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2021

  • 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

  • Edlova, T.; Dvorakova, 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.; Stepankova, N.; Tlusty, M.; Tobrman, T.; Jurasek, B.; Kuchar, M.; Trchova, M.; Fitl, P.; Vrnata, M.:
    Electrochemically oxidized 15-crown-5 substituted thiophene and host-guest interaction with new psychoactive substances
    Electrochimica 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, 255-266. 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, 35109-35120. 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, 10728-10739. 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, 2187─2190 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, 429─436 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.
    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, 90-95 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, 2175-2181 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, 957-968. 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, 4604-4614 DOI: 10.1002/adsc.201801000

2017

  • Polak, P.; Dvorak, D.; Tobrman, T.:
    Cyanogen: A Versatile Reagent for Diversity-​Oriented Synthesis
    Synthesis 2017, 49, 1757-1766 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, 6233-6241 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, 460-4611 DOI: 10.1021/acs.orglett.7b02219

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

2016

  • Vanova, H.; Tobrman, T.; Hoskovcova, I.; Dvorak, D.:
    Modular synthesis of Fischer biscarbene complexes of chromium
    Organometallics 2016, 35, 2999-3006 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, 5037-5044 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, 3684-3693 DOI:10.1016/j.tetlet.2016.07.030 

  • Kotek, V.; Polák, P.; Tobrman, T.
    Efficient and Simple Preparation of Functionalized 1,1-Dibromoenol Phosphates
     
    Monatshefte fuer Chemie 2016, 147, 405-412 DOI:10.1007/s00706-015-1613-6


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Aktualizováno: 13.7.2021 14:30, Autor: Ondřej Kundrát

Skupina doc. Tobrmana

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A BUDOVA A Ústav organické chemie se nachází ve 2. patře budovy A na straně ke Studentské ulici, sekretariát ústavu – místnost A278
B BUDOVA B V 1. patře se nachází Laboratoř forenzní analýzy biologicky aktivních látek
C BUDOVA C
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