P. Kolonits

发表

Synthesis of novel HMG‐CoA reductase inhibitors, II. Heterocyclic analogs of mevinolin

L. Novák, C. Szántay, J. Rohály, 1995 .

Synthesis of novel tryptamine and β-carboline derivatives via palladium-catalyzed reaction of bromotryptamine with organic boronic acids

M. Fekete, L. Novák, N. Hien, 2005 .

Rearrangements of Cycloalkenyl Aryl Ethers

A. Stirling, L. Novák, M. Nagy, 2016, Molecules.

Chemoenzymatic preparation of all the stereoisomers of 2-(1-hydroxyethyl)- and 2,6-bis(1-hydroxyethyl)pyridines and their acetates

L. Poppe, G. Szatzker, L. Novák, 2004 .

Preparation of new vindoline derivatives by palladium-catalyzed cross-coupling reaction

M. Fekete, L. Novák, P. Kolonits, 2005 .

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 .

Optically active 1-(benzofuran-2-yl)ethanols and ethane-1,2-diols by enantiotopic selective bioreductions

Paula Moldovan, L. Poppe, Csaba Paizs, 2003 .

Synthesis of protoemetine. A new total synthesis of emetine.

C. Szántay, P. Kolonits, L. Töke, 1966, The Journal of organic chemistry.

Simultaneous displacement of a nitro group during coupling of diazotized o-nitroaniline with phenols

J. Fekete, L. Novák, R. Farkas, 2010 .

One-pot synthesis of benzotriazoles and benzotriazole 1-oxides by reductive cyclization of o-nitrophenylazo compounds with benzyl alcohol

L. Novák, R. Farkas, P. Kolonits, 2009 .

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

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

Rearrangement of allyl aryl ethers; IV: Reaction of trimethylhydroquinone with cycloalkanediols

J. Fekete, L. Novák, C. Szántay, 2000 .

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 .

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 .

Preparation of new imidacloprid analogues

L. Novák, C. Szántay, J. Rohály, 2001 .

PREFERRED CARBON VS. NITROGEN SULFONYLATION ON β-CARBOLINES

A. Dobó, C. Szántay, M. Milen, 2001 .

Rearrangement of allyl aryl ethers III reaction of alkoxyhydroquinone with cycloalkenediols

L. Novák, C. Szántay, Péter Kovács, 1997 .

Studies on stereoselective approaches to β-carboline derivatives

C. Szántay, Á. Gömöry, M. Milen, 2005 .

Convenient synthetic route to (+)-faranal and (+)-13-norfaranal : The trail pheromone of pharaoh's ant and its congener 1

L. Poppe, L. Novák, C. Szántay, 1988 .

A convenient synthetic route to (+)-faranal; The trail pheromone of pharaoh's ant

L. Poppe, L. Novák, C. Szántay, 1986 .

A Convenient Route To Cyanoguanidines

L. Novák, C. Szántay, C. Kovacs, 1999 .

Synthesis of optically active 3-substituted-10-alkyl-10H-phenothiazine-5-oxides by enantioselective biotransformations

L. Poppe, Csaba Paizs, M. Toșa, 2002 .

Rearrangement Reactions for the Synthesis of Some Oxa- and Aza-tricyclic Rings Heterocyclic Compounds

L. Novák, Gábor Hornyánszky, P. Kolonits, 2015 .

A Convenient Route to Cyanoguanidines.

L. Novák, C. Szántay, C. Kovacs, 1999 .

Synthesis and further rearrangements of 7-(2-cycloalken-1-yl)-8-quinolinols

L. Novák, P. Kolonits, Mercedesz Törincsi, 2014, Monatshefte für Chemie - Chemical Monthly.

The isolation of Nϵ-formyl-l-lysine from the reaction between formaldehyde and l-lysine and its identification by OPLC and NMR spectroscopy

E. Tyihák, P. Kolonits, L. Trézl, 1985 .

Synthesis of new potential UV-filters

L. Novák, R. Farkas, P. Kolonits, 2012 .

Baker's yeast mediated preparation of (10-alkyl-10H-phenothiazin-3-yl)methanols

Paula Moldovan, L. Poppe, Csaba Paizs, 2002 .

SELECTIVE OXIDATON METHODS FOR PREPARATION OF N-ALKYLPHENOTHIAZINE SULFOXIDES AND SULFONES

L. Poppe, M. Toșa, F. Irimie, 2001 .

Lipase mediated enantiomer and diastereomer separation of 2,2′-[1,2- and 1,3-phenylenebis(oxy)]dicyclohexanols

E. Tőke, L. Poppe, L. Novák, 2006 .

Synthesis of novel tryptamine and azepinoindole derivatives

L. Novák, C. Szántay, J. Rohály, 1997 .

A convenient method for the preparation of cyclohepta[b]indole derivatives

L. Novák, Gábor Hornyánszky, K. Kupai, 2012 .

Synthesis and rearrangement of 13-thiaprostanoids

M. Kajtár, L. Novák, C. Szántay, 1982 .

The base‐catalyzed, low‐temperature interesterification mechanism revisited

A. Dijkstra, E. Tőke, L. Poppe, 2005 .

Structural reinvestigation of two diastereoisomeric aspidosperma–eburnea type bis‐indoles by NMR methods. Detection of a ‘hidden’ exchange partner and implications in noe analysis

Á. Demeter, C. Szantay, P. Kolonits, 1993 .

Rearrangement of Aryl Geranyl Ethers

J. Fekete, L. Novák, P. Kolonits, 2012 .

Stereocontrolled Synthesis of the Insect Growth Regulators — Alkyl (2E,4E)‐Dodecadienoates

J. Fekete, P. Kolonits, Ĺ. Varjas, 1982 .

Synthese des rac-5'-O-Methylphaseollinisoflavans

S. Antus, M. Nógrádi, A. Gottsegen, 1986 .

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

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

Convenient One-Pot Synthesis of Symmetrical Xanthenes

J. Fekete, L. Novák, C. Szántay, 1995 .

Convenient One‐Pot Synthesis of Symmetrical Xanthenes.

J. Fekete, L. Novák, C. Szántay, 2010 .

Structural investigation of a new heterocyclic ring system: NMR and X-ray studies

C. Szántay, L. Párkányi, A. Kălmăn, 1996 .

Formation of a new ring system via addition of acrylonitrile to benzoquinolizines

C. Szántay, A. Kălmăn, P. Kolonits, 1995 .

Synthesis of Reserpine‐type Alkaloids, II. Synthesis of 18‐Hydroxyyohimbine Stereoisomers and Raunescine Analogues with Normal Skeletons

E. Baitz-Gács, G. Blaskó, C. Szantay, 1983 .

Facile synthesis of cycloalkanoindole derivatives by aza-Claisen rearrangement

Gábor Hornyánszky, K. Kupai, P. Kolonits, 2012, Monatshefte für Chemie - Chemical Monthly.

Rearrangement of Allyl Aryl Ethers I. Reaction of hydroquinone with conjugated Dien-ols and Trien-ol

C. Szántay, Péter Kovács, György Pirok, 1995 .

Rearrangement of Allyl Aryl Ethers. Part 1. Reaction of Hydroquinone with Conjugated Dien-ols and Trien-ol.

C. Szántay, Péter Kovács, György Pirok, 1995 .

One-pot route to vinyl-2,3-dihydrobenzofurans

C. Szántay, Péter Kovács, P. Kolonits, 1994 .

Synthesis of novel HMG-CoA reductase inhibitors. I: Naphthalene analogs of mevinolin

J. Fekete, L. Poppe, A. Jávor, 1992 .