@article { ISI:000325738700001,
	title = {Sugar furanoid trans-vicinal diacid as a gamma-turn inducer: synthesis and conformational study},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {11},
	number = {40},
	year = {2013},
	month = {OCT},
	pages = {6874-6878},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A simple method for the synthesis of a sugar furanoid trans vicinal diacid and its incorporation into the N-terminal tetrapeptide sequence (H-Phe-Trp-Lys-Thr-OH) to get glycopeptide 8 has been described. 2D NMR and MD simulation studies of 8 clearly show that the sugar diacid adopts a gamma-turn conformation towards the N-terminus.</p>},
	issn = {1477-0520},
	doi = {10.1039/c3ob41462k},
	author = {Vangala, Madhuri and Dhokale, Snehal A. and Gawade, Rupesh L. and Pattuparambil, Rajamohanan R. and Puranik, Vedavati G. and Dhavale, Dilip D.}
}
