Mikhail Krasavin
0000-0002-0200-4772
78 papers found
Refreshing results…
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
Complexity-Enhancing Acid-Promoted Rearrangement of Tricyclic Products of Tandem Ugi 4CC/Intramolecular Diels—Alder Reaction.
Air-oxidized products of multi-component reactions between 3-amino-1,2,4-triazole, aromatic aldehydes and isonitriles
Synthesis of Tricyclic Pyrazolo[1,5-a]pyrimidin-7(4H)-ones Featuring Regioselective Formation of the Core Structure.
Natural products as templates for bioactive compound libraries: synthesis of biaryl derivatives of (±)-vasicine
Practical Outcome of Azaphthalimide Reduction with Zn/AcOH at Various Temperatures
One-Step Assembly of Carbamoyl-Substituted Heteroannelated [1,4]Thiazepines
Multi-component reactions between 2-aminopyrimidine, aldehydes and isonitriles: the use of a nonpolar solvent suppresses formation of multiple products
Preparation and Chemical Behavior of 2‐(tert‐Butoxycarbonyl)amino‐3‐bromomethyl Pyridine, a Novel Alkylating Agent
Synthesis and Practical Use of 1H ‐1,2,3‐Benzotriazole‐5‐carboxaldehyde for Reductive Amination
One-Step Construction of Peptidomimetic 5-Carbamoyl-4-sulfonyl-2-piperazinones
A Convenient Synthesis of 1‐Amino‐7‐(Piperidin‐4‐yl)Isoquinoline
Preparation of 1-Alkyl-2-aryl-1H-imidazo[4,5-b]pyridines from 2-Alkylamino-3-aminopyridines and Aromatic Aldehydes Using Air as an Oxidant.
Antimalarial Simplified 3-Aryltrioxanes: Synthesis and Preclinical Efficacy/Toxicity Testing in Rodents
Antimalarial sulfide, sulfone, and sulfonamide trioxanes
Antimalarial, Antiproliferative, and Antitumor Activities of Artemisinin-Derived, Chemically Robust, Trioxane Dimers
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