1393381-99-1Relevant articles and documents
Enantioselective vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones: Facile access to chiral trifluoromethyl dihydropyranones
Fu, Chun-Wei,Fu, Jun-Hao,Sha, Feng,Wu, Xin-Yan,Zhang, Zhen-Guo,Zhou, Xue-Ying
, p. 7848 - 7851 (2020)
An efficient asymmetric vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones has been developed. Using a chiral cyclohexanediamine-based tertiary amine-thiourea catalyst, optically active trifluoromethyl dihydropyranones have been constructed in moderate-to-excellent yields (up to 99%) with excellent stereoselectivities (96-> 99.5% ee). This journal is
Oxidative γ-addition of enals to trifluoromethyl ketones: Enantioselectivity control via lewis acid/n-heterocyclic carbene cooperative catalysis
Mo, Junming,Chen, Xingkuan,Chi, Yonggui Robin
supporting information; experimental part, p. 8810 - 8813 (2012/07/02)
An oxidative γ-functionalization of enals under N-heterocyclic carbene (NHC) catalysis to give unsaturated δ-lactones is disclosed. Enantioselectivity control involving the relatively remote enal γ-carbon was achieved via Lewis acid [Sc(OTf)3 or combined Sc(OTf) 3/Mg(OTf)2] and NHC cooperative catalysis.