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Stereoselectivity Williamson synthesis

A much more elaborate synthesis of 4-aryl-2-(benzyloxy)carbonyl-3-hydroxy tetrahydrofurans 88 from aryl epoxides requires the use of benzyl diazoacetate. This methodology can now be extended to a highly stereoselective synthesis of chiral tetrahydrofurans starting from optically active epoxides. The mechanism is believed to involve a Williamson-type cyclization as illustrated below <00TL8059>. [Pg.148]


See other pages where Stereoselectivity Williamson synthesis is mentioned: [Pg.448]    [Pg.152]    [Pg.183]    [Pg.183]    [Pg.281]    [Pg.159]    [Pg.99]    [Pg.105]    [Pg.52]   
See also in sourсe #XX -- [ Pg.346 ]




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Stereoselective synthesis

Stereoselectivity synthesis

Williamson

Williamson synthesis

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