Asymmetric synthesis of (−)-bissetone via a highly enantioselective hetero-Diels–Alder reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference51 articles.
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4. Expedient conversion of d-glucose into 1,5-anhydro-d-fructose and into single stereogenic-center dihydropyranones, suitable six-carbon scaffolds for concise syntheses of the soft-coral constituents (−)-bissetone and (−)-palythazine
5. For reviews, see:
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1. Total synthesis and absolute configuration determination of Ktedonoketone, a benzenoid metabolite from Thermophilic bacterium;Tetrahedron Letters;2020-11
2. Corrigendum to “Asymmetric synthesis of (-)-bissetone via a highly enantioselective hetero-Diels-Alder reaction” [Tetrahedron 69/39 (2013) 8463-8469];Tetrahedron;2018-03
3. Diels-Alder Reaction;Kirk-Othmer Encyclopedia of Chemical Technology;2016-12-15
4. Carbocation Catalysis: Oxa-Diels-Alder Reactions of Unactivated Aldehydes and Simple Dienes;European Journal of Organic Chemistry;2015-09-18
5. The Asymmetric Hetero-Diels-Alder Reaction in the Syntheses of Biologically Relevant Compounds;Angewandte Chemie International Edition;2014-09-12
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