22 results on '"Stepanov, Nikita O."'
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2. Electrocatalytic and chemical assembling of N, N′-dialkylbarbituric acids and aldehydes: efficient cascade approach to the spiro-[furo[2,3- d]pyrimidine-6,5′-pyrimidine]-2,2′,4,4′,6′-(1′ H,3 H,3′ H)-pentone framework
3. A new type of cascade reaction: direct conversion of carbonyl compounds and malononitrile into substituted tetracyanocyclopropanes
4. A new strategy of the chemical route to the cyclopropane structure: direct transformation of benzylidenemalononitriles and malononitrile into 1,1,2,2-tetracyanocyclopropanes
5. Electrocatalytic multicomponent transformation of cyclic 1,3-diketones, isatins, and malononitrile: facile and convenient way to functionalized spirocyclic (5,6,7,8-tetrahydro-4 H-chromene)-4,3′-oxindole system
6. One-pot cascade assembling of 3-substituted tetracyanocyclopropanes from alkylidenemalononitriles and malononitrile by the only bromine direct action
7. Cascade assembly of N, N′-dialkylbarbituric acids and aldehydes: a simple and efficient one-pot approach to the substituted 1,5-dihydro-2 H,2′ H-spiro(furo[2,3- d]pyrimidine-6,5′-pyrimidine)-2,2′,4,4′,6′(1′ H,3 H,3′ H)-pentone framework
8. The first example of the cascade assembly of a spirocyclopropane structure: direct transformation of benzylidenemalononitriles and N, N′-dialkylbarbituric acids into substituted 2-aryl-4,6,8-trioxo-5,7-diazaspiro[2.5]octane-1,1-dicarbonitriles
9. ChemInform Abstract: Electrocatalytic and Chemical Methods in MHIRC Reactions: The First Example of the Multicomponent Assembly of Medicinally Relevant Spirocyclopropylbarbiturates from Three Different Molecules.
10. ChemInform Abstract: Electrocatalytic and Chemical Assembling of N,N′‐Dialkylbarbituric Acids and Aldehydes: Efficient Cascade Approach to the Spiro‐[furo [2,3‐d]pyrimidine‐6,5′‐pyrimidine]‐2,2′,4,4′,6′‐(1′H,3H,3′H)‐pentone Framework.
11. Electrocatalytic and chemical assembling of N,N′-dialkylbarbituric acids and aldehydes: efficient cascade approach to the spiro-[furo[2,3-d]pyrimidine-6,5′-pyrimidine]-2,2′,4,4′,6′-(1′H,3H,3′H)-pentone framework
12. Electrocatalysis in MIRC reaction strategy: facile stereoselective approach to medicinally relevant spirocyclopropylbarbiturates from barbituric acids and activated olefins
13. New Way to Substitute Tetracyanocyclopropanes: One-Pot Cascade Assembling of Carbonyls and Malononitrile by the Only Bromine Direct Action
14. ChemInform Abstract: Cascade Assembly of N,N′-Dialkylbarbituric Acids and Aldehydes: A Simple and Efficient One-Pot Approach to the Substituted 1,5-Dihydro-2H,2′H-spiro(furo [2,3-d]pyrimidine-6,5′-pyrimidine)2,2′,4,4′,6′(1′H,3H,3′H)-pentone Framework.
15. Cascade assembly of N,N′-dialkylbarbituric acids and aldehydes: a simple and efficient one-pot approach to the substituted 1,5-dihydro-2H,2′H-spiro(furo[2,3-d]pyrimidine-6,5′-pyrimidine)-2,2′,4,4′,6′(1′H,3H,3′H)-pentone framework
16. ChemInform Abstract: One-Pot Cascade Assembling of 3-Substituted Tetracyanocyclopropanes from Alkylidenemalononitriles and Malononitrile by the only Bromine Direct Action.
17. The first example of the cascade assembly of a spirocyclopropane structure: direct transformation of benzylidenemalononitriles and N,N′-dialkylbarbituric acids into substituted 2-aryl-4,6,8-trioxo-5,7-diazaspiro[2.5]octane-1,1-dicarbonitriles
18. ChemInform Abstract: A New Type of Cascade Reaction: Direct Conversion of Carbonyl Compounds and Malononitrile into Substituted Tetracyanocyclopropanes.
19. ChemInform Abstract: A New Strategy of the Chemical Route to the Cyclopropane Structure: Direct Transformation of Benzylidenemalononitriles and Malononitrile into 1,1,2,2-Tetracyanocyclopropanes.
20. Electrocatalytic multicomponent transformation of cyclic 1,3-diketones, isatins, and malononitrile: facile and convenient way to functionalized spirocyclic (5,6,7,8-tetrahydro-4H-chromene)-4,3′-oxindole system
21. Electrochemically Induced Chain Transformation of Salicylaldehydes and Alkyl Cyanoacetates into Substituted 4H-Chromenes.
22. Electrochemically induced chain transformation of salicylaldehydes and alkyl cyanoacetates into substituted 4H-chromenes
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