77509-36-5Relevant academic research and scientific papers
Synthesis of Functionalized Dihydrocoumarins by NHC-Catalyzed [3 + 3] Annulation of Enals with 2-Substituted Naphthoquinones
Shee, Sayan,Barik, Soumen,Ghosh, Arghya,Biju, Akkattu T.
supporting information, p. 8039 - 8044 (2021/10/20)
The [3 + 3] annulation of α,β-unsaturated aldehydes with 2-substituted 1,4-naphthoquinones allowing the facile synthesis of functionalized dihydrocoumarins catalyzed by N-heterocyclic carbene (NHC) is reported. The initially formed NHC-homoenolates underwent an efficient Michael-isomerization-lactonization cascade to furnish the products. Preliminary studies on mechanism shed light on the homoenolate pathway over the intermediacy of the α,β-unsaturated acylazolium intermediates. Moreover, using chiral NHCs, the desired products were formed in up to 49% yield and 99:1 er.
Arylation of benzo-fused 1,4-quinones by the addition of boronic acids under dicationic Pd(II)-catalysis
Molina, Maria Teresa,Navarro, Cristina,Moreno, Ana,Csaky, Aurelio G.
supporting information; experimental part, p. 4938 - 4941 (2010/01/16)
The first examples of the direct arylation of benzo-fused 1,4-quinones by the dicationic Pd(II)-catalyzed addition of arylboronic acids are reported. The addition reaction is carried out under very mild conditions (dioxane-H 2O, rt, open air at
