71154-83-1Relevant academic research and scientific papers
Two Syntheses of Pinane Thromboxane A2
Ansell, Martin F.,Caton, Michael P. L.,Stutte, Keith A. J.
, p. 1069 - 1077 (2007/10/02)
The thromboxane analogue (PTA2) (2a) has been synthesized from nopol (3a) and via conjugate addition of the cuprate (18a) to myrtenal (17).
Synthesis of prostanoids with bicyclo[2.2.1]heptane, bicyclo[3.1.1]heptane, and bicyclo[2.2.2]octane bicycloAD2.2.2BDoctane ring systems. Activities of 15-hydroxy epimers on human platelets
Wilson,Peesapati,Jones,Hamilton
, p. 495 - 500 (2007/10/02)
A number of prostanoids with bicyclo[2.2.1]heptane, bicyclo[3.1.1]heptane, and bicyclo[2.2.2]octane ring systems have been prepared by routes which allow the introduction of the ω chain after the α chain. The introduction of a 16-p-halophenoxy substituent confers platelet aggregation activity on both 15α- and 15β-hydroxy epimers. In the case of the pinane thromboxane ring system, the natural ω-chain compound is an inhibitor of aggregation, whereas the 16-p-fluorophenoxy analogue is a potent aggregation agent.
