2 article(s) from Li, Minghao
- Letter
- Published 30 Nov 2020
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Graphical Abstract
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Figure 1: Representative biologically active N-(hetero)aryl-4,5-unsubstituted pyrrole scaffolds.
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Scheme 1: Typical routes to N-(heteroaryl)-4,5-unsubstituted pyrroles.
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Scheme 2: Substrate scope of the pyrrole synthesis.
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Scheme 3: Synthesis of N-heterocyclic pyrroles.
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Scheme 4: Direct synthesis of pyrrole-3-carboxamide derivatives.
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Scheme 5: Plausible mechanism of the three-component reaction.
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Scheme 6: Synthesis of polysubstituted pyrazolo[3,4-b]pyridine derivatives.
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- Full Research Paper
- Published 26 Nov 2020
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Graphical Abstract
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Figure 1: Schematic illustration for the preparation of the catalyst in this work.
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Figure 2: FTIR spectra of LS, LS-FAS, and LS-FAS-Cu.
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Figure 3: Thermogravimetric weight loss of the obtained materials LS-FAS and LS-FAS-Cu.
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Figure 4: 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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Figure 5: 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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Scheme 1: Substrate scope of LS-FAS-Cu catalyzed three-component reactions of 4-aminoindoles, alkynes and ald...
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Figure 6: Recyclability of LS-FAS-Cu, LS-FM-Cu and Resin-Cu in the reaction between compounds 1a, 2a and 3a.
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