M
Michail N. Elinson
Researcher at Russian Academy of Sciences
Publications - 330
Citations - 3408
Michail N. Elinson is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Malononitrile & Catalysis. The author has an hindex of 30, co-authored 306 publications receiving 2898 citations. Previous affiliations of Michail N. Elinson include Russian Academy & Moscow State University.
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Mediator oxidation systems in organic electrosynthesis
TL;DR: In this article, the use of mediator oxidation systems activated by electric current (anodic or parallel anodic and cathodic) in organic electrosynthesis is considered and generalised.
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Catalysis of Salicylaldehydes and Two Different C ? H Acids with Electricity: First Example of an Efficient Multicomponent Approach to the Design of Functionalized Medicinally Privileged 2‐Amino‐4H‐Chromene Scaffold
Michail N. Elinson,Alexander S. Dorofeev,Fedor M. Miloserdov,Alexey I. Ilovaisky,Sergey K. Feducovich,Pavel A. Belyakov,Gennady I. Nikishin +6 more
TL;DR: Fifteen previously inaccessible, close structural analogues of the tumor antagonists HA14-1 and MX58151 have been synthesized and the electrocatalytic process was found to be advantageous in terms of selectivity and yields compared to classic chemical base catalysis.
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Solvent-free cascade reaction: direct multicomponent assembling of 2-amino-4H-chromene scaffold from salicylaldehyde, malononitrile or cyanoacetate and nitroalkanes
Michail N. Elinson,Alexey I. Ilovaisky,Valentina M. Merkulova,Pavel A. Belyakov,Alexander O. Chizhov,Gennady I. Nikishin +5 more
TL;DR: In this paper, a solvent-free cascade reaction was found for substituted medicinally privileged 2-amino-4H-chromene scaffolds from such simple and reasonable starting compounds as salicylaldehyde, malononitrile or cyanoacetate and nitroalkanes.
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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
Michail N. Elinson,Alexey I. Ilovaisky,Alexander S. Dorofeev,Valentina M. Merkulova,Nikita O. Stepanov,Fedor M. Miloserdov,Yuri N. Ogibin,Gennady I. Nikishin +7 more
TL;DR: An electrochemically induced catalytic multicomponent transformation of cyclic 1,3-diketones, isatins, and malononitrile in alcohols in an undivided cell in the presence of sodium bromide as an electrolyte results in the formation of spirooxindoles with fused functionalized 5,6,7,8-tetrahydro-4 H -chromene system in 83-98% yields.
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Facile and Convenient Synthesis of 4,4′-(Arylmethylene)bis(1H-pyrazol-5-ols) by Electrocatalytic Tandem Knoevenagel-Michael Reaction
TL;DR: In this article, an electrochemically induced catalytic tandem Knoevenagel-Michael reaction of two equivalents of 5-methyl-2-phenyl-2,4-dihydro-3 H-pyrazol-3-one with various aromatic aldehydes in ethanol in an undivided cell in the presence of sodium bromide as an electrolyte was demonstrated.