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AuthorMloston, Grzegorz (3)Baranovskii, Viktor I. (2)Mereshchenko, Andrey S. (2)Nikolaev, Valerij A. (2)Rodina, Ludmila L. (2)Alexey, V. Ivanov (1)Grzelak, Paulina (1)Heimgartner, Heinz (1)Ivanov, Alexey V. (1)Linden, Anthony (1)... View MoreSubject
thioketones (3)
1,3-dipolar cycloaddition (2)1,3-oxathioles (2)diazocarbonyl compounds (2)thiiranes (2)thiocarbonyl ylides (2)dimethyl acetylenedicarboxylate (DMAD) (1)hetero-Diels–Alder reactions (1)high pressure reactions; methyl propiolate (1)thiopyrans (1)... View MoreDate Issued2015 (3)Has File(s)Yes (3)

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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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