Total Synthesis of (−)-Hymenosetin

Biological Products Cycloaddition Reaction Molecular Structure Stereoisomerism 01 natural sciences Pyrrolidinones 0104 chemical sciences
DOI: 10.1021/acs.joc.5b02526 Publication Date: 2015-12-04T22:39:08Z
ABSTRACT
AbstractHymenosetin (I) and its N‐methyl analogue are prepared in 11 and 8 steps, respectively, from citronellal employing an intramolecular Diels‐Alder reaction as the key step.
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