@article {45947,
	title = {Chirality induction and chiron approaches to enantioselective total synthesis of alpha-lipoic acid},
	journal = {Tetrahedron},
	volume = {71},
	year = {2015},
	month = {JUN },
	pages = {4213-4218},
	type = {Article},
	abstract = {<p>An efficient, short and convenient asymmetric synthesis of (R)-(+)-lipoic acid in seven steps from chiral hydroxy aldehyde with 32.5\% overall yield is described. Synthesis of S and R enantiomers of a-lipoic acid from cis-1,4-butene diol derived chiral lactone is reported with 34 \% overall yield. The present synthesis involves use of simple reaction conditions making it a convenient synthesis. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Chiral pool, Chirality induction, enantioselective, Lipoic acid, sharpless asymmetric dihydroxylation},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2015.04.090},
	author = {Chavan, Subhash P. and Pawar, Kailash P. and Praveen, Ch and Patil, Niteen B.}
}
@article { ISI:000377612300010,
	title = {Asymmetric total synthesis of L-allo-1-deoxynojirimycin},
	journal = {Arkivoc},
	number = {2},
	year = {2016},
	month = {OCT},
	pages = {137-147},
	publisher = {ARKAT USA INC},
	address = {C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA},
	abstract = {<p>Asymmetric total synthesis of L-allo-1-deoxynojirimycin (L-allo-DNJ) was achieved from cis-butene-1,4-diol by employing Sharpless asymmetric dihydroxylation, stereoselective flash dihydroxylation and ring enlargement reactions as key steps.</p>},
	keywords = {diastereoselective flash dihydroxylation, ring-enlargement reaction, sharpless asymmetric dihydroxylation},
	issn = {1551-7004},
	doi = {10.3998/ark.5550190.p009.295},
	author = {Chavan, Subhash P. and Dumare, Nilesh B. and Pawar, Kailash P. and Chavan, Prakash N. and Khairnar, Lalit B.}
}
