1616788-07-8Relevant articles and documents
Gold-catalyzed [1,5]-hydride shift onto unactivated alkynes to trigger an intermolecular Diels-Alder reaction
Wu, Xiang,Chen, Shu-Sen,Hu, Yue,Gong, Liu-Zhu
, p. 3820 - 3823 (2014/08/05)
A [1,5]-hydride shift of sp3 C-H onto an unactivated carbon-carbon triple bond catalyzed by a gold(I) complex enabled N-propargylisoindolines to be latent dienes and therefore triggered an intermolecular Diels-Alder reaction with dienophiles. This protocol provides an atom-economical and straightforward approach to access a wide range of polycyclic skeletons in high yields and with excellent diastereoselectivities from easily accessible molecules.