ArticleOrganic letters2013
Aldol reactions in multicomponent reaction based domino pathways: a multipurpose enabling tool in heterocyclic chemistry.
Article in Organic letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Microwave-assisted facile construction of quinoxalinone and benzimidazopyrazinone derivatives via two paths of post-Ugi cascade reaction.Molecular diversity · 2019Article
- One-pot synthesis of novel 1-(1H-tetrazol-5-yl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine derivatives via an Ugi-azide 4CR process.Molecular diversity · 2018Article
- Synthesis of pyrimido[1,6-Beilstein journal of organic chemistry · 2018Article
- Facile microwave-assisted synthesis of benzimidazole scaffolds via Ugi-type three-component condensation (3CC) reactions.Molecular diversity · 2016Article
- New Three-Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4-European journal of organic chemistry · 2016Article
- Transition metal-free one-pot synthesis of nitrogen-containing heterocycles.Molecular diversity · 2016Review
- Four-component bicyclization approaches to skeletally diverse pyrazolo[3,4-b]pyridine derivatives.The Journal of organic chemistry · 2014Article
- Synthesis of isocoumarins with different substituted patterns via Passerini-aldol sequence.Organic letters · 2014Article
- A simple one-pot 2-stepTetrahedron letters · 2013Article
- Metal-free [3 + 2 + 1]/[2 + 2 + 1] biscyclization: stereospecific construction with concomitant functionalization of indolizin-5(1H)-one.The Journal of organic chemistry · 2013Article
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Authors and funding
4 authors.
Funding
Abstract
The aldol reaction has been evaluated in combination with the Ugi multicomponent reaction to assemble richly decorated mono- and polycyclic systems via expeditious cascade pathways. A small collection of pyrrolinones was generated thereof, and the scarcely accessible pyridoquinoxalinedione scaffold was also prepared by designing an additional nucleophilic substitution step in this domino sequence requiring minimal operational effort.
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