<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Lai B</submitter><pubmed_abstract>A waste biomass, sodium lignosulfonate, was treated with sodium 2-formylbenzenesulfonate, and the phenylaldehyde condensation product was then used as a robust supporting material to immobilize a copper species. The so-obtained catalyst was characterized by many physicochemical methods including FTIR, EA, FSEM, FTEM, XPS, and TG. This catalyst exhibited excellent catalytic activity in the synthesis of nitrogen-containing heterocycles such as tricyclic indoles bearing 3,4-fused seven-membered rings, 2‑arylpyridines, aminonaphthalenes and 3-phenylisoquinolines. In addition, this catalyst showed to be recyclable and could be reused several times without significant loss in activity during the course of the reaction process.</pubmed_abstract><journal>Beilstein journal of organic chemistry</journal><pagination>2888-2902</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7705867</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A novel and robust heterogeneous Cu catalyst using modified lignosulfonate as support for the synthesis of nitrogen-containing heterocycles.</pubmed_title><pmcid>PMC7705867</pmcid><pubmed_authors>Ye M</pubmed_authors><pubmed_authors>Bai R</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Lai B</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel and robust heterogeneous Cu catalyst using modified lignosulfonate as support for the synthesis of nitrogen-containing heterocycles.</name><description>A waste biomass, sodium lignosulfonate, was treated with sodium 2-formylbenzenesulfonate, and the phenylaldehyde condensation product was then used as a robust supporting material to immobilize a copper species. The so-obtained catalyst was characterized by many physicochemical methods including FTIR, EA, FSEM, FTEM, XPS, and TG. This catalyst exhibited excellent catalytic activity in the synthesis of nitrogen-containing heterocycles such as tricyclic indoles bearing 3,4-fused seven-membered rings, 2‑arylpyridines, aminonaphthalenes and 3-phenylisoquinolines. In addition, this catalyst showed to be recyclable and could be reused several times without significant loss in activity during the course of the reaction process.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2024-02-15T06:29:00.495Z</modification><creation>2021-02-21T05:24:40Z</creation></dates><accession>S-EPMC7705867</accession><cross_references><pubmed>33299487</pubmed><doi>10.3762/bjoc.16.238</doi></cross_references></HashMap>