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This article is cited in 5 scientific papers (total in 5 papers)
Synthesis and Acid-induced Ring Opening of Modified Glycals. Synthons for (14R,15R)-Lipoxin B and (7S,8R)-( – )-Disparlure
A. G. Tolstikova, O. F. Prokopenkob, L. M. Khalilovc, L. V. Spirikhinb, 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:
The chiral 1,2-unsaturated dihydroxyaldehydes 7 and 11 were synthesized as synthons for (14R,15R)-lipoxin B 12 and (7S,8R)-( – )-cis-disparlure 13, based on new glycals 6 and 10 prepared from α-d-galactose.
Citation:
A. G. Tolstikov, O. F. Prokopenko, L. M. Khalilov, L. V. Spirikhin, G. A. Tolstikov, “Synthesis and Acid-induced Ring Opening of Modified Glycals. Synthons for (14R,15R)-Lipoxin B and (7S,8R)-( – )-Disparlure”, Mendeleev Commun., 1:2 (1991), 51
Linking options:
https://www.mathnet.ru/eng/mendc5490 https://www.mathnet.ru/eng/mendc/v1/i2/p51
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