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Mloston, Grzegorz (8)
Heimgartner, Heinz (4)Linden, Anthony (3)Baranovskii, Viktor I. (2)Grzelak, Paulina (2)Mereshchenko, Andrey S. (2)Nikolaev, Valerij A. (2)Rodina, Ludmila L. (2)Alexey, V. Ivanov (1)Czerwieniec, Rafał (1)... View MoreSubjectthioketones (3)1,3-dipolar cycloaddition (2)1,3-oxathioles (2)crystal structure (2)diazocarbonyl compounds (2)thiiranes (2)thiocarbonyl ylides (2)[3 + 2]-cyclo­addition (1)aldonitrones (1)copper(I) catalysis (1)... View MoreDate Issued2015 (4)2018 (2)2013 (1)2017 (1)Has File(s)Yes (8)

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Chemo- and regioselective [3 + 2]-cyclo­additions of thio­carbonyl ylides: crystal structures of trans-8-benzoyl-1,1,3,3-tetra­methyl-7-tri­fluoro­methyl-5-thia­spiro­[3.4]octan-2-one and trans-3-benzoyl-2,2-di­phenyl-4-(tri­fluoro­meth­yl)tetra­hydro­thio­phene 

Mlostoń, Grzegorz; Grzelak, Paulina; Linden, Anthony; Heimgartner, Heinz (International Union of Crystallography, 2018)
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Crystal structure of (E)-1,2-diferrocenyl-1,2-bis­(furan-2-yl)ethene 

Mloston, Grzegorz; Hamera-Fałdyga, Róża; Linden, Anthony; Heimgartner, Heinz (International Union of Crystallography, 2018)
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Synthesis and (spectro)electrochemistry of mixedvalent diferrocenyl–dihydrothiopyran derivatives 

Kowalski, Konrad; Karpowicz, Rafał; Mloston, Grzegorz; Miesel, Dominique; Hildebrandt, Alexander; Lang, Heinrich; Czerwieniec, Rafał; Therrien, Bruno (Royal Society of Chemistry, 2015-02-20)
Three novel diferrocenyl complexes were prepared and characterised. 2,2-Diferrocenyl-4,5-dimethyl- 3,6-dihydro-2H-thiopyran (1, sulphide) was accessible by the hetero-Diels–Alder reaction of diferrocenyl thioketone with ...
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On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation 

Mereshchenko, Andrey S.; Alexey, V. Ivanov; Baranovskii, Viktor I.; Rodina, Ludmila L.; Nikolaev, Valerij A.; Mloston, Grzegorz (Beilstein-Institut zur Förderung der Chemischen Wissenschaften, 2015-04-20)
The 1,3-dipolar cycloaddition of acyclic 2-diazo-1,3-dicarbonyl compounds (DDC) and thioketones preferably occurs with Z,Econformers and leads to the formation of transient thiocarbonyl ylides in two stages. The ...
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On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation 

Mereshchenko, Andrey S.; Ivanov, Alexey V.; Baranovskii, Viktor I.; Mloston, Grzegorz; Rodina, Ludmila L.; Nikolaev, Valerij A. (Beilstein Institute for the Advancement of Chemical Sciences, 2015-04-20)
The 1,3-dipolar cycloaddition of acyclic 2-diazo-1,3-dicarbonyl compounds (DDC) and thioketones preferably occurs with Z,Econformers and leads to the formation of transient thiocarbonyl ylides in two stages. The ...
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Hetero-Diels–Alder reactions of hetaryl and aryl thioketones with acetylenic dienophiles 

Mloston, Grzegorz; Grzelak, Paulina; Mikina, Maciej; Linden, Anthony; Heimgartner, Heinz (Beilstein Beilstein-Institut zur Förderung der Chemischen Wissenschaften, 2015-04-28)
Selected hetaryl and aryl thioketones react with acetylenecarboxylates under thermal conditions in the presence of LiClO4 or, alternatively, under high-pressure conditions (5 kbar) at room temperature yielding thiopyran ...
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Matrix isolation and spectroscopic properties of the methylsulfinyl radical CH3(O)S˙ 

Reisenauer, Hans Peter; Romański, Jarosław; Mloston, Grzegorz; Schreiner, Peter R. (The Royal Society of Chemistry, 2013-08-15)
The atmospherically highly relevant methylsulfinyl radical CH3(O)S˙ was generated thermally under flash pyrolysis conditions and isolated in Ar matrices at 10 K; the allyl radical is a byproduct. CH3(O)S˙ and its D3- and ...
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Application of diethyl ethynylphosphonate to the synthesis of 3‐phosphonylated β‐lactams via the Kinugasa reaction 

Obijalska, Emilia; Kowalski, Marcin K.; Mlostoń, Grzegorz; Heimgartner, Heinz (ARKAT USA, 2017)
The easily available diethyl ethynylphosphonate reacts with diverse aldonitrones under Kinugasa reaction conditions at room temperature, providing 3‐phosphonylated β‐lactams in good yields. In all cases, the reaction ...

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