@article { ISI:000328606500014,
	title = {One-pot synthesis of cyclic carbonates from aldehydes, sulfur ylide, and CO2},
	journal = {Synlett},
	volume = {25},
	number = {1},
	year = {2014},
	month = {JAN},
	pages = {97-101},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Treatment of aldehydes with sulfur ylide (CH2=SOMe2 or CH2=SMe2), in the presence of CO2 (1 atm) bubbled sequentially under mild conditions, produces cyclic carbonates in preparative yields. Sodium iodide formed in situ promotes the reaction between epoxide as intermediate and CO2 at ambient conditions, thus constituting a powerful metal-free synthesis of organic cyclic carbonates directly from aldehydes.</p>},
	keywords = {Carbon dioxide, cyclic carbonates, cyclization, epoxides, Insertion},
	issn = {0936-5214},
	doi = {10.1055/s-0033-1340072},
	author = {Aher, Ravindra D. and Kumar, B. Senthil and Sudalai, Arumugam}
}
@article { ISI:000359136500087,
	title = {Organocatalytic [4+1]-annulation approach for the synthesis of densely functionalized pyrazolidine carboxylates},
	journal = {RSC Advances},
	volume = {5},
	number = {80},
	year = {2015},
	month = {JUL},
	pages = {65554-65559},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A novel one-pot [4+1]-annulation process for the asymmetric synthesis of densely functionalized pyrazolidine carboxylates is described. The in situ generated gamma-hydrazino-alpha,beta-unsaturated ester obtained via proline catalysis acts as a four-atom component, and Corey{\textquoteright}s sulfur ylide or ethyl bromoacetate acts as a one-atom carbon source to construct pyrazolidine carboxylate units in a highly enantio- and diastereoselective fashion.</p>},
	issn = {2046-2069},
	doi = {10.1039/c5ra09583b},
	author = {Lalwani, Komal G. and Aher, Ravindra D. and Sudalai, Arumugam}
}
