@article { ISI:000352463200027,
	title = {Total synthesis of sinenside A},
	journal = {Organic Letters},
	volume = {17},
	number = {7},
	year = {2015},
	month = {APR},
	pages = {1724-1727},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of norlignan glucoside sinenside A has been accomplished. An intramolecular acetalization reaction has been employed as the key skeletal construct to forge the central cyclic disaccharide core. The trans-1,2-diol configuration present in the cyclic disaccharide of this natural product is unique and has been addressed by setting this configuration at the beginning. A 1,2-orthoester group has been selected as a handle for both sp glycosidation and for differentiation of the C2{\textquoteright}-OH (that participates in the key acetalization reaction) of the sugar unit.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.5b00505},
	author = {Vadhadiya, Paresh M. and Ramana, Chepuri V.}
}
