@article { ISI:000310215400007,
	title = {Conformational modulation of Ant-Pro oligomers using chirality alteration of proline residues},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {10},
	number = {42},
	year = {2012},
	month = {SEP},
	pages = {8426-8433},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Structural modulation of Ant-Pro (anthranilic acid-proline) oligomers has been carried out by chirality alteration of the proline residues. The results suggest that the chirality altered oligomers show well-defined helical conformation featuring nine-membered hydrogen bonding interactions - without compromising conformational rigidity.</p>},
	issn = {1477-0520},
	doi = {10.1039/c2ob26132d},
	author = {Kale, Sangram S. and Kotmale, Amol S. and Dutta, Achintya Kumar and Pal, Sourav and Rajamohanan, P. R. and Sanjayan, Gangadhar J.}
}
