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Pyrrolizidine sulfide

A slightly different approach to 850 takes advantage of an intermolecular carbenoid displacement and intramolecular alkylation to construct the pyrrolizidine ring (Scheme 128) [193,194]. The precursor is prepared from 875 (R==OH — OEt —> SPh) and, for convenience, the protecting acyl group is replaced with a MOM group, which gives 876 as an 8 1 mixture of trans and cis phenyl sulfides. The major ra 5-sulfide is subjected to a carbenoid dis-... [Pg.273]


See other pages where Pyrrolizidine sulfide is mentioned: [Pg.493]    [Pg.493]    [Pg.478]    [Pg.12]    [Pg.22]    [Pg.206]    [Pg.780]    [Pg.237]    [Pg.61]   


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Pyrrolizidin

Pyrrolizidine

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