@article { ISI:000350674400031,
	title = {Reversal of H-bonding direction by N-sulfonation in a synthetic reverse-turn peptide motif},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {13},
	number = {10},
	year = {2015},
	month = {MAR},
	pages = {3064-3069},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>This communication depicts an intriguing example of hydrogen-bonding reversal upon introduction of a sulfonamide linkage at the N-terminus of a synthetic reverse-turn peptide motif. The ready availability of two sulfonyl oxygen atoms, as hydrogen-bonding acceptors, combined with the inherent twisted conformation of sulfonamides are seen to act as switches that engage/disengage the hydrogen-bond at the sticky ends/termini.</p>},
	issn = {1477-0520},
	doi = {10.1039/c4ob02438a},
	author = {Vijayadas, Kuruppanthara N. and Kotmale, Amol S. and Thorat, Shridhar H. and Gonnade, Rajesh G. and Nair, Roshna V. and Rajamohanan, Pattuparambil R. and Sanjayan, Gangadhar J.}
}
