@article { ISI:000242059100038,
	title = {Nazarov reagent: a novel reagent for the synthesis of natural products},
	journal = {Synlett},
	number = {17},
	year = {2006},
	month = {OCT},
	pages = {2853-2854},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	issn = {0936-5214},
	doi = {10.1055/s-2006-950248},
	author = {Kaur, Tanpreet}
}
@article { ISI:000246431300013,
	title = {Efficient one-pot synthesis of alpha-amino phosphonates catalyzed by bismuth nitrate pentahydrate},
	journal = {Synlett},
	number = {5},
	year = {2007},
	month = {MAR},
	pages = {745-748},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A simple, efficient, and environmentally benign method has been developed for the synthesis of alpha-amino phosphonates through a one-pot reaction of aldehydes with amines and diethyl phosphite in the presence of bismuth nitrate pentahydrate as a catalyst. Some of the major advantages of this protocol are: good yields, the involvement of a less-expensive and non-toxic catalyst, mild and solvent-free reaction conditions and also tolerance towards other functional groups present in the substrates. Eighteen examples are described, highlighting the substrate scope of the reaction.</p>},
	keywords = {aldehydes, alkyl phosphite, alpha-amino phosphonates, amines, bismuth nitrate pentahydrate, synthetic methods},
	issn = {0936-5214},
	doi = {10.1055/s-2007-970762},
	author = {Bhattacharya, Asish K. and Kaur, Tanpreet}
}
@article { ISI:000275756700010,
	title = {Synthesis of the antibacterial benzoquinone primin and its water-soluble analogue, primin acid},
	journal = {Synthesis-Stuttgart},
	number = {7},
	year = {2010},
	month = {APR},
	pages = {1141-1144},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The biologically active natural product, primin and its water-soluble acid analogue, primin acid are prepared in 34\% and 25\% overall yields, respectively, from a common intermediate using a Grignard reaction and a Johnson-Claisen rearrangement as the key steps.</p>},
	keywords = {1, 4-benzoquinones, Antibacterial, Johnson-Claisen rearrangement, primin, primin acid},
	issn = {0039-7881},
	doi = {10.1055/s-0029-1218666},
	author = {Bhattacharya, Asish K. and Kaur, Tanpreet and Ganesh, Krishna N.}
}
