Підписатись
Mikhail Krasavin
Mikhail Krasavin
Підтверджена електронна адреса в spbu.ru - Домашня сторінка
Назва
Посилання
Посилання
Рік
Spirocyclic scaffolds in medicinal chemistry
K Hiesinger, D Dar’in, E Proschak, M Krasavin
Journal of Medicinal Chemistry 64 (1), 150-183, 2020
2752020
Antimalarial, antiproliferative, and antitumor activities of artemisinin-derived, chemically robust, trioxane dimers
GH Posner, P Ploypradith, MH Parker, H O'Dowd, SH Woo, J Northrop, ...
Journal of medicinal chemistry 42 (21), 4275-4280, 1999
1941999
Spirocyclic motifs in natural products
E Chupakhin, O Babich, A Prosekov, L Asyakina, M Krasavin
Molecules 24 (22), 4165, 2019
1492019
Discovery of 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-6-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carboxamide (NMS-P118): A Potent, Orally Available, and …
G Papeo, H Posteri, D Borghi, AA Busel, F Caprera, E Casale, M Ciomei, ...
Journal of medicinal chemistry 58 (17), 6875-6898, 2015
1092015
Multi-component reactions between 2-aminopyrimidine, aldehydes and isonitriles: the use of a nonpolar solvent suppresses formation of multiple products
VZ Parchinsky, O Shuvalova, O Ushakova, DV Kravchenko, M Krasavin
Tetrahedron letters 47 (6), 947-951, 2006
972006
Multicomponent reactions of isocyanides in the synthesis of heterocycles
AV Ivachtchenko, YA Ivanenkov, VM Kysil, MY Krasavin, AP Ilyin
Russian Chemical Reviews 79 (9), 787, 2010
932010
Modern Trends of Organic Chemistry in Russian Universities
AI Konovalov, IS Antipin, VA Burilov, TI Madzhidov, AR Kurbangalieva, ...
Russian Journal of Organic Chemistry 54, 157-371, 2018
912018
Complexity-Enhancing Acid-Promoted Rearrangement of Tricyclic Products of Tandem Ugi 4CC/Intramolecular Diels− Alder Reaction
A Ilyin, V Kysil, M Krasavin, I Kurashvili, AV Ivachtchenko
The Journal of organic chemistry 71 (25), 9544-9547, 2006
882006
Continued exploration of 1, 2, 4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: Discovery of subnanomolar inhibitors of membrane-bound hCA IX …
M Krasavin, A Shetnev, T Sharonova, S Baykov, S Kalinin, A Nocentini, ...
European Journal of Medicinal Chemistry 164, 92-105, 2019
772019
Current diversity of cyclic anhydrides for the Castagnoli–Cushman-type formal cycloaddition reactions: Prospects and challenges
M Krasavin, D Dar’in
Tetrahedron Letters 57 (15), 1635-1640, 2016
762016
New heterocyclic product space for the Castagnoli–Cushman three-component reaction
D Dar’in, O Bakulina, M Chizhova, M Krasavin
Organic letters 17 (15), 3930-3933, 2015
742015
Imidazo[1,2-a]quinoxalines Accessed via Two Sequential Isocyanide-Based Multicomponent Reactions
M Krasavin, S Shkavrov, V Parchinsky, K Bukhryakov
The Journal of Organic Chemistry 74 (6), 2627-2629, 2009
732009
Antimalarial simplified 3-aryltrioxanes: Synthesis and preclinical efficacy/toxicity testing in rodents
GH Posner, HB Jeon, MH Parker, M Krasavin, IH Paik, TA Shapiro
Journal of medicinal chemistry 44 (19), 3054-3058, 2001
722001
One-step assembly of carbamoyl-substituted heteroannelated [1, 4] thiazepines
AP Ilyn, MV Loseva, VY Vvedensky, EB Putsykina, SE Tkachenko, ...
The Journal of Organic Chemistry 71 (7), 2811-2819, 2006
622006
Heterocyclic periphery in the design of carbonic anhydrase inhibitors: 1, 2, 4-Oxadiazol-5-yl benzenesulfonamides as potent and selective inhibitors of cytosolic hCA II and …
M Krasavin, A Shetnev, T Sharonova, S Baykov, T Tuccinardi, S Kalinin, ...
Bioorganic Chemistry 76, 88-97, 2018
602018
Mechanism of generation of closo-decaborato amidrazones. Intramolecular non-covalent B–H⋯ π (Ph) interaction determines stabilization of the configuration around the amidrazone …
VK Burianova, DS Bolotin, AS Mikherdov, AS Novikov, PP Mokolokolo, ...
New Journal of Chemistry 42 (11), 8693-8703, 2018
602018
Probing the ‘bipolar’nature of the carbonic anhydrase active site: Aromatic sulfonamides containing 1, 3-oxazol-5-yl moiety as picomolar inhibitors of cytosolic CA I and CA II …
M Krasavin, M Korsakov, M Dorogov, T Tuccinardi, N Dedeoglu, ...
European journal of medicinal chemistry 101, 334-347, 2015
592015
A ‘sulfonyl-azide-free’(SAFE) aqueous-phase diazo transfer reaction for parallel and diversity-oriented synthesis
D Dar’in, G Kantin, M Krasavin
Chemical communications 55 (36), 5239-5242, 2019
552019
Biologically active compounds based on the privileged 2-imidazoline scaffold: The world beyond adrenergic/imidazoline receptor modulators
M Krasavin
European Journal of Medicinal Chemistry 97, 525-537, 2015
512015
1, 2, 4-oxadiazole/2-imidazoline hybrids: multi-target-directed compounds for the treatment of infectious diseases and cancer
A Shetnev, S Baykov, S Kalinin, A Belova, V Sharoyko, A Rozhkov, ...
International Journal of Molecular Sciences 20 (7), 1699, 2019
502019
У даний момент система не може виконати операцію. Спробуйте пізніше.
Статті 1–20