Year |
Citation |
Score |
2023 |
Ibukun OJ, Gumtya M, Singh S, Shit A, Haldar D. Effect of the spacer on the structure and self-assembly of FF peptide mimetics. Soft Matter. 19: 3215-3221. PMID 37074778 DOI: 10.1039/d3sm00339f |
0.437 |
|
2023 |
Roy Chowdhury S, Haldar D. Effect of Symmetry and Increasing Hydrophobicity on the Self-Assembly and Function of Benzoylurea Derivatives. Langmuir : the Acs Journal of Surfaces and Colloids. PMID 36966507 DOI: 10.1021/acs.langmuir.3c00456 |
0.344 |
|
2022 |
Nandi SK, Sarkar R, Jaiswar A, Roy S, Haldar D. Miniature β-Hairpin Mimetic by Intramolecular Hydrogen Bond and C-H···π Interactions. Acs Omega. 7: 17245-17252. PMID 35647431 DOI: 10.1021/acsomega.2c01168 |
0.329 |
|
2020 |
Kumar S, Bera S, Nandi SK, Haldar D. The effect of amide bond orientation and symmetry on the self-assembly and gelation of discotic tripeptides. Soft Matter. PMID 33155010 DOI: 10.1039/d0sm01804j |
0.321 |
|
2020 |
Mondal S, Podder D, Nandi SK, Roy Chowdhury S, Haldar D. Acid-responsive fibrillation and urease-assisted defibrillation of phenylalanine: a transient supramolecular hydrogel. Soft Matter. PMID 32761013 DOI: 10.1039/D0Sm00774A |
0.448 |
|
2020 |
Chowdhury SR, Nandi SK, Podder D, Haldar D. Conformational Heterogeneity and Self-Assembly of α,β,γ-Hybrid Peptides Containing Fenamic Acid: Multistimuli-Responsive Phase-Selective Gelation. Acs Omega. 5: 2287-2294. PMID 32064390 DOI: 10.1021/acsomega.9b03532 |
0.415 |
|
2020 |
Tiwari R, Maji K, Ajmal, Ghosh S, Ghosh N, Haldar D, Banerjee A. Laser assisted self-assembly of diphenylalanine: emergence of robust waveguiding properties and Fano resonances Journal of Materials Chemistry C. 8: 9663-9670. DOI: 10.1039/D0Tc01510E |
0.353 |
|
2020 |
Podder D, Sasmal S, Konar S, Ghorai PK, Haldar D. Topology-Controlled Selective Fe3+ Binding in Water by δ-Peptides with a Dihydropyrimidinone-Containing Amino Acid Crystal Growth & Design. 20: 1760-1770. DOI: 10.1021/Acs.Cgd.9B01492 |
0.501 |
|
2019 |
Podder D, Nandi SK, Sasmal S, Haldar D. Synergistic Tricolor Emission-Based White light from Supramolecular Organic-Inorganic Hybrid Gel. Langmuir : the Acs Journal of Surfaces and Colloids. PMID 30998369 DOI: 10.1021/Acs.Langmuir.9B00456 |
0.337 |
|
2019 |
Sasmal S, Maji K, Díaz DD, Haldar D. Highly selective metallogel from 4-biphenylcarboxy capped diphenylalanine and FeCl3 Crystengcomm. 21: 4289-4297. DOI: 10.1039/C9Ce00695H |
0.404 |
|
2019 |
Podder D, Chowdhury SR, Nandi SK, Haldar D. Tripeptide based super-organogelators: structure and function New Journal of Chemistry. 43: 3743-3749. DOI: 10.1039/C8Nj05578E |
0.404 |
|
2019 |
Paikar A, Podder D, Chowdhury SR, Sasmal S, Haldar D. Bromine–bromine interactions enhanced plasticity for the bending of a single crystal without affecting fluorescent properties Crystengcomm. 21: 589-593. DOI: 10.1039/C8Ce02086H |
0.311 |
|
2019 |
Häring M, Grijalvo S, Haldar D, Saldías C, Díaz DD. Polymer topology-controlled self-healing properties of polyelectrolyte hydrogels based on DABCO-containing aromatic ionenes European Polymer Journal. 115: 221-224. DOI: 10.1016/J.Eurpolymj.2019.03.044 |
0.335 |
|
2018 |
Debnath M, Das T, Podder D, Haldar D. α,ε-Hybrid Peptide Foldamers: Self-Assembly of Peptide with Trans Carbon-Carbon Double Bonds in the Backbone and Its Saturated Analogue. Acs Omega. 3: 8760-8768. PMID 31459008 DOI: 10.1021/acsomega.8b00832 |
0.435 |
|
2017 |
Podder D, Bera S, Debnath M, Das T, Haldar D. Formation of toroids by self-assembly of an α-α corner mimetic: supramolecular cyclization. Journal of Materials Chemistry. B. 5: 7583-7590. PMID 32264233 DOI: 10.1039/C7Tb01711A |
0.442 |
|
2017 |
Debnath M, Sasmal S, Haldar D. Fabrication of egg shell-like nanovesicles from a thiocoumarin-based ε-amino ester: a potential carrier. Journal of Materials Chemistry. B. 5: 5450-5457. PMID 32264084 DOI: 10.1039/C7Tb00025A |
0.427 |
|
2017 |
Das T, Häring M, Haldar D, Díaz Díaz D. Phenylalanine and derivatives as versatile low-molecular-weight gelators: design, structure and tailored function. Biomaterials Science. PMID 29164186 DOI: 10.1039/C7Bm00882A |
0.391 |
|
2017 |
Maji K, Haldar D. 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including . Royal Society Open Science. 4: 170684. PMID 29134076 DOI: 10.1098/Rsos.170684 |
0.342 |
|
2017 |
Paikar A, Debnath M, Podder D, Sasmal S, Haldar D. Synthesis and structural investigation of 2-aminomethyl-3-(4-methoxy-phenyl)-propionic acid containing a peptide analogue of the amyloidogenic AS(6-7) sequence: inhibition of fibril formation. Organic & Biomolecular Chemistry. PMID 28463373 DOI: 10.1039/C7Ob00797C |
0.521 |
|
2017 |
Paikar A, Haldar D. Dynamic self-assembled polymer: HCl responsive inversion of supramolecular polymer handedness Rsc Advances. 7: 47170-47176. DOI: 10.1039/C7Ra08035B |
0.382 |
|
2017 |
Pramanik A, Haldar D. Packing-induced solid-state fluorescence and thermochromic behavior of peptidic luminophores Rsc Advances. 7: 389-395. DOI: 10.1039/C6Ra24799G |
0.444 |
|
2017 |
Paikar A, Pramanik A, Das T, Haldar D. A self-assembled peptide mimetic of a tubular host and a supramolecular polymer Polymer Chemistry. 8: 396-403. DOI: 10.1039/C6Py01955B |
0.439 |
|
2017 |
Maji K, Saha S, Dey R, Ghosh N, Haldar D. Mueller Matrix Fluorescence Spectroscopy for Probing Self-Assembled Peptide-Based Hybrid Supramolecular Structure and Orientation Journal of Physical Chemistry C. 121: 19519-19529. DOI: 10.1021/Acs.Jpcc.7B06725 |
0.436 |
|
2016 |
Pramanik A, Paikar A, Maji K, Haldar D. Photo-responsive modulation of hybrid peptide assembly, charge transfer complex formation and gelation Rsc Advances. 6: 59851-59857. DOI: 10.1039/C6Ra13026G |
0.475 |
|
2016 |
Pramanik A, Paikar A, Das T, Maji K, Haldar D. Self-assembled peptide microspheres for sustainable release of sulfamethoxazole Rsc Advances. 6: 39172-39179. DOI: 10.1039/C6Ra07095G |
0.505 |
|
2016 |
Bera S, Haldar D. A rechargeable self-healing safety fuel gel Journal of Materials Chemistry. 4: 6933-6939. DOI: 10.1039/C5Ta08010J |
0.322 |
|
2016 |
Podder D, Sasmal S, Maji K, Haldar D. Supramolecular tryptophan-zipper forms a tripeptide as a regular proton transporter Crystengcomm. 18: 4109-4114. DOI: 10.1039/C5Ce02005K |
0.473 |
|
2015 |
Bera S, Ambast DK, Pal B, Haldar D. Assembly, growth and nonlinear thermo-optical properties of nitropeptides. Physical Chemistry Chemical Physics : Pccp. 17: 16983-90. PMID 26061359 DOI: 10.1039/C5Cp02218E |
0.439 |
|
2015 |
Sarkar R, Debnath M, Maji K, Haldar D. Solvent assisted structural diversity: Supramolecular sheet and double helix of a short aromatic γ-peptide Rsc Advances. 5: 76257-76262. DOI: 10.1039/C5Ra12831E |
0.536 |
|
2015 |
Sarkar R, Maji K, Haldar D. An efficient one pot ipso-nitration: structural transformation of a dipeptide by N-terminus modification Rsc Advances. 5: 59570-59575. DOI: 10.1039/C5Ra09789D |
0.311 |
|
2015 |
Pramanik A, Paikar A, Haldar D. Sonication-induced instant fibrillation and fluorescent labeling of tripeptide fibers Rsc Advances. 5: 53886-53892. DOI: 10.1039/C5Ra07864D |
0.496 |
|
2015 |
Paikar A, Pramanik A, Haldar D. Influence of side-chain interactions on the self-assembly of discotic tricarboxyamides: a crystallographic insight Rsc Advances. 5: 31845-31851. DOI: 10.1039/C5Ra03864B |
0.483 |
|
2015 |
Bera S, Maity S, Haldar D. Assembly of encapsulated water in hybrid bisamides: Helical and zigzag water chains Crystengcomm. 17: 1569-1575. DOI: 10.1039/C4Ce01950D |
0.395 |
|
2014 |
Maji K, Sarkar R, Bera S, Haldar D. A small molecule peptidomimetic of spider silk and webs. Chemical Communications (Cambridge, England). 50: 12749-52. PMID 25204650 DOI: 10.1039/C4Cc04475D |
0.32 |
|
2014 |
Jana P, Paikar A, Bera S, Maity SK, Haldar D. Porous organic material from discotic tricarboxyamide: side chain-core interactions. Organic Letters. 16: 38-41. PMID 24350641 DOI: 10.1021/Ol402865T |
0.416 |
|
2014 |
Bera S, Maity SK, Haldar D. Photoelectrochemical properties of CdSe quantum dots doped disk-like tripeptide capsule Crystengcomm. 16: 4834-4841. DOI: 10.1039/C3Ce42582G |
0.417 |
|
2014 |
Maity SK, Bera S, Paikar A, Pramanik A, Haldar D. Fabrication of self-assembled peptidomimetic microspheres and hydrogen peroxide responsive release of nicotinamide Crystengcomm. 16: 2527-2534. DOI: 10.1039/C3Ce41796D |
0.388 |
|
2014 |
Jana P, Bera S, Paikar A, Haldar D. Terminal Peptide Directed Assembly of Naphthalene-Bisimides Crystal Growth & Design. 14: 3918-3922. DOI: 10.1021/Cg500501R |
0.492 |
|
2014 |
Bera S, Jana P, Maity SK, Haldar D. Inhibition of Fibril Formation by Tyrosine Modification of Diphenylalanine: Crystallographic Insights Crystal Growth & Design. 14: 1032-1038. DOI: 10.1021/Cg4015042 |
0.529 |
|
2013 |
Maity SK, Bera S, Paikar A, Pramanik A, Haldar D. Halogen bond induced phosphorescence of capped γ-amino acid in the solid state. Chemical Communications (Cambridge, England). 49: 9051-3. PMID 23985996 DOI: 10.1039/C3Cc44231D |
0.404 |
|
2013 |
Maity SK, Bera S, Paikar A, Pramanik A, Haldar D. Fabrication of microspheres from self-assembled γ-peptides Crystengcomm. 15: 5860-5866. DOI: 10.1039/C3Ce40689J |
0.493 |
|
2013 |
Jana P, Maity SK, Bera S, Ghorai PK, Haldar D. Hierarchical self-assembly of naphthalene bisimides to fluorescent microspheres and fluoride sensing Crystengcomm. 15: 2512-2518. DOI: 10.1039/C3Ce26700H |
0.469 |
|
2013 |
Maity S, Kumar R, Maity SK, Jana P, Bera S, Haldar D. Synthesis and study of 2-acetyl amino-3-[4-(2-amino-5-sulfo-phenylazo)-phenyl]-propionic acid: a new class of inhibitor for hen egg white lysozyme amyloidogenesis Medchemcomm. 4: 530-536. DOI: 10.1039/C2Md20236K |
0.344 |
|
2012 |
Maity SK, Maity S, Jana P, Haldar D. Supramolecular double helix from capped γ-peptide. Chemical Communications (Cambridge, England). 48: 711-3. PMID 22129621 DOI: 10.1039/C1Cc15570A |
0.53 |
|
2012 |
Maity S, Sarkar S, Jana P, Maity SK, Bera S, Mahalingam V, Haldar D. Sonication-responsive organogelation of a tripodal peptide and optical properties of embedded Tm3+ nanoclusters Soft Matter. 8: 7960-7966. DOI: 10.1039/C2Sm25981H |
0.395 |
|
2012 |
Jana P, Maity S, Maity SK, Ghorai PK, Haldar D. Photo-induced charge-transfer complex formation and organogelation by a tripeptide Soft Matter. 8: 5621-5628. DOI: 10.1039/C2Sm25062D |
0.351 |
|
2012 |
Maity SK, Kumar R, Ambast DKS, Pal B, Haldar D. Self-assembly and nonlinear optical properties of a synthetic dipeptide Journal of Materials Chemistry. 22: 22198-22203. DOI: 10.1039/C2Jm34338J |
0.474 |
|
2012 |
Jana P, Maity S, Maity SK, Ghorai PK, Haldar D. Insights into H-aggregates and CH⋯O hydrogen bond mediated self-assembly of pyromellitic bisimide Crystengcomm. 14: 6586-6592. DOI: 10.1039/C2Ce25778E |
0.485 |
|
2012 |
Maity SK, Maity S, Jana P, Haldar D. CdS quantum dots doped with a peptide matrix: structural and photoelectrochemical properties Crystengcomm. 14: 3156-3162. DOI: 10.1039/C2Ce06355G |
0.441 |
|
2012 |
Maity SK, Maity S, Jana P, Haldar D. Luminescent nanoparticles from tripeptide–CdS conjugate Crystengcomm. 14: 4034-4040. DOI: 10.1039/C2Ce05786G |
0.474 |
|
2012 |
Maity S, Jana P, Maity SK, Kumar P, Haldar D. Conformational Heterogeneity, Self-Assembly, and Gas Adsorption Studies of Isomeric Hybrid Peptides Crystal Growth & Design. 12: 422-428. DOI: 10.1021/Cg201268X |
0.509 |
|
2011 |
Maity S, Kumar P, Haldar D. An amyloid-like fibril-forming supramolecular cross-β-structure of a model peptide: a crystallographic insight. Organic & Biomolecular Chemistry. 9: 3787-91. PMID 21448469 DOI: 10.1039/C0Ob01033B |
0.455 |
|
2011 |
Maity S, Jana P, Maity SK, Haldar D. Fabrication of hollow self-assembled peptide microvesicles and transition from sphere-to-rod structure. Langmuir : the Acs Journal of Surfaces and Colloids. 27: 3835-41. PMID 21381778 DOI: 10.1021/La104461M |
0.417 |
|
2011 |
Jana P, Maity S, Maity SK, Haldar D. A new peptide motif in the formation of supramolecular double helices. Chemical Communications (Cambridge, England). 47: 2092-4. PMID 21186386 DOI: 10.1039/C0Cc04244G |
0.513 |
|
2011 |
Maity S, Jana P, Maity SK, Haldar D. Mesoporous vesicles from supramolecular helical peptide as drug carrier Soft Matter. 7: 10174-10181. DOI: 10.1039/C1Sm05958K |
0.418 |
|
2011 |
Maity S, Kumar P, Haldar D. Sonication-induced instant amyloid-like fibril formation and organogelation by a tripeptide Soft Matter. 7: 5239-5245. DOI: 10.1039/C1Sm05277B |
0.454 |
|
2011 |
Maity S, Jana P, Haldar D. Fabrication of nanoporous material from a hydrophobic peptide Crystengcomm. 13: 3064-3071. DOI: 10.1039/C0Ce00701C |
0.479 |
|
2011 |
Jana P, Maity S, Haldar D. Insights into self-assembling nanoporous peptide and in situ reducing agent Crystengcomm. 13: 973-978. DOI: 10.1039/C0Ce00143K |
0.534 |
|
2010 |
Baptiste B, Zhu J, Haldar D, Kauffmann B, Léger JM, Huc I. Hybridization of long pyridine-dicarboxamide oligomers into multi-turn double helices: slow strand association and dissociation, solvent dependence, and solid state structures. Chemistry, An Asian Journal. 5: 1364-75. PMID 20376877 DOI: 10.1002/Asia.200900713 |
0.698 |
|
2010 |
Jana P, Maity S, Haldar D. Developments in the Synthesis of Organometallic Amino Acids and Analogues Current Organic Synthesis. 7: 224-234. DOI: 10.2174/157017910791162995 |
0.302 |
|
2009 |
Haldar D, Schmuck C. Metal-free double helices from abiotic backbones. Chemical Society Reviews. 38: 363-71. PMID 19169454 DOI: 10.1039/B803553A |
0.412 |
|
2008 |
Haldar D. Recent Developments in the Synthesis of Amino Acids and Analogues for Foldamers Study Current Organic Synthesis. 5: 61-80. DOI: 10.2174/157017908783497527 |
0.304 |
|
2008 |
Haldar D. Two component hydrogel with γ-amino butyric acid as potential receptor and neurotransmitter delivery system Tetrahedron. 64: 186-190. DOI: 10.1016/J.Tet.2007.10.074 |
0.39 |
|
2007 |
Haldar D, Drew MGB, Banerjee A. Conformational heterogeneity of tripeptides containing Boc–Leu–Aib as corner residues in the solid state Tetrahedron. 63: 5561-5566. DOI: 10.1016/J.Tet.2007.04.026 |
0.452 |
|
2007 |
Haldar D, Jiang H, Léger J, Huc I. Double versus single helical structures of oligopyridine-dicarboxamide strands. Part 2: The role of side chains Tetrahedron. 63: 6322-6330. DOI: 10.1016/J.Tet.2007.02.114 |
0.634 |
|
2007 |
Haldar D, Banerjee A. Intrinsic Amyloidogenic Behavior of Terminally Protected Alzheimer’s Aβ 17–21 Peptide: Self-Aggregation and Amyloid-Like Fibril Formation International Journal of Peptide Research and Therapeutics. 13: 439-446. DOI: 10.1007/S10989-006-9072-X |
0.452 |
|
2006 |
Haldar D, Jiang H, Léger JM, Huc I. Interstrand interactions between side chains in a double-helical foldamer. Angewandte Chemie (International Ed. in English). 45: 5483-6. PMID 16850517 DOI: 10.1002/Anie.200600698 |
0.584 |
|
2006 |
Ray S, Drew MG, Das AK, Haldar D, Banerjee A. Nanozipper formation in the solid state from a self-assembling tripeptide with a single tryptophan residue Tetrahedron Letters. 47: 2771-2774. DOI: 10.1016/J.Tetlet.2006.02.070 |
0.443 |
|
2006 |
Haldar D, Drew MGB, Banerjee A. α-Aminoisobutyric acid modified protected analogues of β-amyloid residue 17–20: a change from sheet to helix Tetrahedron. 62: 6370-6378. DOI: 10.1016/J.Tet.2006.04.036 |
0.407 |
|
2006 |
Haldar D, Banerjee A. l-Ala Modified Analogues of Amyloid β-Peptide Residue 17-20: Self-Association and Amyloid-like Fibril Formation International Journal of Peptide Research and Therapeutics. 12: 341-348. DOI: 10.1007/S10989-006-9037-0 |
0.472 |
|
2005 |
Das AK, Drew MG, Haldar D, Banerjee A. The role of the disulfide bond in amyloid-like fibrillogenesis in a model peptide system. Organic & Biomolecular Chemistry. 3: 3502-7. PMID 16172687 DOI: 10.1039/B509083K |
0.495 |
|
2005 |
Bhattacharjee RR, Das AK, Haldar D, Si S, Banerjee A, Mandal TK. Peptide-assisted synthesis of gold nanoparticles and their self-assembly. Journal of Nanoscience and Nanotechnology. 5: 1141-7. PMID 16108441 DOI: 10.1166/Jnn.2005.166 |
0.354 |
|
2005 |
Das AK, Haldar D, Hegde RP, Shamala N, Banerjee A. X-ray crystallographic signature of supramolecular triple helix formation from a water soluble synthetic tetrapeptide. Chemical Communications (Cambridge, England). 1836-8. PMID 15795759 DOI: 10.1039/B417726F |
0.49 |
|
2005 |
Das AK, Banerjee A, Drew MG, Ray S, Haldar D, Banerjee A. Can a consecutive double turn conformation be considered as a peptide based molecular scaffold for supramolecular helix in the solid state? Tetrahedron. 61: 5027-5036. DOI: 10.1016/J.Tet.2005.03.057 |
0.506 |
|
2004 |
Ray S, Haldar D, Drew MG, Banerjee A. A new motif in the formation of peptide nanotubes: the crystallographic signature. Organic Letters. 6: 4463-5. PMID 15548051 DOI: 10.1021/Ol048253A |
0.493 |
|
2004 |
Das AK, Banerjee A, Drew MG, Haldar D, Banerjee A. Stepwise Self-assembly of a Tripeptide from Molecular Dimers to Supramolecular β-sheets in Crystals and Amyloid-like Fibrils in the Solid State Supramolecular Chemistry. 16: 331-335. DOI: 10.1080/1061027042000213047 |
0.469 |
|
2004 |
Banerjee A, Maji SK, Drew MG, Haldar D, Das AK, Banerjee A. Hydrogen-bonded dimer can mediate supramolecular β-sheet formation and subsequent amyloid-like fibril formation: a model study Tetrahedron. 60: 5935-5944. DOI: 10.1016/J.Tet.2004.05.041 |
0.468 |
|
2004 |
Maji SK, Haldar D, Drew MG, Banerjee A, Das AK, Banerjee A. Self-assembly of β-turn forming synthetic tripeptides into supramolecular β-sheets and amyloid-like fibrils in the solid state Tetrahedron. 60: 3251-3259. DOI: 10.1016/J.Tet.2004.02.019 |
0.458 |
|
2003 |
Haldar D, Banerjee A, Drew MG, Das AK, Banerjee A. First crystallographic signature of an acyclic peptide nanorod: molecular mechanism of nanorod formation by a self-assembled tetrapeptide. Chemical Communications (Cambridge, England). 1406-7. PMID 12841264 DOI: 10.1039/B302472P |
0.468 |
|
2003 |
Maji SK, Haldar D, Banerjee A, Mukhopadhyay C, Banerjee A. Conformational Heterogeneity of a Tripeptide in the Solid State and in Solution: Characterization of a g-Turn Containing Incipient Hairpin in Solution Journal of Structural Chemistry. 44: 790-795. DOI: 10.1023/B:Jory.0000029816.31278.7B |
0.444 |
|
2003 |
Banerjee A, Maji SK, Drew MG, Haldar D, Banerjee A. An amyloid-like fibril forming antiparallel supramolecular β-sheet from a synthetic tripeptide: a crystallographic signature Tetrahedron Letters. 44: 6741-6744. DOI: 10.1016/S0040-4039(03)01642-3 |
0.51 |
|
2003 |
Banerjee A, Maji SK, Drew MG, Haldar D, Banerjee A. Supramolecular peptide helix from a novel double turn forming peptide containing a β-amino acid Tetrahedron Letters. 44: 699-702. DOI: 10.1016/S0040-4039(02)02675-8 |
0.502 |
|
2003 |
Banerjee A, Maji SK, Drew MG, Haldar D, Banerjee A. Amyloid-like fibril-forming supramolecular β-sheets from a β-turn forming tripeptide containing non-coded amino acids: the crystallographic signature Tetrahedron Letters. 44: 335-339. DOI: 10.1016/S0040-4039(02)02570-4 |
0.44 |
|
2003 |
Maji SK, Haldar D, Bhattacharyya D, Banerjee A. Conformational heterogeneity of a turn mimetic pseudo-peptide: comparison of crystal state, solution and theoretically derived structures Journal of Molecular Structure. 646: 111-123. DOI: 10.1016/S0022-2860(02)00619-1 |
0.446 |
|
2003 |
Banerjee A, Maji SK, Drew MGB, Haldar D, Banerjee A. Supramolecular Peptide Helix from a Novel Double Turn Forming Peptide Containing a β-Amino Acid. Cheminform. 34. DOI: 10.1002/CHIN.200314198 |
0.351 |
|
2002 |
Maji SK, Banerjee A, Drew MG, Haldar D, Banerjee A. Self-assembly of a tetrapeptide in which a unique supramolecular helical structure is formed via intermolecular hydrogen bonding in the solid state Tetrahedron Letters. 43: 6759-6762. DOI: 10.1016/S0040-4039(02)01521-6 |
0.511 |
|
2002 |
Haldar D, Maji SK, Drew MG, Banerjee A, Banerjee A. Self-assembly of a short peptide monomer into a continuous hydrogen bonded supramolecular helix: the crystallographic signature Tetrahedron Letters. 43: 5465-5468. DOI: 10.1016/S0040-4039(02)01050-X |
0.532 |
|
2002 |
Haldar D, Maji SK, Sheldrick WS, Banerjee A. First crystallographic signature of the highly ordered supramolecular helical assemblage from a tripeptide containing a non-coded amino acid Tetrahedron Letters. 43: 2653-2656. DOI: 10.1016/S0040-4039(02)00283-6 |
0.449 |
|
2002 |
Maji SK, Haldar D, Banerjee A, Banerjee A. Fibril-forming model synthetic peptides containing 3-aminophenylacetic acid Tetrahedron. 58: 8695-8702. DOI: 10.1016/S0040-4020(02)01093-1 |
0.484 |
|
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