B
Baoguo Li
Researcher at Inner Mongolia University
Publications - 37
Citations - 309
Baoguo Li is an academic researcher from Inner Mongolia University. The author has contributed to research in topics: Ferrocene & Catalysis. The author has an hindex of 10, co-authored 37 publications receiving 257 citations.
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Ferrocene and [3]ferrocenophane-based β-diketonato copper(II) and zinc(II) complexes: synthesis, crystal structure, electrochemistry and catalytic effect on thermal decomposition of ammonium perchlorate
TL;DR: In this article, Ferrocene and ferrocenophane-based β-diketones and their Cu(II) and Zn-II complexes have been synthesized and characterized.
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Construction of 9H-Pyrrolo[1,2-a]indoles by a Copper-Catalyzed Friedel–Crafts Alkylation/Annulation Cascade Reaction
TL;DR: An efficient and concise Cu(OTf)2-catalyzed Friedel-Crafts alkylation/annulation cascade reaction of substituted indoles with 1,2-dicarbonyl-3-enes has been established, representing a practical method for the construction of diverse 9H-pyrrolo[1, 2-a]indoles bearing a carbonyl group.
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CuBr-Promoted Formal Hydroacylation of 1-Alkynes with Glyoxal Derivatives: An Unexpected Synthesis of 1,2-Dicarbonyl-3-enes
TL;DR: An efficient and concise protocol has been developed for the highly regio- and stereoselective synthesis of E-1,2-dicarbonyl-3-ene derivatives by a copper-promoted reaction of 1-alkynes with α-carbonyl aldehydes in the presence of morpholine.
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Ce(OTf)3-catalyzed multicomponent domino cyclization–aromatization of ferrocenylacetylene, aldehydes, and amines: a straightforward synthesis of ferrocene-containing quinolines
TL;DR: In this article, a straightforward and economic method for the synthesis of ferrocene-containing quinolines by the Ce(OTf)3-catalyed one-pot three-component domino cyclization/aromatization reaction was developed.
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Y(OTf)3-Catalyzed Cascade Propargylic Substitution/Aza-Meyer–Schuster Rearrangement: Stereoselective Synthesis of α,β-Unsaturated Hydrazones and Their Conversion into Pyrazoles
TL;DR: In this article, a straightforward and concise method for the highly stereoselective synthesis of α,β-unsaturated hydrazones by the Y(OTf)3-catalyzed cascade propargylic substitution/aza-Meyer-Schuster rearrangement reaction of tertiary propargyl alcohols and p-toluenesulfonyl hydrazide under an air atmosphere is developed.