Asymmetrical synthesis of lysine derivatives

Asymmetrical synthesis of lysine derivatives Full article

Journal

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
ISSN: 2376-8444 , E-ISSN: 0568-5230

Output data

Year: 1986, Volume: 35, Number: 4, Pages: 842-844 Pages count : 3 DOI: 10.1007/bf00954244

Authors

Levitina E.S. ^1,2 , Godunova L.F. ^1,2 , Kaigorodova L.N. ^1,2 , Karpeiskaya E.I. ^1,2 , Klabunovskii E.I. ^1,2 , Gogoladze D.D. ^1,2

Affiliations

1	N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, Moscow
2	P. G. Melikishvili Institute of Physical and Organic Chemistry, Academy of Sciences of the Georgian SSR, Tbilisi

The stereoselective aminolysis of the azlactone of DL-diacetyllysine by the action of S-α-phenylethylamine in t-BuOH leads to an excess of the SS-diastereomer of the α-phenylethylamine or diaceyllysine. Crystallization of the mixture of diastereomeric amides gave the optically pure S-α-phenylethylamide of S-diacetyllysine.

Levitina E.S. , Godunova L.F. , Kaigorodova L.N. , Karpeiskaya E.I. , Klabunovskii E.I. , Gogoladze D.D.
Asymmetrical synthesis of lysine derivatives
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1986. V.35. N4. P.842-844. DOI: 10.1007/bf00954244 OpenAlex

OpenAlex:

W2995290558

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