P. Zhmurov

发表

A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides

A. Sukhorukov, S. Ioffe, R. Novikov, 2018, Synlett.

A General Metal‐Assisted Synthesis of α‐Halo Oxime Ethers from Nitronates and Nitro Compounds

V. A. Tartakovsky, A. Sukhorukov, S. Ioffe, 2014 .

Synthesis of PDE IV inhibitors. First asymmetric synthesis of two of GlaxoSmithKline's highly potent Rolipram analogues.

V. Chupakhin, V. A. Tartakovsky, A. Sukhorukov, 2013, Organic & biomolecular chemistry.

Construction of bis-, tris- and tetrahydrazones by addition of azoalkenes to amines and ammonia

Y. Nelyubina, V. A. Tartakovsky, A. Sukhorukov, 2016, Beilstein journal of organic chemistry.

Divergent Reactivity of In Situ Generated Metal Azides: Reaction with N,N-Bis(oxy)enamines as a Case Study.

A. Sukhorukov, S. Ioffe, R. Novikov, 2017, Chemistry.

Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane

A. Sukhorukov, S. Ioffe, A. Mikhaylov, 2015 .

Synthesis of phosphodiesterase IVb inhibitors 2. Stereoselective synthesis of hexahydro-3H-pyrrolo[1,2-c]imidazol-3-one and tetrahydro-1H-pyrrolo[1,2-c][1,3]oxazol-3-one derivatives

V. A. Tartakovsky, A. Sukhorukov, S. Ioffe, 2011 .

One-pot preparation of methyl 2-diazo-3-oxopropionates comprising an aqueous ‘sulfonyl-azide-free’ (SAFE) diazo transfer step

M. Krasavin, O. Bakulina, D. Dar'in, 2020 .

Taking diazo transfer to water: α-diazo carbonyl compounds from in situ generated mesyl azide

M. Krasavin, D. Dar'in, P. Zhmurov, 2020 .

Sulfocoumarins as dual inhibitors of human carbonic anhydrase isoforms IX/XII and of human thioredoxin reductase

C. Supuran, A. Grandane, R. Žalubovskis, 2020, Journal of enzyme inhibition and medicinal chemistry.

Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile

C. Supuran, M. Ferraroni, A. Angeli, 2022, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of novel glutarimide ligands for the E3 ligase substrate receptor Cereblon (CRBN): Investigation of their binding mode and antiproliferative effects against myeloma cell lines.

A. Bunev, M. Hartmann, M. Krasavin, 2023, European journal of medicinal chemistry.

1-Oxo-3,4-dihydroisoquinoline-4-carboxamides as novel druglike inhibitors of poly(ADP-ribose) polymerase (PARP) with favourable ADME characteristics

M. Krasavin, D. Dar'in, Alexander Safrygin, 2021, Journal of enzyme inhibition and medicinal chemistry.

Three-component Castagnoli-Cushman reaction with ammonium acetate delivers 2-unsubstituted isoquinol-1-ones as potent inhibitors of poly(ADP-ribose) polymerase (PARP)

M. Krasavin, D. Dar'in, Alexander Safrygin, 2021, Journal of enzyme inhibition and medicinal chemistry.

Patterning of various materials by the photochemical reaction of [(C5H5)Fe(C6H6)]+ complex with salicylate dyes

D. Perekalin, P. Zhmurov, A. Shved, 2020 .

α-Diazoacetamides in Sc(OTf)3-Catalyzed Tiffeneau–Demjanov Ring Expansion: Application towards the Synthesis of Rare Bicyclic Pyrazoles

M. Krasavin, D. Dar'in, G. Kantin, 2020, Synlett.