Article ID Journal Published Year Pages File Type
9565944 Tetrahedron Letters 2005 4 Pages PDF
Abstract
An enantioselective synthesis of substituted 2-methyl chromans was accomplished in four steps using four sequential Pd-catalyzed reactions. A study in the key palladium-catalyzed regioselective aryl ether ring formation of two different substrates was also carried out.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
A highly efficient enantioselective synthesis of 2-methyl chromans via four sequential palladium-catalyzed reactions
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