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Homochiral diol auxiliaries

The use of C2-symmetric 1,2- and 1,3-diols as chiral auxiliaries is a reliable method for asymmetric allylation of acetals [382]. Acyclic acetals derived from homochiral 1-phenylethanol undergo the Hosomi-Sakurai allylation with high diastereoselectivity [383]. Tietze et al. have, on the other hand, reported that the TMSOTf-catalyzed successive acetalization-allylation reaction of aliphatic aldehydes with homochiral silyl ethers 123 and allyltrimethylsilane gives the corresponding homoallyl ethers with complete diastereocontrol these ethers can be readily converted into enantiomerically pure homoallyl alcohols without epimerization (Scheme 10.135) [384]. This method is applicable to asymmetric allylation of methyl ketones [385]. [Pg.499]


See other pages where Homochiral diol auxiliaries is mentioned: [Pg.1177]    [Pg.247]    [Pg.122]   
See also in sourсe #XX -- [ Pg.579 , Pg.580 , Pg.581 ]

See also in sourсe #XX -- [ Pg.579 , Pg.580 , Pg.581 ]




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Homochiral

Homochiral auxiliary

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