the Research Grants Council of Hong Kong(GRF:14308121);cUHK Direct Fund(4053503)for financial support.We also thank the Guangdong Basic and Applied Basic Research Foundation(2022A1515010955);Shenzhen Virtual University Park Fund(2021Szvup147)for their support;thankful for the Innovation and Technology Commission(HKSAR,China)to the State Key Laboratory of Synthetic Chemistry;thank Guangdong Province Zhu Jiang Talents Plan(Project code:2016ZT06C090);Guangzhou City Talents Plan(Project code:CYLJTD-201609)for their support.
Sonogashira cross-coupling protocol,typically showing the reaction between aryl/vinyl halide and terminal alkyne,has been a widely used protocol for constructing C(sp2)-C(sp)bond.The resulting internal alkynes are hig...
support from the National Natural Science Foundation of China(nos.21702184,21772175,and 91956117).
Highly enantioselective and diastereoselective 1,2-diarylation and 1,2-arylalkynylation of trisubstituted alkenes are reported via the palladium-catalyzed Heck/Suzuki or Heck/Sonogashira domino sequence.These alkenes ...
financially supported by the Natural Science Foundation of Jiangsu Higher Education Institutions (No. 18KJA430014);the Natural Science Foundation of Jiangsu Province (No. BK20181441);the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
Sonogashira coupling of two different diketopyrrolopyrrole (DPP)-containing dihaloarenes with the same aromatic bisalkyne resulted in two new conjugated polymers with the same backbone but different pendant groups on ...
Palladium-catalyzed the Sonogashira coupling reaction of 3-halogen-2-aminopyridines 1 with terminal alkynes 2 afforded the corresponding 21 target products 3a-3u in the presence of palladium catalyst. The structure of...