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Dabco Subject

Subjection of this material to a formylation protocol involving a Rh catalyst, a bulky phosphite and DABCO (l,4-diazabicyclo[2.2.2]octane) in the presence of H2/CO gas mixture, gives a high yield of the desired aldehyde. Iteration of these steps leads to the synthesis of Tolypothrix pentaether. [Pg.2604]

An efficient method for the oxidative cleavage of solid-supported peptide olefins into aldehydes using a combination of OsOa/NalOa/DABCO system was described by Meldal and coworkers. The resulting aldehydes are subjected to intermolec-ular (V-acylium Pictet-Spengler reactions to furnish pyrroloiso-quinoline derivatives in high purity (eq 76). ... [Pg.279]

Using optimized reaction conditions, other substrates were subjected to tritylation reaction in ball mill (Scheme 4.7). Yields vary from moderate to good, and uridine besides being converted to its 5 -0-trityl derivative 27 was also converted to 5 -0-dimethoxytrityl derivative 28 by milling with DMTCl (2.5 mol equiv.), respectively, in the presence of DABCO (2.5mol equiv.). [Pg.239]


See other pages where Dabco Subject is mentioned: [Pg.675]    [Pg.471]    [Pg.408]    [Pg.380]    [Pg.284]    [Pg.1023]    [Pg.57]    [Pg.487]    [Pg.504]    [Pg.1552]    [Pg.375]    [Pg.377]    [Pg.15]    [Pg.915]    [Pg.524]    [Pg.531]    [Pg.915]    [Pg.100]    [Pg.380]   
See also in sourсe #XX -- [ Pg.395 ]




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