Selective bis-hydride reduction of tosylmethyl-substituted tricyclic enones by lithium aluminium hydride synthesis of α-methylene cyclopentenoids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Silver(I)-Catalyzed Ring-Contractive Rearrangement: A New Entry to 5-Alkylidene-2-cyclopentenones;Organic Letters;2014-12-01
2. Derivatives of 7-oxabicyclo[2.2.1]heptane in nature and as useful synthetic intermediates;Tetrahedron;1999-11
3. Synthetic applications of flash vacuum pyrolysis;Contemporary Organic Synthesis;1996
4. ChemInform Abstract: Selective Bis-hydride Reduction of Tosylmethyl-Substituted Tricyclic Enones by Lithium Aluminum Hydride. Synthesis of α-Methylene Cyclopentenoids.;ChemInform;1990-03-13
5. Menthol mediated optical resolution of 10-oxatricyclodecadienones. Application in the enantioselective synthesis of cyclopentenoids;Tetrahedron;1990
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