Enantioselective organocatalytic domino synthesis of tetrahydropyridin-2-ols.
摘要：
A series of tetrahydropyridin-2-ols (III) is obtained by a Michael addition-hemiaminalization reaction sequence of enaminones (I) with enals (II).
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关键词：
pyridine derivatives diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism organocatalysis
DOI：
10.1002/chin.201303141
被引量：
年份：
2013
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