@article {43308,
	title = {Antimicrobial activity of a new series of Bis(isoxazoline),Bis(isoxazole)and their derivatives},
	journal = {International Journal of Chemical and Physical Sciences},
	volume = {1},
	year = {2014},
	month = {JAN},
	pages = {1-4},
	type = {Article},
	abstract = {<p>A series of 1,1-bis [2-hydroxy-3-(5{\textquoteright}-aryl-isoxazoline-3-yl)-5-methyl phenyl] methane and 1,1-bis [2-hydroxy-3-(5{\textquoteright}-aryl-isoxazol-3-yl)-5-methyl phenyl] methane derivatives were evaluated for their antimicrobial activity against some selected pathogenic micro-organisms such as Gram-positive bacteria, Staphylococcus aureus, Citrobacter frundii, Bacillus megatherium and Gram-negative bacteria Staphyloccus aureus, Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Enterobacter aerogenes, Salmonella typhi, Proteus vulgaris.</p>},
	author = {Gajbhiye, Jayant M. and Chopade, A. U.}
}
@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.}
}
