1312922-72-7Relevant academic research and scientific papers
One-Pot Copper-Catalyzed Three-Component Reaction of Sulfonyl Azides, Alkynes, and Allylamines to Access 2,3-Dihydro-1 H-imi-dazo[1,2-a]indoles
Jin, Hongwei,Liu, Daohong,Liu, Yunkui,Zhou, Bingwei
, p. 1417 - 1424 (2020)
A copper-catalyzed multicomponent reaction of sulfonyl azides, alkynes, and allylamines affording 2,3-dihydro-1 H-imidazo-[1,2-a]indoles in moderate yields is reported. Four C-N bonds are constructed- by way of azide-alkyne cycloaddition (CuAAC) and double Ullmann-type coupling reactions in a one-pot process.
Gold-catalyzed intermolecular oxidation of o-alkynylbiaryls: An easy and practical access to functionalized fluorenes
Pan, Fei,Liu, Shuang,Shu, Chao,Lin, Rong-Kun,Yu, Yong-Fei,Zhou, Jin-Mei,Ye, Long-Wu
supporting information, p. 10726 - 10729 (2014/10/15)
A novel gold-catalyzed intermolecular oxidation of o-alkynylbiaryls has been developed. A variety of functionalized fluorenes are readily accessed by utilizing this non-diazo approach, thus providing a viable alternative to synthetically useful fluorenes. This journal is the Partner Organisations 2014.
Palladium-catalyzed, one-pot, three-component approach to α-alkynyl indoles from o-bromo-(2,2-dibromovinyl)benzenes, terminal alkynes and arylamines
Liang, Yun,Meng, Tianhao,Zhang, Hui-Jun,Xi, Zhenfeng
supporting information; experimental part, p. 911 - 914 (2011/06/10)
α-Alkynyl indoles were efficiently synthesized in one pot from o-bromo-(2,2-dibromovinyl)benzenes, terminal alkynes, and arylamines via a palladium-catalyzed three-component coupling process. Georg Thieme Verlag Stuttgart · New York.
