We focus on the development of a new selective reductive methods.
Moscow, Russia
Joined April 2019
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Not always the desirable is the truth.
The common catalytic pair of a metal catalyst and an organic cocatalyst in the CO₂ fixation reaction turned out to be redundant in most cases.
The real performance of organic salts has been underestimated.
doi.org/10.1007/s11426-026-3…
Another approach to discovering new chemical reactions
Chemists are no longer pouring promising reactions down the drain just because the product is hard to isolate and understand the structure. They now use OdanChem to analyze the complex mixture directly from the flask and discover novel reactions.
doi.org/10.26434/chemrxiv-20…
What occurs when THF is pressurized under syngas? Does this yield a "THF-based soda" or another product? We extend our sincere gratitude to the @OdanChem platform, which facilitates the #DiscoveryOfNewReactions, and for the access that made this research possible
Reductive amination with NaH₂PO₂ − now under mild conditions with the help of Ru-catalysis! Learn more in this #OrgLett article from @chusovgroup
@ACSPublications
doi.org/10.1021/acs.orglett.…
🆕♻️ Aldehydes reimagined: used as internal reductants and as electrophiles — enabling neat, Ru-catalyzed reductive alkylations with no external reductant.
From ketones to amines, amides & nitriles — a unified and sustainable C–C/C–N strategy.
🔗 doi.org/10.1016/j.jcat.2025.…
🆕 Catalyst‑free reductive amination with non‑toxic, cheap NaH₂PO₂!♻️
16 amine–carbonyl combos covered, tunable conditions & kinetic insights.
Check out our #JOC guide📘
👉 doi.org/10.1021/acs.joc.5c00…
@ChusovGroup @ACSPublications @JOC_OL
Recently we have noticed the literature trend and confirmed it together with Prof. Liao's research group through the discovery of one of the most active catalysts for polymerisation of caprolactone
doi.org/10.1016/j.eurpolymj.…
Recently Organic Chemistry Portal has highlighted our work on simplifying the Eschweiler Clark reaction, published in JOC this year. You can read more by clicking on the link below:
organic-chemistry.org/abstra…
Unexplored class of manganese catalysts. Fine tuning can be easily accomplished by changing arenes in one step. It can be active in a variety of reactions. Hopefully, other researchers will develop new catalytic reactions using such catalysts. doi.org/10.1021/acs.joc.4c00…
ALT https://doi.org/10.1021/acs.joc.4c00842
Chusovgroup retweeted
We all dreamed about it and it’s finally real. Organic chemists-made spectral database that can solve problems. Let’s explore what @OdanChem can do! @NMRspectroscopy @nmr900 @nmronline #ChemTwitter
There are 3 reagents in the Eschweiler-Clarke reaction. Isn't that too many? Our new article can be found below
doi.org/10.1021/acs.joc.3c02…
Chusovgroup retweeted
This is really cool! Well done from @SarpongGroup
@Sigman_Lab and @Charles_chem #MerckChemistry 14N-15N swap in pyridines and pyrimidines! @ChemRxiv #SkeletalEditing chemrxiv.org/engage/chemrxiv…
Our work on the use of converter gas in reductive transformations for the synthesis of pharmaceuticals just published @ChemicalScience! Giving a second breath to the industrial waste gas!
pubs.rsc.org/en/content/arti…
Here is our review on the use of osmium catalysts in reductive processes @RussChemRev! russchemrev.org/RCR5045
We recommend you to manipulate with CIA agent — Sodium Hypophosphite — Cheap, Innovative & Alternative agent for reductive amination. Find more in #OrgLett new article from @chusovgroup. pubs.acs.org/doi/10.1021/acs…
Chusovgroup retweeted
Now recommended to carry out your chemical manipulations with a CIA agent — Sodium Hypophosphite — a Cheap, Innovative & Alternative agent for reductive amination. Find more in this #OrgLett new article from @chusovgroup pubs.acs.org/doi/10.1021/acs…
Chusovgroup retweeted
Breaking News! Fluoride additive helps to qualitatively improve organometallic catalyst performance! Learn more in this #JOC article from @chusovgroup pubs.acs.org/doi/10.1021/acs…
Many catalysts have been developed for the hydrogen borrowing reaction. Many of them work under rather harsh conditions in which the reaction can be carried out without a catalyst. So when is a catalyst really necessary?
sciencedirect.com/science/ar…
Interesting research from Saihu Liao group
pubs.acs.org/doi/10.1021/acs…
Our systematic analysis of current research data in the field of Borrowing Hydrogen Amination Reactions is published in @ACSCatalysis!
pubs.acs.org/doi/10.1021/acs…
