@article {47408,
	title = {Enantioselective reduction of ketones and synthesis of 2-methyl-2,3-dihydro-1-benzofuran catalyzed by chiral spiroborate ester},
	journal = {Russian Journal of Organic Chemistry},
	volume = {57},
	year = {2021},
	month = {APR},
	pages = {611-618},
	type = {Article},
	abstract = {<p>Asymmetric reduction of homobenzylic ketones was achieved through the use of chiral spiroborate ester catalyst. The catalyst is applicable for both analytical and industrial purposes since it is not sensitive to air and moisture. A rapid synthetic route has been developed for the preparation of (S)-2-methyl-2,3-dihydro-1-benzofuran via enantioselective reduction of homobenzylic ketone in the presence of a chiral spiroborate catalyst as the key step.</p>},
	keywords = {2-methyl-2, 3-dihydro-1-benzofuran, asymmetric reduction, spiroborate ester},
	issn = {1070-4280},
	doi = {10.1134/S1070428021040163},
	author = {Patil, H. S. and Nikalje, M. D. and Chopade, A. U. and Chopade, M. U.}
}
