Search Results - "Kürti, László"

Aza-Rubottom Oxidation: Synthetic Access to Primary α‑Aminoketones by Zhou, Zhe, Cheng, Qing-Qing, Kürti, László

“…An aza analogue of the Rubottom oxidation is reported. This facile transformation takes place at ambient temperature and directly converts silyl enol ethers to…”
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Symmetry in Cascade Chirality-Transfer Processes: A Catalytic Atroposelective Direct Arylation Approach to BINOL Derivatives by Wang, Jin-Zheng, Zhou, Jin, Xu, Chang, Sun, Hongbin, Kürti, László, Xu, Qing-Long

“…Herein we disclose a scalable organocatalytic direct arylation approach for the regio- and atroposelective synthesis of non-C 2-symmetric…”
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Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines by Guo, Lirong, Liu, Fengting, Wang, Liying, Yuan, Hairui, Feng, Lei, Kürti, László, Gao, Hongyin

“…A transition-metal free synthesis of highly functionalized 2-hydroxy-2′-amino-1,1′-biaryls from N-arylhydroxylamines has been developed. This operationally…”
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Oxidative Nitrogen Insertion into Silyl Enol Ether CC Bonds by Lin, Alex, Ghosh, Arghya, Yellen, Simon, Ball, Zachary T., Kürti, László

“…Here, we demonstrate a fundamentally new reactivity of the silyl enol ether functionality utilizing an in situ-generated iodonitrene-like species. The present…”
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Copper-Catalyzed Synthesis of Hindered Ethers from α‑Bromo Carbonyl Compounds by Zhou, Zhe, Behnke, Nicole Erin, Kürti, László

“…A catalytic method for the synthesis of sterically hindered ethers and thioethers from α-bromo carbonyl compounds and the corresponding nucleophiles using an…”
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Organocatalytic Aryl–Aryl Bond Formation: An Atroposelective [3,3]‑Rearrangement Approach to BINAM Derivatives by Li, Gong-Qiang, Gao, Hongyin, Keene, Craig, Devonas, Michael, Ess, Daniel H, Kürti, László

“…Herein we disclose an organocatalytic aryl–aryl bond-forming process for the regio- and atropo­selective synthesis of 2,2′-diamino-1,1′-binaphthalenes…”
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Enantioselective Catalytic Allylation of Acyclic Ketiminoesters: Synthesis of α‑Fully-Substituted Amino Esters by Bhakta, Urmibhusan, Kattamuri, Padmanabha V, Siitonen, Juha H, Alemany, Lawrence B, Kürti, László

“…We report the first direct catalytic enantioselective allylation of acyclic α-ketiminoesters to afford α-allyl-α-aryl and α-allyl-α-trifluoromethyl amino…”
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Fejős, Zoltán. 2020. “Kaper Kóntri.” Magyar rézbányászok Amerikában (‘“Kaper Kóntri.” Hungarian Copper Miners in America’). Budapest: Korall. 286 pp by Kürti, László

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Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation by Lu, Shenci, Ng, Shawn Voon Hwee, Lovato, Kaitlyn, Ong, Jun-Yang, Poh, Si Bei, Ng, Xiao Qian, Kürti, László, Zhao, Yu

“…The importance of axial chirality in enantioselective synthesis has been widely recognized for decades. The practical access to certain structures such as…”
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Directing-Group-Free Arene C(sp2)–H Amination Using Bulky Aminium Radicals and DFT Analysis of Regioselectivity by Behnke, Nicole Erin, Kwon, Young-Do, Davenport, Michael T., Ess, Daniel H., Kürti, László

“…A hydroxylamine-derived electrophilic aminating reagent produces a transient and bulky aminium radical intermediate upon in situ activation by either TMSOTf or…”
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“DO YOU WANT TO BE KRAMPUS?” Santa Claus, globality and locality of Christmas tradition by Kürti, László

“…Abstract In this paper the author argues that the Christmas holidays, notwithstanding their international standing as a religious and commercial season, are…”
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Transition-Metal-Free Direct Arylation: Synthesis of Halogenated 2‑Amino-2′-hydroxy-1,1′-biaryls and Mechanism by DFT Calculations by Gao, Hongyin, Ess, Daniel H, Yousufuddin, Muhammed, Kürti, László

“…A transition-metal-free, regioselective direct aryl–aryl bond-forming process for the synthesis of halogenated 2-amino-2′-hydroxy-1,1′-biaryls that are…”
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Synthesis of (±)‐Setigerumine I: Biosynthetic Origins of the Elusive Racemic Papaveraceae Isoxazolidine Alkaloids by Serna, Ana V., Kürti, László, Siitonen, Juha H.

“…The biosynthetic origins of the structurally related racemic isoxazolidine Papaveraceae alkaloids Setigerumine I, Dactylicapnosinine and Dactylicapnosine have…”
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Arylboronic Acid-Catalyzed C‑Allylation of Unprotected Oximes: Total Synthesis of N‑Me-Euphococcine by Siitonen, Juha H, Kattamuri, Padmanabha V, Yousufuddin, Muhammed, Kürti, László

“…O-Unprotected keto- and aldoximes are readily C-allylated with allyl diisopropyl boronate in the presence of arylboronic acid catalysts to yield highly…”
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Elusive Metal-Free Primary Amination of Arylboronic Acids: Synthetic Studies and Mechanism by Density Functional Theory by Zhu, Chen, Li, Gongqiang, Ess, Daniel H, Falck, John R, Kürti, László

“…Herein, we disclose the first metal-free synthesis of primary aromatic amines from arylboronic acids, a reaction that has eluded synthetic chemists for…”
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Aza-Quasi-Favorskii Reaction: Construction of Highly Substituted Aziridines through a Concerted Multibond Rearrangement Process by Kattamuri, Padmanabha V., Zhao, Jidong, Das, Tamal Kanti, Siitonen, Juha H., Morgan, Nathan, Ess, Daniel H., Kürti, László

“…A new molecular rearrangement, the aza-Quasi-Favorskii rearrangement, has been developed for the construction of highly substituted aziridines…”
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Plasmon-Generated Solvated Electrons for Chemical Transformations by Solti, David, Chapkin, Kyle D., Renard, David, Bayles, Aaron, Clark, Benjamin D., Wu, Gang, Zhou, Jingyi, Tsai, Ah-Lim, Kürti, László, Nordlander, Peter, Halas, Naomi J.

“…Methods for generating solvated electronsfree electrons in solutionhave focused primarily on alkali metal ionization or high-energy electrons or photons…”
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Streamlining amine synthesis by Kuerti, Laszlo

“…Bulky amine groups that help make many drugs more bioavailable can be added readily to organic compounds [Also see Research Article by Gui et al. ] Amines, a…”
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Synthesis of Highly Substituted Cyclopropanes via the Quasi-Favorskii Rearrangement of α,α-Dichlorocyclobutanols by Behnke, Nicole Erin, Siitonen, Juha H, Chamness, Stephen A, Kürti, László

“…A method for the synthesis of highly substituted cyclopropanes via a quasi-Favorskii rearrangement is described. The method includes the combination two…”
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Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon–Nitrogen Bond Formation by Kattamuri, Padmanabha V, Yin, Jun, Siriwongsup, Surached, Kwon, Doo-Hyun, Ess, Daniel H, Li, Qun, Li, Guigen, Yousufuddin, Muhammed, Richardson, Paul F, Sutton, Scott C, Kürti, László

“…Given the importance of amines in a large number of biologically active natural products, active pharmaceutical ingredients, agro­chemicals, and functional…”
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