@article { ISI:000288848900018,
	title = {Efficient convergent access to spiroketal segment of (+)-spiroxaline methyl ether},
	journal = {Synthesis-Stuttgart},
	volume = {2},
	number = {7},
	year = {2011},
	month = {APR},
	pages = {1137-1141},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Starting from trimethylsilylacetylene, a facile synthesis of optically pure spiroketal unit of (+)-spiroxaline methyl ether has been described. The synthesis entails stepwise alkylation and acylation of an alkyne with two different readily available chiral building blocks followed by the reductive in situ regio- and stereoselective spiroketalization pathway.</p>},
	keywords = {(+)-spiroketal segment synthesis, (R)-gamma-valerolactone, (R)-oxirane, alkyne, nucleophilic reactions},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1258456},
	author = {Singh, Mandeep and N. P. Argade}
}
@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}
}
