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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c00630
Abstract: Ylidenenorbornadienes (YNDs), prepared by [4 + 2] cycloadditions between fulvenes and acetylene carboxylates, react with beta-mercaptoethanol to yield a mixture of four diastereomers. These four diastereomers fragment via a retro-[4 + 2] cycloaddition at differing…
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Keywords:
fragmentation;
ylidenenorbornadiene carboxylates;
experimental kinetic;
analysis nucleophile ... See more keywords