Generation of Molecular Diversity Using a Complexity-generating MCR-platform Towards Triazinane Diones
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Chemistry
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Triazinane diones, readily generated by a recently reported multicomponent reaction, can be easily alkylated with various alkyl halides, allowing a wide variety of complexity-generating secondary reactions. Because of the high variability of the initial multicomponent reactions and the multiple possibilities for participation of substituents in the secondary reactions, a highly diverse set of complex products was obtained in short and efficient reaction sequences.
Poplevin D, Zubkov F, Dorovatovskii P, Zubavichus Y, Khrustalev V Acta Crystallogr E Crystallogr Commun. 2016; 72(Pt 10):1429-1433.
PMID: 27746935 PMC: 5050770. DOI: 10.1107/S2056989016014420.
Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.
Koopmanschap G, Ruijter E, Orru R Beilstein J Org Chem. 2014; 10:544-98.
PMID: 24605172 PMC: 3943360. DOI: 10.3762/bjoc.10.50.
Direct Dynamic Protein-Affinity Selection Mass-Spectrometry.
Jonker N, Lingeman H, Irth H Chromatographia. 2010; 72(1-2):7-13.
PMID: 20628447 PMC: 2889285. DOI: 10.1365/s10337-010-1586-x.
Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds.
Sunderhaus J, Martin S Chemistry. 2009; 15(6):1300-8.
PMID: 19132705 PMC: 2803615. DOI: 10.1002/chem.200802140.