Year |
Citation |
Score |
2021 |
Bahadur V, Gonnade RG, Tamboli MI, Krishnaswamy S, Shashidhar MS. Construction of Two-Component Chemically Reactive Supramolecular Assemblies-Acyl Migration Reactions in Cocrystals of Napthalene-2,3-Diol and Its Diesters. Chempluschem. 86: 1128-1134. PMID 34402211 DOI: 10.1002/cplu.202100139 |
0.393 |
|
2019 |
Shashidhar MS, Krishnaswamy S. Intermolecular Acyl-Transfer Reactions in Molecular Crystals. Accounts of Chemical Research. 52: 437-446. PMID 30698945 DOI: 10.1021/acs.accounts.8b00557 |
0.379 |
|
2018 |
Sarkar N, Sardessai RS, Shashidhar MS, Tamboli MI, Gonnade RG. Lithium hydride as an efficient reagent for the preparation of 1,2-anhydro inositols: Does the reaction proceed through 'axial rich' conformation? Carbohydrate Research. 463: 32-36. PMID 29751207 DOI: 10.1016/j.carres.2018.04.014 |
0.352 |
|
2018 |
Gurale BP, Shashidhar MS, Sardessai RS, Gonnade RG. Inositol to aromatics -benzene free synthesis of poly oxygenated aromatics. Carbohydrate Research. 461: 38-44. PMID 29574293 DOI: 10.1016/j.carres.2018.03.007 |
0.348 |
|
2018 |
Krishnaswamy S, Shashidhar MS. Correlation of Intermolecular Acyl Transfer Reactivity with Noncovalent Lattice Interactions in Molecular Crystals: Toward Prediction of Reactivity of Organic Molecules in the Solid State. The Journal of Organic Chemistry. 83: 3952-3959. PMID 29537268 DOI: 10.1021/acs.joc.8b00293 |
0.344 |
|
2018 |
Tamboli MI, Karothu DP, Shashidhar MS, Gonnade RG, Naumov P. Effect of Crystal Packing on the Thermosalient Effect of the Pincer-Type Diester Naphthalene-2,3-diyl-bis(4-fluorobenzoate): A New Class II Thermosalient Solid. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29315895 DOI: 10.1002/Chem.201705586 |
0.294 |
|
2017 |
Gonnade RG, Shashidhar MS. Acyl-transfer reactions in molecular crystals: reactivity correlation with crystal structure Acta Crystallographica Section a Foundations and Advances. 73: C771-C771. DOI: 10.1107/S2053273317088039 |
0.319 |
|
2017 |
Patil NT, Shashidhar MS, Tamboli MI, Gonnade RG. Clues from Crystal Structures Pave the Way to Access Chiral myo-Inositol Derived Versatile Synthons: Resolution of Racemic 4-O-Allyl-myo-Inositol-1,3,5-Orthoesters via Corresponding Dicamphanates by Crystallization Crystal Growth & Design. 17: 5432-5440. DOI: 10.1021/ACS.CGD.7B00895 |
0.411 |
|
2016 |
Tamboli MI, Krishanaswamy S, Gonnade RG, Shashidhar MS. Engineering crystals that facilitate the acyl-transfer reaction: insight from a comparison of the crystal structures of myo-inositol-1,3,5-orthoformate-derived benzoates and carbonates. Acta Crystallographica. Section C, Structural Chemistry. 72: 875-881. PMID 27811429 DOI: 10.1107/S205322961601603X |
0.423 |
|
2016 |
Krishnaswamy S, Shashidhar MS, Bhadbhade MM. Helical Preorganization of Molecules Drives Solid-State Intermolecular Acyl-Transfer Reactivity in Crystals: Structures and Reactivity Studies of Solvates of Racemic 2,6-Di-O-(4-fluorobenzoyl)-myo-inositol 1,3,5-Orthoformate Crystal Growth & Design. 17: 117-126. DOI: 10.1021/ACS.CGD.6B01322 |
0.419 |
|
2015 |
Tamboli MI, Shashidhar MS, Gonnade RG, Krishnaswamy S. Intramolecular Cyclization of Carbonate and Thiocarbonate Derivatives of myo-Inositol in the Solid State: Implications for Acyl Group Transfer Reactions in Molecular Crystals. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 13676-82. PMID 26260187 DOI: 10.1002/chem.201501480 |
0.417 |
|
2014 |
Tamboli MI, Bahadur V, Gonnade RG, Shashidhar MS. Correlation of the solid-state reactivities of racemic 2,4(6)-di-O-benzoyl-myo-inositol 1,3,5-orthoformate and its 4,4'-bipyridine cocrystal with their crystal structures. Acta Crystallographica. Section C, Structural Chemistry. 70: 1040-5. PMID 25370103 DOI: 10.1107/S2053229614021834 |
0.478 |
|
2014 |
Gurale BP, Sardessai RS, Shashidhar MS. myo-Inositol 1,3-acetals as early intermediates during the synthesis of cyclitol derivatives. Carbohydrate Research. 399: 8-14. PMID 25216930 DOI: 10.1016/j.carres.2014.08.010 |
0.341 |
|
2013 |
Tamboli MI, Krishnaswamy S, Gonnade RG, Shashidhar MS. Identification of molecular crystals capable of undergoing an acyl-transfer reaction based on intermolecular interactions in the crystal lattice. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 12867-74. PMID 23934729 DOI: 10.1002/chem.201301058 |
0.369 |
|
2012 |
Gurale BP, Shashidhar MS, Gonnade RG. Synthesis of the aminocyclitol units of (-)-hygromycin A and methoxyhygromycin from myo-inositol. The Journal of Organic Chemistry. 77: 5801-7. PMID 22663090 DOI: 10.1021/jo300444b |
0.329 |
|
2012 |
Gurale BP, Gonnade RG, Shashidhar MS. Chiral crystals from an achiral molecule: 4,6-di-O-benzyl-1,3-O-benzylidene-2-O-(4-methoxybenzyl)-myo-5-inosose. Acta Crystallographica. Section C, Crystal Structure Communications. 68: o183-7. PMID 22552307 DOI: 10.1107/S0108270112010001 |
0.468 |
|
2012 |
Gurale BP, Vanka K, Shashidhar MS. Radical mediated deoxygenation of inositol benzylidene acetals: conformational analysis, DFT calculations, and mechanism. Carbohydrate Research. 351: 26-34. PMID 22316428 DOI: 10.1016/J.Carres.2012.01.001 |
0.337 |
|
2012 |
Sardessai R, Krishnaswamy S, Shashidhar MS. Achieving molecular stability of racemic 4-O-benzyl-myo-inositol-1,3,5- orthoformate through crystal formation Crystengcomm. 14: 8010-8016. DOI: 10.1039/c2ce26199e |
0.434 |
|
2012 |
Manoj K, Gonnade RG, Shashidhar MS, Bhadbhade MM. Solvent induced crystallization of 1,2,3,4(6),5-penta-O-acetyl-6(4)-O-[(1S)-10-camphor sulfonyl]-myo-inositol diastereomers associated via weak trifurcated C–H⋯O interactions Crystengcomm. 14: 1716-1722. DOI: 10.1039/C2CE06287A |
0.439 |
|
2011 |
Krishnaswamy S, Patil MT, Shashidhar MS. Comparison of racemic epi-inosose and (-)-epi-inosose. Acta Crystallographica. Section C, Crystal Structure Communications. 67: o435-8. PMID 22051958 DOI: 10.1107/S0108270111039412 |
0.436 |
|
2011 |
Krishnaswamy S, Shashidhar MS, Bhadbhade MM. Intermolecular benzoyl group transfer reactivity in crystals of racemic 2,6-di-O-benzoyl-myo-inositol 1,3,5-orthobenzoate: Controlling reactivity by solvate (pseudopolymorph) formation Crystengcomm. 13: 3258. DOI: 10.1039/C1CE05054K |
0.451 |
|
2011 |
Jagdhane RC, Shashidhar MS. A formal synthesis of valiolamine from myo-inositol Tetrahedron. 67: 7963-7970. DOI: 10.1016/J.TET.2011.08.027 |
0.279 |
|
2011 |
Gurale BP, Krishnaswamy S, Vanka K, Shashidhar MS. Thermal epimerization of inositol 1,3-benzylidene acetals in the molten state Tetrahedron. 67: 7280-7288. DOI: 10.1016/J.Tet.2011.07.044 |
0.396 |
|
2010 |
Krishnaswamy S, Gonnade RG, Shashidhar MS, Bhadbhade MM. Helical self-assembly of molecules in pseudopolymorphs of racemic 2,6-di-O-(4-halobenzoyl)-myo-inositol 1,3,5-orthoformates: clues for the construction of molecular assemblies for intermolecular acyl transfer reaction Crystengcomm. 12: 4184. DOI: 10.1039/B924482D |
0.346 |
|
2010 |
Gonnade RG, Bhadbhade MM, Shashidhar MS. Crystal-to-crystal thermal phase transition amongst dimorphs of hexa-O-p-toluoyl-myo-inositol conserving two-dimensional isostructurality Crystengcomm. 12: 478-484. DOI: 10.1039/B910546H |
0.352 |
|
2010 |
Manoj K, Gonnade RG, Bhadbhade MM, Shashidhar MS. Conformational Polymorphism in Racemic 2,4-Di-o-Benzoyl-6-o-Tosyl myo-Inositol 1,3,5-Orthoacetate Journal of Structural Chemistry. 51: 725-730. DOI: 10.1007/S10947-010-0107-Y |
0.423 |
|
2010 |
Jagdhane RC, Shashidhar MS. Orthogonally Protected Cyclohexanehexols by a “One Reaction - One Product” Approach: Efficient Access to Cyclitols and Their Analogs European Journal of Organic Chemistry. 2010: 2945-2953. DOI: 10.1002/EJOC.201000009 |
0.27 |
|
2010 |
Murali C, Gurale BP, Shashidhar MS. Intramolecular Hydrogen Abstraction in Radicals Derived from Inositol 1,3-Acetals: Efficient Access to Cyclitols European Journal of Organic Chemistry. 2010: 755-764. DOI: 10.1002/EJOC.200901156 |
0.28 |
|
2009 |
Manoj K, Gonnade RG, Bhadbhade MM, Shashidhar MS. Dipolar S=O...C=O and C-H...O interactions in the molecular organization of 4,6-di-O-acetyl-2-O-tosyl-myo-inositol 1,3,5-orthoesters. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o335-8. PMID 19578267 DOI: 10.1107/S0108270109017211 |
0.447 |
|
2009 |
Devaraj S, Jagdhane RC, Shashidhar MS. Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation. Carbohydrate Research. 344: 1159-66. PMID 19508911 DOI: 10.1016/j.carres.2009.04.007 |
0.396 |
|
2009 |
Krishnaswamy S, Gonnade RG, Bhadbhade MM, Shashidhar MS. Two modes of O--H...O hydrogen bonding utilized in dimorphs of racemic 6-O-acryloyl-2-O-benzoyl-myo-inositol 1,3,5-orthoformate. Acta Crystallographica. Section C, Crystal Structure Communications. 65: o54-7. PMID 19190388 DOI: 10.1107/S0108270109000225 |
0.471 |
|
2009 |
Murali C, Shashidhar MS, Gonnade RG, Bhadbhade MM. Enhancing intermolecular benzoyl-transfer reactivity in crystals by growing a "reactive" metastable polymorph by using a chiral additive. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 261-9. PMID 19035584 DOI: 10.1002/chem.200801484 |
0.449 |
|
2009 |
Manoj K, Gonnade RG, Bhadbhade MM, Shashidhar MS. Isostructural molecular strings linked via conserved dipolar (ether) O⋯CO short contacts in conformational polymorphs of racemic 2,4-di-O-acetyl-6-O-tosyl-myo-inositol 1,3,5-orthoesters Crystengcomm. 11: 1022. DOI: 10.1039/B818888B |
0.432 |
|
2008 |
Gonnade RG, Bhadbhade MM, Shashidhar MS. Crystal-to-crystal transformation amongst dimorphs of racemic 2,6-di-O-(p-halo benzoyl)-myo-inositol 1,3,5-orthoformates that achieves halogen bonding contacts Crystengcomm. 10: 288-296. DOI: 10.1039/B712528C |
0.39 |
|
2007 |
Manoj K, Gonnade RG, Bhadbhade MM, Shashidhar MS. Different interaction motifs of dipolar S=O...C=O contacts that associate diastereomers of 2,4(6)-di-O-benzoyl-6(4)-O-{[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-ylmethyl]sulfonyl}-myo-inositol 1,3,5-orthoacetate. Acta Crystallographica. Section C, Crystal Structure Communications. 63: o555-8. PMID 17762132 DOI: 10.1107/S0108270107035858 |
0.454 |
|
2007 |
Murali C, Shashidhar MS, Gonnade RG, Bhadbhade MM. Investigating Organization of Molecules that Facilitates Intermolecular Acyl Transfer in Crystals: Reactivity and X-ray Structures ofO-Benzoyl-myo-inositol 1,3,5-Orthoesters European Journal of Organic Chemistry. 2007: 1153-1159. DOI: 10.1002/EJOC.200600765 |
0.279 |
|
2006 |
Manoj K, Gonnade RG, Bhadbhade MM, Shashidhar MS. Subtle Crossover from C−H···O to SO···CO Short Contacts in the Association of Diastereomers of 2,4(6)-Di-O-benzoyl-6(4)-O-[(1S)-10-camphorsulfonyl]-myo-inositol 1,3,5-Orthoformate upon Formation of Pseudopolymorphs Crystal Growth & Design. 6: 1485-1492. DOI: 10.1021/CG060127L |
0.416 |
|
2005 |
Gonnade RG, Bhadbhade MM, Shashidhar MS, Sanki AK. Concomitant dimorphs of tri-O-[p-halobenzoyl]-myo-inositol 1,3,5-orthoformates with different halogen bonding contacts: first order crystal-to-crystal thermal phase transition of kinetic form to the thermodynamic form. Chemical Communications (Cambridge, England). 5870-2. PMID 16317458 DOI: 10.1039/b511754b |
0.447 |
|
2005 |
Manoj K, Devaraj S, Gonnade RG, Bhadbhade MM, Shashidhar MS. O-H...O-bridged dimers linked via C-H...O and C-H...pi interactions in 4,6-di-O-benzyl-myo-inositol 1,3,5-orthoformate. Acta Crystallographica. Section C, Crystal Structure Communications. 61: o628-30. PMID 16272594 DOI: 10.1107/S0108270105029422 |
0.427 |
|
2005 |
Sarmah MP, Gonnade RG, Shashidhar MS, Bhadbhade MM. Benzoyl transfer reactivities of racemic 2,4-di-O-acyl-myo-inosityl 1,3,5-orthoesters in the solid state: molecular packing and intermolecular interactions correlate with the ease of the reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 2103-10. PMID 15714536 DOI: 10.1002/chem.200400851 |
0.502 |
|
2005 |
Gonnade RG, Sanki AK, Shashidhar MS, Bhadbhade MM. Concomitant polymorphs exhibiting differences in the halogen bonding contacts Acta Crystallographica Section a Foundations of Crystallography. 61: c279-c279. DOI: 10.1107/S0108767305088136 |
0.246 |
|
2005 |
Bhosekar G, Murali C, Gonnade RG, Shashidhar MS, Bhadbhade MM. Identical Molecular Strings Woven Differently by Intermolecular Interactions in Dimorphs ofmyo-Inositol 1,3,5-Orthobenzoate Crystal Growth & Design. 5: 1977-1982. DOI: 10.1021/CG050272J |
0.233 |
|
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 |
0.619 |
|
2004 |
Gonnade RG, Bhadbhade MM, Shashidhar MS. Capturing a metastable chiral polymorph of an achiral molecule--hexa-O-benzoyl-myo-inositol. Chemical Communications (Cambridge, England). 2530-1. PMID 15543264 DOI: 10.1039/b410051d |
0.371 |
|
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 |
0.562 |
|
2003 |
Sarmah MP, Shashidhar MS. Sulfonate protecting groups. Improved synthesis of scyllo-inositol and its orthoformate from myo-inositol. Carbohydrate Research. 338: 999-1001. PMID 12681925 |
0.43 |
|
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 |
0.65 |
|
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 |
0.656 |
|
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 |
0.551 |
|
2002 |
Shashidhar MS. Regioselective protection of myo-inositol orthoesters – recent developments Arkivoc. 2002: 63-75. DOI: 10.3998/ARK.5550190.0003.708 |
0.231 |
|
2001 |
Praveen T, Shashidhar MS. Convenient synthesis of 4,6-di-O-benzyl-myo-inositol and myo-inositol 1,3,5-orthoesters. Carbohydrate Research. 330: 409-11. PMID 11270820 |
0.455 |
|
1998 |
Samanta U, Puranik VG, Chakrabarti P, Thoniyot P, Shashidhar MS. 2-O-Benzoyl-myo-inositol-1,3,5-orthoformate Acta Crystallographica Section C Crystal Structure Communications. 54: 1289-1291. DOI: 10.1107/S0108270197017721 |
0.417 |
|
1991 |
Shashidhar MS, Volwerk JJ, Griffith OH, Keana JF. A chromogenic substrate for phosphatidylinositol-specific phospholipase C: 4-nitrophenyl myo-inositol-1-phosphate. Chemistry and Physics of Lipids. 60: 101-10. PMID 1814635 DOI: 10.1016/0009-3084(91)90032-7 |
0.573 |
|
1991 |
Shashidhar MS, Volwerk JJ, Keana JF, Griffith OH. A fluorescent substrate for the continuous assay of phosphatidylinositol-specific phospholipase C: synthesis and application of 2-naphthyl myo-inositol-1-phosphate. Analytical Biochemistry. 198: 10-4. PMID 1789410 DOI: 10.1016/0003-2697(91)90498-I |
0.569 |
|
1990 |
Shashidhar MS, Keana JF, Volwerk JJ, Griffith OH. Synthesis of phosphonate derivatives of myo-inositol for use in biochemical studies of inositol-binding proteins. Chemistry and Physics of Lipids. 53: 103-13. PMID 2354541 DOI: 10.1016/0009-3084(90)90138-H |
0.577 |
|
1990 |
Volwerk JJ, Shashidhar MS, Kuppe A, Griffith OH. Phosphatidylinositol-specific phospholipase C from Bacillus cereus combines intrinsic phosphotransferase and cyclic phosphodiesterase activities: a 31P NMR study. Biochemistry. 29: 8056-62. PMID 2175645 DOI: 10.1021/Bi00487A010 |
0.578 |
|
1990 |
Shashidhar MS, Volwerk JJ, Keana JF, Griffith OH. Inhibition of phosphatidylinositol-specific phospholipase C by phosphonate substrate analogues. Biochimica Et Biophysica Acta. 1042: 410-2. PMID 2106349 DOI: 10.1016/0005-2760(90)90172-T |
0.588 |
|
1990 |
Shashidhar MS, Keana JF, Volwerk JJ, Griffith OH. Preparation and application of an affinity matrix for phosphatidylinositol-specific phospholipase C. Chemistry and Physics of Lipids. 56: 159-67. PMID 1965711 DOI: 10.1016/0009-3084(90)90098-C |
0.566 |
|
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