@article {42616,
	title = {Efficient amano PS-catalyzed chemo-, regio- and enantioselective hydrolysis of (+/-)-2,3-di-O-acetyl-2-C-methyl-D-erythrono-1,4-lactone: a facile preparation of bioactive natural products (-)-saccharinic acid lactone and potassium (2R,3R)-2,3,4-trihydr},
	journal = {Tetrahedron-Asymmetry},
	volume = {17},
	year = {2006},
	month = {MAR},
	pages = {927-932},
	type = {Article},
	doi = {10.1016/j.tetasy.2006.02.025},
	author = {Gogoi, Sanjib and N. P. Argade}
}
@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:000321605900046,
	title = {Enantioselective total synthesis of desbromoarborescidines A-C and the formal synthesis of (S)-deplancheine},
	journal = {Journal of Organic Chemistry},
	volume = {78},
	number = {13},
	year = {2013},
	month = {JUL},
	pages = {6802-6808},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Starting from Boc-protected tryptamine and (S)-tetrahydro-5-oxo-2-furancarboxylic acid, facile enantioselective total synthesis of desbromoarborescidines A-C and the formal synthesis of (S)-deplancheine have been accomplished via a common intermediate (S)-indolo[2,3-a]quinolizine. Synthesis of enantiomerically pure (S)-acetoxyglutarimide, stereoselective reductive intramolecular cyclization, hydroxyl group assisted in situ N-Boc-deprotection, selective deoxygenation, of the xanthate ester, and lactam hydrolysis followed by an appropriate exchange of nitrogen regioselectivity in intramolecular cyclization were the decisive steps.</p>},
	issn = {0022-3263},
	doi = {10.1021/jo401079v},
	author = {Mondal, Pravat and N. P. Argade}
}
