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Published in 2019 at "Synthetic Communications"
DOI: 10.1080/00397911.2019.1704009
Abstract: Abstract A series of spirooxindoles have been synthesized through 1,3-dipolar cycloaddition of an azomethine ylide generated from isatin and sarcosine or L-proline with the dipolarophile (E)-3-(2-cyclopropyl-5-(4-fluorophenyl) quinolin-3-yl)-1-phenylprop-2-en-1-one derivatives. The stereochemistry of the cycloadducts was assigned…
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Keywords:
fluorophenyl quinoline;
cyclopropyl fluorophenyl;
analogues cyclopropyl;
synthesis spirooxindole ... See more keywords