Year: 2025
Type: article
Abstract: ) bond of the 1,3-diene, leading to a pentadienyl cation. Regioselective attack on the latter species leads to the formation of multi-substituted 1,3-dienes or 1,4-dienes with a broad range of carbon and heteroatomic nucleophiles.
Source: Chemical Science
DOI: 10.1039/d5sc03161c
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: diamond
Funders: Ministerio de Ciencia, Innovación y Universidades, Centres de Recerca de Catalunya, European Commission, Institució Catalana de Recerca i Estudis Avançats, Institut Català d'Investigació Química, Agencia Estatal de Investigación, H2020 European Research Council, H2020 Marie Skłodowska-Curie Actions
Awards: G1105844351, G110640233, G114204955, Carbyne transfer catalysis for C(sp2)–C(sp2) bond (radio)fluorinations, G2262748287, G2338646650, G2601397997, Carbyne transfer catalysis for C(sp2)–C(sp2) bond (radio)fluorinations, G300979063, G3480869486, G3681454997, G4027493804, G4042783231, G425668148, G4643134928, G4890640476, G5080475149, G5555131222, G5807460470, G6656126374, G7805626310, G7863371703, G8053623925, G8118268009, G8497050386, G8684520763, New carbon reactivity rules for molecular editing
OpenAlex ID: W4411456452