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Alexander N. Chernega
Researcher at National Academy of Sciences of Ukraine
Publications - 213
Citations - 1250
Alexander N. Chernega is an academic researcher from National Academy of Sciences of Ukraine. The author has contributed to research in topics: Crystal structure & Alkylation. The author has an hindex of 15, co-authored 213 publications receiving 1201 citations. Previous affiliations of Alexander N. Chernega include Pedagogical University.
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Acentric Extended Solids by Self Assembly of 4,4′-Bipyrazolyls
Ishtvan Boldog,Eduard B. Rusanov,Alexander N. Chernega,Joachim Sieler,Konstantin V. Domasevitch +4 more
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Heterocondensed 1,4-diphosphinines
TL;DR: A reaction of phosphorus tribromide with a compound containing two 2,5-dimethyl-1-arylpyrrolyl-3 residues bound through a phosphorus atom gave rise to a new phosphorus-containing heterocyclic system, 1,4-diphosphinine as discussed by the authors.
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Peculiarities of pπ ? pπ conjugation in aminosubstituted phosphaalkenes
Alexander N. Chernega,Alexander V. Ruban,V. D. Romanenko,Leonid N. Markovski,A. A. Korkin,Mikhail Yu. Antipin,Yuri T. Struchkov +6 more
TL;DR: In this paper, the effects of conjugation in phosphaalkenes were investigated by taking into account the results of X-ray structural studies and ab initio quantum-chemical calculations.
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Aliphatic aldehydes in multicomponent syntheses of 4-alkyl-substituted partially hydrogenated quinolines, fused 4H-pyrans, and 2-amino-4-ethyl-5-methylbenzene-1,3-dicarbonitrile
TL;DR: The Knoevenagel condensation of aliphatic aldehydes with CH acids, malonodinitrile, cyanothioacetamide, cyclohexane-1,3-dione, dimedone, 4-hydroxycoumarin, 3-aminophenol, and N-(cyclohex-1-enyl)-morpholine leads to formation of 4-alkyl-substituted partially hydrogenated quinolines, fused 4H-pyrans, and 2-amino-4-ethyl-
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The Aza Curtius Rearrangement
Lev M. Yagupolskii,Svetlana V. Shelyazhenko,I. I. Maletina,Vitalij N. Petrik,Eduard B. Rusanov,Alexander N. Chernega +5 more
TL;DR: On interaction of N-(trifluoromethylsulfonyl)carboximidoyl chlorides with sodium azide in glyme or acetonitrile at −5 to +10 °C, dinitrogen is eliminated quantitatively and carbodiimides RN=C=NSO2CF3 are formed in high yield.