Article ID Journal Published Year Pages File Type
5276339 Tetrahedron Letters 2007 6 Pages PDF
Abstract
An unusual syn-selective cyclisation of a TIPS-protected malic acid derived lactam is employed as the key step in an asymmetric synthesis of 3-demethoxyerythratidinone.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
An enantiospecific synthesis of (+)-demethoxyerythratidinone from (S)-malic acid: key observations concerning the diastereocontrol in malic acid-derived N-acyliminium ion cyclisations
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