@article { ISI:000339494600024,
	title = {Stereoselective approach to 2,6-disubstituted piperidin-3-ol: synthesis of (-)-deoxoprosopinine and (+)-deoxoprosophylline},
	journal = {European Journal of Organic Chemistry},
	number = {22},
	year = {2014},
	month = {AUG},
	pages = {4897-4902},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>A simple and highly efficient approach to an enantioenriched 2,6-disubstituted piperidin-3-ol skeleton is developed from an aldehyde as a starting material by using organocatalytic and asymmetric dihydroxylation as the key steps. Its application to the total synthesis of (-)-deoxoprosopinine and (+)-deoxoprosophylline is also reported.</p>},
	keywords = {alkaloids, Amination, Amino alcohols, synthetic methods, Wittig reactions},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201402363},
	author = {Jha, Vishwajeet and Kauloorkar, Shruti Vandana and Kumar, Pradeep}
}
