Asymmetric synthesis of 1,2-amino alcohols using tert-butanesulfinimines as chiral auxiliary
Facile and highly stereoselective synthesis of 1,2-amino alcohols has been achieved by the addition of [(dimethylphenyl-silyl)methyl] magnesium chloride to the tert-butanesulfinimines, followed by Fleming-Tamao oxidation of the silicon moiety.
Ko, Chang Hong,Jung, Doo Young,Kim, Min Kyun,Kim, Yong Hae
p. 304 - 308
(2007/10/03)
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