@article { ISI:000276804800005,
	title = {Synthesis of (-)-galantinic acid via iterative hydrolytic kinetic resolution and tethered aminohydroxylation},
	journal = {Tetrahedron},
	volume = {66},
	number = {17},
	year = {2010},
	month = {APR},
	pages = {3159-3164},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new synthetic strategy for (-)-galantinic acid is reported using iterative hydrolytic kinetic resolution and tethered aminohydroxylation as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {1, 2-Aminoalcohol, 3-Diol, Iterative hydrolytic kinetic resolution, selectivity, Tethered aminohydroxylation},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2010.02.093},
	author = {Dubey, Abhishek and Kauloorkar, Shruti Vandana and Kumar, Pradeep}
}
@article {46091,
	title = {Tf2NH catalyzed 1,6-conjugate addition of 2-hydroxy-p-quinone methides with -functionalized ketones: access to 2,3,4,9-Tetrahydro-1H-xanthenones and 4H-Chromene Derivatives},
	journal = {European Journal of Organic Chemistry},
	year = {2019},
	month = {JUN },
	pages = {3127-3133},
	type = {Article},
	abstract = {<p>A Bronsted acid catalyzed tandem 1,6-conjugate sequential cycloaddition reaction using 2-hydroxy-p-quinone methides and -functionalized ketones is reported. The method allows xanthenones and chromenes to be accessed in moderate to excellent yield with broad substrate scope, which could be further functionalized to give a versatile set of products.</p>
},
	keywords = {-Functionalized ketone, 1, 6-Conjugated addition, Bronsted acid, Chromenes, Xanthenones},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201900370},
	author = {Satbhaiya, Shruti and Khonde, Nilesh S. and Rathod, Jayant and Gonnade, Rajesh and Kumar, Pradeep}
}
@article {47588,
	title = {Metal-free, Tf2NH-catalyzed 1, 6-conjugate addition of imidazopyridine to para-quinone methides: easy access to C3-functionalized triarylmethane imidazopyridine},
	journal = {Tetrahedron},
	volume = {101},
	year = {2021},
	month = {NOV},
	pages = {132510},
	type = {Article},
	abstract = {An inexpensive and commercially available Tf2NH-catalyzed 1,6-conjugate addition of imidazopyridine (IMPY) heterocycles to para-quinone methides (p-QMs) is reported. The present transformation provides a diverse class of C3-functionalized triarylmethanes heterocyclic derivatives of imidazopyridine. These metal-free transformations provided a very broad substrate scope of conjugate addition product with a high yield up to 97\% within a short duration. (C) 2021 Elsevier Ltd. All rights reserved.},
	keywords = {1, 6-Conjugate addition, Bronsted acid, C3-functionalization, Imidazopyridine, para-Quinone methide},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2021.132510},
	author = {Khonde, Nilesh S. and Said, Madhukar S. and Sabane, Jagjivan K. and Gajbhiye, Jayant M. and Kumar, Pradeep}
}
