Year |
Citation |
Score |
2014 |
Naini SR, Ranganathan S, Yadav JS, Ramakrishna KVS, Gayatri G, Sastry GN, Roy KB, Shamala N. The exploration of Kemp's triacid (KTA) as the core for the synthesis of 3-fold symmetric 23-cyclophane, 22-cyclophane and novel linker directed designs Rsc Advances. 4: 5322-5328. DOI: 10.1039/C3Ra44327B |
0.547 |
|
2014 |
Naini SR, Ranganathan S, Yadav JS, Sarma AVS, Ramakrishna KVS, Nagaraj R, Premkumar JR, Sastry GN. The trans opening of ethylene diamine tetra acetic acid bis anhydride (EDTAA) with cystine-di-OMe: One-step synthesis of bihelical systems Respectfully dedicated to Professor M.V. George on the occasion of his 85th birthday Tetrahedron Letters. 55: 1132-1135. DOI: 10.1016/J.Tetlet.2013.11.078 |
0.529 |
|
2014 |
Ranganathan S. Think it over Resonance. 19: 654-657. DOI: 10.1007/S12045-014-0068-0 |
0.46 |
|
2014 |
Babu SM, Ranganathan S. The total synthesis of Cephalosporin C Resonance. 19: 649-653. DOI: 10.1007/S12045-014-0067-1 |
0.511 |
|
2014 |
Babu SM, Ranganathan S. The total synthesis of chlorophyll Resonance. 19: 645-648. DOI: 10.1007/S12045-014-0066-2 |
0.526 |
|
2014 |
Babu SM, Ranganathan S. The total synthesis of strychnine Resonance. 19: 641-644. DOI: 10.1007/S12045-014-0065-3 |
0.529 |
|
2014 |
Babu SM, Ranganathan S. The spirit of adventure and the art of creation: Camphor to vitamin B12 Resonance. 19: 593-623. DOI: 10.1007/S12045-014-0063-5 |
0.491 |
|
2014 |
Ranganathan S. Robert Burns Woodward (1917-1979): A personal profile Resonance. 19: 586-589. DOI: 10.1007/S12045-014-0061-7 |
0.429 |
|
2014 |
Naini SR, Lalancette RA, Gorlova O, Ramakrishna KVS, Yadav JS, Ranganathan S. Sulfate encapsulation in supramolecular structures from L-asparagine-derived 2,5-diketopiperazine scaffolds: Anion binding European Journal of Organic Chemistry. 2014: 7015-7022. DOI: 10.1002/Ejoc.201402610 |
0.506 |
|
2013 |
Sujatha KB, Babu SM, Ranganathan S, Rao DN, Ravichandran S, Voleti SR. SILICON ACCUMULATION AND ITS INFLUENCE ON SOME OF THE LEAF CHARACTERISTICS, MEMBRANE STABILITY AND YIELD IN RICE HYBRIDS AND VARIETIES GROWN UNDER AEROBIC CONDITIONS Journal of Plant Nutrition. 36: 963-975. DOI: 10.1080/01904167.2012.759973 |
0.467 |
|
2011 |
Ranganathan S, Babu SM, Bangal PR, Madhavendra S, Voleti SR. The Novel Formation of Ordered and Varied Silica-Imidazole Complexes from Silicic Acid Phosphorus Sulfur and Silicon and the Related Elements. 186: 1835-1843. DOI: 10.1080/10426507.2010.540727 |
0.526 |
|
2011 |
Ranganathan S. Fascinating organic transformations: 2. The ubiquitous hydrogen bond Resonance. 16: 1307-1314. DOI: 10.1007/S12045-011-0148-3 |
0.499 |
|
2011 |
Ranganathan S. A tale of two topologies: Woodward-hoffmann rules at your fingertips! Resonance. 16: 1211-1222. DOI: 10.1007/S12045-011-0136-7 |
0.486 |
|
2010 |
Ranganathan S, Venkateshwarlu P, Babu SM, Reddy NS, Basha SJ, Sarma AVS, Vijay D, Sastry GN. Triply bridged (1,3,5) cyclophanes from cystine and lanthionine linkers-a comparison Tetrahedron. 66: 3923-3929. DOI: 10.1016/J.Tet.2010.03.091 |
0.526 |
|
2010 |
RANGANATHAN S, JAYARAMAN N, ROY R, MADHUSUDANAN KP. ChemInform Abstract: A Short Serendipitous Synthesis of Minimal Glucocorticoid Receptor Zinc Template. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199409239 |
0.494 |
|
2010 |
RANGANATHAN S, JAYARAMAN N. ChemInform Abstract: A General and Versatile Route to “Zinc Finger” Templates. Cheminform. 24: no-no. DOI: 10.1002/CHIN.199312238 |
0.491 |
|
2009 |
Karle IL, Huang L, Venkateshwarlu P, Sarma AV, Ranganathan S. SUBTLE CONTROL IN SOLUTION AND CRYSTAL STRUCTURES WITH WEAK HYDROGEN BONDS: THE UNUSUAL PROFILE OF DIMETHYL 3, 12-DIOXO-7, 8 DITHIA 4, 11-DIAZABICYCLO[12.2.2]OCTADECA-1(16), 14, 17-TRIENE 5, 10-DICARBOXYLATE (TDA1). Heterocycles. 79: 471-486. PMID 19688029 DOI: 10.3987/Com-08-S(D)4 |
0.505 |
|
2009 |
Rao VS, Babu SM, Ranganathan S. Biocompatible Small Molecules that Enhance Silica Solubilization Under Ambient Conditions: Chemical Profile of Such Complexes, Possible Mechanism for Enhancement, and Their Effect on the Growth and Protection from Pests in the Rice Plant (Oryza sativa L.) Phosphorus Sulfur and Silicon and the Related Elements. 184: 1975-1990. DOI: 10.1080/10426500802417208 |
0.529 |
|
2009 |
Karle IL, Butcher RJ, Rajesh YBRD, Ranganathan S. Crystal engineering: A salt of mellitate ion, MA-2, with hydronium, H3O+, containing π-π stacks of neutral phenazine, PZ, in the crystal Journal of Chemical Crystallography. 39: 309-314. DOI: 10.1007/S10870-008-9468-X |
0.529 |
|
2009 |
Karle IL, Rajesh YBRD, Ranganathan S. Crystal engineering: A unique cyclic assembly of a 40 membered module composed from two alternating units each of benzenehexacarboxylic acid (mellitic acid, MA) and 2,5-bis-(4-pyridyl)-1,3,4-oxadiazole (4-BPO): Assembly of modules to macromolecules by intermolecular hydrogen bonding Journal of Chemical Crystallography. 39: 201-208. DOI: 10.1007/S10870-008-9458-Z |
0.532 |
|
2008 |
Voleti SR, Padmakumari AP, Raju VS, Babu SM, Ranganathan S. Effect of silicon solubilizers on silica transportation, induced pest and disease resistance in rice (Oryza sativa L.) Crop Protection. 27: 1398-1402. DOI: 10.1016/J.Cropro.2008.05.009 |
0.482 |
|
2008 |
Rajesh YBRD, Ranganathan S, Gilardi RD, Karle IL. Differing patterns in the self-assembly of radially anchored imidazoles, 1,3,5-tris(1H-imidazol-2-yl)benzene and 1,3-Bis(1H-imidazol-2-yl)benzene Journal of Chemical Crystallography. 38: 39-48. DOI: 10.1007/S10870-007-9286-6 |
0.528 |
|
2007 |
Karle IL, Venkateshwarlu P, Nagaraj R, Sarma AV, Vijay D, Sastry NG, Ranganathan S. Diphenic acid as a general conformational lock in the design of bihelical structures. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 4253-63. PMID 17343288 DOI: 10.1002/Chem.200601393 |
0.508 |
|
2007 |
Ranganathan S, Rajesh YBRD, Karle IL. Novel and efficient synthesis of 2- and 4-N-substituted pyridine N-oxides under solvent-free conditions Synlett. 1215-1218. DOI: 10.1055/S-2007-977445 |
0.498 |
|
2006 |
Karle IL, Venkateshwarlu P, Ranganathan S. A robust hybrid peptide crystal formed with weak hydrogen bonds. Biopolymers. 84: 502-7. PMID 16680719 DOI: 10.1002/Bip.20535 |
0.534 |
|
2006 |
Ranganathan S, Suvarchala V, Rajesh YBRD, Prasad MS, Padmakumari AP, Voleti SR. Effects of silicon sources on its deposition, chlorophyll content, and disease and pest resistance in rice Biologia Plantarum. 50: 713-716. DOI: 10.1007/S10535-006-0113-2 |
0.464 |
|
2005 |
Karle IL, Rajesh YBRD, Ranganathan S. Conformational variability exhibited by mellitic acid anions (MA -n) with organic amine cations: Structures with an abundance of NH⋯OC hydrogen bonds and a paucity of hydrogen bonds Journal of Chemical Crystallography. 35: 835-845. DOI: 10.1007/S10870-005-4554-9 |
0.542 |
|
2004 |
Ranganathan S, Cheruku P, P MK, George KS. One-step transformation of 2-oxa-3-azabicyclo[2.2.1]heptene and 2-carbomethoxy–2,3-diazabicyclo[2.2.1]heptane to ion uptake systems Arkivoc. 2004. DOI: 10.3998/Ark.5550190.0005.805 |
0.485 |
|
2004 |
Ranganathan S, Muraleedharan K, Vaish NK, Jayaraman N. Halo- and selenolactonisation: the two major strategies for cyclofunctionalisation Tetrahedron. 60: 5273-5308. DOI: 10.1016/J.Tet.2004.04.014 |
0.67 |
|
2004 |
Ranganathan S, Rao CC, Vudayagiri SD, Rajesh YBRD, Jagadeesh B. Solubilization of silica: Synthesis, characterization and study of penta-coordinated pyridine N-oxide silicon complexes # Journal of Chemical Sciences. 116: 169-174. DOI: 10.1007/Bf02708221 |
0.511 |
|
2004 |
Ranganathan S, Muraleedharan KM, Vaish NK, Jayaraman N. Halo- and Selenolactonization: The Two Major Strategies for Cyclofunctionalization Cheminform. 35. DOI: 10.1002/CHIN.200435245 |
0.445 |
|
2003 |
Ranganathan S, Kundu D, Vudayagiri SD. Protein evolution: intrinsic preferences in peptide bond formation: a computational and experimental analysis. Journal of Biosciences. 28: 683-90. PMID 14660867 DOI: 10.1007/Bf02708428 |
0.512 |
|
2003 |
Karle I, Gilardi RD, Chandrashekhar Rao C, Muraleedharan KM, Ranganathan S. Unique assemblies of alternating positively and negatively charged layers, directed by hydrogen bonds, ionic interactions, and π-stacking in the crystal structures of complexes between mellitic acid (benzenehexacarboxylic acid) and five planar aromatic bases Journal of Chemical Crystallography. 33: 727-749. DOI: 10.1023/A:1026151222486 |
0.53 |
|
2003 |
Ranganathan S. Structural origami: A geodesic dome from five postcards Resonance. 8: 52-56. DOI: 10.1007/Bf02867130 |
0.451 |
|
2003 |
Ranganathan S. Origami, modular packing and the Soma puzzle Resonance. 8: 71-77. DOI: 10.1007/Bf02837959 |
0.47 |
|
2002 |
Ranganathan S, Muraleedharan KM, Vairamani M, Kunwar AC, Sankar AR. Unusual cyclo-tetra and hexa peptidation of bis-boc-cystine with cystine-di-OMe: one step preparation of the novel 32- and 48-membered cyclotetracystine and cyclohexacystine. Chemical Communications (Cambridge, England). 314-5. PMID 12120051 DOI: 10.1039/B109749K |
0.513 |
|
2002 |
Ranganathan S, Muraleedharan KM, Bharadwaj P, Chatterji D, Karle I. The design and synthesis of redox core-alpha amino acid composites based on thiol-disulfide exchange mechanism and a comparative study of their zinc abstraction potential from [CCXX] boxes in proteins Tetrahedron. 58: 2861-2874. DOI: 10.1016/S0040-4020(02)00159-X |
0.527 |
|
2002 |
Ranganathan S, Ranganathan A. The modular construction of DNA double helix Resonance. 7: 39-44. DOI: 10.1007/Bf02834390 |
0.46 |
|
2001 |
Ranganathan S, Muraleedharan KM, Rao CC, Vairamani M, Karle IL. One-step transformation of tricyclopentabenzene (trindane, C(15)H(18)) to bicyclo(10.3.0)pentadec-1(12)ene- 2,6,7,11-tetrone (C(15)H(18)O(4)) and its aldol product, 12-hydroxy-16-oxatetracyclo(10.3.1.0.(1,5)0(7,11))hexadec-7(11)ene-2,6-dione (C(15)H(18)O(4)). Organic Letters. 3: 2447-9. PMID 11483031 DOI: 10.1021/Ol010086G |
0.535 |
|
2001 |
Ranganathan S, Muraleedharan KM, Rao CHC, Vairamani M, Karle IL, Gilardi RD. Stacking of a benzenehexacarboxylic acid core in the crystal structure of benzenehexacarboxylic acid α-aminomethyl isobutyrate amide (MA-Aib6)–sodium nitrate complex Chemical Communications. 2544-2545. DOI: 10.1039/B109465N |
0.53 |
|
2000 |
Ranganathan S. Molecular origami: Modular construction of platonic solids as models for reversible assemblies Resonance. 5: 82-91. DOI: 10.1007/Bf02836220 |
0.467 |
|
1999 |
Ranganathan S, Tamilarasu N. Protein Engineering: Design of Single-Residue-Anchored Metal-Uptake Systems. Inorganic Chemistry. 38: 1019-1023. PMID 11670877 DOI: 10.1021/Ic980263I |
0.516 |
|
1999 |
Ranganathan S, Singh G. A Design for Peptidation in the Crystal Lattice Research On Chemical Intermediates. 25: 551-566. DOI: 10.1163/156856799X00554 |
0.507 |
|
1999 |
Ranganathan S, Kundu D, Tamilarasu N. Protein Evolution : The Deciphering Of Latent Facets - Correlation Of Synthesis Profiles Of Ribosomally Directed Proteins And Enzyme Directed Peptides Journal of Biosciences. 24: 103-113. DOI: 10.1007/Bf02941114 |
0.529 |
|
1998 |
Ranganathan S, Muraleedharan KM, Bharadwaj P, Madhusudanan KP. One step transformation of tricyclopentabenzene (trindane) [C15H18] to 4-[1R,2S,4R,5S)-1,2,5-trihydroxy-3-oxabicyclo[3.3.0]octane-4 spiro-1′-(2′-oxocyclopentan)-2-yl]butanoic acid [C15H22O7] Chemical Communications. 2239-2240. DOI: 10.1039/A805906C |
0.526 |
|
1998 |
Ranganathan S. Nobel Prize in Chemistry — 1997 Resonance. 3: 45-52. DOI: 10.1007/Bf02838984 |
0.457 |
|
1997 |
Ranganathan S, George KS. 2-Aza-3-Oxabicyclo[2.2.1]heptene hydrochloride: An exceptionally versatile synthon for carbocyclic sugars and nucleosides Tetrahedron. 53: 3347-3362. DOI: 10.1016/S0040-4020(97)00057-4 |
0.557 |
|
1997 |
Ranganathan S, Jayaraman N, Chatterji D. DNA recognition by Zn [Cysteinyl-His-OMe]2: A minimal zinc finger docking unit Biopolymers. 41: 407-418. DOI: 10.1002/(Sici)1097-0282(19970405)41:4<407::Aid-Bip5>3.0.Co;2-Q |
0.631 |
|
1996 |
Ranganathan S, Kundu D, Tamilarasu N, Nagaraj R, Dhople VM, Jaganadham MV. The gramicidin pore: Selective tryptophan replacement with aspartic acid Tetrahedron Letters. 37: 5199-5202. DOI: 10.1016/0040-4039(96)01050-7 |
0.493 |
|
1996 |
Ranganathan S, Tamilarasu N, Roy R. Protein folding: The synthesis and conformational studies on cystinyl-cystinyl-cystine [-CSSCCSSCCSSC-] a novel cross linking motif Tetrahedron. 52: 9823-9834. DOI: 10.1016/0040-4020(96)00514-5 |
0.54 |
|
1996 |
Ranganathan S. Fascinating organic transformations. 2. The ubiquitous hydrogen bond Resonance. 1: 23-30. DOI: 10.1007/Bf02896194 |
0.499 |
|
1996 |
Ranganathan S. Fascinating organic transformations: Rational mechanistic analysis Resonance. 1: 28-33. DOI: 10.1007/Bf02838855 |
0.495 |
|
1996 |
Ranganathan S. Jeans and means: 3. The story of indigo Resonance. 1: 22-27. DOI: 10.1007/Bf02837019 |
0.476 |
|
1994 |
Luthra M, Ranganathan D, Ranganathan S, Balasubramanian D. Protein-associated pigments that accumulate in the brunescent eye lens. Identification of a quinoline derivative. Febs Letters. 349: 39-44. PMID 8045299 DOI: 10.1016/0014-5793(94)00635-0 |
0.486 |
|
1994 |
Ranganathan S, Tamilarasu N. The crafting of peptide segments with CuII uptake potential Tetrahedron Letters. 35: 447-450. DOI: 10.1016/0040-4039(94)85077-1 |
0.498 |
|
1993 |
Ranganathan S, Jayaraman N, Roy R, Madhusudanan K. A short serendipitous synthesis of minimal glucocorticoid receptor zinc template Tetrahedron Letters. 34: 7801-7804. DOI: 10.1016/S0040-4039(00)61571-X |
0.655 |
|
1993 |
Ranganathan S, Patel BK. Lysine-sandwiched ionophores Tetrahedron Letters. 34: 2533-2536. DOI: 10.1016/S0040-4039(00)60461-6 |
0.616 |
|
1993 |
Ranganathan D, Ranganathan S, Singh GP, Patel BK. Demonstration of exclusive α-pep tidation at the micellar interface Tetrahedron Letters. 34: 525-528. DOI: 10.1016/0040-4039(93)85118-G |
0.639 |
|
1992 |
Ranganathan S, Jayaraman N. A general and versatile route to "zinc finger" templates Tetrahedron Letters. 33: 6681-6682. DOI: 10.1016/S0040-4039(00)61018-3 |
0.648 |
|
1992 |
Ranganathan S, Jayaraman N, Roy R. Synthesis of “ zinc finger ” template Tetrahedron. 48: 931-938. DOI: 10.1016/S0040-4020(01)88195-3 |
0.661 |
|
1991 |
Ranganathan S, Jayaraman N. Highly efficient propane-1,3-dithiol mediated thiol-disulphide interchange: A facile and clean methodology for S-S reduction in peptides Journal of the Chemical Society, Chemical Communications. 934-936. DOI: 10.1039/C39910000934 |
0.632 |
|
1991 |
Ranganathan S, Ranganathan D, Bhattacharyya D. The transformation of histidine side chain to non-coded asparagines Tetrahedron Letters. 32: 5615-5618. DOI: 10.1016/0040-4039(91)80099-R |
0.536 |
|
1990 |
Ranganathan S, Ranganathan D, Bamezai S, Singh WP, Bhattacharyya D, Sing GP, Rathi R, Saini S, Jayaraman N, Patel BK. Chemical approaches to the re-structuring of proteins Pure and Applied Chemistry. 62: 1437-1440. DOI: 10.1351/Pac199062071437 |
0.7 |
|
1989 |
Ranganathan D, Singh GP, Ranganathan S. Peptide bond formation at the micellar interface Journal of the American Chemical Society. 111: 1144-1145. DOI: 10.1021/Ja00185A063 |
0.493 |
|
1988 |
Ranganathan S, Singh WP. Convenient synthesis of 2-thionaphthylmethyl isocyanide: A useful reagent for methyl isocyanide transfer Tetrahedron Letters. 29: 1435-1436. DOI: 10.1016/S0040-4039(00)80317-2 |
0.52 |
|
1988 |
Ranganathan S, Ranganathan D, Singh W. Spontaneous cyclization of a chain shortened lysine analog Tetrahedron Letters. 29: 3111-3114. DOI: 10.1016/0040-4039(88)85099-8 |
0.506 |
|
1987 |
Ranganathan S, Ranganathan D, Singh S, Bhattacharyya D. Oxidative transformations of coded aromatic amino acids with 4-t-butyl lodylbenzene Journal of the Chemical Society, Chemical Communications. 1887-1888. DOI: 10.1039/C39870001887 |
0.521 |
|
1987 |
Ranganathan S, Ranganathan D, Bhattacharyya D. The transformation of tryptophan to aspartic acid in peptides Journal of the Chemical Society, Chemical Communications. 1085-1086. DOI: 10.1039/C39870001085 |
0.538 |
|
1987 |
Ranganathan S, Ranganathan D, Singh SK. A practical and convenient synthesis of the nitroethylene transfer reagent, 2-nitroethyl phenyl sulfoxide Tetrahedron Letters. 28: 2893-2894. DOI: 10.1016/S0040-4039(00)96237-3 |
0.509 |
|
1987 |
Ranganathan S, Ranganathan D, Singh S, Bhattacharyya D, Shanthy S, Singh G. L-methionine oxidation : novel and unanticipated transformations with 4-t butyl iodoxybenzene Tetrahedron. 43: 5363-5366. DOI: 10.1016/S0040-4020(01)87715-2 |
0.531 |
|
1985 |
Ranganathan S, Ranganathan D, Singh SK. 4-tbutyl iodoxybenzene : an effective ozone equivalent Tetrahedron Letters. 26: 4955-4956. DOI: 10.1016/S0040-4039(00)94995-5 |
0.535 |
|
1985 |
Ranganathan S, Maniktala V, Kumar R, Singh GP. Metamorphosis Of Castor Oil To Insect Sex-Pheromones And Useful Synthons Cheminform. 16. DOI: 10.1002/Chin.198521356 |
0.446 |
|
1984 |
Ranganathan S, Kumar R, Maniktala V. On the mechanism and synthetic applications of the thermal and alkaline degradation of C-18 castor oil Tetrahedron. 40: 1167-1178. DOI: 10.1016/S0040-4020(01)99322-6 |
0.531 |
|
1984 |
Ranganathan S, Ranganathan D, Ramachandran PV. Iodoxybenzene. A remarkably close ozone equivalent Tetrahedron. 40: 3145-3151. DOI: 10.1016/S0040-4020(01)82441-8 |
0.559 |
|
1983 |
Ranganathan D, Ranganathan S, Bamezai S, Mehrotra S, Ramachandran PV. 2-Nitroethyl Phenyl Sulfoxide. A Novel Reagent For Facile Nitroethylene Transfer Cheminform. 14. DOI: 10.1002/Chin.198327172 |
0.48 |
|
1982 |
Ranganathan D, Ranganathan S, Bamezai S. Nitroethylene nitroethylation of amines Tetrahedron Letters. 23: 2789-2792. DOI: 10.1016/S0040-4039(00)87459-6 |
0.534 |
|
1982 |
Ranganathan S, Kumar R, Maniktala V. A Practical, Convenient, And Highly Stereospecific Synthesis Of 1‐Acetoxy‐(E)‐9,11‐Dodecadiene. The Insect Sex Pheromone Of Bollworm Moth Cheminform. 14: 921-926. DOI: 10.1002/Chin.198326354 |
0.487 |
|
1982 |
Ranganathan S, Maniktala V, Kumar R. Synthesis of the Insect Sex Pheromone of Achroia Grisella via the Novel Synthon, 1-Tetrahydro-Pyranyloxy Dodec 11-Yne Cheminform. 14: 959-966. DOI: 10.1002/Chin.198326353 |
0.508 |
|
1981 |
Ranganathan D, Ranganathan S, Rao CB. Novel thermolytic transformations of n-benzoyl 2-aza 3-oxa bicyclo(2.2.1)hept-5-ene and n-benzoyl 2-aza 3-oxa bicyclo(2.2.1)heptane Tetrahedron. 37: 637-641. DOI: 10.1016/S0040-4020(01)92441-X |
0.523 |
|
1981 |
Ranganathan D, Ranganathan S, Rao CB, Raman K. The preparation and transformations of 2-aza-3-oxabicyclo [2.2.1] heptene hydrochloride Tetrahedron. 37: 629-635. DOI: 10.1016/S0040-4020(01)92440-8 |
0.556 |
|
1981 |
Ranganathan S, Ranganathan D, Ramachandran PV, Mahanty MK, Bamezai S. A chemical and thermochemical study of non-observed symmetry allowed reactions Tetrahedron. 37: 4171-4184. DOI: 10.1016/0040-4020(81)85008-9 |
0.559 |
|
1981 |
RANGANATHAN D, RANGANATHAN S, RAO CB, KESAVAN K. ChemInform Abstract: NITROETHYLENE: A NOVEL SYNTHON FOR N-(2-NITROETHYL)AMINO COMPOUNDS Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198112200 |
0.502 |
|
1980 |
Ranganathan D, Ranganathan S, Rao CB, Kesavan K. Nitroethylene: A Novel Synthon forN-(2-Nitroethyl)-amino Compounds Synthesis. 1980: 884-886. DOI: 10.1055/S-1980-29251 |
0.494 |
|
1980 |
Ranganathan D, Rao C, Ranganathan S, Mehrotra A, Iyengar R. Additions and Corrections - Nitroethylene: A Stable, Clean and Reactive Agent for Organic Synthesis. The Journal of Organic Chemistry. 45: 5433-5434. DOI: 10.1021/Jo01314A618 |
0.512 |
|
1980 |
Ranganathan D, Rao CB, Ranganathan S, Mehrotra AK, Iyengar R. Nitroethylene: a stable, clean, and reactive agent for organic synthesis The Journal of Organic Chemistry. 45: 1185-1189. DOI: 10.1021/Jo01295A003 |
0.508 |
|
1980 |
Ranganathan D, Ranganathan S, Mehrotra MM. The synthesis of PGF1α by re-structuring of castor oil Tetrahedron. 36: 1869-1875. DOI: 10.1016/0040-4020(80)80089-5 |
0.534 |
|
1980 |
RANGANATHAN D, RAO CB, RANGANATHAN S, MEHROTRA AK, IYENGAR R. ChemInform Abstract: NITROETHYLENE: A STABLE, CLEAN, AND REACTIVE AGENT FOR ORGANIC SYNTHESIS Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198029178 |
0.544 |
|
1980 |
Ranganathan G, Tao CB, Ranganathan S. Nitroethylene: Synthesis Of Novel 2-Nitroethylphosphonates Cheminform. 11. DOI: 10.1002/Chin.198009279 |
0.536 |
|
1979 |
Ranganathan D, Rao CB, Ranganathan S. Nitroethylene: Synthesis of novel 2-nitroethylphosphonates Journal of the Chemical Society, Chemical Communications. 975-976. DOI: 10.1039/C39790000975 |
0.51 |
|
1978 |
Ranganathan S, Ranganathan D, Mehrotra MM. A versatile synthon from castor oil: a direct, practical and novel route to 9,11-etheno-PGH Tetrahedron Letters. 19: 1851-1852. DOI: 10.1016/S0040-4039(01)94688-X |
0.468 |
|
1978 |
Ranganathan S, Raman H, Srinivasan CV. A novel stereochemical control. A persistent preference for exo electrophile acceptance in 2-bornanes Tetrahedron. 34: 3129-3132. DOI: 10.1016/0040-4020(78)87010-0 |
0.516 |
|
1978 |
RANGANATHAN S, RANGANATHAN D, MEHROTRA MM. ChemInform Abstract: A NOVEL, PRACTICAL AND BIOGENETIC-TYPE SYNTHESIS OF A RARE FURANOID FATTY ACID FROM CASTOR OIL Chemischer Informationsdienst. 9. DOI: 10.1002/Chin.197811184 |
0.512 |
|
1977 |
Ranganathan S, Singh BB, Panda CS. α,β-Unsaturated nitroso system—I : The generation and transformations of ω-nitroso camphene Tetrahedron. 33: 2415-2421. DOI: 10.1016/0040-4020(77)80256-1 |
0.485 |
|
1977 |
Ranganathan S, Ranganathan D, Mehrotra AK. A novel facet of the halolactonisation reaction Tetrahedron. 33: 807-812. DOI: 10.1016/0040-4020(77)80197-X |
0.521 |
|
1976 |
RANGANATHAN S, RANGANATHAN D, MEHROTRA AK. Synthesis of 3,5-Dioxo-2-oxatricyclo[4.2.1.04,8]-nonane (2,4-Dioxo-5-oxabrendane) Synthesis. 1976: 620-621. DOI: 10.1055/S-1976-24145 |
0.54 |
|
1976 |
Ranganathan S, Ranganathan D, Iyengar R. A simple and convenient route to 11-desoxyprostaglandins Tetrahedron. 32: 961-964. DOI: 10.1016/0040-4020(76)85057-0 |
0.537 |
|
1975 |
Ranganathan S, Ranganathan D, Mehrotra AK. An unanticipated, facile, regiospecific and stereospecific a → f prostanoid transformation Tetrahedron Letters. 16: 1215-1216. DOI: 10.1016/S0040-4039(00)72098-3 |
0.468 |
|
1975 |
Ranganathan S, Kar SK. Fascinating problems in organic reaction mechanisms-VII. Novel sodium nitrite-aqueous acid cis-hydroxylation reaction Tetrahedron. 31: 1391-1398. DOI: 10.1016/0040-4020(75)87069-4 |
0.551 |
|
1974 |
Ranganathan S, Ranganathan D, Mehrotra AK. Nitroethylene as a versatile ketene equivalent. Novel one-step preparation of prostaglandin intermediates by reduction and abnormal nef reaction Journal of the American Chemical Society. 96: 5261-5262. DOI: 10.1021/Ja00823A047 |
0.522 |
|
1974 |
Ranganathan S, Raman HH. Fascinating problems in organic reaction mechanisms—VI : Bromonitrocamphane anhydrobromonitrocamphane rearrangement Tetrahedron. 30: 63-72. DOI: 10.1016/S0040-4020(01)97217-5 |
0.528 |
|
1973 |
Ranganathan S, Raman H. Fascinating problems in organic reaction mechanisms V: Pyrolysis of bromonitrobornane Tetrahedron Letters. 14: 411-412. DOI: 10.1016/S0040-4039(01)95822-8 |
0.47 |
|
1973 |
Ranganathan S, Ranganathan D, Mehrotra AK. The "hassner-ritter" reaction in iodine azide additions to pinenes with solvent participation Tetrahedron Letters. 14: 2265-2266. DOI: 10.1016/S0040-4039(01)87611-5 |
0.492 |
|
1973 |
Ranganathan S, Ranganathan D, Sidhu RS, Mehrotra AK. [2,3] vs [3,3]: the novel [2,3] sigmatropic rearrangement of oxime-o-allyl ethers Tetrahedron Letters. 14: 3577-3578. DOI: 10.1016/S0040-4039(01)86974-4 |
0.486 |
|
1973 |
RANGANATHAN D, RANGANATHAN S, MEHROTRA AK. ChemInform Abstract: A NOVEL ROUTE TO 1-(AZIDOALKYL)-TETRAZOLES BY ′HASSNER-RITTER′ REACTION Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197342296 |
0.511 |
|
1972 |
Shechter H, Ranganathan S, Panda CS, Page T. Actions of bases and of zinc and acids on trans-2,3-dibenzoylspiro(cyclopropane-1,9'-fluorene The Journal of Organic Chemistry. 37: 1071-1073. DOI: 10.1021/Jo00972A041 |
0.628 |
|
1972 |
RANGANATHAN S, PANDA CS, PAGE T, SHECHTER H. ChemInform Abstract: WEITERE UNTERSUCHUNGEN UEBER DIE EINWIRKUNG VON BASEN UND VON ZINK UND SAEUREN AUF TRANS-2,3-DIBENZOYL-SPIRO-(CYCLOPROPAN-1,9′-FLUOREN) Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197231273 |
0.598 |
|
1971 |
Ranganathan S, Panda CS. Novel transformations of nitrocyclopropanes with triisopropylphosphite Tetrahedron Letters. 12: 3841-3842. DOI: 10.1016/S0040-4039(01)97303-4 |
0.488 |
|
1971 |
Ranganathan S, Kar SK. On the transformation of tetraphenylcyclopentadienone to pentaphenylpyrrole in boiling nitrobenzene Tetrahedron Letters. 12: 1855-1858. DOI: 10.1016/S0040-4039(01)87480-3 |
0.48 |
|
1970 |
Ranganathan S, Singh BB. A new reaction of an αβ-unsaturated nitro-compound Journal of the Chemical Society D: Chemical Communications. 218-219. DOI: 10.1039/C29700000218 |
0.517 |
|
1970 |
Ranganathan S, Kar SK. Novel cis-hydroxylation with nitrous acid Journal of Organic Chemistry. 35: 3962-3964. DOI: 10.1021/Jo00836A085 |
0.502 |
|
1970 |
Ranganathan S, Raman H. A reinterpretation of the transformation of bromonitrocompounds to ketones Tetrahedron Letters. 11: 3331-3332. DOI: 10.1016/S0040-4039(01)98466-7 |
0.495 |
|
1970 |
Ranganathan S, Singh BB, Panda CS. The preparation and transformations of an interesting bridgehead nitrile oxide Tetrahedron Letters. 11: 1225-1228. DOI: 10.1016/S0040-4039(01)91594-1 |
0.493 |
|
1970 |
Ranganathan S, Singh BB, Panda CS. Herstellung Und Umwandlungsrk. Eines Interessanten Brueckenkopfnitriloxids Cheminform. 1. DOI: 10.1002/Chin.197028238 |
0.44 |
|
1969 |
Ranganathan S, Singh BB, Divekar PV. Synthesis of caerulomycin Canadian Journal of Chemistry. 47: 165-166. DOI: 10.1139/V69-021 |
0.535 |
|
1969 |
Ranganathan S, Raman H. On the mechanism of the bromonitrocamphane-anhydrobromonitrocamphane rearrangement Tetrahedron Letters. 10: 3747-3750. DOI: 10.1016/S0040-4039(01)88503-8 |
0.457 |
|
1968 |
Ranganathan S, Goel A, Singh BB. On the mechanism of the unusual transformation of ω-nitrocamphene to 7,7-dimethyl tricyclo(2,2,1,02,6)Heptane-1-carboxylic acid Tetrahedron Letters. 9: 3299-3302. DOI: 10.1016/S0040-4039(00)89551-9 |
0.529 |
|
1966 |
Woodward RB, Heusler K, Gosteli J, Naegeli P, Oppolzer W, Ramage R, Ranganathan S, Vorbrüggen H. The Total Synthesis of Cephalosporin C1 Journal of the American Chemical Society. 88: 852-853. DOI: 10.1021/Ja00956A051 |
0.6 |
|
1962 |
Ranganathan S, Shechter H. Investigation of a Reported Synthesis of 1,3-Diphenylcyclobutadiene The Journal of Organic Chemistry. 27: 2947-2948. DOI: 10.1021/Jo01055A525 |
0.629 |
|
1957 |
Swaminathan S, Ranganathan S. Synthesis of DL-α-amino-β-(1-skatyl)propionic acid Journal of Organic Chemistry. 22: 70-72. DOI: 10.1021/Jo01352A019 |
0.513 |
|
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