Synthesis of enatiomerically enriched β-amino alcohol derivatives via chiral base mediated-asymmetric deprotonation of (benzyl methyl ether) tricarbonylchromium(0) complex and electrophilic trapping with imines
Free accessResearch articleFirst published online September, 2004
Synthesis of enatiomerically enriched β-amino alcohol derivatives via chiral base mediated-asymmetric deprotonation of (benzyl methyl ether) tricarbonylchromium(0) complex and electrophilic trapping with imines
Deprotonation of (benzyl methyl ether)tricarbonylchromium(0) complex 1 by chiral base 2 followed by quenching reaction with imines 3 and subsequent decomplexation give β-amino alcohol derivatives 5 in good yields and high enantioselectivities (up to 96% e.e.).
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