2-Amino-1-phenyl-propan-1,3-diol as chir
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Tamas E Gunda; Ferenc Sztaricskai
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Article
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1997
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Elsevier Science
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French
โ 686 KB
were obtained in optically pure form by chiral Staudinger reaction. The cis-al~-ratio could be influenced by the protective groups of the diol moiety. Removal of the chiral auxiliarity could be accomplished by direct oxidation, or by previous double bond formation, thus the 2-amino-l-phenyl-propan-l