%0 Journal Article
%T Monopyrrolische VorHiufer fur die Synthese des Uroporp hyrinogen -octani trils
%A Eschenmoser
%A Albert
%A Fruh
%A Thomas
%A Inomata
%A Katsuhiko
%A Lattmann
%A Rene
%A Lehmann
%A Christian
%A Ono
%A Mitsunori
%J -
%D 1985
%X Sa£żetak Syntheses of the pre-uroporphinoid monopyrrolic derivatives porphobilinogen dinitrile, deaminomethyl-porphobilinogen dinitrile and 5-deaminomethyl-2-hydroxymethyl-porphobilinogen dinitrile make multiple use of the crystalline Mannich salt dimethyl- -methylidene-iminiumjodide as areagent for the introduction of cyanomethyl and ,B-cyanoethylside chains at the ,B-positionof the pyrrol nucleus. The paper is the first in a series of reports on the chemistry of uroporphyrinogen octanitrile
%U https://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=262377