A very nice application of our boronate-TAADtriol click-declick chemistry (pubs.acs.org/doi/abs/10.102…). Congrats to Smulders et al from Wageningen UR

Delighted to share that I have been awarded the full academic title of Professor after more than 15 years of research at Zelinsky Institute and teaching students at Mendeev University

Crown-hydroxylamines are pH-dependent chelating N,O-ligands with a potential for aerobic oxidation catalysis nature.com/articles/s4146…

Our new paper on the domino synthesis of pyrrolizidinone scaffold is published in JOC. Congrats to everyone involved! #chemtwitter #OrganicChemistry

Our paper on a nitroso version of the Meerwein-Ponndorf-Verley reaction is now out in OrgLett. Congrats to everyone involved! #chemtwitter #OrganicChemistry #nitroso

Happy to see our paper is well-cited! Thank you, OrgChemFront for publishing it. doi.org/10.1039/D2QO00…

Tomorrow is THE day. The winners of the 2023 EurJOC-Society Award will present their research at this Virtual Symposium: Join us! ▪️Register here: register.gotowebinar.com/register/35149… ▪️Check out our Special Collection featuring their work: …mistry-europe.onlinelibrary.wiley.com/doi/toc/10.100…

Congratulations to Vladislav Lesnikov (Владислав Лесников) for successfully defending his PhD on crown-hydroxylamines today! 🎉 Already 5th Doctor from my group!

Lab members photo, retro-style. 90th anniversary of Zelinsky Institute and already 4th birthday of our Lab.

Our recent paper on the synthesis of 3-aryl NH pyrroles combines many things reviewers don't like - the use of stoichiometric transition metal reagents, yields far from excellent, and substrate restrictions... But there's no better way to make most of these pyrroles

Our new paper on an umpolung approach to pyrazoles from halohydrazones and alkynes is now out in #OrgLett pubs.acs.org/doi/10.1021/ac…

#OnTheCover Front Cover: Accessing Polysubstituted NH Pyrroles from Nitroalkenes via [4+2]-Cycloaddition/Reductive Ring Contraction Strategy by Alexey Sukhorukov and co-workershttps://onlinelibrary.wiley.com/doi/10.1002/ejoc.202400627 onlinelibrary.wiley.com/doi/10.1002/ej…

Ever thought about umpolung of aldol reaction? Our new paper in J Org Chem/Org Lett demonstrates a simple way to couple enolonium cation and carbinol C-anion synthons: pubs.acs.org/doi/10.1021/ac… #chemtwitter #OrganicChemistry #chemistry

Quantum chemical calculations of the Nef reaction mechanism reveal an unusual nitrosocarbenium ion possessing three contiguous electrophilic centers! Check out our recent paper in J Org Chem/Org Lett pubs.acs.org/doi/10.1021/ac… #chemtwitter #OrganicChemistry #chemistry

Isoxazoline route to aldols is a powerful strategy in natural product synthesis. In our recent review in Nat. Prod. Reports, we discuss >50 total syntheses developed since 2000 along with basic methodological aspects and stereochemical models pubs.rsc.org/en/content/art… #chemtwitter

Happy to meet Prof. Goverdhan Mehta (a foreign member of Russian Academy of Sciences) and Prof. Vinod K. Singh (President of the National Academy of Sciences, India) Vinod K Singh at NCIMM-2015 held by UniMysore! Thanks to Prof. K.S. Rangappa for the invitation! University of Mysore Online

The α-effect refers to the increased reactivity of a nucleophile due to the presence of an adjacent heteroatom. We found that α-effect stabilizes atypical higher oxidation states of d-metals thus extending this phenomenon to coordination #chemistry bit.ly/4dR854t

organic-chemistry.org/abstracts/lit9… The reaction of aromatic α-halohydrazones with terminal alkynes regioselectively provides N-protected polysubstituted pyrazoles

The formation of prebiotic organic molecules in space and on early Earth is a pivotal scientific question. In this Perspective published in JACS Au, I examine this question through the prizm of N-O bond chemistry #chemistry #astrobiology #OrganicChemistry dx.doi.org/10.1021/jacsau…