Abstract:
Starting from (2R,3S)-2,3-dihydroxybutanolide, (4S,5S)-5-hydroxydecan-4-olide (l-factor) was synthesized, the latter being an autoregulator in the biosynthesis of the anthracycline antibiotic leukaemomycin.
Document Type:
Article
Language: English
Citation:
A. G. Tolstikov, R. Kh. Yamilov, N. V. Khakhalina, E. E. Savateeva, L. V. Spirikhin, G. A. Tolstikov, “Enantiospecific Synthesis of (4S,5S)-5-Hydroxydecan-4-olide (L-Factor)”, Mendeleev Commun., 2:2 (1992), 53–54
Linking options:
https://www.mathnet.ru/eng/mendc5399
https://www.mathnet.ru/eng/mendc/v2/i2/p53
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K. Siva Nagi Reddy, Gowravaram Sabitha, Y. Poornachandra, C. Ganesh Kumar, “Synthesis and biological evaluation of sapinofuranones A,B and 1,2,3-triazole-sapinofuranone hybrids as cytotoxic agents”, RSC Adv., 6:103 (2016), 101501
Sandip Chatterjee, Avrajit Manna, Tanurima Bhaumik, “A convenient chiron approach to (4R,5R)-5-hydroxyalkylbutan-4-olides and the corresponding 7-oxa analogues from d-(+)-mannitol via an advanced common precursor: syntheses of (-)-muricatacin, 7-oxa-(-)-muricatacin, (4R,5R)-(-)-5-hydroxy-4-decanolide, and (4R,5R)-(-)-7-oxa-5-hydroxy-4-dodecanolide”, Tetrahedron: Asymmetry, 25:24 (2014), 1624
A. G. TOLSTIKOV, R. KH. YAMILOV, N. V. KHAKHALINA, E. E. SAVATEEVA, L. V. SPIRIKHIN, G. A. TOLSTIKOV, “ChemInform Abstract: Enantiospecific Synthesis of (4S,5S)‐5‐Hydroxydecan‐4‐olide (I) (L‐ Factor).”, ChemInform, 23:39 (1992)
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