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ACS Omega|June 28, 2021
Unsaturated Vinyl-Type Carbocation [(CH3)2C=CH]+ in Its Carborane SaltsEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
ACS Omega|September 27, 2021
Isomers of the Allyl Carbocation C3H5 + in Solid Salts: Infrared Spectra and StructuresEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
Molecules (Basel, Switzerland)|February 11, 2023
Interaction of Vinyl-Type Carbocations, C3H5+ and C4H7+ with Molecules of Water, Alcohols, and AcetoneEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
International Journal of Molecular Sciences|July 14, 2023
Substitution of H Atoms in Unsaturated (Vinyl-Type) Carbocations by Cl or O AtomsEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
ACS Omega|August 15, 2022
IR-Spectroscopic and X-ray-Structural Study of Vinyl-Type Carbocations in Their Carborane SaltsEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
Scientific Reports|April 10, 2024
A new type of C+⋯Hδ-(C=) bond in adducts of vinyl carbocations with alkenesEvgenii S Stoyanov, Irina Yu Bagryanskaya, Irina V Stoyanova
Chemistryopen|November 22, 2018
Efficient Synthesis of the N-(buta-2,3-dienyl)carboxamide of Isopimaric Acid and the Potential of This Compound towards Heterocyclic Derivatives of DiterpenoidsMarya A Gromova, Yurii V Kharitonov, Irina Yu Bagryanskaya, et al.
Dalton Transactions (Cambridge, England : 2003)|December 22, 2021
Pyridylarsine-based Cu(I) complexes showing TADF mixed with fast phosphorescence: a speeding-up emission rate using arsine ligandsAlexander V Artem'ev, Yan V Demyanov, Marianna I Rakhmanova, et al.
Chemistryopen|June 17, 2016
Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid DerivativesMariya A Timoshenko, Yurii V Kharitonov, Makhmut M Shakirov, et al.
Dalton Transactions (Cambridge, England : 2003)|September 10, 2025
A tetraphosphino-bis(s-triazine) from cyanuric chloride and Ph2PH: new unexpected tandem C-C/C-P coupling reactionAlexander V Artem'ev, Maria P Davydova, Anton V Kuzmin, et al.
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