Enantiospecific synthesis of tetrasubstituted δ-lactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Metabolic Products of Microorganisms. Part 265. Prelactones C and B, oligoketides fromStreptomyces producing concanamycins and bafilomycins
2. Biosynthesis of Erythromycin and Rapamycin
3. Repositioning of a Domain in a Modular Polyketide Synthase to Promote Specific Chain Cleavage
4. Engineered biosynthesis of a triketide lactone from an incomplete modular polyketide synthase
5. A mutant generated by expression of an engineered DEBS 1 protein from the erythromycin-producing polyketide synthase (PKS) in Streptomyces coelicolor produces the triketide as a lactone, but the major product is the nor-analogue derived from acetate as starter acid
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3. Rapid access to the synthesis of polysubstituted delta-lactones via tandem stereoselective conjugate addition/a-alkylation of unsaturated 7,3-1actone-alpha-D-xy1ofuranose derivative;TETRAHEDRON LETT;2013
4. Rapid access to the synthesis of polysubstituted δ-lactones via tandem stereoselective conjugate addition/α-alkylation of unsaturated 7,3-lactone-α-d-xylofuranose derivative;Tetrahedron Letters;2013-10
5. Aldol reactions mediated by a tetrahedral boronate;Chem. Commun.;2013
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