| Literature DB >> 31885406 |
Hang T Dang1, Viet D Nguyen1, Hoang H Pham1, Hadi D Arman1, Oleg V Larionov1.
Abstract
Conjugated dienes and polyenes are central structural motifs of natural products, and key synthetic intermediates in organic synthesis and materials science. We describe herein a palladium-catalyzed dienylation of aryl, heteroaryl, and vinyl triflates, nonaflates and iodides that were previously identified as recalcitrant substrates for the sulfolene-mediated catalytic dienylation. The method has now been successfully expanded to C-O and C-I dienylation, demonstrating broad scope with respect to sulfonates, iodides and sulfolenes. The reactions proceed with high regio- and stereoselectivity, and efficiency that are strongly influenced by basic additives, whose influence on the reaction performance was systematically studied.Entities:
Keywords: Cross-coupling; Desulfitation; Dienes; Palladium catalysis; Polyenes; Sulfinates; Sulfolenes
Year: 2019 PMID: 31885406 PMCID: PMC6934257 DOI: 10.1016/j.tet.2019.04.012
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457