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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02860
Abstract: In the presence of TiCl3, the reductive cyclization of tetrasubstituted enol esters bearing a 2-(ortho-nitroaryl) substituent affords 3-acyloxy-2,3-disubstituted indolenines in good yields. A domino process involving the partial reduction of nitro to a nitroso group…
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Keywords:
reductive cyclization;
acyloxyindolenines ticl3;
synthesis acyloxyindolenines;
ortho nitroaryl ... See more keywords