147687-45-4Relevant articles and documents
Factors influencing the cytotoxicity of α-methylene-γ-hydroxy esters against pancreatic cancer
Ramachandran, P. Veeraraghavan,Helppi, Matthew A.,Lehmkuhler, Arlie L.,Marchi, Jennifer M.,Schmidt, C. Max,Yip-Schneider, Michele T.
, p. 4270 - 4273 (2015/11/03)
A systematic study to identify the factors influencing the cytotoxicity of α-methylene-γ-hydroxy esters against three pancreatic cancer cell lines (Panc-1, MIA-PaCa-2, and BxPC-3) has established that, in addition to Michael acceptor abilities, the possibility to lactonize to α-methylene-γ-butyrolactones is as important. The substitution pattern and the number of carbons between the hydroxy and ester moieties also influence the bio-activity.
Decarboxylative heck reaction of aryl iodide with baylis-hillman adduct using PD/C as a catalyst in aqueous media
Kim, Hyun-Soo,Lee, Sang-Jin,Yoon, Cheol Min
, p. 325 - 327 (2013/08/24)
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A novel liquid-phase synthesis of Baylis-Hillman products using PEG-supported α-phenylselenopropionate ester
Sheng, Shou-Ri,Wang, Qiong,Wang, Qiu-Ying,Guo, Lei,Liu, Xiao-Ling,Huang, Xian
, p. 1887 - 1890 (2008/02/08)
Treatment of the lithio derivative of novel PEG-supported α-phenylselenopropionate ester with aldehydes and subsequent cleavage from the PEG support by oxidative elimination with 30% hydrogen peroxide efficiently afforded Baylis-Hillman products in good y