Year |
Citation |
Score |
2019 |
Kalita M, Archana A, Dimri A, Vasudev PG, Ramapanicker R. Synthesis of peptides containing oxo amino acids and their crystallographic analysis. Journal of Peptide Science : An Official Publication of the European Peptide Society. e3148. PMID 30697868 DOI: 10.1002/Psc.3148 |
0.621 |
|
2019 |
Gorde AB, Ramapanicker R. D-prolyl-2-(trifluoromethylsulfonamidopropyl)pyrrolidine: An Organocatalyst for Asymmetric Michael Addition of Aldehydes to β-Nitroalkenes at Ambient Conditions. The Journal of Organic Chemistry. PMID 30609351 DOI: 10.1021/Acs.Joc.8B02945 |
0.73 |
|
2019 |
Gorde AB, Ramapanicker R. Enantioselective Michael Addition of Aldehydes to β-Nitrostyrenes Catalyzed by (S)-N
-(D-Prolyl)-1-triflicamido-3-phenylpropan-2-amine European Journal of Organic Chemistry. 2019: 4745-4751. DOI: 10.1002/Ejoc.201900719 |
0.73 |
|
2018 |
Ansari A, Ramapanicker R. Enantioselective Synthesis of 2-Aminomethyl and 3-Amino Pyrrolidines and Piperidines through 1,2-Diamination of Aldehydes. The Journal of Organic Chemistry. PMID 30004231 DOI: 10.1021/Acs.Joc.8B00933 |
0.797 |
|
2018 |
Sengupta G, Pandey P, De S, Ramapanicker R, Bera JK. A bromo-capped diruthenium(i,i) N-heterocyclic carbene compound for in situ bromine generation with NBS: catalytic olefin aziridination reactions. Dalton Transactions (Cambridge, England : 2003). PMID 29964290 DOI: 10.1039/C8Dt01851K |
0.403 |
|
2018 |
Ansari A, Ramapanicker R. Enantioselective Synthesis of (R)-Antofine and (R)-Cryptopleurine Chemistryselect. 3: 12591-12594. DOI: 10.1002/SLCT.201803529 |
0.718 |
|
2017 |
Jain VK, Ramapanicker R. Diastereoselective synthesis of D-threo-sphinganine, L-erythro-sphinganine and (−)-spisulosine through asymmetric α-hydroxylation of a higher homologue of Garner's aldehyde Tetrahedron. 73: 1568-1575. DOI: 10.1016/J.Tet.2017.02.001 |
0.51 |
|
2016 |
Petakamsetty R, Ansari A, Ramapanicker R. Diastereoselective synthesis of furanose and pyranose substituted glycine and alanine derivatives via proline-catalyzed asymmetric α-amination of aldehydes. Carbohydrate Research. 435: 37-49. PMID 27693912 DOI: 10.1016/J.Carres.2016.09.011 |
0.799 |
|
2016 |
Chandrasekaran S, Ramapanicker R. Click Chemistry Route to the Synthesis of Unusual Amino Acids, Peptides, Triazole-Fused Heterocycles and Pseudodisaccharides. Chemical Record (New York, N.Y.). PMID 27411087 DOI: 10.1002/Tcr.201600093 |
0.666 |
|
2016 |
Saha P, Yadav K, Chacko S, Philip AT, Ramapanicker R, Gopakumar TG. Controlling Growth to One Dimension in Nanoislands of Ferrocene-Sugar Derivatives The Journal of Physical Chemistry C. 120: 9223-9228. DOI: 10.1021/Acs.Jpcc.6B00774 |
0.594 |
|
2016 |
Philip AT, Raju E, Ramapanicker R. Stereoselective Synthesis of Hydroxy Diamino Acid Derivatives and the Caprolactam Unit of Bengamide A through Organocatalytic α-Hydroxylation and Reductive Amination of Aldehydes European Journal of Organic Chemistry. 2016: 5502-5510. DOI: 10.1002/Ejoc.201600842 |
0.694 |
|
2015 |
Philip AT, Chacko S, Ramapanicker R. Synthesis of stable C-linked ferrocenyl amino acids and their use in solution-phase peptide synthesis. Journal of Peptide Science : An Official Publication of the European Peptide Society. PMID 26477332 DOI: 10.1002/Psc.2831 |
0.696 |
|
2015 |
Petakamsetty R, Jain VK, Majhi PK, Ramapanicker R. Divergent synthesis of various iminocyclitols from D-ribose. Organic & Biomolecular Chemistry. 13: 8512-23. PMID 26158408 DOI: 10.1039/C5Ob01042J |
0.552 |
|
2015 |
Chacko S, Ramapanicker R. Diastereoselective Synthesis of 1-Deoxygalactonojirimycin, 1-Deoxyaltronojirimycin, and N-Boc-(2S,3S)-3-Hydroxypipecolic Acid via Proline Catalyzed α-Aminoxylation of Aldehydes. The Journal of Organic Chemistry. 80: 4776-82. PMID 25860296 DOI: 10.1021/Acs.Joc.5B00424 |
0.673 |
|
2015 |
Chacko S, Ramapanicker R. Proline catalyzed, one-pot three component Mannich reaction and sequential cyclization toward the synthesis of 2-substituted piperidine and pyrrolidine alkaloids Tetrahedron Letters. 56: 2023-2026. DOI: 10.1016/J.Tetlet.2015.03.001 |
0.584 |
|
2015 |
Chacko S, Kalita M, Ramapanicker R. Chelation controlled reduction of N-protected β-amino ketones toward the synthesis of HPA-12 and analogues Tetrahedron Asymmetry. DOI: 10.1016/J.Tetasy.2015.04.016 |
0.755 |
|
2015 |
Yadav P, Chacko S, Kumar G, Ramapanicker R, Verma V. Click chemistry route to covalently link cellulose and clay Cellulose. 22: 1615-1624. DOI: 10.1007/S10570-015-0594-2 |
0.596 |
|
2015 |
Chacko S, Ramapanicker R. Enantiospecific Synthesis of (-)-Cuspareine and (-)-Galipinine Journal of Heterocyclic Chemistry. 52: 1902-1906. DOI: 10.1002/Jhet.2112 |
0.611 |
|
2015 |
Chacko S, Kalita M, Ramapanicker R. ChemInform Abstract: Chelation Controlled Reduction of N-Protected β-Amino Ketones Toward the Synthesis of HPA-12 and Analogues. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201543070 |
0.742 |
|
2015 |
Chacko S, Ramapanicker R. ChemInform Abstract: Proline Catalyzed, One-Pot Three Component Mannich Reaction and Sequential Cyclization Toward the Synthesis of 2-Substituted Piperidine and Pyrrolidine Alkaloids. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201530203 |
0.606 |
|
2015 |
Petakamsetty R, Das RP, Ramapanicker R. ChemInform Abstract: Synthesis of Bis-α-amino Acids Through Proline Catalyzed Asymmetric α-Amination of Higher Homologues of Garner′s Aldehyde. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201517261 |
0.422 |
|
2014 |
Daw P, Petakamsetty R, Sarbajna A, Laha S, Ramapanicker R, Bera JK. A highly efficient catalyst for selective oxidative scission of olefins to aldehydes: abnormal-NHC-Ru(II) complex in oxidation chemistry. Journal of the American Chemical Society. 136: 13987-90. PMID 25237828 DOI: 10.1021/Ja5075294 |
0.378 |
|
2014 |
Petakamsetty R, Das RP, Ramapanicker R. Synthesis of bis-α-amino acids through proline catalyzed asymmetric α-amination of higher homologs of Garner's aldehyde Tetrahedron. 70: 9554-9563. DOI: 10.1016/J.Tet.2014.10.048 |
0.568 |
|
2013 |
Ramapanicker R, Sun X, Viljanen J, Baltzer L. Powerful binders for the D-dimer by conjugation of the GPRP peptide to polypeptides from a designed set--illustrating a general route to new binders for proteins. Bioconjugate Chemistry. 24: 17-25. PMID 23151063 DOI: 10.1021/Bc300186Z |
0.327 |
|
2013 |
Philip AT, Chacko S, Ramapanicker R. Unusual Reactions of the 1,3-Dithiane Derivative of the Garner Aldehyde and Related Compounds Synthesis (Germany). 45: 1997-2002. DOI: 10.1055/S-0033-1338874 |
0.681 |
|
2013 |
Chacko S, Ramapanicker R. ChemInform Abstract: Synthesis of γ-Oxo γ-Aryl and γ-Aryl α-Amino Acids from Aromatic Aldehydes and Serine. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201320087 |
0.611 |
|
2012 |
Ślósarczyk AT, Ramapanicker R, Norberg T, Baltzer L. Mixed pentafluorophenyl and o-fluorophenyl esters of aliphatic dicarboxylic acids: efficient tools for peptide and protein conjugation Rsc Adv.. 2: 908-914. DOI: 10.1039/C1Ra00530H |
0.44 |
|
2012 |
Chacko S, Ramapanicker R. Synthesis of γ-oxo γ-aryl and γ-aryl α-amino acids from aromatic aldehydes and serine European Journal of Organic Chemistry. 7120-7128. DOI: 10.1002/Ejoc.201201128 |
0.664 |
|
2011 |
Ramapanicker R, Gupta R, Megha R, Chandrasekaran S. Applications of propargyl esters of amino acids in solution-phase Peptide synthesis. International Journal of Peptides. 2011: 854952. PMID 21760822 DOI: 10.1155/2011/854952 |
0.62 |
|
2010 |
Ramapanicker R, Mishra R, Chandrasekaran S. An improved procedure for the synthesis of dehydroamino acids and dehydropeptides from the carbonate derivatives of serine and threonine using tetrabutylammonium fluoride. Journal of Peptide Science : An Official Publication of the European Peptide Society. 16: 123-5. PMID 20112295 DOI: 10.1002/Psc.1210 |
0.627 |
|
2009 |
Chakrabarty SP, Ramapanicker R, Mishra R, Chandrasekaran S, Balaram H. Development and characterization of lysine based tripeptide analogues as inhibitors of Sir2 activity. Bioorganic & Medicinal Chemistry. 17: 8060-72. PMID 19861237 DOI: 10.1016/J.Bmc.2009.10.003 |
0.539 |
|
2009 |
Ramapanicker R, Baig NB, De K, Chandrasekaran S. One-pot protection and activation of amino acids using pentafluorophenyl carbonates. Journal of Peptide Science : An Official Publication of the European Peptide Society. 15: 849-55. PMID 19856278 DOI: 10.1002/Psc.1187 |
0.608 |
|
Low-probability matches (unlikely to be authored by this person) |
2019 |
Saha P, Yadav VK, Gurunarayanan V, Ramapanicker R, Singh JK, Gopakumar TG. Revealing the Limits of Intermolecular Interactions: Molecular Rings of Ferrocene Derivatives on Graphite Surface. The Journal of Physical Chemistry Letters. 297-302. PMID 31842542 DOI: 10.1021/Acs.Jpclett.9B03357 |
0.267 |
|
2018 |
Saha P, Gurunarayanan V, Korolkov VV, Vasudev PG, Ramapanicker R, Beton PH, Gopakumar TG. Selection of Adlayer Patterns of 1,3-Dithia Derivatives of Ferrocene by the Nature of the Solvent The Journal of Physical Chemistry C. 122: 19067-19074. DOI: 10.1021/Acs.Jpcc.8B06036 |
0.25 |
|
2011 |
Tegler LT, Nonglaton G, Büttner F, Caldwell K, Christopeit T, Danielson UH, Fromell K, Gossas T, Larsson A, Longati P, Norberg T, Ramapanicker R, Rydberg J, Baltzer L. Powerful protein binders from designed polypeptides and small organic molecules--a general concept for protein recognition. Angewandte Chemie (International Ed. in English). 50: 1823-7. PMID 21328648 DOI: 10.1002/Anie.201005059 |
0.219 |
|
2021 |
Gurunarayanan V, Ramapanicker R. Amphiphilic conjugates of ferrocene with amino acids and peptides: Design, synthesis, and studies on their aggregation behavior. Journal of Peptide Science : An Official Publication of the European Peptide Society. e3332. PMID 33884698 DOI: 10.1002/psc.3332 |
0.208 |
|
2019 |
Saha P, Yadav VK, Gurunarayanan V, Ramapanicker R, Singh JK, Gopakumar TG. Understanding the Adsorption Energetics of Growth Polymorphs of Ferrocene Derivatives: Microscopic Thermal Desorption Analysis The Journal of Physical Chemistry C. 123: 18488-18494. DOI: 10.1021/Acs.Jpcc.9B05557 |
0.197 |
|
2023 |
Ahlawat M, Ramapanicker R, Govind Rao V. Enhancing Photocatalytic Attributes of Perovskite Nanocrystals in Aqueous Media via Ligand Engineering. Acs Applied Materials & Interfaces. 16: 623-632. PMID 38112532 DOI: 10.1021/acsami.3c14321 |
0.136 |
|
Hide low-probability matches. |