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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b02881
Abstract: A highly regio- and diastereoselective visible-light-promoted [2 + 2] cycloaddition between readily available 1,4-dihydropyridines and olefins has been developed. This strategy is operationally simple and atom-economical and enables the construction of strained polysubstituted 2-azabicyclo[4.2.0]octanes with…
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Keywords:
cycloaddition dihydropyridines;
energy transfer;
intermolecular cycloaddition;
dihydropyridines olefins ... See more keywords