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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1991 Volume 1, Issue 2, Pages 52–53 (Mi mendc5491)

This article is cited in 1 paper

Synthesis of Unsaturated Polyhydroxycarboxylic Acids as Structural Analogues of an Arachidonic Acid Metabolite

A. G. Tolstikova, O. F. Prokopenkob, L. M. Khalilovc, L. V. Spirikhinb, A. A. Bergb, V. R. Sultanmuratovab, G. A. Tolstikovd

a G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
c Institute of Petrochemistry and Catalysis, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
d N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: (5Z,10Z,9R,12R,13R)-12-Acetoxy-9,13-epoxyoctadeca-5,10-dienoicacid 1, (2E,7Z,6R,9R,10R)-9-acetoxy-6,10-epoxypentadeca-2,7-dienoic acid methyl ester 12 and (5Z,10Z,9R,12R,13R,14R)-12,14-diacetoxy-9,13-epoxyicosa-5,10-dienoic acid 3 have been synthesized, starting from modified glycals 5 and 12α prepared from 1,2,3,4-di-O-isopropylidene-α-d-galactopyranose.

Language: English

DOI: 10.1070/MC1991v001n02ABEH000030



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