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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c01341
Abstract: Here, a facile and selective synthesis method for cationic azatriphenylene derivatives was established by electrochemical intramolecular cyclization, where atom-economical C–H pyridination without a transition-metal catalyst or an oxidant is a key step. The proposed protocol…
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Keywords:
cationic azatriphenylene;
azatriphenylene derivatives;
pyridination;
synthesis cationic ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b03164
Abstract: A novel domino oxidative annulation of 2-vinylanilines with internal alkynes was developed to constitute a rare class of cyclopentaquinoline derivatives. This transformation encompasses four σ bonds formation, one quaternary carbon center construction, and pyridination steps…
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Keywords:
domino;
pyridination;
palladium catalyzed;
alkenylation amination ... See more keywords