Regioselective reductions of 23-epoxy acetals with lithium aluminum hydride: A reinvestigation.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Losco, P.; PhD Thesis, in preparation.
2. Regioselective reductions of 2,3-epoxy acetals with zinc-chlorotrimethylsilane and lithium aluminium hydride: convenient synthesis of 1,2 and 1,3-diones
3. 1,3‐Cyclopentandion — ein vielbegehrtes Reagens
4. Conversion of 3-Acetoxy-6-acetoxymethyl-2H-pyran-2-one to Cyclopentenone Derivatives and 1,3-Cyclopentanedione
5. Bromohydrin formation in dimethyl sulfoxide
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2. 8.29 Reduction of Epoxides;Comprehensive Organic Synthesis II;2014
3. ChemInform Abstract: Regioselective Reductions of 2,3-Epoxy Acetals with Lithium Aluminum Hydride: A Reinvestigation.;ChemInform;2010-08-20
4. Total synthesis of (±)-stemonamide, (±)-isostemonamide, (±)-stemonamine, and (±)-isostemonamine using a radical cascade;Tetrahedron;2008-09
5. Total Synthesis of (±)-Stemonamide and (±)-Isostemonamide Using a Radical Cascade;Organic Letters;2007-12-20
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