Drupal-Biblio17<style face="normal" font="default" size="100%">Preorganizing linear (self-complementary) quadruple hydrogen-bonding arrays using intramolecular hydrogen bonding as the sole force</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hybrid foldamer with unique architecture from conformationally constrained aliphatic-aromatic amino acid conjugate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of 4-aminomethyl-tetrahydrofuran-2-carboxylates with 2,4-cis and 2,4-trans relationships</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective syntheses of (-)-pinellic acid, alpha- and beta-dimorphecolic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enforcing periodic secondary structures in hybrid peptides: a novel hybrid foldamer containing periodic gamma-turn motifs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">N,N `,N `'-Tri-Boc-guanidine (TBG): a common starting material for both N-alkyl guanidines and amidinoureas</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Di-tert-butyl N,N `-(octahydropentalene-2,5-diyl) dicarbamate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Foldamers with unusual structural architecture from spirobi(indane) building blocks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pre-organization-mediated macrocylization: efficient synthesis and structural investigations of BINOL-m-phenylenediamine-derived macrocycles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rigid bicyclo[3.3.0]octane (octahydropentalene): a heavily constrained novel aliphatic template for molecular self-assembly</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sequence-specific unusual (1 -> 2)-type helical turns in alpha/beta-hybrid peptides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sheet-forming abiotic hetero foldamers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tandem non-polymerizing strategy to higher order acrylamide oligomers; potential intermediates for conformational correlations of poly-N-acrylamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel foldamer structural architecture from cofacial aromatic building blocks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sterically controlled naphthalene homo-oligoamides with novel structural architectures</style>Drupal-Biblio17<style face="normal" font="default" size="100%">1,8-Bis(4-methoxy-3-nitrophenyl)naphthalene</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Bicyclic amino acid-carbohydrate-conjugates as conformationally restricted hydroxyethylamine (HEA) transition-state isosteres</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concurrent display of both alpha- and beta-turns in a model peptide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conformationally rigid aromatic amino acids as potential building blocks for abiotic foldamers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diversifying the structural architecture of synthetic oligomers: the hetero foldamer approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carbohydrate-derived conformationally restricted bicyclic dipeptides as potential hetero foldamer building blocks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conformational modulation of Ant-Pro oligomers using chirality alteration of proline residues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Expanding the structural repertoire of beta/alpha Ant-Pro (anthranilic acid-proline) oligomers into gamma/alpha 2-Amb-Pro (2-aminomethyl benzoic acid-proline) oligomers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Foldamers: they're not just for biomedical applications anymore</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Helical folding in heterogeneous foldamers without inter-residual backbone hydrogen-bonding</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multifaceted folding in a foldamer featuring highly cooperative folds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Sugar-amino acid cyclic conjugates as novel conformationally constrained hydroxyethylamine transition-state isosteres</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unusual conformational similarity of two peptide folds featuring sulfonamide and carboxamide on the backbone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ant-pro reverse-turn motif. structural features and conformational characteristics</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carboxamide versus sulfonamide in peptide backbone folding: a case study with a hetero foldamer</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Correlation of hydrogen-bonding propensity and anticancer profile of tetrazole-tethered combretastatin analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Easy and multigram-scale synthesis of pillar[5]quinone by the hypervalent iodine oxidation of 1,4-dimethoxypillar[5]arene</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ester vs. amide on folding: a case study with a 2-residue synthetic peptide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Orthanilic acid-promoted reverse turn formation in peptides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Switching the H-bonding network of a foldamer by modulating the backbone chirality and constitutional ratio of amino acids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthetic zipper peptide motif orchestrated via co-operative interplay of hydrogen bonding, aromatic stacking, and backbone chirality</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conformational modulation of peptide secondary structures using beta-aminobenzenesulfonic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formation of a pseudo-beta-hairpin motif utilizing the Ant-Pro reverse turn: consequences of stereochemical reordering</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Heterogeneous foldamers from aliphatic-aromatic amino acid building blocks: current trends and future prospects</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nucleophilic ring-opening of benzoxazinones by dbu: some observations</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Probing the folding induction ability of orthanilic acid in peptides: some observations</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthetic turn mimetics and hairpin nucleators: quo vadimus?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conformational modulation of peptides using beta-amino benzenesulfonic acid ((S)Ant)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exploiting powder x-ray diffraction to establish the solvent-assisted solid-state supramolecular assembly of pillar[5]quinone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel hybrid nocodazole analogues as tubulin polymerization inhibitors and their antiproliferative activity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Reversal of H-bonding direction by N-sulfonation in a synthetic reverse-turn peptide motif</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Role of N-terminal proline in stabilizing the Ant-Pro zipper motif</style>Drupal-Biblio17<style face="normal" font="default" size="100%">3-Aminothiophenecarboxylic acid (3-Atc)-induced folding in peptides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Angiotensin II analogs comprised of pro-amb (gamma-turn scaffold) as angiotensin II type 2 (AT(2)) receptor agonists</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Disruption of native beta-turns: consequence of folding competition between native and orthanilic acid proline-based pseudo beta-turn</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Residue dependent hydrogen-bonding preferences in orthanilic acid-based short peptide beta-turn motifs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Self-assembled vesicles of urea-tethered foldamers as hydrophobic drug carriers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Coumarin-appended stable fluorescent self-complementary quadruple-hydrogen-bonded molecular duplexes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exploring the gem-dimethyl effect in the formation of imine-based macrocycles and cages</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mixed-stack charge transfer crystals of pillar[5]quinone and tetrathiafulvalene exhibiting ferroelectric features</style>
Drupal-Biblio17<style face="normal" font="default" size="100%">Modular approach towards functionalized highly stable self-complementary quadruple hydrogen bonded systems</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel silaproline (Sip)-incorporated close structural mimics of potent antidepressant peptide drug rapastinel (GLYX-13)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rigid peptide scaffold-incorporated structural analogs of the potent antidepressant peptide drug rapastinel (GLYX-13)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Structural insights into the hydrogen-bonding and folding pattern in ant-ant-pro-gly tetrapeptides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Three in one: prototropy-free highly stable AADD-type self-complementary quadruple hydrogen-bonded molecular duplexes with built-in fluorophore</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Triazine-based highly stable AADD-type self-complementary quadruple hydrogen-bonded systems devoid of prototropy</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conducting nanofibres of solvatofluorochromic cyclohexanetrione-dithiolylidene-based C-3 symmetric molecule</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conformational studies of Ant-Pro motif-incorporated cyclic peptides: gramicidin S and avellanin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of 2-amino-thiophene-tethered ureidopenicillin analogs with potentantibacterial and antitubercular activity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Helically structured peptide architecture engineered using dimedone as a rigid organic scaffold</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and anticancer activity of conformationally constrained Smac mimetics containing pseudo beta turns</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Three-dimensional metal-organic polymer of multivalent hexaphenylbenzene</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> Twelve-armed hexaphenylbenzene-based giant supramolecular framework for entrapping guest molecules</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Conducting nanofibres of solvatofluorochromic cyclohexanetrione-dithiolylidene-based C-3 symmetric molecule (vol 54, pg 212, 2018)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of 2-amino-thiophene-proline-conjugates and their anti-tubercular activity against mycobacterium tuberculosis H37Ra</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dimedone-based rigid organic scaffold for organizing symmetrical helical peptide chains.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and convenient route for the synthesis of thiophene-2-carboxamidines as potential inhibitors of nitric oxide synthase (NOS)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel cilengitide-based cyclic RGD peptides as alpha nu beta(3) integrin inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Three in one: triple G-C-T base-coded brahma nucleobase amino acid: synthesis, peptide formation, and structural features</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Triazine-based janus G-C nucleobase as a building block for self-assembly, peptide nucleic acids, and smart polymers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Janus cross-links in supramolecular networks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-purpose synthetic alpha-amino acid featuring coumarin and ureidopyrimidinone motifs on its backbone: Synthesis and peptide formation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carbamate-Protected (BOC and O-NB) 2-Aminopyrimidinedione-based janus G-C nucleobase motifs as building blocks for supramolecular assembly and smart polymers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Discovery of SARS-CoV-2 inhibitors featuring novel histidine α-nitrile motif</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Histidinal-based potent antimalarial agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Block copolymer self-assembly: exploitation of hydrogen bonding for nanoparticle morphology control via incorporation of triazine based comonomers by RAFT polymerization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Creep resistance in doubly crosslinked dynamic covalent networks</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and film formation of aqueous emulsion polymer latexes featuring hydrogen bonding via a janus guanine-cytosine base monomer</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Morphology rearrangement by mixing of internally hydrogen-bonded nanoparticles comprising triazine-based amphiphilic diblock copolymers</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Triple G-C-T base-coded self-assembling water-soluble nucleobase monomers with a broad scope for biomaterial and protein bioconjugation applications</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dynamic janus hydrogen bond mimicry unlocks tough, flexible supramolecular elastomers for strain sensing</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Repurposed ciprofloxacin derivatives as potent autophagic-type anticancer agents</style>