@article { ISI:000264061100021,
	title = {Cobalt(II) chloride hexahydrate-diisopropylamine catalyzed mild and chemoselective reduction of carboxylic esters with sodium borohydride},
	journal = {Synthesis-Stuttgart},
	number = {4},
	year = {2009},
	month = {FEB},
	pages = {660-664},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The cobalt-catalyzed reduction of unsaturated alpha-cyano carboxylic esters using sodium borohydride (NaBH(4)) leads to the corresponding saturated cyano alcohols in high yields. In particular, the new catalytic system cobalt(II) chloride-diisopropylamine in combination with NaBH(4) showed excellent activity in the chemoselective reduction of a variety of carboxylic esters to their corresponding alcohols in good to excellent yields under mild conditions.</p>},
	keywords = {Alcohols, amines, catalysis, Esters, reductions},
	issn = {0039-7881},
	doi = {10.1055/s-0028-1083353},
	author = {Jagdale, Arun R. and Paraskar, Abhimanyu S. and Sudalai, Arumugam}
}
@article { ISI:000350056800015,
	title = {Proline-catalyzed alpha-aminooxylation of beta-amino aldehydes: access to enantiomerically pure syn- and anti-3-amino-3-aryl-1,2-alkanediols},
	journal = {Synlett},
	volume = {26},
	number = {3},
	year = {2015},
	month = {FEB},
	pages = {355-358},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A new synthetic method for enantioselective synthesis of syn 3-amino-3-aryl-1,2-alkanediols via praline catalyzed alpha-aminaoxn y ylation of beta-amino aldehydes des are described. This methodology is successfully applied to a concise and protecting group-free asymmetric synthesis of (-)-cytoxazone (+)-epi-cytoxazone and formal synthesis of N-thiolated 2-oxazolidinone.</p>},
	keywords = {amino aldehydes, Asymmetric synthesis, catalysis, diastereoselectivity, Enantioselectivity, Natural product},
	issn = {0936-5214},
	doi = {10.1055/s-0034-1379735},
	author = {Venkataramasubramanian, V. and Kiran, I. N. Chaithanya and Sudalai, Arumugam}
}
