Stereospecific construction of substituted piperidines. Synthesis of (−)-paroxetine and (+)-laccarin
Chemical Communications2007Iss. 7, pp. 728–730
Citations Over TimeTop 10% of 2007 papers
Abstract
Short and efficient enantioselective syntheses of (-)-paroxetine and (+)-laccarin are described based on the highly stereospecific cleavage of C(3)-substituted 1,3-cyclic sulfamidates.
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