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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02658
Abstract: A highly efficient method for the enantioselective build of spiro[1-indanone-5,2'-γ-butyrolactones] has been developed through the tandem Michael/transesterification reaction of α-hydroxy-1-indanone and α,β-unsaturated esters. A broad range of spiro(1-indanone-butyrolacones) with contiguous stereocenters have been synthesized with…
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Keywords:
hydroxy indanone;
spiro indanone;
reaction hydroxy;
indanone butyrolactones ... See more keywords