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Published in 2025 at "Organic Letters"
DOI: 10.1021/acs.orglett.5c02006
Abstract: We report a new method for the enantio- and diastereoselective synthesis of α-allene quaternary centers in fully substituted cyclohexanones at the α-positions. This reaction involves asymmetric 1,2-carbonyl addition to 2-O-propargyl enones using a mixture of…
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Keywords:
addition propargyl;
synthesis allene;
allene quaternary;
propargyl claisen ... See more keywords