@article { ISI:000325006600012,
	title = {Synthesis of indolizidine, pyrrolizidine and quinolizidine ring systems by proline-catalyzed sequential alpha-amination and HWE olefination of an aldehyde},
	journal = {RSC Advances},
	volume = {3},
	number = {40},
	year = {2013},
	month = {AUG},
	pages = {18288-18291},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A general procedure for the synthesis of azabicyclic ring systems viz. indolizidine, pyrrolizidine and quinolizidine has been developed utilizing proline-catalyzed sequential alpha-amination and Horner-Wadsworth-Emmons (HWE) olefination of an aldehyde as the key step. This method can be further extended to the synthesis of various biologically active natural products containing azabicyclic ring systems.</p>},
	issn = {2046-2069},
	doi = {10.1039/c3ra42001a},
	author = {Kauloorkar, Shruti Vandana and Jha, Vishwajeet and Kumar, Pradeep}
}
