@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}
}
