| Year |
Citation |
Score |
| 2024 |
Khazeber R, Kana GS, Sureshan KM. Massive Molecular Motion in Crystal Leads to an Unexpected Helical Covalent Polymer in a Solid-state Polymerization. Angewandte Chemie (International Ed. in English). e202316513. PMID 38224551 DOI: 10.1002/anie.202316513 |
0.323 |
|
| 2023 |
Rai R, Khazeber R, Sureshan KM. Single-Crystal-to-Single-Crystal Topochemical Synthesis of a Collagen-inspired Covalent Helical Polymer. Angewandte Chemie (International Ed. in English). e202315742. PMID 37861464 DOI: 10.1002/anie.202315742 |
0.631 |
|
| 2023 |
Pathan JR, Bhandary S, Sureshan KM. Two Structurally Different Polymers from a Single Monomer. Journal of the American Chemical Society. PMID 37788217 DOI: 10.1021/jacs.3c07767 |
0.795 |
|
| 2023 |
Raju C, Mridula K, Srinivasan N, Kunnikuruvan S, Sureshan KM. Topochemical Syntheses of Polyarylopeptides Involving Large Molecular Motions: Frustrated Monomer Packing Leads to the Formation of Polymer Blends. Angewandte Chemie (International Ed. in English). e202306504. PMID 37486334 DOI: 10.1002/anie.202306504 |
0.802 |
|
| 2023 |
Ravi A, Pathigoolla A, Balan H, Gupta R, Raj G, Varghese R, Sureshan KM. Adamantoid Scaffolds for Multiple Cargo Loading and Cellular Delivery as β-Cyclodextrin Inclusion Complexes. Angewandte Chemie (International Ed. in English). e202307324. PMID 37384430 DOI: 10.1002/anie.202307324 |
0.538 |
|
| 2023 |
Raju C, Ramteke GR, Jose KVJ, Sureshan KM. Cascading Effect of Large Molecular Motion in Crystals: A Topotactic Polymorphic Transition Paves the Way to Topochemical Polymerization. Journal of the American Chemical Society. PMID 37078975 DOI: 10.1021/jacs.3c00132 |
0.798 |
|
| 2022 |
Hema K, Raju C, Bhandary S, Sureshan KM. Tuning the Regioselectivity of Topochemical Polymerization through Cocrystallization of the Monomer with an Inert Isostere. Angewandte Chemie (International Ed. in English). PMID 35947531 DOI: 10.1002/anie.202210733 |
0.806 |
|
| 2022 |
Khazeber R, Sureshan KM. Single-crystal-to-single-crystal translation of a helical supramolecular polymer to a helical covalent polymer. Proceedings of the National Academy of Sciences of the United States of America. 119: e2205320119. PMID 35858342 DOI: 10.1073/pnas.2205320119 |
0.316 |
|
| 2022 |
Raju C, Kunnikuruvan S, Sureshan KM. Topochemical Cycloaddition Reaction between an Azide and an Internal Alkyne. Angewandte Chemie (International Ed. in English). e202210453. PMID 35857815 DOI: 10.1002/anie.202210453 |
0.808 |
|
| 2022 |
Ravi A, Hassan SZ, Bhandary S, Sureshan KM. Topochemical Postulates: Are They Relevant for Topochemical Reactions Occurring at Elevated Temperatures? Angewandte Chemie (International Ed. in English). e202200954. PMID 35258143 DOI: 10.1002/anie.202200954 |
0.628 |
|
| 2022 |
Rai R, Sureshan KM. Topochemical Synthesis of a Heterochiral Peptide Polymer in Different Polymorphic Forms from Crystals and Aerogels. Angewandte Chemie (International Ed. in English). 61: e202111623. PMID 35076971 DOI: 10.1002/anie.202111623 |
0.616 |
|
| 2021 |
Ravi A, Shijad A, Sureshan KM. Single-crystal-to-single-crystal synthesis of a pseudostarch topochemical azide-alkyne cycloaddition polymerization. Chemical Science. 12: 11652-11658. PMID 34659700 DOI: 10.1039/d1sc03727g |
0.634 |
|
| 2021 |
Hema K, Ravi A, Raju C, Sureshan KM. Polymers with advanced structural and supramolecular features synthesized through topochemical polymerization. Chemical Science. 12: 5361-5380. PMID 34168781 DOI: 10.1039/d0sc07066a |
0.786 |
|
| 2021 |
Hema K, Ravi A, Raju C, Pathan JR, Rai R, Sureshan KM. Topochemical polymerizations for the solid-state synthesis of organic polymers. Chemical Society Reviews. PMID 33543741 DOI: 10.1039/d0cs00840k |
0.763 |
|
| 2020 |
Bursch M, Kunze L, Vibhute AM, Hansen A, Sureshan KM, Jones PG, Grimme S, Werz DB. Quantification of Non-covalent Interactions in Azide-Pnictogen, -Chalcogen, and -Halogen Contacts. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33078853 DOI: 10.1002/chem.202004525 |
0.73 |
|
| 2020 |
Vibhute AM, Sureshan KM. How Far Are We in Combating Marine Oil Spills by Using Phase-Selective Organogelators? Chemsuschem. PMID 32808717 DOI: 10.1002/Cssc.202001285 |
0.733 |
|
| 2020 |
Athiyarath V, Sureshan KM. Designed Synthesis of a 1D Polymer in Twist-Stacked Topology via Single-Crystal-to-Single-Crystal Polymerization. Angewandte Chemie (International Ed. in English). PMID 32779302 DOI: 10.1002/Anie.202006758 |
0.415 |
|
| 2020 |
Sureshan KM, Hema K. β-Sheet to Helical-sheet Evolution Induced by Topochemical Polymerization: Cross-α-amyloid-like Packing in a Pseudoprotein with Gly-Phe-Gly Repeats. Angewandte Chemie (International Ed. in English). PMID 32149438 DOI: 10.1002/Anie.201914975 |
0.369 |
|
| 2020 |
Mohanrao R, Hema K, Sureshan KM. Topochemical synthesis of different polymorphs of polymers as a paradigm for tuning properties of polymers. Nature Communications. 11: 865. PMID 32054844 DOI: 10.1038/S41467-020-14733-Y |
0.388 |
|
| 2020 |
Hema K, Gonnade RG, Sureshan KM. Crystal‐to‐Crystal Synthesis of Helically Ordered Polymers of Trehalose by Topochemical Polymerization Angewandte Chemie. 132: 2919-2925. DOI: 10.1002/Ange.201914164 |
0.42 |
|
| 2019 |
Sureshan KM, Hema K, Gonnade RG. Crystal-to-crystal synthesis of helically ordered polymers of trehalose via topochemical polymerization. Angewandte Chemie (International Ed. in English). PMID 31804011 DOI: 10.1002/anie.201914164 |
0.319 |
|
| 2019 |
Hema K, Sureshan KM. Topochemical Azide-Alkyne Cycloaddition Reaction. Accounts of Chemical Research. PMID 31600046 DOI: 10.1021/Acs.Accounts.9B00398 |
0.389 |
|
| 2019 |
Prathap A, Sureshan KM. Sugar-Based Organogelators for Various Applications. Langmuir : the Acs Journal of Surfaces and Colloids. 35: 6005-6014. PMID 30983352 DOI: 10.1021/Acs.Langmuir.9B00506 |
0.782 |
|
| 2019 |
Hema K, Sureshan KM. Solid-State Synthesis of Two Different Polymers in a Single Crystal: A Miscible Polymer Blend from a Topochemical Reaction. Angewandte Chemie (International Ed. in English). 58: 2754-2759. PMID 30609210 DOI: 10.1002/Anie.201813198 |
0.399 |
|
| 2019 |
Athiyarath V, Sureshan KM. Spontaneous Single-Crystal-to-Single-Crystal Evolution of Two Cross-Laminated Polymers. Angewandte Chemie (International Ed. in English). 58: 612-617. PMID 30461147 DOI: 10.1002/Anie.201812094 |
0.39 |
|
| 2019 |
Prathap A, Ravi A, Pathan JR, Sureshan KM. Halobenzyl alcohols as structurally simple organogelators Crystengcomm. 21: 5310-5316. DOI: 10.1039/C9Ce01008D |
0.74 |
|
| 2018 |
Mohanrao R, Sureshan KM. Synthesis and Reversible Hydration of a Pseudoprotein, a Fully Organic Polymeric Desiccant by Multiple Single-Crystal-to-Single-Crystal Transformations. Angewandte Chemie (International Ed. in English). 57: 12435-12439. PMID 30044034 DOI: 10.1002/Anie.201806451 |
0.399 |
|
| 2018 |
Vibhute AM, Priyakumar UD, Ravi A, Sureshan KM. Correction: Model molecules to classify CHO hydrogen-bonds. Chemical Communications (Cambridge, England). 54: 8136. PMID 29975379 DOI: 10.1039/C8Cc90298D |
0.76 |
|
| 2018 |
Ravi A, Sureshan KM. Tunable Mechanical Response from a Crystal Undergoing Topochemical Dimerization: Instant Explosion at a Faster Rate and Chemical Storage of a Harvestable Explosion at a Slower Rate. Angewandte Chemie (International Ed. in English). 57: 9362-9366. PMID 29870594 DOI: 10.1002/Anie.201804589 |
0.629 |
|
| 2018 |
Vibhute AM, Deva Priyakumar U, Ravi A, Sureshan KM. Model molecules to classify CHO hydrogen-bonds. Chemical Communications (Cambridge, England). 54: 4629-4632. PMID 29671427 DOI: 10.1039/C8Cc01653D |
0.764 |
|
| 2018 |
Prathap A, Raju C, Sureshan KM. Organogel-Derived Covalent-Noncovalent Hybrid Polymers as Alkali Metal-Ion Scavengers for Partial Deionization of Water. Acs Applied Materials & Interfaces. PMID 29648776 DOI: 10.1021/Acsami.8B03150 |
0.76 |
|
| 2018 |
Rai R, Krishnan BP, Sureshan KM. Chirality-controlled spontaneous twisting of crystals due to thermal topochemical reaction. Proceedings of the National Academy of Sciences of the United States of America. PMID 29507233 DOI: 10.1073/Pnas.1718965115 |
0.789 |
|
| 2018 |
Hema K, Sureshan KM. Three-way competition in a topochemical reaction: permutative azide–alkyne cycloaddition reactions leading to a vast library of products in the crystal Crystengcomm. 20: 1478-1482. DOI: 10.1039/C8Ce00131F |
0.351 |
|
| 2017 |
Krishnan BP, Sureshan KM. A Library of Multipurpose Supramolecular Supergelators: Fabrication of Structured Silica, Porous Plastics, and Fluorescent Gels. Chemistry, An Asian Journal. PMID 29195010 DOI: 10.1002/Asia.201701657 |
0.777 |
|
| 2017 |
Prathap A, Sureshan KM. Organogelator-Cellulose Composite for Practical and Eco-Friendly Marine Oil-Spill Recovery. Angewandte Chemie (International Ed. in English). 56: 9405-9409. PMID 28640482 DOI: 10.1002/Anie.201704699 |
0.773 |
|
| 2017 |
Ravi A, Hassan SZ, Vanikrishna AN, Sureshan KM. Regioselective SN2 reactions for rapid syntheses of azido-inositols by one-pot sequence-specific nucleophilysis. Chemical Communications (Cambridge, England). PMID 28327767 DOI: 10.1039/C7Cc01219E |
0.614 |
|
| 2017 |
Krishnan BP, Sureshan KM. Topochemical Azide-Alkyne Cycloaddition Reaction in Gels: Size-Tunable Synthesis of Triazole-Linked Polypeptides. Journal of the American Chemical Society. PMID 28068764 DOI: 10.1021/Jacs.6B11549 |
0.783 |
|
| 2017 |
Rai R, Sureshan KM. Thermal topochemical synthesis of pseudo-polypeptide leading to crystal cracking Acta Crystallographica Section a Foundations and Advances. 73: C485-C485. DOI: 10.1107/S205327331709088X |
0.592 |
|
| 2017 |
Sureshan K. Topochemical azide–alkyne cycloaddition reactions in crystals and organogels Acta Crystallographica Section a Foundations and Advances. 73: C758-C758. DOI: 10.1107/S2053273317088167 |
0.347 |
|
| 2016 |
Vibhute AM, Dhaka A, Athiyarath V, Sureshan KM. Correction: A versatile glycosylation strategy Au(iii) catalyzed activation of thioglycoside donors. Chemical Science. 7: 6282. PMID 30123469 DOI: 10.1039/C6Sc90051H |
0.726 |
|
| 2016 |
Vibhute AM, Dhaka A, Athiyarath V, Sureshan KM. A versatile glycosylation strategy Au(iii) catalyzed activation of thioglycoside donors. Chemical Science. 7: 4259-4263. PMID 30090287 DOI: 10.1039/C6Sc00633G |
0.75 |
|
| 2016 |
Vibhute AM, Pushpanandan P, Varghese M, Koniecnzy V, Taylor CW, Sureshan KM. Synthesis of dimeric analogs of adenophostin A that potently evoke Ca(2+) release through IP3 receptors. Rsc Advances. 6: 86346-86351. PMID 28066549 DOI: 10.1039/C6Ra19413C |
0.739 |
|
| 2016 |
Krishnan BP, Raghu S, Mukherjee S, Sureshan KM. Organogel-assisted topochemical synthesis of multivalent glyco-polymer for high-affinity lectin binding. Chemical Communications (Cambridge, England). PMID 27853762 DOI: 10.1039/C6Cc07993H |
0.767 |
|
| 2016 |
Mondal S, Sureshan KM. Carbasugar synthesis via vinylogous ketal: Total syntheses of (+)-MK7607, (-)-MK7607, (-)-Gabosine A, (-)-Epoxydine B, (-)-Epoxydine C, epi-(+)-Gabosine E and epi-(+)-MK7607. The Journal of Organic Chemistry. PMID 27808513 DOI: 10.1021/Acs.Joc.6B01876 |
0.768 |
|
| 2016 |
Krishnan BP, Rai R, Asokan A, Sureshan KM. Crystal-to-Crystal Synthesis of Triazole-linked Pseudo-proteins via Topochemical Azide-Alkyne Cycloaddition Reaction. Journal of the American Chemical Society. PMID 27791357 DOI: 10.1021/Jacs.6B07538 |
0.801 |
|
| 2016 |
Krishnan BP, Sureshan KM. A Molecular Level Study of Metamorphosis and Strengthening of Gel via Spontaneous Polymorphic Transition. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. PMID 27384543 DOI: 10.1002/Cphc.201600590 |
0.759 |
|
| 2016 |
Krishnan BP, Mukherjee S, Aneesh PM, Namboothiry MA, Sureshan KM. Semiconducting Fabrics by In Situ Topochemical Synthesis of Polydiacetylene: A New Dimension to the Use of Organogels. Angewandte Chemie (International Ed. in English). 55: 2345-9. PMID 26840212 DOI: 10.1002/Anie.201507475 |
0.764 |
|
| 2016 |
Vibhute AM, Muvvala V, Sureshan KM. A Sugar-Based Gelator for Marine Oil-Spill Recovery. Angewandte Chemie (International Ed. in English). 55: 7782-5. PMID 26821611 DOI: 10.1002/Anie.201510308 |
0.735 |
|
| 2016 |
Prathap A, Shaijumon MM, Sureshan KM. CaO nanocrystals grown over SiO2 microtubes for efficient CO2 capture: organogel sets the platform. Chemical Communications (Cambridge, England). 52: 1342-5. PMID 26621485 DOI: 10.1039/C5Cc07636F |
0.747 |
|
| 2015 |
Vidyasagar A, Sureshan KM. Stoichiometric sensing to opt between gelation and crystallization. Angewandte Chemie (International Ed. in English). 54: 12078-82. PMID 26329982 DOI: 10.1002/Anie.201506544 |
0.34 |
|
| 2015 |
Vibhute AM, Konieczny V, Taylor CW, Sureshan KM. Triazolophostins: a library of novel and potent agonists of IP3 receptors. Organic & Biomolecular Chemistry. 13: 6698-710. PMID 25869535 DOI: 10.1039/C5Ob00440C |
0.741 |
|
| 2015 |
Vidyasagar A, Sureshan KM. Total syntheses of five uvacalols: structural validation of uvacalol A, uvacalol B and uvacalol C and disproval of the structures of uvacalol E and uvacalol G. Organic & Biomolecular Chemistry. 13: 3900-10. PMID 25655990 DOI: 10.1039/C4Ob02663B |
0.307 |
|
| 2015 |
Krishnan BP, Sureshan KM. A spontaneous single-crystal-to-single-crystal polymorphic transition involving major packing changes. Journal of the American Chemical Society. 137: 1692-6. PMID 25585170 DOI: 10.1021/Ja512697G |
0.77 |
|
| 2015 |
Mondal S, Sureshan KM. ChemInform Abstract: Total Syntheses and Structural Validation of Lincitol A (Ia), Lincitol B (Ib), Uvacalol I (IIa), Uvacalol J (IIb), and Uvacalol K (IIc). Cheminform. 46: no-no. DOI: 10.1002/CHIN.201509275 |
0.741 |
|
| 2014 |
Saha T, Dasari S, Tewari D, Prathap A, Sureshan KM, Bera AK, Mukherjee A, Talukdar P. Hopping-mediated anion transport through a mannitol-based rosette ion channel. Journal of the American Chemical Society. 136: 14128-35. PMID 25203165 DOI: 10.1021/Ja506278Z |
0.763 |
|
| 2014 |
Mondal S, Sureshan KM. Total syntheses and structural validation of lincitol A, lincitol B, uvacalol I, uvacalol J, and uvacalol K. Organic & Biomolecular Chemistry. 12: 7279-89. PMID 25110185 DOI: 10.1039/C4Ob01329H |
0.775 |
|
| 2014 |
Pathigoolla A, Sureshan KM. Synthesis of triazole-linked homonucleoside polymers through topochemical azide-alkyne cycloaddition. Angewandte Chemie (International Ed. in English). 53: 9522-5. PMID 25044244 DOI: 10.1002/Anie.201404797 |
0.381 |
|
| 2014 |
Vibhute AM, Sureshan KM. Strength from weakness: conformational divergence between solid and solution states of substituted cyclitols facilitated by CH···O hydrogen bonding. The Journal of Organic Chemistry. 79: 4892-908. PMID 24784727 DOI: 10.1021/Jo5004778 |
0.759 |
|
| 2013 |
Mondal S, Prathap A, Sureshan KM. Vinylogy in orthoester hydrolysis: total syntheses of cyclophellitol, valienamine, gabosine K, valienone, gabosine G, 1-epi-streptol, streptol, and uvamalol A. The Journal of Organic Chemistry. 78: 7690-700. PMID 23879653 DOI: 10.1021/Jo401272J |
0.75 |
|
| 2013 |
Vidyasagar A, Pathigoolla A, Sureshan KM. Chemoselective alcoholysis/acetolysis of trans-ketals over cis-ketals and its application in the total synthesis of the cellular second messenger, D-myo-inositol-1,4,5-trisphosphate. Organic & Biomolecular Chemistry. 11: 5443-53. PMID 23851711 DOI: 10.1039/C3Ob40789F |
0.323 |
|
| 2013 |
Pathigoolla A, Sureshan KM. A crystal-to-crystal synthesis of triazolyl-linked polysaccharide. Angewandte Chemie (International Ed. in English). 52: 8671-5. PMID 23818337 DOI: 10.1002/Anie.201303372 |
0.338 |
|
| 2013 |
Krishnan BP, Ramakrishnan S, Sureshan KM. Supramolecular design of a bicomponent topochemical reaction between two non-identical molecules. Chemical Communications (Cambridge, England). 49: 1494-6. PMID 23208380 DOI: 10.1039/C2Cc37067K |
0.758 |
|
| 2013 |
Vibhute AM, Sureshan KM. H2SO4-silica: an eco-friendly heterogeneous catalyst for the differential protection of myo-inositol hydroxyl groups Rsc Advances. 3: 7321. DOI: 10.1039/C3Ra40506K |
0.76 |
|
| 2012 |
Prathap A, Sureshan KM. A mannitol based phase selective supergelator offers a simple, viable and greener method to combat marine oil spills. Chemical Communications (Cambridge, England). 48: 5250-2. PMID 22513880 DOI: 10.1039/C2Cc31631E |
0.759 |
|
| 2012 |
Vibhute AM, Vidyasagar A, Sarala S, Sureshan KM. Regioselectivity among six secondary hydroxyl groups: selective acylation of the least reactive hydroxyl groups of inositol. Chemical Communications (Cambridge, England). 48: 2448-50. PMID 22266806 DOI: 10.1039/C2Cc17241K |
0.749 |
|
| 2012 |
Sureshan KM, Riley AM, Thomas MP, Tovey SC, Taylor CW, Potter BV. Contribution of phosphates and adenine to the potency of adenophostins at the IP₃ receptor: synthesis of all possible bisphosphates of adenophostin A. Journal of Medicinal Chemistry. 55: 1706-20. PMID 22248345 DOI: 10.1021/Jm201571P |
0.475 |
|
| 2012 |
Vibhute AM, Gonnade RG, Swathi RS, Sureshan KM. Strength from weakness: opportunistic CH···O hydrogen bonds differentially dictate the conformational fate in solid and solution states. Chemical Communications (Cambridge, England). 48: 717-9. PMID 22116387 DOI: 10.1039/C1Cc15051K |
0.746 |
|
| 2012 |
Shivakumar K, Vidyasagar A, Naidu A, Gonnade RG, Sureshan KM. Strength from weakness: The role of CH…N hydrogen bond in the formation of wave-like topology in crystals of aza-heterocycles Crystengcomm. 14: 519-524. DOI: 10.1039/C1Ce05997A |
0.336 |
|
| 2009 |
Sureshan KM, Riley AM, Rossi AM, Tovey SC, Dedos SG, Taylor CW, Potter BV. Activation of IP(3) receptors by synthetic bisphosphate ligands. Chemical Communications (Cambridge, England). 1204-6. PMID 19240874 DOI: 10.1039/B819328B |
0.464 |
|
| 2008 |
Sureshan KM, Trusselle M, Tovey SC, Taylor CW, Potter BV. 2-Position base-modified analogues of adenophostin A as high-affinity agonists of the D-myo-inositol trisphosphate receptor: in vitro evaluation and molecular modeling. The Journal of Organic Chemistry. 73: 1682-92. PMID 18247493 DOI: 10.1021/Jo702617C |
0.506 |
|
| 2007 |
Sureshan KM, Riley AM, Potter BV. Rapid and efficient routes to phosphatidylinositol 3,4,5-trisphosphates via myo-inositol orthobenzoate Tetrahedron Letters. 48: 1923-1926. DOI: 10.1016/J.Tetlet.2007.01.095 |
0.514 |
|
| 2006 |
Sureshan KM, Trusselle M, Tovey SC, Taylor CW, Potter BV. Guanophostin A: Synthesis and evaluation of a high affinity agonist of the D-myo-inositol 1,4,5-trisphosphate receptor. Chemical Communications (Cambridge, England). 2015-7. PMID 16767260 DOI: 10.1039/B517911D |
0.495 |
|
| 2005 |
Manoj K, Sureshan KM, Gonnade RG, Bhadbhade MM, Shashidhar MS. Short SO···CO Contacts Associate Diastereomers of 2,4(6)-Di-O-benzoyl-6(4)-O-[(1S)-10-camphorsulfonyl]-myo-inositol 1,3,5-Orthoformate in Their Inclusion Complexes Crystal Growth & Design. 5: 833-836. DOI: 10.1021/Cg049621K |
0.63 |
|
| 2005 |
Sureshan KM, Kiyosawa Y, Han F, Hyodo S, Uno Y, Watanabe Y. Resolution of synthetically useful myo-inositol derivatives using the chiral auxiliary O-acetylmandelic acid Tetrahedron: Asymmetry. 16: 231-241. DOI: 10.1016/J.Tetasy.2004.11.030 |
0.313 |
|
| 2004 |
Sureshan KM, Murakami T, Miyasou T, Watanabe Y. Topochemical transketalization reaction driven by hydrogen bonding. Journal of the American Chemical Society. 126: 9174-5. PMID 15281794 DOI: 10.1021/Ja0483847 |
0.383 |
|
| 2004 |
Sureshan KM, Miyasou T, Watanabe Y. Solid and solution state conformation of 1L-1-O-acetyl-2,3:5,6-di-O-isopropylidene-chiro-inositol. Carbohydrate Research. 339: 1803-7. PMID 15220090 DOI: 10.1016/J.Carres.2004.05.005 |
0.309 |
|
| 2004 |
Sureshan KM, Miyasou T, Watanabe Y. Crystal structure of 1L-1,2:4,5-di-O-isopropylidene-allo-inositol: a comparison of its conformation in solid and solution states. Carbohydrate Research. 339: 1551-5. PMID 15178400 DOI: 10.1016/J.Carres.2004.03.031 |
0.33 |
|
| 2004 |
Sureshan KM, Miyasou T, Watanabe Y. Crystal structure, solid state and solution conformation of 1d-1,4-di-O-[(S)-O-acetylmandeloyl]-2,3:5,6-di-O-isopropylidene-myo-inositol. Carbohydrate Research. 339: 807-11. PMID 14980823 DOI: 10.1016/J.Carres.2003.12.018 |
0.311 |
|
| 2004 |
Sureshan KM, Watanabe Y. Simple and Efficient Routes to Optically Active chiro- and allo-Inositol Derivatives from myo-Inositol Synlett. 2004: 493-496. DOI: 10.1055/S-2004-815443 |
0.305 |
|
| 2004 |
Sureshan KM, Watanabe Y. An efficient route to optically active inositol derivatives via the resolution of myo-inositol 1,3,5-orthoformate: a short synthesis of d-myo-inositol-4-phosphate Tetrahedron: Asymmetry. 15: 1193-1198. DOI: 10.1016/J.Tetasy.2004.02.020 |
0.31 |
|
| 2004 |
Sureshan KM, Miyasou T, Hayashi M, Watanabe Y. Is O-acetylmandelic acid a reliable chiral anisotropy reagent? Tetrahedron: Asymmetry. 15: 3-7. DOI: 10.1016/J.Tetasy.2003.10.012 |
0.308 |
|
| 2004 |
Sureshan KM, Yamaguchi K, Sei Y, Watanabe Y. Probing gelation at the molecular level: Head-to-tail hydrogen-bonded self-assembly of an inositol-based organogelator European Journal of Organic Chemistry. 4703-4709. DOI: 10.1002/Ejoc.200400368 |
0.344 |
|
| 2003 |
Sureshan KM, Shashidhar MS, Praveen T, Das T. Regioselective protection and deprotection of inositol hydroxyl groups. Chemical Reviews. 103: 4477-503. PMID 14611268 DOI: 10.1021/Cr0200724 |
0.634 |
|
| 2003 |
Sureshan KM, Yamasaki T, Hayashi M, Watanabe Y. A simple and practical resolution of 1,2:4,5-di-O-isopropylidene-myo-inositol Tetrahedron: Asymmetry. 14: 1771-1774. DOI: 10.1016/S0957-4166(03)00402-6 |
0.313 |
|
| 2003 |
Sureshan K, Das T, Shashidhar M, Gonnade R, Bhadbhade M. Sulfonate Protecting Groups: Synthesis of D- and L-myo-Inositol-1,3,4,5-tetrakisphosphate Precursors by a Novel Silver(I) Oxide-Mediated O-Alkylation of 2,4(6)-Di-O-acyl-6(4)-O-sulfonyl-myo-Inositol 1,3,5-Orthoformate Derivatives Through Intramolecular Assistance of the Sulfonyl Group European Journal of Organic Chemistry. 2003: 1035-1041. DOI: 10.1002/Ejoc.200390145 |
0.651 |
|
| 2002 |
Sureshan KM, Shashidhar MS, Praveen T, Gonnade RG, Bhadbhade MM. Sulfonate protecting groups. Regioselective sulfonylation of myo-inositol orthoesters-improved synthesis of precursors of D- and L-myo-inositol 1,3,4,5-tetrakisphosphate, myo-inositol 1,3,4,5,6-pentakisphosphate and related derivatives. Carbohydrate Research. 337: 2399-410. PMID 12493224 DOI: 10.1016/S0008-6215(02)00298-7 |
0.672 |
|
| 2002 |
Sureshan KM, Shashidhar MS, Varma AJ. Cyclitol-based metal-complexing agents. Effect of the relative orientation of oxygen atoms in the ionophoric ring on the cation-binding ability of myo-inositol-based crown ethers. The Journal of Organic Chemistry. 67: 6884-8. PMID 12353978 DOI: 10.1021/Jo025783G |
0.639 |
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| 2001 |
Sureshan KM, Gonnade RG, Shashidhar MS, Puranik VG, Bhadbhade MM. A highly selective host–guest system formed and stabilized due to concerted halogen⋯oxygen and C-H⋯O non-bonded interactions: X-ray structures of racemic 1,2,3,4,5-penta-O-benzoyl-6-O-tosyl myo-inositol–dihalomethane (CH2X2, X = Cl and Br) inclusion complexes Chemical Communications. 881-882. DOI: 10.1039/B101394G |
0.301 |
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