2 article(s) from Gu, Yanlong
Representative biologically active N-(hetero)aryl-4,5-unsubstituted pyrrole scaffolds.
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Typical routes to N-(heteroaryl)-4,5-unsubstituted pyrroles.
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Substrate scope of the pyrrole synthesis.
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Synthesis of N-heterocyclic pyrroles.
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Direct synthesis of pyrrole-3-carboxamide derivatives.
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Plausible mechanism of the three-component reaction.
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Synthesis of polysubstituted pyrazolo[3,4-b]pyridine derivatives.
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Beilstein J. Org. Chem. 2020, 16, 2920–2928, doi:10.3762/bjoc.16.241
Schematic illustration for the preparation of the catalyst in this work.
FTIR spectra of LS, LS-FAS, and LS-FAS-Cu.
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Thermogravimetric weight loss of the obtained materials LS-FAS and LS-FAS-Cu.
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FSEM imagine of LS-FAS-Cu in different scale label a) 1 μm, b) 200 nm; FTEM images of LS-FAS-Cu in ...
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XPS spectra of LS-FAS-Cu in the regions of C 1s, O 1s, Cu 2p3/2 and Cu LMM (inset).
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Substrate scope of LS-FAS-Cu catalyzed three-component reactions of 4-aminoindoles, alkynes and ald...
Recyclability of LS-FAS-Cu, LS-FM-Cu and Resin-Cu in the reaction between compounds 1a, 2a and 3a.
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Beilstein J. Org. Chem. 2020, 16, 2888–2902, doi:10.3762/bjoc.16.238
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