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5-Bromo-norborn-2-en-7-one derivatives as a carbon monoxide source for palladium catalyzed carbonylation reactions.
Payne, China M; Cho, Kyulee; Larsen, David S.
Affiliation
  • Payne CM; Department of Chemistry, University of Otago P.O. Box 56 Dunedin 9054 New Zealand david.larsen@otago.ac.nz.
  • Cho K; Department of Chemistry, University of Otago P.O. Box 56 Dunedin 9054 New Zealand david.larsen@otago.ac.nz.
  • Larsen DS; Department of Chemistry, University of Otago P.O. Box 56 Dunedin 9054 New Zealand david.larsen@otago.ac.nz.
RSC Adv ; 9(53): 30736-30740, 2019 Sep 26.
Article in En | MEDLINE | ID: mdl-35529407
ABSTRACT
Norbornenone (5b), obtained from the reaction of 2,5-dimethyl-3,4-diphenylcyclopentadienone dimer (3) with bromomaleic anhydride (4b), provides an excellent base-triggered source of carbon monoxide for palladium-catalysed carbonylation reactions. Aminocarbonylation, ketoamide synthesis, and Suzuki-Miyaura reactions of aryl iodides carried out in a two-chamber reaction vessel gave good to excellent yields of carbonylated products.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2019 Document type: Article Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: RSC Adv Year: 2019 Document type: Article Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM