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3- cyclopentane- 2-alkenoate ester

Addition of the chelated enolate of the S-oxo ester moiety of a 2,8-dioxo-6-alkenoate 1 under thermodynamic control at 25 °C using stoichiometric or catalytic amounts of sodium hydride in benzene results in the formation of tram-2-oxo-5-(2-oxoalkyl)-l-cyclopentane-carboxylate 2 exclusively. [Pg.968]

See other pages where 3- cyclopentane- 2-alkenoate ester is mentioned: [Pg.2453]    [Pg.1999]    [Pg.1999]    [Pg.2134]    [Pg.2166]    [Pg.2185]    [Pg.2329]    [Pg.2367]    [Pg.2420]    [Pg.2453]    [Pg.2507]    [Pg.2572]    [Pg.1114]    [Pg.2479]    [Pg.2482]    [Pg.2500]   
See also in sourсe #XX -- [ Pg.172 ]



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