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Prostaglandin synthesis endoperoxide analogs

Similar dicarborating cis-exo additions are achieved with up to 99 % yield if aryl or vinyl halides and various organotin compounds, such as vinyl-, phenyl-, ethynyl- and allyl(tributyl)tin systems, are added to norbornene in the presence of tetrakis(triphenylphosphane)palladium(0) or di-chlorobis(triphenylphosphane) as catalyst precursor7,30,80-81. Also reported are cis-exo dicarbo-rative additions to the norbornene skeleton, and their application to the synthesis of prostaglandin endoperoxide analogs, which employ stoichiometric amounts of palladium compounds16. [Pg.439]

Bundy, G. (1975). The synthesis of prostaglandin endoperoxide analogs. Tetrahedron Lett., 24, 1957-1960... [Pg.226]

Synthesis of Several Analogs of the Prostaglandin Endoperoxide PGH2... [Pg.286]

Jeremy, J.Y., Mikhailidis, D.P. and Dandona, P. (1985). Thromboxane A analog (U46619) stimulates vascular PGI synthesis. Eur. ]. Pharmacol, 107, 259-262 Schafer, A.I., Crawford, D.D. and Gimbrone, M.M. (1984). Unidirectional transfer of prostaglandin endoperoxides between platelets and endothelial cells. ]. Clin. Invest., 73, 1105-1108... [Pg.150]

See other pages where Prostaglandin synthesis endoperoxide analogs is mentioned: [Pg.9]    [Pg.153]    [Pg.341]    [Pg.396]   
See also in sourсe #XX -- [ Pg.286 , Pg.287 , Pg.288 , Pg.289 , Pg.297 , Pg.298 , Pg.299 , Pg.300 , Pg.301 ]

See also in sourсe #XX -- [ Pg.286 , Pg.287 , Pg.288 , Pg.289 , Pg.297 , Pg.298 , Pg.299 , Pg.300 , Pg.301 ]



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Analogs synthesis

Endoperoxidation

Endoperoxide

Endoperoxides synthesis

Endoperoxides/endoperoxidation

Prostaglandin endoperoxide synthesis

Prostaglandine analog

Prostaglandines, synthesis

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