@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: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.}
}
@article { ISI:000342927000001,
	title = {Concise account of the chemistry of valuable alkyl(methyl)maleic anhydrides},
	journal = {Synthesis-Stuttgart},
	volume = {46},
	number = {20},
	year = {2014},
	month = {OCT},
	pages = {2683-2700},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Review},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A large number of significant bioactive natural and synthetic alkyl(methyl)maleic anhydrides are known in the contemporary literature. A broad range of suitably functionalized substrates have been tailored to accomplish concise and efficient syntheses of an array of alkyl(methyl)maleic anhydrides employing a variety of elegant synthetic strategies. This review presents a brief literature account of the isolation and activity of these important target compounds with a special emphasis on their synthesis.</p>},
	keywords = {alkyl(methyl)maleic anhydrides, bioactivity, dimethylmaleic anhydride, isolation, nucleophilic reactions, Total synthesis},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1378665},
	author = {Deore, Prashant S. and Haval, Kishan P. and Gadre, Smita R. and N. P. Argade}
}
