Maria D. Matveeva

A novel multi-component approach to the synthesis of pyrrolo[2,1-a]isoquinoline derivatives

Leonid G. Voskressensky, Maria D. Matveeva, Victor N. Khrustalev et al. · RSC Advances · 2016 · 27 citations

Combinatorial Chemistry, Bioorganic Chemistry, Heterocyclic +11

A New Class of 1‐Aryl‐5,6‐dihydropyrrolo[2,1‐<i>a</i>]isoquinoline Derivatives as Reversers of P‐Glycoprotein‐Mediated Multidrug Resistance in Tumor Cells

Alisa A. Nevskaya, Maria D. Matveeva, Mauro Niso et al. · ChemMedChem · 2018 · 24 citations · Full text

A facile synthesis of 1-oxo-pyrrolo[2,1-a]isoquinolines

Leonid G. Voskressensky, Maria D. Matveeva, Victor N. Khrustalev et al. · Tetrahedron Letters · 2017 · 21 citations

Heterocyclic, Facile Synthesis, Organic Chemistry +3

Domino Reactions of 1-Aroyl-3,4-dihydroisoquinolines with α,β-Unsaturated Aldehydes

Maria D. Matveeva, Alexander А. Titov, Svetlana V. Dyachenko et al. · Synthesis · 2017 · 21 citations

Asymmetric Catalysis, Chemical Engineering, Engineering +12

[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4‐Disubstituted Pyrroles

Ilya V. Efimov, Maria D. Matveeva, Rafael Luque et al. · European Journal of Organic Chemistry · 2019 · 21 citations

Diversity Oriented Synthesis, Derivatives, Strong Base +14