iodides with isocyanides to afford alkyl amide, which proceeds via the selective monomigratory insertion of isocyanides with alkyl iodides, subsequent β-hydride elimination, and hydrolysis process. The reaction features wide functional group tolerance under mild conditions. Additionally, the selective, one-pot hydrolysis of reaction mixture under acid conditions allows for expedient synthesis of the corresponding
Nickel-Catalyzed Multicomponent Coupling Reaction of Alkyl Halides, Isocyanides and H2O: An Expedient Way to Access Alkyl Amides
作者:Yunkui Liu、Bingwei Zhou、Qiao Li、Hongwei Jin
DOI:10.1055/s-0040-1707229
日期:2020.11
multicomponent coupling reaction of alkylhalides, isocyanides, and H2O to access alkyl amides. Bench-stable NiCl2(dppp) is competent to initiate this transformation under mild reaction conditions, thus allowing easy operation and adding practical value. Substrate scope studies revealed a broad functional group tolerance and generality of primary and secondary alkylhalides in this protocol. A plausible
4-AZA INDOLE DERIVATIVES AND THEIR USE AS FUNGICIDES
申请人:Selles Patrice
公开号:US20100184598A1
公开(公告)日:2010-07-22
The present invention relates to a method of preventing and/or controlling fungal infection in plants and/or plant propagation material comprising applying to the plant or plant propagation material a fungicidally effective amount of a compound of formula (I) or a salt of N-oxide thereof. In addition, the present invention also relates to a compound of formula (I).
Cyclic peptide epitopes and small-molecule mimics for inducing autophagy
申请人:TRUSTEES OF TUFTS COLLEGE
公开号:US10993983B2
公开(公告)日:2021-05-04
Disclosed herein are cyclic peptides that induce cellular autophagy and have significant cell penetration activity. Methods for inducing autophagy and thereby treating various diseases and conditions associated with impaired autophagy are provided.