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Published in 2019 at "Communications Chemistry"
DOI: 10.1038/s42004-019-0236-y
Abstract: Although azomethine ylides have been fully exploited as versatile reactive intermediates in dipolar cycloaddition reactions to construct a variety of heterocyclic compounds involving a nitrogen atom, little is known about their structural and electronic properties.…
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Keywords:
ylide;
phenyl butyl;
stable azaphenalenyl;
azomethine ylide ... See more keywords
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Published in 2017 at "Chemical communications"
DOI: 10.1039/c6cc08996h
Abstract: A protocol for the direct functionalization of N-H/α,α,β,β-C(sp3)-H of piperidine without any metal or external oxidants is reported. This reaction is promoted by 4-(trifluoromethyl)benzoic acid via an azomethine ylide intermediate. This is a simple method…
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Keywords:
via azomethine;
bearing substituted;
synthesis spirooxindoles;
azomethine ylide ... See more keywords
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Published in 2022 at "Chemical communications"
DOI: 10.1039/d2cc02071h
Abstract: A 1,3-cycloaddition reaction of 2-(tert-butyl)-8H-isoquinolino[4,3,2-de]phenanthridin-9-ium chloride to NiII norcorrole in the presence of base is shown to produce a family of chiral derivatives of polycyclic system(s) fused with pyrrole subunit(s) of the macrocycle. Dehydrogenation of…
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Keywords:
dipolar cycloaddition;
ylide norcorroles;
azomethine ylide;
polycyclic azomethine ... See more keywords
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Published in 2023 at "New Journal of Chemistry"
DOI: 10.1039/d3nj01018j
Abstract: Nitrogen-containing heterocyclic compounds are some of the most significant that are produced artificially or naturally. These heterocyclic rings are virtually always present in biological systems, from the smallest eukaryotes to...
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Keywords:
cycloaddition azomethine;
azomethine ylide;
chemistry;
recent advances ... See more keywords