226915-53-3Relevant articles and documents
Improved large-scale synthesis of(R)-benzyl 4-hydroxyl-2-pentynoate from (R)-3-butyn-2-ol
Fu, Xiaoyong,Yin, Jianguo,Thiruvengadam,McAllister, Timothy L.,Tann, Chou-Hong,Colon, Cesar
, p. 308 - 310 (2002)
A reliable one-pot process for the title compound has been developed for large-scale productions. The effect of reaction conditions such as temperature, order of addition, and amount of the lithiation reagent has been extensively investigated, giving rise to an optimal process with highest attainable yield.
Metabolism-based identification of a potent thrombin receptor antagonist
Clasby, Martin C.,Chackalamannil, Samuel,Czarniecki, Michael,Doller, Dario,Eagen, Keith,Greenlee, William,Kao, Grace,Lin, Yan,Tsai, Hsingan,Xia, Yan,Ahn, Ho-Sam,Agans-Fantuzzi, Jacqueline,Boykow, George,Chintala, Madhu,Foster, Carolyn,Smith-Torhan, April,Alton, Kevin,Bryant, Matthew,Hsieh, Yunsheng,Lau, Janice,Palamanda, Jairam
, p. 129 - 138 (2008/02/03)
The metabolism of our prototypical thrombin receptor antagonist 1, K i = 2.7 nM, was studied and three major metabolites (2, 4, and 5) were found. The structures of the metabolites were verified independently by synthesis. Compound 4 was shown