Enantiospecific Synthesis of (4S,5S)-5-Hydroxydecan-4-olide (L-Factor)
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference6 articles.
1. Isolation and structure of novel autoregulators from Streptomyces griseus.
2. Synthesis of (4s,5r)-(+)-factor, a proposed autoregulator of anthracycline biosynthesis
3. The enantiospecific synthesis of (4S,5R)-and (4S,5S)-4,5-dihydroxydecanoic acid γ-lactones, proposed autoregulators from
4. An enantiospecific synthesis of (4R,5R)-5-hydroxy-4-decanolide from d-glucose
5. Simple synthesis of all of the four stereoisomers of 5-hydroxy-4-decanolide (l-factors), the proposed autoregulators from
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1. Chiron approach from D-mannitol to access a diastereomer of the reported structure of an acetogenin, an amide alkaloid and a sex pheromone;Carbohydrate Research;2019-02
2. Synthesis and biological evaluation of sapinofuranones A,B and 1,2,3-triazole-sapinofuranone hybrids as cytotoxic agents;RSC Advances;2016
3. 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;2014-12
4. ChemInform Abstract: Enantiospecific Synthesis of (4S,5S)-5-Hydroxydecan-4-olide (I) (L- Factor).;ChemInform;2010-08-21
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