@article { ISI:000323132100073,
	title = {Highly concise and practical route to clavaminols, sphinganine and (+)-spisulosine via indium mediated allylation of alpha-hydrazino aldehyde and a theoretical insight into the stereochemical aspects of the reaction},
	journal = {RSC Advances},
	volume = {3},
	number = {35},
	year = {2013},
	month = {JUL},
	pages = {15442-15448},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A conceptually different approach has been employed for the synthesis of 1,2-amino alcohols by proline-catalyzed alpha-amination of aldehyde and one-pot indium mediated allylation of the crude alpha-hydrazino aldehydes. DFT based quantum chemical calculations have been performed to obtain a quantitative explanation of the stereoselectivity of the reaction.</p>},
	issn = {2046-2069},
	doi = {10.1039/c3ra43048k},
	author = {Pandey, Menaka and Chowdhury, Partha Sarathi and Dutta, Achintya Kumar and Kumar, Pradeep and Pal, Sourav}
}
