1190949-12-2Relevant academic research and scientific papers
Stereoselective Biginelli-like reaction catalyzed by a chiral phosphoric acid bearing two hydroxy groups
Hu, Xiaoyun,Guo, Jianxin,Wang, Cui,Zhang, Rui,Borovkov, Victor
, p. 1875 - 1880 (2020)
To develop new efficient stereoselective catalysts for Biginelli-like reactions, a chiral phosphoric acid bearing two hydroxy groups derived from L-tartaric acid was successfully synthesized via highly regioselective transformations of enantiopure 1,1,4,4
Highly enantioselective organocatalytic Biginelli and Biginelli-like condensations: Reversal of the stereochemistry by tuning the 3,3′-disubstituents of phosphoric acids
Li, Nan,Chen, Xiao-Hua,Song, Jin,Luo, Shi-Wei,Fan, Wu,Gong, Liu-Zhu
supporting information; experimental part, p. 15301 - 15310 (2010/01/30)
Organocatalytic enantioselective Biginelli and Biginelli-like reactions by chiral phosphoric acids derived from 3,3′-disubstituted binaphthols have been investigated. The size of 3,3′-substituents of the catalysts is able to control the stereochemistry of
