314289-74-2Relevant academic research and scientific papers
Practical synthesis of PGI2 agonist: Resolution-inversion- recycle approach of its chiral intermediate
Ohigashi, Atsushi,Kanda, Atsushi,Moriki, Shigeru,Baba, Yukihisa,Hashimoto, Norio,Okada, Minoru
, p. 658 - 665 (2013/07/05)
Practical synthesis of ((2R)-5-benzyloxy-2-hydroxy-1,2,3,4- tetrahydronaphth-2-yl)methanol ((R)-7b), a key chiral intermediate for the synthesis of the novel PGI2 agonist, (R)-[6-[(diphenylcarbamoyloxy) methyl]-6-hydroxy-5,6,7,8-tetrahydronapht
Discovery of diphenylcarbamate derivatives as highly potent and selective IP receptor agonists: Orally active prostacyclin mimetics. Part 3
Hattori, Kouji,Tanaka, Akira,Okitsu, Osamu,Tabuchi, Seiichiro,Taniguchi, Kiyoshi,Nishio, Mie,Koyama, Satoshi,Higaki, Masahide,Seki, Jiro,Sakane, Kazuo
, p. 3091 - 3095 (2007/10/03)
The new classes of diphenylcarbamate derivatives with a tetrahydronaphthalene skeleton as highly potent and selective IP agonists have been discovered. The optimized diphenylcarbamate type compound FK-788: (R)-4 exhibited potent antiaggregative potency wi
