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Published in 2020 at "Chemical communications"
DOI: 10.1039/d0cc03285a
Abstract: An unprecedented gold(i)-catalyzed cyclization of cyclopropylidene-tethered propargylic alcohols via a 6-endo-dig enyne cyclization followed by a ring-opening of cyclopropane and nucleophilic closure reaction to construct naphtho[2,3-c]pyrans was developed. This transformation represents a highly efficient method…
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Keywords:
cyclization cyclopropylidene;
tethered propargylic;
cyclization;
propargylic alcohols ... See more keywords