62747-51-7Relevant academic research and scientific papers
Ming-Phos/Gold(I)-Catalyzed Diastereo- and Enantioselective Synthesis of Indolyl-Substituted Cyclopenta[ c]furans
Wang, Yidong,Zhang, Zhan-Ming,Liu, Feng,He, Yinyan,Zhang, Junliang
, p. 6403 - 6406 (2018)
A highly enantioselective gold(I)-catalyzed intermolecular tandem cyclization/[3 + 2] cycloaddition of 2-(1-alkynyl)-2-alken-1-ones with 3-stylindoles was achieved by using Ming-Phos as a chiral ligand. A variety of chiral highly substituted cyclopenta[c]
Gold(I)-catalyzed, highly diastereoselective, tandem heterocyclizations/ [3+2] cycloadditions: Synthesis of highly substituted cyclopenta[c]furans
Gao, Hongyin,Wu, Xingxing,Zhang, Junliang
, p. 2838 - 2841 (2011)
The domino effect: A novel, cationic, gold(I)-catalyzed [3+2], tandem bicyclization, which provides rapid, efficient, and diastereoselective access to highly substituted cyclopenta[c]furans from simple, readily available 2-(1-alkynyl)-2-alken-1-ones and 3-styrylindoles under mild conditions, is described (see scheme).
Rhenium-catalyzed regiodivergent addition of indoles to terminal alkynes
Xia, Dexin,Wang, Yin,Du, Zhenting,Zheng, Qi-Yu,Wang, Congyang
supporting information; experimental part, p. 588 - 591 (2012/03/09)
An efficient rhenium-catalyzed site-switchable addition of indoles to terminal alkynes is described. A variety of bisindolylalkane derivatives are expeditiously synthesized in high yields with excellent regioselectivity. Preliminary mechanistic study shed
