| Year |
Citation |
Score |
| 2022 |
Gupta SK, Banerjee S, Prabhakaran EN. Understanding the anomaly of cis-trans isomerism in Pro-His sequence. Bioorganic & Medicinal Chemistry Letters. 76: 128985. PMID 36165914 DOI: 10.1016/j.bmcl.2022.128985 |
0.725 |
|
| 2021 |
Pal S, Banerjee S, Prabhakaran EN. α-Helices Propagating from Stable Nucleators Exhibit Unconventional Thermal Folding. Febs Letters. PMID 34716991 DOI: 10.1002/1873-3468.14216 |
0.681 |
|
| 2021 |
Prabhakaran EN, Reddy SS, Pal S, Ghosh S. Hydrogen Bond Surrogate-Constrained Dynamic Anti-parallel β-Sheets. Chembiochem : a European Journal of Chemical Biology. PMID 33751754 DOI: 10.1002/cbic.202100028 |
0.563 |
|
| 2020 |
Prabhakaran EN, Tumminakatti S, Vats K, Ghosh S. Spectral evidence for generic charge → acceptor interactions in carbamates and esters. Rsc Advances. 10: 11871-11875. PMID 35496580 DOI: 10.1039/d0ra00313a |
0.667 |
|
| 2020 |
Pal S, Banerjee S, Prabhakaran EN. Helix-Coil Transition at a Glycine Following a Nascent α-Helix: A Synergetic Guidance Mechanism for Helix Growth. The Journal of Physical Chemistry. A. PMID 32877193 DOI: 10.1021/Acs.Jpca.0C05489 |
0.696 |
|
| 2020 |
Pal S, Banerjee S, Kumar A, Prabhakaran EN. H-Bond Surrogate-Stabilized Shortest Single-Turn α-Helices: sp Constraints and Residue Preferences for the Highest α-Helicities. Acs Omega. 5: 13902-13912. PMID 32566857 DOI: 10.1021/acsomega.0c01277 |
0.687 |
|
| 2020 |
Prabhakaran EN, Tumminakatti S, Vats K, Ghosh S. Spectral evidence for generic charge → acceptor interactions in carbamates and esters Rsc Advances. 10: 11871-11875. DOI: 10.1039/D0Ra00313A |
0.766 |
|
| 2018 |
Pal S, Prabhakaran EN. Hydrogen bond surrogate stabilized water soluble 310-helix from a disordered pentapeptide containing coded α-amino acids Tetrahedron Letters. 59: 2515-2519. DOI: 10.1016/J.Tetlet.2018.05.029 |
0.427 |
|
| 2015 |
Tumminakatti S, Reddy DN, Prabhakaran EN. Exploring the consequences of a representative "disallowed" conformation of Aib on a 310 -helical fold. Biopolymers. 104: 21-36. PMID 25488434 DOI: 10.1002/Bip.22599 |
0.759 |
|
| 2015 |
Tumminakatti S, Khatri B, Krishnamurti V, Athavale V, Prabhakaran EN. Solution structural features of N-acyl homoserine lactones Tetrahedron Letters. 56: 5771-5775. DOI: 10.1016/J.Tetlet.2015.08.078 |
0.784 |
|
| 2014 |
Reddy DN, Prabhakaran EN. Steric and electronic interactions controlling the cis/trans isomer equilibrium at X-pro tertiary amide motifs in solution. Biopolymers. 101: 66-77. PMID 23653336 DOI: 10.1002/Bip.22278 |
0.778 |
|
| 2014 |
Tumminakatti S, Reddy DN, Lakshmi AN, Prabhakaran EN. Synthesis of 5,6-dihydro-4H-1,3-thiazine containing peptide mimics from N-(3-hydroxypropyl)thioamides and epimerization studies Tetrahedron Letters. 4731-4735. DOI: 10.1016/J.Tetlet.2014.06.084 |
0.768 |
|
| 2014 |
Thirupathi R, Prabhakaran EN. Estimation of the 2.05 helix type i→i hydrogen bond energy at Aib*-Oxa motif: An isodesmic approach Tetrahedron Letters. 55: 3418-3421. DOI: 10.1016/J.Tetlet.2014.04.064 |
0.429 |
|
| 2013 |
Reddy DN, George G, Prabhakaran EN. Crystal-structure analysis of cis-X-Pro-containing peptidomimetics: understanding the steric interactions at cis X-Pro amide bonds. Angewandte Chemie (International Ed. in English). 52: 3935-9. PMID 23450815 DOI: 10.1002/Anie.201209517 |
0.775 |
|
| 2012 |
Reddy DN, Thirupathi R, Tumminakatti S, Prabhakaran EN. A method for stabilizing the cis prolyl peptide bond: Influence of an unusual n→π * interaction in 1,3-oxazine and 1,3-thiazine containing peptidomimetics Tetrahedron Letters. 53: 4413-4417. DOI: 10.1016/J.Tetlet.2012.06.031 |
0.764 |
|
| 2011 |
Reddy DN, Thirupathi R, Prabhakaran EN. Accessing the disallowed conformations of peptides employing amide-to-imidate modification. Chemical Communications (Cambridge, England). 47: 9417-9. PMID 21773612 DOI: 10.1039/C1Cc13515E |
0.798 |
|
| 2011 |
Reddy DN, Prabhakaran EN. Synthesis and isolation of 5,6-dihydro-4H-1,3-oxazine hydrobromides by autocyclization of N-(3-bromopropyl)amides. The Journal of Organic Chemistry. 76: 680-3. PMID 21171661 DOI: 10.1021/Jo101955Q |
0.778 |
|
| 2009 |
Thirupathi R, Reddy DN, Brinda S, Prabhakaran EN. N-{1-[(3-Bromo-prop-yl)amino-carbon-yl]eth-yl}-2-(2-nitro-benzene-sulfonamido)propionamide. Acta Crystallographica. Section E, Structure Reports Online. 65: o2308-9. PMID 21577780 DOI: 10.1107/S1600536809034291 |
0.78 |
|
| 2008 |
Viswanathan R, Smith CR, Prabhakaran EN, Johnston JN. Free radical-mediated aryl amination: convergent two- and three-component couplings to chiral 2,3-disubstituted indolines. The Journal of Organic Chemistry. 73: 3040-6. PMID 18351776 DOI: 10.1021/Jo702523U |
0.65 |
|
| 2004 |
Pace CN, Treviño S, Prabhakaran E, Scholtz JM. Protein structure, stability and solubility in water and other solvents. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 359: 1225-34; discussion . PMID 15306378 DOI: 10.1098/Rstb.2004.1500 |
0.672 |
|
| 2003 |
Rao IN, Prabhakaran EN, Das SK, Iqbal J. Cobalt-catalyzed one-pot three-component coupling route to beta-acetamido carbonyl compounds: a general synthetic protocol for gamma-lactams. The Journal of Organic Chemistry. 68: 4079-82. PMID 12737595 DOI: 10.1021/Jo020559C |
0.442 |
|
| 2003 |
Nandy JP, Prabhakaran EN, Kumar SK, Kunwar AC, Iqbal J. Reverse turn induced pi-facial selectivity during polyaniline-supported cobalt(II) salen catalyzed aerobic epoxidation of N-cinnamoyl L-proline derived peptides. The Journal of Organic Chemistry. 68: 1679-92. PMID 12608779 DOI: 10.1021/Jo020352J |
0.571 |
|
| 2003 |
Viswanathan R, Prabhakaran EN, Plotkin MA, Johnston JN. Free radical-mediated aryl amination and its use in a convergent [3 + 2] strategy for enantioselective indoline alpha-amino acid synthesis. Journal of the American Chemical Society. 125: 163-8. PMID 12515518 DOI: 10.1021/Ja0284308 |
0.688 |
|
| 2003 |
Nugent BM, Williams AL, Prabhakaran EN, Johnston JN. Free radical-mediated vinyl amination: A mild, general pyrrolidinyl enamine synthesis Tetrahedron. 59: 8877-8888. DOI: 10.1016/J.Tet.2003.04.003 |
0.772 |
|
| 2003 |
Prabhakaran EN, Nugent BM, Williams AL, Nailor KE, Johnston JN. Free Radical Mediated Vinyl Amination: Access-to N,N-Dialkyl Enamines and Their β-Stannyl and β-Thio Derivatives. Cheminform. 34. DOI: 10.1002/chin.200315118 |
0.676 |
|
| 2002 |
Prabhakaran EN, Nugent BM, Williams AL, Nailor KE, Johnston JN. Free radical-mediated vinyl amination: access to N,N-dialkyl enamines and their beta-stannyl and beta-thio derivatives. Organic Letters. 4: 4197-200. PMID 12443057 DOI: 10.1021/Ol027064U |
0.775 |
|
| 2002 |
Prabhakaran EN, Rao IN, Boruah A, Iqbal J. Synthesis of small cyclic peptides via reverse turn induced ring closing metathesis of tripeptides. The Journal of Organic Chemistry. 67: 8247-50. PMID 12423162 DOI: 10.1021/Jo0200320 |
0.523 |
|
| 2002 |
Prabhakaran EN, Nandy JP, Shukla S, Tewari A, Kumar Das S, Iqbal J. Synthesis and conformation of proline containing tripeptides constrained with phenylalanine-like aziridine and dehydrophenylalanine residues Tetrahedron Letters. 43: 6461-6466. DOI: 10.1016/S0040-4039(02)01236-4 |
0.502 |
|
| 2001 |
Johnston JN, Plotkin MA, Viswanathan R, Prabhakaran EN. Nonconventional carbon additions to azomethines. aryl amination/indoline synthesis by direct aryl radical addition to azomethine nitrogen. Organic Letters. 3: 1009-11. PMID 11277782 DOI: 10.1021/Ol007065R |
0.689 |
|
| 2001 |
Prabhakaran EN, Rajesh V, Dubey S, Iqbal J. Synthesis of cyclic peptides as mimics for the constrained conformation of structural analogues of HIV protease inhibitors Tetrahedron Letters. 42: 339-342. DOI: 10.1016/S0040-4039(00)01951-1 |
0.513 |
|
| 2001 |
Prabhakaran EN, Nandy JP, Shukla S, Iqbal J. π-Facial selectivity in polyaniline supported cobalt catalysed aerobic epoxidation of N-cinnamoyl proline derivatives Tetrahedron Letters. 42: 333-337. DOI: 10.1016/S0040-4039(00)01949-3 |
0.573 |
|
| 1999 |
Prabhakaran EN, Iqbal J. Polyaniline-Supported Cobalt Catalyst: A Three-Component Condensation Route to beta-Amino Acid Derivatives. The Journal of Organic Chemistry. 64: 3339-3341. PMID 11674441 DOI: 10.1021/Jo981239P |
0.408 |
|
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