The intramolecular enyne diels-alder reaction. Stereoselective construction of tricyclic dioxadienones and mechanistic outline
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
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4. Improved procedure for the synthesis of 6-alkoxy-2,3-dihydro-6h-pyran-3-ones (2,3-dideoxy-dl-pent-2-enopyranos-4-uloses). Neat conversion into polyfunctionalized cyclopentenones
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1. Sequential Morita–Baylis–Hillman/Achmatowicz reactions: an expeditious access to pyran-3(6H)-ones with a unique substitution pattern;Tetrahedron Letters;2015-11
2. The Achmatowicz Rearrangement – Oxidative Ring Expansion of Furfuryl Alcohols;Synthesis;2015-09-28
3. Recent Advances in Transition Metal-Catalyzed Glycosylation;ACS Catalysis;2012-07-05
4. ChemInform Abstract: Intramolecular Enyne Diels-Alder Reaction. Stereoselective Construction of Tricyclic Dioxadienones and Mechanistic Outline.;ChemInform;2010-08-19
5. Double Dehydro-Diels-Alder Reactions of 1,5-Dien-3-ynes;Chemistry - A European Journal;2009-12-02
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