supported by the Natural Science Foundation of Shandong Province(ZR2019BB011);the Scientific Research Foundation of Qingdao University of Science&Technology(010029022).
A Ru(II)-catalyzed ortho allylation reaction of N-aryl-7-azaindole with readily available 2-methylidene cyclic carbonate has been developed.This reaction is an effective pathway for synthesizing 7-azaindole derivative...
supported by the National Natural Science Foundation of China(22271100,21973113);the Key-Area Research and Development Program of Guangdong Province(2020-B010188001);the Guangdong Basic and Applied Basic Research Foundation(2023A1515010070);the China Postdoctoral Science Foundation(2021M701243)。
We disclose the development of the Rh-catalyzed amine-directed remote 5,6-carboamination protocol of pyridines via dual Csp^(2)-H functionalizations.A variety of readily available 2-aminopyridines and 1,2,3-triazoles ...
support from the National Natural Science Foundation of China(51802001);Education Committee of Anhui Province(KJ2018A0037).
A transition-metal free three-component coupling reaction of azaindoles,C_(60),and bromoalkanes/triphenylamines has been developed to provide an efficient access to diverse azaindole functionalized 1,4-C_(60) adducts....
the financial support from the National Natural Science Foundation of China(No.21503161);the Key Research&Development Project in Shaanxi Province(No.2017ZDXM-GY-040);the Doctoral Scientific Research Foundation of Xi'an Polytechnic University(No.107020336).
We reported for the first time that ethyl bromodifluoroacetate directly reacts with azaindole without transition metal catalysis to produce a difluoromethyl protected 5-aldehyde group product in one step.It is worth m...
financial support from the NSFC(21572135 and 21321061)
A mild and efficient dearomatic [3+2] annulation reaction of 3-nitro-7-azaindoles and Morita Baylis Hillman carbonates from isatins was developed catalyzed by DMAP, affording the corresponding polycyclic spirooxindol...