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The Journal of Organic Chemistry|January 5, 2023
Diazo Tetramic Acids Provide Access to Natural-Like Spirocyclic Δα,β-Butenolides through Rh(II)-Catalyzed O-H Insertion/Base-Promoted CyclizationDmitry Dar'in, Grigory Kantin, Daria Glushakova, et al.
Organic & Biomolecular Chemistry|December 5, 2025
Elucidating the mechanism, origin of regioselectivity and substrate scope of the synthesis of structurally diverse 1,2,4-triazoles via a rare type of diazo compound reactivityRoman Kuznetsov, Grigory Kantin, Alexander Sapegin, et al.
The Journal of Organic Chemistry|November 23, 2020
Spirocyclizations Involving Oxonium Ylides Derived from Cyclic α-Diazocarbonyl Compounds: An Entry into 6-Oxa-2-azaspiro[4.5]decane ScaffoldDmitry Dar'in, Grigory Kantin, Olga Bakulina, et al.
Organic Letters|June 24, 2022
Unexpected Ring Contraction of Homophthalic Anhydrides under Diazo Transfer ConditionsAlexander Kazantsev, Olga Bakulina, Dmitry Dar'in, et al.
Organic & Biomolecular Chemistry|May 5, 2021
Unexpected formal [4 + 2]-cycloaddition of chalcone imines and homophthalic anhydrides: preparation of dihydropyridin-2(1H)-onesNatalia Guranova, Pavel Golubev, Olga Bakulina, et al.
Beilstein Journal of Organic Chemistry|December 26, 2022
A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael additionAnastasia Vepreva, Alexander Yanovich, Dmitry Dar'in, et al.
The Journal of Organic Chemistry|August 22, 2019
α-Acyl-α-diazoacetates in Transition-Metal-Free β-Lactam SynthesisJudith Synofzik, Dmitry Dar'in, Mikhail S Novikov, et al.
Beilstein Journal of Organic Chemistry|May 26, 2022
Unusual highly diastereoselective Rh(II)-catalyzed dimerization of 3-diazo-2-arylidenesuccinimides provides access to a new dibenzazulene scaffoldAnastasia Vepreva, Alexander S Bunev, Andrey Yu Kudinov, et al.
The Journal of Organic Chemistry|March 1, 2019
Rh(II)-Catalyzed Spirocyclization of α-Diazo Homophthalimides with Cyclic EthersNatalia I Guranova, Dmitry Dar'in, Grigory Kantin, et al.
Bioorganic & Medicinal Chemistry|February 19, 2017
New nitrofurans amenable by isocyanide multicomponent chemistry are active against multidrug-resistant and poly-resistant Mycobacterium tuberculosisMikhail Krasavin, Vladislav Parchinsky, Grigory Kantin, et al.
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