Total synthesis of (+)-decarestrictine L
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
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3. Secondary metabolites by chemical screening. 9. Decarestrictines, a new family of inhibitors of cholesterol biosynthesis from Penicillium. II. Structure elucidation of the decarestrictines A to D.
4. Improved Syntheses of Both Enantiomers of 1,2,5,6-Diepoxyhexane from (2S,5S)-1,2,5,6-Hexanetetrol
5. General entry to the 3,5-disubstituted indolizidine class of dendrobatid alkaloids. Total syntheses of both enantiomers of indolizidines 195B, 223AB, 239AB, and 239CD from a common chiral synthon
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1. Synthesis and stereochemistry of decarestrictines H and J;Tetrahedron;2017-03
2. Preparation of cis-Fused Tetrahydropyranyl Lactones via Palladium-Catalysed Cyclocarbonylation of Enediols;Synthesis;2016-10-14
3. Stereoselective synthesis of (−)-decarestrictine G;Tetrahedron;2015-05
4. Asymmetric Hydroformylation-Initiated Tandem Sequences for Syntheses of (+)-Patulolide C, (−)-Pyrenophorol, (+)-Decarestrictine L, and (+)-Prelog Djerassi Lactone;The Journal of Organic Chemistry;2014-12-01
5. A Chemoenzymatic Synthesis of Hept-6-ene-2,5-diol Stereomers: Application to Asymmetric Synthesis of Decarestrictine L, Pyrenophorol, and Stagonolide E;The Journal of Organic Chemistry;2014-08-19
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