215544-03-9Relevant articles and documents
Structure-activity relationship (SAR) studies of 3-(2-amino-ethyl)-5-(4-ethoxy-benzylidene)-thiazolidine-2,4-dione: Development of potential substrate-specific ERK1/2 inhibitors
Li, Qianbin,Al-Ayoubi, Adnan,Guo, Tailiang,Zheng, Hui,Sarkar, Aurijit,Nguyen, Tri,Eblen, Scott T.,Grant, Steven,Kellogg, Glen E.,Zhang, Shijun
scheme or table, p. 6042 - 6046 (2010/05/18)
A series of analogs of 3-(2-amino-ethyl)-5-(4-ethoxy-benzylidene)-thiazolidine-2,4-dione, a putative substrate-specific ERK1/2 inhibitor, were synthesized and biologically characterized in human leukemia U937 cells to define its pharmacophore. It was disc
Preparation of chiral propargylic alcohols from α,β-unsaturated esters
Chun, Jiong,Byun, Hoe-Sup,Bittman, Robert
, p. 8043 - 8045 (2007/10/03)
A series of chiral propargylic alcohols with high enantiomeric excess was prepared by asymmetric dihydroxylation of α,β-unsaturated esters, conversion of the diols to 4-(chloromethyl)-1,3-dioxolane intermediates, and base-induced elimination.