Mikhail Krasavin
0000-0002-0200-4772
75 papers found
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A Convenient Preparation of Diastereomerically Pure, Diversely Substituted Piperazine-2,5-diones from N-Protected α-Amino Acids
Hydrazinopeptide Motifs Synthesized via the Ugi Reaction: An Insight into the Secondary Structure
Proline-like β-turn mimics accessed via Ugi reaction involving monoprotected hydrazines
Thiophene-containing products of the Ugi reaction in an oxidation-triggered IMDA/aromatization cascade: a simple access to 3-oxoisoindolines
Dihydro-resveratrol—A potent dietary polyphenol
Discovery and SAR exploration of N-aryl-N-(3-aryl-1,2,4-oxadiazol-5-yl)amines as potential therapeutic agents for prostate cancer
Diversity-oriented pyrazol-3-one synthesis based on hydrazinodipeptide-like units prepared via the Ugi reaction
Trimethylsilyl Chloride as a Promoter for the Groebke–Blackburn Reaction: Preparation of Imidazo[2,1-b][1,3]Benzothiazoles
Efficient entry into hydrazinopeptide-like structures via sequential Ugi reactions
BF3·OEt2-promoted reaction of isocyanides with o-aminobenzophenones
Streamlined access to 2,3-dihydropyrazino[1,2-a]indole-1,4-diones via Ugi reaction followed by microwave-assisted cyclization
Development of Privileged Groebke-Blackburn-Type 4-(3-aminoimidazo [1,2-a]pyridin-2-yl)benzoic Acid Core into a Combinatorial Library on Solid Phase
Discovery and Potency Optimization of 2-Amino-5-arylmethyl-1,3-thiazole Derivatives as Potential Therapeutic Agents for Prostate Cancer
Imidazo[1,2-a]quinoxalines Accessed via Two Sequential Isocyanide-Based Multicomponent Reactions
Asymmetric Lewis Acid Catalysis in Water: α-Amino Acids as Effective Ligands in Aqueous Biphasic Catalytic Michael Additions
tert-Butyl Isocyanide as a Convertible Reagent in Ugi Reaction: Microwave-Assisted Preparation of 5,6-Dihydropyrazolo[1,5-a]pyrazine-4,7-diones
tert-Butyl isocyanide revisited as a convertible reagent in the Groebke–Blackburn reaction
Greater variety in Groebke–Blackburn type 3-arylaminoimidazo[1,2-a]azines accessed via Pd-catalyzed arylation of a primary amine precursor
Poorly reactive 5-piperazin-1-yl-1,3,4-thiadiazol-2-amines rendered as valid substrates for Groebke–Blackburn type multi-component reaction with aldehydes and isocyanides using TMSCl as a promoter
Expedient Entry into 1,4-Dihydroquinoxalines and Quinoxalines via a Novel Variant of Isocyanide-Based MCR
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