Synthesis of Prolylproline


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Resumo

Prolylproline has been synthesized by both classical peptide synthesis method utilizing tert-butoxycarbonyl or trifluoroacetyl protection of the NH group and carbodiimide-promoted peptide bond formation and by opening of the dioxopiperazine ring in octahydrodipyrrolo[1,2-a:1′,2′-d]pyrazine-5,10-dione obtained by thermolysis of proline methyl ester.

Sobre autores

V. Gaidukevich

Institute of Physical Organic Chemistry

Email: knizh@ifoch.bas-net.by
Belarus, Minsk

L. Popova

Institute of Physical Organic Chemistry

Email: knizh@ifoch.bas-net.by
Belarus, Minsk

Z. Zubreichuk

Institute of Physical Organic Chemistry

Email: knizh@ifoch.bas-net.by
Belarus, Minsk

V. Knizhnikov

Institute of Physical Organic Chemistry

Autor responsável pela correspondência
Email: knizh@ifoch.bas-net.by
Belarus, Minsk

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