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Molecular Diversity|April 22, 2009
One hundred years of Meldrum's acid: advances in the synthesis of pyridine and pyrimidine derivativesVictoria V Lipson, Nikolay Yu GorobetsOrganic Letters|April 12, 2003
High-throughput synthesis of N3-acylated dihydropyrimidines combining microwave-assisted synthesis and scavenging techniquesDoris Dallinger, Nikolay Yu Gorobets, C Oliver KappeMolecular Diversity|February 12, 2004
Microwave-assisted scavenging of electrophiles utilizing polymer-supported sequestration reagents. Application to the synthesis of N3-acylated dihydropyrimidine librariesDoris Dallinger, Nikolay Yu Gorobets, C Oliver KappeJournal of Combinatorial Chemistry|December 9, 2008
Rapid three-step one-pot microwave-assisted synthesis of 2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarbonitrile librarySergey A Yermolayev, Nikolay Yu Gorobets, Sergey M DesenkoCurrent Topics in Medicinal Chemistry|April 9, 2015
Self-assembled peptide nanoarchitectures: applications and future aspectsPrem Prakash Sharma, Brijesh Rathi, Joao Rodrigues, et al.Acta Crystallographica. Section E, Crystallographic Communications|May 17, 2018
Crystal structure and Hirshfeld surface analysis of 7-eth-oxy-5-methyl-2-(pyridin-3-yl)-11,12-di-hydro-5,11-methano-[1,2,4]triazolo[1,5-c][1,3,5]benzoxadiazo-cineErcan Aydemir, Sevgi Kansiz, Mustafa Kemal Gumus, et al.Molecules (Basel, Switzerland)|December 25, 2009
Generation of 500-member library of 10-alkyl-2-R(1),3-R(2)-4,10-dihydrobenzo[4,5]imidazo[1,2-alpha]pyrimidin-4-onesSvetlana M Sirko, Nikolay Yu Gorobets, Vladimir I Musatov, et al.Journal of Combinatorial Chemistry|August 22, 2008
Efficient ytterbium triflate catalyzed microwave-assisted synthesis of 3-acylacrylic acid building blocksNikita V Tolstoluzhsky, Nikolay Yu Gorobets, Nadezhda N Kolos, et al.Current Topics in Medicinal Chemistry|February 1, 2017
An Overview of Currently Available AntimalarialsNikolay Yu Gorobets, Yuriy V Sedash, Brajendra K Singh, et al.Molecular Diversity|September 13, 2006
An easy access to 2-Amino-5,6-dihydro-3H-pyrimidin-4-one building blocks: the reaction under conventional and microwave conditionsKonstantin S Ostras, Nikolay Yu Gorobets, Sergey M Desenko, et al.Pageof 2