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    [platne_od] => 31.10.2023 17:15:00
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            [paticka_budova_a_nadpis] => BUILDING A
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FCT Dean’s Office, 
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Bursar
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Crèche Zkumavka, 
General Practitioner, 
Department of Economics and Management, 
Department of Mathematics
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            [paticka_adresa] => UCT Prague
Technická 5
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Czech Post certified digital mail code: sp4j9ch

Copyright: UCT Prague 2015
Information provided by the Department of Organic Chemistry. Technical support by the Computing Centre. [paticka_odkaz_mail] => mailto:kundrato@vscht.cz [social_fb_title] => Facebook of Department [social_tw_title] => Twitter of Department [social_yt_title] => [aktualizovano] => Updated [autor] => Author [paticka_mapa_alt] => [drobecky] => You are here: VŠCHT PrahaFCHTÚOCH [intranet_odkaz] => http://intranet.vscht.cz/ [intranet_text] => Intranet [logo_mobile_href] => / [logo_mobile] => [mobile_over_nadpis_menu] => Menu [mobile_over_nadpis_search] => Search [mobile_over_nadpis_jazyky] => Languages [mobile_over_nadpis_login] => Login [menu_home] => Homepage [zobraz_desktop_verzi] => switch to desktop version [zobraz_mobilni_verzi] => switch to mobile version [more_info] => more information [paticka_mapa_odkaz] => [nepodporovany_prohlizec] => For full access, please use different browser. [preloader] => Wait a second... [social_in_odkaz] => [den_kratky_4] => [archiv_novinek] => [novinky_servis_archiv_rok] => [novinky_kategorie_1] => [novinky_kategorie_2] => [novinky_kategorie_3] => [novinky_kategorie_4] => [novinky_kategorie_5] => [novinky_archiv_url] => [novinky_servis_nadpis] => [novinky_dalsi] => [hledani_nadpis] => hledání [hledani_nenalezeno] => Nenalezeno... [hledani_vyhledat_google] => vyhledat pomocí Google [social_li_odkaz] => ) [poduzel] => stdClass Object ( [6525] => stdClass Object ( [obsah] => [poduzel] => stdClass Object ( [6532] => stdClass Object ( [obsah] => [iduzel] => 6532 [canonical_url] => //uoch.vscht.cz [skupina_www] => Array ( ) [url] => [sablona] => stdClass Object ( [class] => [html] => [css] => [js] => [autonomni] => ) ) [6530] => stdClass Object ( [obsah] => [iduzel] => 6530 [canonical_url] => //uoch.vscht.cz [skupina_www] => Array ( ) [url] => [sablona] => stdClass Object ( [class] => [html] => [css] => [js] => [autonomni] => ) ) [6531] => stdClass Object ( [obsah] => [iduzel] => 6531 [canonical_url] => //uoch.vscht.cz [skupina_www] => Array ( ) [url] => [sablona] => stdClass Object ( [class] => [html] => [css] => [js] => [autonomni] => ) ) ) [iduzel] => 6525 [canonical_url] => [skupina_www] => Array ( ) [url] => [sablona] => stdClass Object ( [class] => [html] => [css] => [js] => [autonomni] => ) ) [6526] => stdClass Object ( [obsah] => [poduzel] => stdClass Object ( [21923] => stdClass Object ( [nazev] => Department of Organic Chemistry [seo_title] => Department of Organic Chemistry [seo_desc] => [autor] => [autor_email] => [obsah] =>

New PhD topics of our department: here

 All publications of our authors (since 2015): here

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k Phonebook of the Department    
     

Professors:

   
     

Prof. Radek Cibulka

e +420 22044 4182

d A 278c

b Radek.Cibulka@vscht.cz 

Head of Department www ResearcherID
     

Prof. Pavel Lhoták

e +420 22044 5055

d A 249

b Pavel.Lhotak@vscht.cz

  www  
     

Prof. Jaroslav Kvíčala

e +420 22044 4240

d A 278d

b Jaroslav.Kvicala@vscht.cz

  www  
     

Prof. Jiří Svoboda

e +420 22044 3688

d A 278e

b Jiri.Svoboda@vscht.cz

  www  
     

Associate Professors:

   
     

Assoc. Prof. Jan Budka

e +420 22044 4284

d A 251

b Jan.Budka@vscht.cz

DOC web editor www  
     

Assoc. Prof. Jana Hodačová

e +420 22044 4173

d A 270

b Jana.Hodacova@vscht.cz

  www  
     

Assoc. Prof. Michal Kohout

e +420 22044 5012

d A 258

b Michal.Kohout@vscht.cz

  www  
     

Assoc. Prof. Igor Linhart

e +420 22044 4165

d A 266

b Igor.Linhart@vscht.cz

  www  
     

Assoc. Prof. Tomáš Tobrman

e +420 22044 4245

d A 271

b Tomas.Tobrman@vscht.cz

 RIT www  
     

Assistant Professors:

   

Dr. Michal Himl

e +420 22044 4165

d A 266

b Michal.Himl@vscht.cz

  www  
     

Dr. Roman Holakovský

e +420 22044 4279

d A 255

b Roman.Holakovsky@vscht.cz

  www  
     

Dr. Petr Kovaříček

e +420 22044 2040

d B3 207

b Petr.Kovaricek@vscht.cz

www

Dr. Václav Kozmík

e +420 22044 4118

d A 308

b Vaclav.Kozmik@vscht.cz

  www  
     

Dr. Martin Krupička

e +420 220 444 173
d A 268
b Martin.Krupicka@vscht.cz

  www  
     

Dr. Ondřej Kundrát

e +420 22044 4280

d A 253

b Ondrej.Kundrat@vscht.cz

www ResearcherID 
     

Dr. Petra Ménová

e +420 22044 3686

d A 268

b Petra.Menova@vscht.cz

  www  

Dr. Pavla Perlíková

e +420 22044 2039

d B3 206

b Pavla.Perlikova@vscht.cz

www
     

Dr. Markéta Rybáčková

e +420 22044 4242

d A 259

b Marketa.Rybackova@vscht.cz

Secretary of Department

www  
     

Dr. Eva Svobodová

e +420 22044 4249

d A 260

b Eva.Svobodova@vscht.cz

  www  
     

Technicians:

   

Květa Bártová

e +420 22044 3686

d A 268

b Kveta.Bartova@vscht.cz

   
     

Ivana Bocková, MSc.

e +420 22044 4280

d A 250

b Ivana.Bockova@vscht.cz

   
     
Michaela Kadlecová 

e +420 22044 4276

d A 262

b Michaela.Kadlecova@vscht.cz
   
     

Martina Kovandová

e +420 22044 4279

d A 255

b Martina.Kovandova@vscht.cz

   
     

Vladimír Kuneš

e +420 22044 4277

d A L06

b Vladimir.Kunes@vscht.cz

   
     

Jana Netušilová

e +420 22044 4164

d A 278a

b Jana.Netusilova@vscht.cz

Administrative Support of Department  
     

Markéta Slabochová, MSc.

e +420 22044 4059 

d A 308  

b Marketa.Slabochova@vscht.cz

Economist of Department  
     

Helena Štenglová 

e +420 22044 4278 

d A 257 

b Helena.Stenglova@vscht.cz

   
     

Ing. David Tetour

e +420 22044 4173

d A270

b David.Tetour@vscht.cz

Marta Tokárová 

e +420 220 444 245 

d A 271 

b Marta.Tokarova@vscht.cz

   
     

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Essential Information for Current Students



Bachelor Students

Master Students

PhD Students

Lectures delivered by members of the Department

  • Toxicology and ecology
  • Organic chemistry I, II and III
  • Structural analysis
  • Reactivity of organic compounds
  • Molecular design
  • Organic synthesis I and II
  • Quantum organic chemistry
  • Farmacochemistry
  • Organic stereochemistry
  • Organometallic chemistry
  • Organic chemistry of selected elements

Repository of the theses

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DATA


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2024

2023

  • J. Koudelka, M. Vosmanská and T. Tobrman, Synthesis of Sulfonic Acid Salts and Sulfonic Acids by Advanced Cross-Coupling Reaction of Vinyl Sulfonates. ChemistrySelect 2023, 8, e202304246. DOI:10.1002/slct.202304246

  • T. Tobrman, Vinyl Esters and Vinyl Sulfonates as Green Alternatives to Vinyl Bromide for the Synthesis of Monosubstituted Alkenes via Transition-Metal-Catalyzed Reactions. Chemistry 2023, 5, 2288–2321. DOI:10.3390/chemistry5040153

  • L. Koláčná, P. Polák, A. Liška, T. Tobrman and J. Ludvík, Pentasubstituted Phospholes with extended π-conjugated Arm – Synthesis, electrochemistry, spectra and quantum chemical calculations. Electrochim. Acta 2023, 468, 143073. DOI: 10.1016/j.electacta.2023.143073

  • M. Čubiňák, N. Varma, P. Oeser, A. Pokluda, T. Pavlovska, R. Cibulka, M. Sikorski, T. Tobrman, Tuning the Photophysical Properties of Flavins by Attaching an Aryl Moiety via Direct C–C Bond Coupling. J. Org. Chem. 2023, 88, 218–229. DOI: 10.1021/acs.joc.2c02168

2022

  • Tobrman, T.; Mrkobrada, S., Palladium-Catalyzed Cross-Coupling Reactions of Borylated Alkenes for the Stereoselective Synthesis of Tetrasubstituted Double Bond. Organics 2022, 3, 210.10.3390/org3030017

  • Shishkanova, T. V.; Tobrman, T.; Otta, J.; Broncová, G.; Fitl, P.; Vrňata, M., Substituted polythiophene-based sensor for detection of ammonia in gaseous and aqueous environment. J. Mater. Sci. 2022, 57, 1787017882. DOI: 10.1007/s10853-022-07694-8

  • Oeser, P.;  Petrenko, A.; Edlová, T.; Čubiňák, M.; Koudelka, J.; Tobrman, T., Halocyclobutanol Dehydration En Route to Halocyclobutenes. Synthesis 2022, 54, 3239–3248. DOI: 10.1055/a-1794-0685

  • Koláčná, L.; Klíma, J.; Polák, P.; Tobrman, T.; Liška, A.; Ludvík, J., Electrochemical, EPR, and computational study of pyrene conjugatesprecursors for novel type of organic semiconductors. J. Solid State Electrochem. 2022, 26, 503514. DOI: 10.1007/s10008-021-05094-7

2021

  • Oeser, P; Koudelka, J.; Petrenko, A.; T. Tobrman, Recent Progress Concerning the N-Arylation of Indoles. Molecules 2021, 26, 5079. DOI: 10.3390/molecules26165079  
  • Čubiňák, M.; Bigeon, J.; Galář, P.; Ondič, L.; Tobrman, T., The Synthesis of Tetrasubstituted Cycloalkenes Bearing π-Conjugated Substituents and Their Optical Properties. ChemistrySelect 2021, 6, 99049910. DOI: 10.1002/slct.202103122
  • Oeser, P.; Edlová, T.; Čubiňák, M.; Tobrman, T., Transition-Metal-Free Ring-Opening Reaction of 2-Halocyclobutanols through Ring Contraction. Eur. J. Org. Chem. 2021, 49584967. DOI: 10.1002/ejoc.202100837
  • Koudelka, J.; Tobrman, T., Synthesis of 2-Substituted Cyclobutanones by a Suzuki Reaction and Dephosphorylation Sequence. Eur. J. Org. Chem. 2021, 3260–3269 DOI:10.1002/ejoc.202100464

  • Edlová, T.; Dvořáková, H.; Eigner, V.; Tobrman, T., Substrate-Controlled Regioselective Bromination of 1,2-Disubstituted Cyclobutenes: An Application in the Synthesis of 2,3-Disubstituted Cyclobutenones.
    J. Org. Chem. 2021, 86, 5820–5831 DOI:10.1021/acs.joc.1c00261

  • Shishkanova, T.; Stepánková, N.; Tlustý, M.; Tobrman, T.; Jurásek, B.; Kuchař, M.; Trchová, M.; Fitl, P.; Vrňata, M., Electrochemically oxidized 15-crown-5 substituted thiophene and host-guest interaction with new psychoactive substances Electrochim. Acta 2021, 737, 137862 DOI:10.1016/j.electacta.2021.137862

  • Edlová, T.; Čubiňák, M.; Tobrman, T., Cross-Coupling Reactions of Double or Triple Electrophilic Templates for Alkene Synthesis. Synthesis 2021, 53, 255266. DOI: 10.1055/s-0040-1707270

2020

  • Oeser, P.; Koudelka, J.; Dvořáková, H.; Tobrman, T., Formation of trisubstituted buta-1,3-dienes and α,β-unsaturated ketones via the reaction of functionalized vinyl phosphates and vinyl phosphordiamidates with organometallic reagents. RSC Adv. 2020, 10, 3510935120. DOI: 10.1039/D0RA07472A

  • Čubiňák, M.; Tobrman, T., Room-Temperature Negishi Reaction of Trisubstituted Vinyl Phosphates for the Synthesis of Tetrasubstituted Alkenes. J. Org. Chem. 2020, 85, 1072810739. DOI: 10.1021/acs.joc.0c01254

  • Polák, P.; Čejka, J.; Tobrman, T., Formal Transition-Metal-Catalyzed Phosphole C–H Activation for the Synthesis of Pentasubstituted Phospholes. Org. Lett. 2020, 22, 21872190. DOI: 10.1021/acs.orglett.0c00359

  • Tobrman, T; Krupička, M.; Polák, P.; Dvořáková, H.; Čubiňák, M.; Babor, M.; Dvořák, D., Diastereoselective Cyclopropanation through Michael Addition‐Initiated Ring Closure between α,α‐Dibromoketones and α,β‐Unsaturated Fischer Carbene Complexes. Eur. J. Org. Chem. 2020, 429436. DOI: 10.1002/ejoc.201901503

  • Guricová, M.; Tobrman, T; Pižl, M.; Žižková, S.; Hoskovcová, I.; Dvořák, D., Synthesis, characterisation and electrochemical properties of Cr(0) aminocarbene complexes containing condensed heteroaromatic moiety. J. Organomet. Chem. 2020, 905, 121023 DOI: 10.1016/j.jorganchem.2019.121023

2019

  • Tobrman, T.; Čubiňák, M.; Dvořák, D., Stereoselective synthesis of trisubstituted alkenyl Fischer aminocarbenes through self-mediated α-haloketone olefination. J. Organomet. Chem. 2019, 902, 120971. DOI: 10.1016/j.jorganchem.2019.120971

  • Čubiňák, M.; Edlová, T.; Polák, P.; Tobrman, T., Indolylboronic Acids: Preparation and Applications.
    Molecules 2019, 24, 3523 DOI: 10.3390/molecules24193523

  • Váňová, H.; Tobrman, T.; Babor, M.; Dvořák, D., Reaction of lithiated thiophene-derived aminocarbene complexes with inorganic halides: Preparation of a heteroatom containing mono- and multicarbene complexes. J. Organomet. Chem. 2019, 882, 9095 DOI: 10.1016/j.jorganchem.2018.12.015

  • Tobrman, T.; Polák, P.; Čubiňák, M.; Dvořáková, H.; Dvořák, D., Dichotomy within 1,4-addition of organolithium and Grignard reagents to α,β-unsaturated Fischer alkoxycarbenes: A new synthesis of Fischer carbenes. Tetrahedron 2019, 75, 21752181 DOI: 10.1016/j.tet.2019.02.038

  • Polák, P.; Tobrman, T., Novel Selective Approach to Terminally Substituted [n]Dendralenes
    Eur. J. Org. Chem. 2019, 957968. DOI:10.1002/ejoc.201801522

2018

  • Čubiňák, M.; Eigner, V.; Tobrman, T., Bench-Stable Sulfoxide-Based Boronates: Preparation and Application in a Tandem Suzuki Reaction. Adv. Synth. Catal. 2018, 360, 46044614 DOI: 10.1002/adsc.201801000

2017

  • Polak, P.; Dvorak, D.; Tobrman, T., Cyanogen: A Versatile Reagent for Diversity-​Oriented Synthesis
    Synthesis 2017, 49, 17571766 DOI:10.1055/s-0036-1588410

  • Polak, P.; Tobrman, T., The synthesis of polysubstituted indoles from 3-​bromo-​2-​indolyl phosphates. Org. Biomol. Chem. 2017, 15, 62336241 DOI:10.1039/C7OB01127J

  • Polak, P.; Tobrman, T., Dearomatization Strategy for the Synthesis of Arylated 2H-​Pyrroles and 2,​3,​5-​Trisubstituted 1H-​Pyrroles. Org. Lett. 2017, 19, 4604611 DOI: 10.1021/acs.orglett.7b02219

  • Šimůnková, N.; Tobrman, T.; Eigner, V.; Dvořák, D., A Study on the Intramolecular Mitsunobu Reaction of N6-(ω-hydroxyalkyl)adenines. J. Heterocyclic Chem 2017, asap DOI: 10.1002/jhet.2982

2016

  • Váňová, H.; Tobrman, T.; Hoskovcova, I.; Dvořák, D., Modular synthesis of Fischer biscarbene complexes of chromium. Organometallics 2016, 35, 29993006. DOI:10.1021/acs.organomet.6b00527

  • Kotek, V.; Polák, P.; Dvořáková, H.; Tobrman, T., Aluminium Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues. Eur. J. Org. Chem. 2016, 50375044. DOI:10.1002/ejoc.201600959

  • Polák, P.; Váňová, H.; Dvořák, D.; Tobrman, T., Recent Progress in Transition Metal-Catalyzed Stereoselective Synthesis of Acyclic All-Carbon Tetrasubstituted Alkenes. Tetrahedron Lett. 2016, 57, 36843693. DOI:10.1016/j.tetlet.2016.07.030 

  • Kotek, V.; Polák, P.; Tobrman, T., Efficient and Simple Preparation of Functionalized 1,1-Dibromoenol Phosphates. Monat. Chem. 2016, 147, 405412. DOI:10.1007/s00706-015-1613-6


2015

  • Kotek V., Dvořáková H., Tobrman T., Modular and highly stereoselective approach to all-carbon tetrasubstituted alkenes. Org. Lett., 2015, 17, 608611. DOI: 10.1021/ol503624v
  • Křováček M., Dvořák D.: Synthesis of potentially biologically active 6-(1,3-butadiynyl)purines. J. Heterocyclic Chem., 2015, 52, 4047. DOI: 10.1002/jhet.1938

 

2014

  • Tobrman T., Jurásková I., Dvořák D., Negishi cross-coupling reaction as a simple and efficient route to functionalized amino and alkoxy carbene complexes of chromium, molybdenum, and tungsten. Organometallics, 2014, 33, 65936603. DOI: 10.1021/om500925m
  • Kvapilová H., Eigner V., Hoskovcová I., Tobrman T., Čejka J., Záliš S., Structural flexibility of 2-hetaryl chromium aminocarbene complexes: Experimental and theoretical evidence. Inorg. Chim. Acta, 2014, 421, 439445. DOI: 10.1016/j.ica.2014.06.028
  • Vrzal L., Flídrová K., Tobrman T, Dvořáková H., Lhoták, P., Use of residual dipolar couplings in conformational analysis of meta-disubstituted calix[4]arenes. Chem. Commun., 2014, 50, 75907592. DOI: 10.1039/C4CC02274B
  • Tobrman T, Jurásková I., Váňová H., Dvořák D, Lithiation of chromium and tungsten aminocarbene complexes: An easy approach to functionalized aminocarbene complexes. Organometallics, 2014, 33, 29902996. DOI: 10.1021/om500182p
  • Tobrman T., Dvořák D., Regioselective and facile synthesis of 7,9-dialkyl-8-oxopurines from 7,9-dialkyl-7,8-dihydropurines: Total synthesis of Heteromines I and J. Synthesis, 2014, 46, 660668. DOI: 10.1055/s-0033-1340499

 

2013

  • Maryška M., Chudíková N., Kotek V., Dvořák D., Tobrman T., Regioselective and efficient synthesis of N7-substituted adenines, guanines, and 6-mercaptopurines. Monatsh. Chem. 2013, 144, 501507. DOI: 10.1007/s00706-012-0899-x
  • Koukal P., Dvořáková H., Dvořák D., Tobrman T., Palladium-Catalyzed Claisen Rearrangement of Allyloxypurines. Chem. Pap., 2013, 67, 38. DOI: 10.2478/s11696-012-0239-y

 

2012

  • Metelková R., Tobrman T., Kvapilová H., Hoskovcová I., Ludvík J., Synthesis, characterization and electrochemical investigation of hetaryl chromium(0) aminocarbene complexes. Electrochim. Acta, 2012, 82, 470477. DOI: 10.1016/j.electacta.2012.05.027
  • Kotek V., Tobrman T., Dvořák D., Highly Efficient and Broad-Scope Protocol for the Preparation of 7-Substituted 6-halopurines via N9-Boc-Protected 7,8-dihydropurines. Synthesis 2012, 44, 610618. DOI: 10.1055/s-0031-1290068

 

2011

  • Hoskovcová I., Zvěřinová R., Roháčová J., Dvořák D., Tobrman T., Záliš S., Ludvík J, Fischer aminocarbene complexes of chromium and iron: Anomalous electrochemical reduction of p-carbonyl substituted derivatives. Electrochim. Acta 2011, 56, 68536859. DOI: 10.1016/j.electacta.2011.05.096
  • Tobrmanová M., Tobrman T., Dvořák D., Pd-Catalyzed Allylic Substitution of Purin-8-yl(allyl) Acetate: Route to (E)-Alkenylpurines. Collect. Czech. Chem. Commun. 2011, 76, 311326. DOI: 10.1135/cccc2011030

 

2010

  • Negishi E.-i., Tobrman T., Rao H., Xu S., Lee Ch.-T., Highly (98 %) Selective Alkene Synthesis of Wide Applicability via Fluride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes. Isr. J. Chem. 2010, 50, 696701. DOI: 10.1002/ijch.201000051
  • Kotek V., Chudíková N., Tobrman T., Dvořák D., Selective Synthesis of 7-substituted Purines via 7,8-dihydropurines. Org. Lett. 2010, 12, 57245727. DOI: 10.1021/ol1025525
  • Pařík P., Kulhánek J., Ludwig M., Wagner R., Rotrekl I., Drahoňovský D., Meca L., Šmídková M., Tobrman T., Dvořák D., Acidity of Benzoic Acids Bearing the (CO)5Cr=CN(CH3)2 Group. Organometallics 2010, 29, 41354138. DOI: 10.1021/om100608x
  • Hoskovcová I., Roháčová J., Dvořák D., Tobrman T., Záliš S., Zvěřinová R., Ludvík J., Synthesis and electrochemical study of iron, chromium and tungsten aminocarbenes: Role of ligand structure and central metal nature. Electrochim. Acta, 2010, 55, 83418351. DOI: 10.1016/j.electacta.2010.02.057
  • Klečka M., Křováček M., Tobrman T., Dvořák D., Synthesis of (E)-6-Alkenylpurines via Pd-Catalyzed Stannation/Protodestannation Tandem Process of Alkynylpurines. Collect. Czech. Chem. Commun. 2010, 75, 313332. DOI: 10.1135/cccc2009563
  • Wang C., Xu Z., Tobrman T., Negishi E.-i., Arylethyne Bromoboration-Negishi Coupling Route to E- or Z-Aryl-Substituted Trisubstituted Alkenes of >98% Isomeric Purity. New Horizon in the Highly Selective Synthesis of Trisubstituted Alkenes. Adv. Synth Catal., 2010, 352, 627631. DOI: 10.1002/adsc.200900766

  

2009-1996

  • Wang C., Tobrman T., Xu Z., Negishi E.-i., Highly Regio- and Stereoselective Synthesis of (Z)-Trisubstituted Alkenes via Propyne Bromoboration and Tandem Pd-Catalyzed Cross-Coupling. Org. Lett. 2009, 11, 40924095. DOI: 10.1021/ol901566e
  • Keder R., Dvořáková H., Dvořák D., New Approach to the Synthesis of N-7-Arylguanines and N-7-Aryladenines. Eur. J. Org. Chem. 2009, 15221531. DOI: 10.1002/ejoc.200801002
  • Tobrman T., Dvořák D., Heck reactions of 6- and 2-halopurines. Eur. J. Org. Chem. 2008, 2923–2928. DOI: 10.1002/ejoc.200800091
  • Krouželka J., Linhart I., Tobrman T., Synthesis of 3-(2-hydroxy-1-phenylethyl)- and 3-(2-hydroxy-2-phenylehtyl)adenine, DNA adducts derived from styrene. J. Heterocyclic Chem. 2008, 45, 789–795. DOI: 10.1002/chin.200838155
  • Tobrman T., Štepnička P., Císařová I., Dvořák D., Preparation and crystal structures of purine 2,2’-, 6,6’-, and 8,8’-dimers. Eur. J. Org. Chem. 2008, 2167–2174. DOI: 10.1002/ejoc.200800017
  • Tobrman T., Dvořák D., Reductive Dimerization of 2- and 6-Iodopurines: Side reaction in Pd-Catalyzed Cross Coupling of Iodopurines. Collect. Czech Chem. Comm. 2007, 72, 13651374. DOI: 10.1135/cccc20071365
  • Tobrman T., Dvořák D., Selective magnesiation of chloro-iodopurines: An efficient approach to new purine derivatives. Org. Lett. 2006, 8, 12911294. DOI: 10.1021/ol053013w
  • Tobrman T., Meca L., Dvořáková H., Černý J., Dvořák D., Study of the Origin of the Hindered Rotation of an Aryl Ring in the Chromium Aminocarbene Complexes Bearing Aromatic Ring Atteched to the Carbene Carbon Atom. Organometalics 2006, 25, 55405548. DOI: 10.1021/om0605837
  • Klečka M., Tobrman T., Dvořák D., Cu(I)-catalyzed coupling of (9-benzylpurin-6-yl)magnesium chloride with allyl halides: an approach to 6-allylpurine derivatives. Collect. Czech Chem. Comm. 2006, 71, 12211228. DOI: 10.1135/cccc20061221
  • Hoskovcová I., Roháčová J., Meca L., et al., Electrochemistry of chromium(0)-aminocarbene complexes: The use of intramolecular interaction LFER for characterization of the oxidation and reduction centre of the complex. Electrochim. Acta 2005, 50, 49114915. DOI: 10.1016/j.electacta.2004.12.047
  • Drahoňovský D., Štěpnička P., Dvořák D., P-chiral 2-{1 '-[butyl(phenyl)phosphanyl]ferrocen-1-yl} -4-isopropyl-4,5-dihydrooxazoles: A second chirality center in catalytic system. Collect. Czech Chem. Comm. 2005, 70, 361369. DOI: 10.1135/cccc20050361
  • Meca L., Dvořák D., Ludvík J., et al., Synthesis, structures, and electrochemistry of group 6 aminocarbenes with a P-chelating 1'-(Diphenylphosphino)ferrocenyl substituent Organometallics 2004, 23, 25412551. DOI: 10.1021/om040007f
  • Tobrman T., Dvořák D., 'Reductive Heck reaction' of 6-halopurines. Tetrahedron Lett. 2004, 45, 273276. DOI: 10.1016/j.tetlet.2003.10.181
  • Tobrman T., Dvořák D., 6-Magnesiated purines: Preparation and reaction with aldehydes. Org. Lett. 2003, 5, 42894291. DOI: 10.1021/ol0355027
  • Hocek M., Dvořák D., Havelková M., Covalent analogues of nucleobase-pairs. Nucleoside Nucleotides & Nucleic Acids 2003, 22, 775777. DOI: 10.1081/NCN-120022632
  • Meca L., Císařová I., Dvořák D., Thermolysis of iron N-allylaminocarbene complexes: Formation of eta(3)-1-azaallylirontricarbonyl complexes. Synthetic and theoretical study. Organometallics 2003, 22, 37033709. DOI: 10.1021/om0301280
  • Drahoňovský D., Borgo V., Dvořák D., Fischer chromium carbene complexes as nucleophiles in palladium-catalyzed allylic substitution reactions. Tetrahedron Lett. 2002, 43, 78677869. DOI: 10.1016/S0040-4039(02)01913-5
  • Havelková M., Dvořák D., Hocek M., Covalent analogues of DNA base-pairs and triplets. Part 3: Synthesis of 1 ,4-and 1,3-bis(purin-6-yl)benzenes and 1-(1,3-dimethyluracil-5-yl)-3 or 4-(purin-9-yl)benzenes. Tetrahedron 2002, 58, 74317435. DOI: 10.1016/S0040-4020(02)00833-5
  • Havránek M., Dvořák D., 3,3-disubstituted allyl alcohols from palladium-catalyzed coupling of hydroaluminated propargyl alcohols with aryl iodides. J. Org. Chem. 2002, 67, 21252130. DOI: 10.1021/jo0162235
  • Vyklický L., Dvořáková H., Dvořák D., Iron aminocarbene complexes containing a double C=C bond in the N-substituent: Preparation and reactivity. Organometallics 2001, 20, 54195424. DOI: 10.1021/om010533w
  • Havelková M., Dvořák D., Hocek M., The Suzuki-Miyaura cross-coupling reactions of 2-, 6-or 8-halopurines with boronic acids leading to 2-, 6-or 8-aryl- and -alkenylpurine derivatives. Synthesis 2001, 17041710. DOI: 10.1055/s-1999-2753
  • Drahoňovský D., Císařová I., Štěpnička P., et al., An alternative approach to chiral 2-[1 '-(diphenylphosphanyl)ferrocenyl]-4,5-dihydrooxazoles. Collect. Czech. Chem. Commun. 2001, 66, 588604. DOI: 10.1135/cccc20010588
  • Rotrekl I., Vyklický L., Dvořák D., Reaction of iron aminocarbene complexes with electronically deficient alkenes. J. Organometallic Chem. 2001, 617, 329333. DOI: 10.1016/S0022-328X(00)00707-5
  • Havelková M., Studenovský M., Dvořák D., N-1-substituted hypoxanthine derivatives from the reaction of 6-halopurines with Michael acceptors under the conditions of Heck reaction. Collect. Czech. Chem. Commun. 2000, 65, 797804. DOI: 10.1135/cccc20000797
  • Havránek M., Dvořák D., 3-(tributylstannyl)allyl alcohols: Useful building blocks for solid-phase synthesis of skipped dienes and trienes. Collect. Czech. Chem. Commun. 2000, 65, 434454. DOI: 10.1135/cccc20000434
  • Havelková M., Hocek M., Česnek M., et al., The Suzuki-Miyaura cross-coupling reactions of 6-halopurines with boronic acids leading to 6-aryl- and 6-alkenylpurines. Synlett 1999, 11451147. DOI: 10.1055/s-1999-2753
  • Suchý P., Dvořák D., Havelková M., Unexpected course of the reaction of 1,3-bis(dimethylamino)trimethinium perchlorate with 3-substituted prop-2-ynals leading to 1-aryl-2,4,6-triformylbenzenes. Collect. Czech. Chem. Commun. 1999, 64, 119129. DOI: 10.1135/cccc19990119
  • Dvořáková H., Dvořák D., Holý A., Synthesis of acyclic nucleotide analogues derived from 6-(sec- or tert-alkyl)purines via coupling of 6-chloropurine derivatives with organocuprates. Collect. Czech. Chem. Commun. 1998, 63, 20652074. DOI: 10.1135/cccc19982065
  • Havránek M., Dvořák D., Transmetallation from aluminum to tin: A facile preparation of tributylstannylprop-2-en-1-ols. Synthesis 1998, 12641268. DOI: 10.1055/s-1998-6101
  • Dvořák D., Ludwig M., [(N,N-dimethylamino)carboxymethylene]pentacarbonyl-chromium(0): The first Fischer carbene complex with a free carboxyl group attached directly to the carbene atom. Organometallics 1998, 17, 36273629. DOI: 10.1021/om980082o
  • Dvořák D., Transition metals in organic synthesis - Basic principles. Chemické Listy 1997, 91, 216226.
  • Arnold Z., Dvořák D., Havránek M., Convenient preparation of 1,3-bis(dimethylamino)trimethinium perchlorate, tetrafluoroborate and hexafluorophosphate. Collect. Czech. Chem. Commun. 1996, 61, 16371641. DOI: 10.1135/cccc19961637
  • Wagner R., Dvořák D., Holý A.: New application of the Stille coupling in the synthesis of 5-substituted uracils. Collect. Czech. Chem. Commun. 1996, 61, S118S119 Sp. Iss. SI. DOI: 10.1135/cccc1996s118
  • Dvořáková H., Dvořák D., Holý A., Coupling of 6-chloropurines with organocuprates derived from Grignard reagents: A convenient route to sec and tert 6-alkylpurines. Tetrahedron Lett. 1996, 37, 12851288. DOI: 10.1016/0040-4039(95)02375-5
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