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Application of the Asymmetric Synthesis in the Determination of the Configuration of Amino Alcohols and Diamines with Two Adjacent Asymmetric Carbon Atoms

M. Proštenik ; Department of Chemistry, Faculty of Medicine, University of Zagreb , Zagreb, Croatia, Yugoslavia
P. Alaupović ; Department of Chemistry, Faculty of Medicine, University of Zagreb , Zagreb, Croatia, Yugoslavia


Puni tekst: engleski pdf 13.836 Kb

str. 393-402

preuzimanja: 144

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Sažetak

Optically active a-amino ketones of known configuration (D-) can be prepared by virtue of the Bowman ketone synthesis starting with optically active, natural a-amino acids as acylating components. By reduction of a-amino ketones and of their oximes with lithium aluminum ,hydride the hydroxy and the second amino group were induced asymmetrically yielding in both cases predominantly the erythro epimers of corresponding a- amino alcohols and a-diamines. This is in agreement with Cram's rule of the steric control of the asymmetric induction.

Ključne riječi

Hrčak ID:

246319

URI

https://hrcak.srce.hr/246319

Datum izdavanja:

30.12.1957.

Posjeta: 382 *