biblio
“Conformational modulation of Ant-Pro oligomers using chirality alteration of proline residues”, Organic & Biomolecular Chemistry, vol. 10, no. 42, pp. 8426-8433, 2012.
, “Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding”, Chemical Communications, vol. 48, no. 71, pp. 8922-8924, 2012.
, “Multifaceted folding in a foldamer featuring highly cooperative folds”, Chemical Communications, vol. 48, no. 91, pp. 11205-11207, 2012.
, “Unusual conformational similarity of two peptide folds featuring sulfonamide and carboxamide on the backbone”, Chemical Communications, vol. 48, no. 78, pp. 9747-9749, 2012.
, “Carboxamide versus sulfonamide in peptide backbone folding: a case study with a hetero foldamer”, Organic Letters, vol. 15, no. 7, pp. 1504-1507, 2013.
, “Ester vs. amide on folding: a case study with a 2-residue synthetic peptide”, Organic & Biomolecular Chemistry, vol. 11, no. 48, pp. 8348-8356, 2013.
, “Orthanilic acid-promoted reverse turn formation in peptides”, Chemical Communications, vol. 49, no. 22, pp. 2222-2224, 2013.
, “Synthetic zipper peptide motif orchestrated via co-operative interplay of hydrogen bonding, aromatic stacking, and backbone chirality”, Journal of the American Chemical Society, vol. 135, no. 31, pp. 11477-11480, 2013.
, “Formation of a pseudo-beta-hairpin motif utilizing the Ant-Pro reverse turn: consequences of stereochemical reordering”, Organic & Biomolecular Chemistry, vol. 12, no. 5, pp. 774-782, 2014.
, “Probing the folding induction ability of orthanilic acid in peptides: some observations”, RSC Advances, vol. 4, no. 25, pp. 13018-13025, 2014.
, “Bile acid hydrazides: gelation, structural, physical and spectroscopic properties”, New Journal of Chemistry, vol. 39, no. 1, pp. 453-460, 2015.
, “Conformational modulation of peptides using beta-amino benzenesulfonic acid ((S)Ant)”, Organic & Biomolecular Chemistry, vol. 13, no. 7, pp. 2087-2091, 2015.
, “Reversal of H-bonding direction by N-sulfonation in a synthetic reverse-turn peptide motif”, Organic & Biomolecular Chemistry, vol. 13, no. 10, pp. 3064-3069, 2015.
, “Role of N-terminal proline in stabilizing the Ant-Pro zipper motif”, New Journal of Chemistry, vol. 39, no. 5, pp. 3327-3332, 2015.
, “3-Aminothiophenecarboxylic acid (3-Atc)-induced folding in peptides”, New Journal of Chemistry, vol. 40, no. 11, pp. 9205-9210, 2016.
, “Angiotensin II analogs comprised of pro-amb (gamma-turn scaffold) as angiotensin II type 2 (AT(2)) receptor agonists”, Chemical Communications, vol. 52, no. 8, pp. 1645-1648, 2016.
, “Bronsted-acid-mediated divergent reactions of betti bases with indoles: an approach to chromeno[2,3-b]indoles through intramolecular dehydrogenative C2-alkoxylation of indole”, European Journal of Organic Chemistry, no. 20, pp. 3441-3448, 2016.
, “Disruption of native beta-turns: consequence of folding competition between native and orthanilic acid proline-based pseudo beta-turn”, European Journal of Organic Chemistry, no. 7, pp. 1380-1388, 2016.
, “Residue dependent hydrogen-bonding preferences in orthanilic acid-based short peptide beta-turn motifs”, RSC Advances, vol. 6, no. 42, pp. 35328-35331, 2016.
, “Coumarin-appended stable fluorescent self-complementary quadruple-hydrogen-bonded molecular duplexes”, Journal of Organic Chemistry, vol. 82, no. 12, pp. 6403-6408, 2017.
, “Structural insights into the hydrogen-bonding and folding pattern in ant-ant-pro-gly tetrapeptides”, European Journal of Organic Chemistry, no. 20, pp. 2944–2949, 2017.
, “Three in one: prototropy-free highly stable AADD-type self-complementary quadruple hydrogen-bonded molecular duplexes with built-in fluorophore”, Chemical Communications, vol. 53, no. 18, 2017.
, “Triazine-based highly stable AADD-type self-complementary quadruple hydrogen-bonded systems devoid of prototropy”, Chemistry-A European Journal, vol. 23, no. 4, pp. 783-787, 2017.
, “Conformational studies of Ant-Pro motif-incorporated cyclic peptides: gramicidin S and avellanin”, New Journal of Chemistry, vol. 42, no. 2, pp. 1197-1201, 2018.
, “Helically structured peptide architecture engineered using dimedone as a rigid organic scaffold”, ChemistrySelect, vol. 3, no. 10, pp. 2776-2780, 2018.
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