{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13(1)"],"submitter":["Huang JQ"],"pubmed_abstract":["Isocyanides are common compounds in fine and bulk chemical syntheses. However, the direct addition of isocyanide to simple unactivated cyclopropene via transition metal catalysis is challenging. Most of the current approaches focus on 1,1-insertion of isocyanide to M-R or nucleophilc insertion. That is often complicated by the competitive homo-oligomerization reactivity occurring at room temperature, such as isocyanide 1,1-insertion by Ni(II). Here we show a (N-heterocyclic carbene)Ni(II) catalyst that enables cyclopropene-isocyanide [5 + 1] benzannulation. As shown in the broad substrate scope and a [trans-(N-heterocyclic carbene)Ni(isocyanide)Br<sub>2</sub>] crystal structure, the desired cross-reactivity is cooperatively controlled by the high reactivity of the cyclopropene, the sterica"],"journal":["Nature communications"],"pagination":["4145"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9288548"],"repository":["biostudies-literature"],"pubmed_title":["NHC-Ni(II)-catalyzed cyclopropene-isocyanide [5 + 1] benzannulation."],"pmcid":["PMC9288548"],"pubmed_authors":["Yu M","Ho CY","Yong X","Huang JQ"],"additional_accession":[]},"is_claimable":false,"name":"NHC-Ni(II)-catalyzed cyclopropene-isocyanide [5 + 1] benzannulation.","description":"Isocyanides are common compounds in fine and bulk chemical syntheses. However, the direct addition of isocyanide to simple unactivated cyclopropene via transition metal catalysis is challenging. Most of the current approaches focus on 1,1-insertion of isocyanide to M-R or nucleophilc insertion. That is often complicated by the competitive homo-oligomerization reactivity occurring at room temperature, such as isocyanide 1,1-insertion by Ni(II). Here we show a (N-heterocyclic carbene)Ni(II) catalyst that enables cyclopropene-isocyanide [5 + 1] benzannulation. As shown in the broad substrate scope and a [trans-(N-heterocyclic carbene)Ni(isocyanide)Br<sub>2</sub>] crystal structure, the desired cross-reactivity is cooperatively controlled by the high reactivity of the cyclopropene, the sterica","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jul","modification":"2025-04-04T03:06:09.995Z","creation":"2025-04-04T03:06:09.995Z"},"accession":"S-EPMC9288548","cross_references":{"pubmed":["35842422"],"doi":["10.1038/s41467-022-31896-y"]}}