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Bromoenol lactone

J Balsinde, EA Dennis. Bromoenol lactone inhibits magnesium-dependent phospha-tidate phosphohydrolase and blocks triacylglycerol biosynthesis in mouse P388D1 macrophages. J Biol Chem 271 31937-31941, 1996. [Pg.396]

An example of bromocyclization is the stereoselective bromoenol lactonization of alkynoic acids that furnishes either the Z or the E isomer according to the reaction conditions (equation 59)467>468. [Pg.561]

Chiral 8-lactones are formed in the condensation of keteneacetals with a-diketones (2 1 stoichiometry) in the presence of the bis(oxazoline)-Cu(OTf)2 complex 49. Aldol adducts derived from a-bromoenolates are precursors of chiral a,p-epoxyalkanoic esters. ... [Pg.105]

See other pages where Bromoenol lactone is mentioned: [Pg.970]    [Pg.46]    [Pg.81]    [Pg.210]    [Pg.96]    [Pg.390]    [Pg.392]    [Pg.970]    [Pg.323]    [Pg.323]    [Pg.352]    [Pg.114]    [Pg.122]    [Pg.33]    [Pg.970]    [Pg.46]    [Pg.81]    [Pg.210]    [Pg.96]    [Pg.390]    [Pg.392]    [Pg.970]    [Pg.323]    [Pg.323]    [Pg.352]    [Pg.114]    [Pg.122]    [Pg.33]    [Pg.104]    [Pg.1683]   
See also in sourсe #XX -- [ Pg.45 , Pg.212 ]

See also in sourсe #XX -- [ Pg.122 ]



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