@article { ISI:000321573300021,
	title = {Total synthesis of umuravumbolide and hyptolide through silicon-tethered ring-closing metathesis},
	journal = {European Journal of Organic Chemistry},
	volume = {2013},
	number = {21},
	year = {2013},
	month = {JUL},
	pages = {4586-4593},
	publisher = {WILEY-V C H VERLAG GMBH},
	address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY},
	abstract = {<p>The total synthesis of umuravumbolide and hyptolide has been achieved in a efficient manner by using temporary silicon-tethered ring-closing metathesis and cross-coupling reactions as key steps. The stereogenic centres were generated by means of proline-catalysed -aminoxylation of aldehydes and Brown{\textquoteright}s asymmetric allylation method.</p>},
	keywords = {lactones, Metathesis, Silanes, synthetic methods, Total synthesis, Wittig reactions},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201300302},
	author = {Chowdhury, Partha Sarathi and Kumar, Pradeep}
}
@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}
}
