Stereoselective synthesis of 5-alkyliden-6-aminotetrahydro-2-pyranones through an unexpected isomerization of the hydroxytetrahydro-2-pyridinones obtained by the selective reduction of acylated enaminones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. Selectivity in C-alkylation of dianions of acyclic β-enamino ketones
2. Reaction of dianions of acyclic β-enamino ketones with electrophiles. Part 2. Oxiranes: synthesis of γ′- and ε-hydroxy-β-enamino ketones and of α-tetrahydrofurylidene ketones
3. Reaction of dianion β-enamino ketones with electrophiles. Part 4. Synthesis of β′- and δ-hydroxy-β-enamino ketones.
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2. Selective Reduction ofortho-Acylated β-Enaminones of Homoveratryamine and Their Cyclization to 1,2,3,4-Tetrahydroisoquinolines with β-Enaminone Moiety;Synthetic Communications;2013-01
3. ChemInform Abstract: Stereoselective Synthesis of 5-Alkylidene-6-aminotetrahydro-2-pyranones Through an Unexpected Isomerization of the Hydroxytetrahydro-2-pyridinones Obtained by the Selective Reduction of Acylated Enaminones.;ChemInform;2010-06-22
4. α-Acyloxynitroso dienophiles in [4+2] hetero Diels–Alder cycloadditions: mechanistic insights;Tetrahedron;2010-04
5. Aza-annulation of β-enaminolactones: application to the synthesis of enantiopure difunctionalized bicyclic lactams;Tetrahedron Letters;2009-02
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