@article { ISI:000341938100024,
	title = {Total syntheses of D-allo-1-deoxynojirimycin and L-talo-1-deoxynojirimycin via reductive cyclization},
	journal = {RSC Advances},
	volume = {4},
	number = {77},
	year = {2014},
	month = {AUG},
	pages = {40852-40858},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Synthesis of a polyhydroxypiperidine framework for L-talo-1-deoxynojirimycin and D-allo-1-deoxynojirimycin was achieved from L-tartaric acid by employing flash dihydroxylation and reductive lactamisation as the key steps.</p>},
	issn = {2046-2069},
	doi = {10.1039/c4ra06884j},
	author = {Chavan, Subhash P. and Dumare, Nilesh B. and Pawar, Kailash P.}
}
@article { ISI:000352671600006,
	title = {Total synthesis of (R)-lipoic acid and (S)-lipoic acid via an Mn (III)-salen-catalyzed oxidative kinetic resolution},
	journal = {Tetrahedron-Asymmetry},
	volume = {26},
	number = {5-6},
	year = {2015},
	month = {MAR},
	pages = {281-287},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The asymmetric synthesis of both the antipodes of alpha-lipoic acid is described. The total synthesis of racemic and asymmetric lipoic acid is achieved from propane 1,3-diol. This work reports the use of Mn (III)-salen-catalyzed oxidative kinetic resolution as the key step to obtain enantiomerically pure (R)- and (S)-lipoic acid. The undesired product formed during the resolution can be recycled to achieve the desired isomer. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2015.02.001},
	author = {Purude, Abhijeet N. and Pawar, Kailash P. and Patil, Niteen B. and Kalkote, Uttam R. and Chavan, Subhash P.}
}
