Gold(I)-Catalyzed Addition of Carboxylic Acids to Alkynes
摘要:
Au(I)-catalyzed hydroacyloxylation of alkynes with carboxylic acids is described PPh3AuCl/AgPF6 catalyst affords the Markonikov addition products, whereas PPh3AuCl/AgOTf catalyst gives the more stable isomerized products via the Markonikov products
this article is a palladium(II)/copper(II)‐ or palladium(II)‐catalyzed intermolecular cyclization of acrylic acid with alkenes to produce α‐methylene‐γ‐butyrolactone derivatives using molecular oxygen as an environmentally benign oxidant. In this system, the carboxylato, especially trifluoroacetato, or trimethylacetato ligand, plays a quite important role to afford a high catalytic activity by suppressing
Gold(I)-Catalyzed Addition of Carboxylic Acids to Alkynes
作者:Bathoju Chandra Chary、Sunggak Kim
DOI:10.1021/jo101543q
日期:2010.11.19
Au(I)-catalyzed hydroacyloxylation of alkynes with carboxylic acids is described PPh3AuCl/AgPF6 catalyst affords the Markonikov addition products, whereas PPh3AuCl/AgOTf catalyst gives the more stable isomerized products via the Markonikov products