4(1H)‐Quinazolone Oximes to 3,5‐Disubstituted 1,2,4‐Oxadiazoles

K. Simon, P. Kolonits, D. Korbonits, 1989 .

Synthesis of 4‐Aminopyrimidines from 1,2,4‐Oxadiazoles, V[1]. Reductive Formation of 2‐(Benzoylamino)indole from 3‐(2‐Aminobenzyl)‐5‐phenyl‐1,2,4‐oxadiazole and Its Transformation to 6‐Phenyl‐8H‐pyrimido‐[1,6‐a: 4,5‐b']diindole, a New Heterocyclic Ring System

B. Podányi, P. Kolonits, I. Bata, 1993 .

Synthesis of 4-Aminopyrimidines from 1,2,4-Oxadiazoles, III A Novel Type of Formation of Olefins from Amines

K. Simon, P. Kolonits, D. Korbonits, 1991 .

Chemistry of the Heterocyclic Pseudobasic Amino Alcohols, XXXVIII Ring-Chain Tautomerism of Pyrimido[6,1-a]isoquinolines

K. Simon, P. Kolonits, D. Korbonits, 1990 .

Formation of α-(acylamino)butyramide oximes from 5-substituted 3-(1-aminopropyl)-1,2,4-oxadiazoles: an astonishing hydrolytic transformation

K. Horváth, D. Korbonits, E. M. Bako, 1988 .

Synthesis of 4-Aminopyrimidines from 1,2,4-Oxadiazoles, II A General Method for the Preparation of 4-Substituted 6,7-Dihydro-9,10-dialkoxy-2H-pyrimido[6,1-a]isoquinolin-2-imine Hydrochlorides

G. Héja, P. Kolonits, I. Bata, 1987 .

SYNTHESIS OF 4-AMINOPYRIMIDINES FROM 1,2,4-OXADIAZOLES. I. NEW GENERAL METHOD D FOR THE PREPARATION OF 4-AMINOQUINAZOLINES AND THEIR HETERO ANALOGS

K. Simon, P. Kolonits, D. Korbonits, 1985 .

Synthesis of new condensed nitrogen heterocyclic systems

B. Podányi, I. Hermecz, K. Simon, 2008 .

Theophylline derivatives 5. Selective alternative reactivity of 7-chloromethyl-oxazolopurine towards potassium phtalimide☆

D. Korbonits, R. Szebeni, 1978 .

DissimilarMechanisms of Action of AnticalmodulinDrugs: Quantitative Analysis

J. Ovádi, F. Orosz, K. Liliom, 1990 .

DIPHENYLPROPYLAMINE DERIVATIVES. I. N-SUBSTITUTED 3,3-DIPHENYLPROPYLAMINES.

K. Harsányi, D. Korbonits, P. Kiss, 1964, Journal of medicinal chemistry.

Solvent‐dependent reversible rearrangement of 4‐(hydroxyimino)hexahydro‐pyrimidines to 4‐aminotetrahydropyrimidine 3‐oxides

K. Simon, P. Kolonits, D. Korbonits, 1994 .

Dissimilar mechanisms of action of anticalmodulin drugs: quantitative analysis.

J. Ovádi, F. Orosz, K. Liliom, 1990, Molecular Pharmacology.

Theobromine inhibits sensory nerve activation and cough

O. Usmani, P. Barnes, M. Korbonits, 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Ring transformation of 3-(2-aminoaryl)-1,2,4-oxadiazoles into 3-acylaminoindazoles; extension of the Boulton–Katritzky scheme

K. Horváth, D. Korbonits, Ida Kanzel-Szvoboda, 1982 .