» Articles » PMID: 18698475

Generation of Molecular Diversity Using a Complexity-generating MCR-platform Towards Triazinane Diones

Overview
Journal Org Biomol Chem
Specialties Biochemistry
Chemistry
Date 2008 Aug 14
PMID 18698475
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Crystal structures of the two epimers from the unusual thermal C6-epimerization of 5-oxo-1,2,3,5,5a,6,7,9b-octa-hydro-7,9a-ep-oxy-pyrrolo-[2,1-]iso-indole-6-carb-oxy-lic acid, 5a(),6(),7(),9a(),9b() and 5a(),6(),7(),9a(),9b().

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.