@article { ISI:000241906100003,
	title = {Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides},
	journal = {Chemical Reviews},
	volume = {106},
	number = {11},
	year = {2006},
	month = {NOV},
	pages = {4484-4517},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	issn = {0009-2665},
	doi = {10.1021/cr050011g},
	author = {Pandey, Ganesh and Banerjee, Prabal and Gadre, Smita R.}
}
@article { ISI:000241435600021,
	title = {Convergent approach toward the synthesis of the stereoisomers of C-6 homologues of 1-deoxynojirimycin and their analogues: evaluation as specific glycosidase inhibitors},
	journal = {Journal of Organic Chemistry},
	volume = {71},
	number = {22},
	year = {2006},
	month = {OCT},
	pages = {8481-8488},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A new and stereoselective strategy is developed to synthesize an appropriate template 9 to obtain C-6 homologues of 1-deoxyazasugars such as 1-deoxy-D-galactohomonojirimycin ( 5), 1-deoxy-4-hydroxymethyl-D-glucohomonojirimycin (6), and their enantiomers. The template 9 is also used to obtain neutral nonbasic pseudo-glyconolactam (8), C-4 amino, and methyl analogues of 1-deoxy- homonojirimycin as new analogues of 1- deoxyhomoazasugars. Compound 5 is found to be a potent and specific inhibitor to alpha-galactosidase (K-i = 1.7 mu M). Similarly compounds 6 (K-i = 28 mu M), ent-5 (K-i = 129 mu M), and ent-6 K-i = 12 mu M) exhibited specific inhibition of beta-glucosidase.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo061455v},
	author = {Pandey, Ganesh and Dumbre, Shrinivas G. and Khan, Mohammad Islam and Shabab, M.}
}
@article { ISI:000287163000011,
	title = {Construction of the 5,10b-phenanthridine skeleton using [3+2]-cycloaddition of a non-stabilized azomethine ylide: total synthesis of (+/-)-maritidine and (+/-)-crinine alkaloids},
	journal = {European Journal of Organic Chemistry},
	number = {4},
	year = {2011},
	month = {FEB},
	pages = {740-750},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY},
	abstract = {<p>Vicinal quaternary and tertiary stereocenters of the 5,10b-phenanthridine skeleton 1 are constructed simultaneously in one step by the [3+2]-cycloaddition of non-stabilized azomethine ylide 9, generated by sequential double desilylation of 10 utilizing silver(I) fluoride as a one-electron oxidant. The regioas well as stereochemical origin of this cycloaddition reaction is explained through a favorable transition state 9{\textquoteright}{\textquoteright}. The strategy is successfully applied for the total synthesis of the biologically active alkaloids (+/-)-maritidine (1a), (+/-)-crinine (1b), and their analogues (1d, 1e, and 1f).</p>},
	keywords = {alkaloids, Azomethine ylides, Cycloaddition, Natural products, Ylides},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201001263},
	author = {Pandey, Ganesh and Gupta, Nishant R. and Gadre, Smita R.}
}
