Mikhail Krasavin
0000-0002-0200-4772
78 papers found
Refreshing results…
Naturally occurring scaffolds for compound library design: convenient access to bis-aryl 1-azaadamantanes carrying a vicinal amino alcohol motif
Atom-Economical Construction of a Rare 6,7-Dihydropyrido[3′,2′:4,5]imidazo[1,2-d][1,4]benzodiazepine Scaffold
Antiproliferative 4-(1,2,4-oxadiazol-5-yl)piperidine-1-carboxamides, a new tubulin inhibitor chemotype
Potent, orally available, selective COX-2 inhibitors based on 2-imidazoline core
Convenient access to novel functionalized pyrazino[1,2-b]isoquinolin-6-one and diazepino[1,2-b]isoquinolin-7-one scaffolds via the Cushman multicomponent reaction followed by post-condensation
New Tetracyclic 1,4-Oxazepines Constructed via Practically Simple Tandem Condensation Strategy from Readily Available Synthons
A simple, three-component synthesis of 2-aminothiazoles using trimethylsilyl isothiocyanate
A simple two-step access to diversely substituted imidazo[4,5-b]pyridines and benzimidazoles from readily available 2-imidazolines
Pd-Catalyzed N-arylation of 2-imidazolines Provides Convenient Access to Selective Cyclooxygenase-2 Inhibitors
Synthesis of 1,2,4-triazoles employing isocyanides
Identification of Diaryl 5-Amino-1,2,4-oxadiazoles as Tubulin Inhibitors: the Special Case of 3-(2-Fluorophenyl)-5-(4-methoxyphenyl)amino-1,2,4-oxadiazole
Amine (Imine) Component Surrogates in the Ugi Reaction and Related Isocyanide-Based Multicomponent Reactions
Increased dipeptoid diversity resulting from post-condensational manipulation of the Ugi reaction products
Dibenzo[b,f]pyrazolo[1,5-d][1,4]oxazepines: facile construction of a rare heterocyclic system via tandem aromatic nucleophilic substitution - Smiles rearrangement – denitrocyclization
Natural Products as Templates for Bioactive Compound Libraries. 3. Novel Heterocycles and Peptidomimetics Generated from Anabasine by Isocyanide-Based Multicomponent Reactions
Synthesis of N1,N3-disubstituted formamidrazones via the TMSCl-promoted reaction of isocyanides with thiosemicarbazones
Novel diversely substituted 1-heteroaryl-2-imidazolines for fragment-based drug discovery
Microwave-assisted aza-Prins reaction. Part 1: facile preparation of natural-like 3-azabicyclo[3.3.1]non-6-enes
Microwave-assisted aza-Prins reaction. Part 2: Straightforward access to 2,6-disubstituted 1-azaadamantanes
Carnosine protects neurons against oxidative stress and modulates the time profile of MAPK cascade signaling
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