Year |
Citation |
Score |
2023 |
Kotha S, Mehta G. Molecular Acrobatics in Polycyclic Frames: Synthesis of "Kurmanediol" via Post-synthetic Modification of Cage Molecules by Olefinic Metathesis. The Journal of Organic Chemistry. 88: 11650-11660. PMID 37506281 DOI: 10.1021/acs.joc.3c00968 |
0.359 |
|
2022 |
Kotha S, Mehta G. Late-stage Modification of Cage Diones by Tandem Metathesis. Chemistry, An Asian Journal. e202201022. PMID 36382422 DOI: 10.1002/asia.202201022 |
0.44 |
|
2022 |
Kotha S, Keesari RR. An Intramolecular Cycloetherification of Unactivated Olefinic Substrates Bearing endo-Alcohol: Access to Diversely Alkylated Oxa-Cage Derivatives Useful for Olefin-Metathesis. Chemistry, An Asian Journal. e202200848. PMID 36278824 DOI: 10.1002/asia.202200848 |
0.432 |
|
2022 |
Kotha S, Solanke BU, Agarwala PK, Kapoor S. Design and synthesis of hetero-steroids via ring-closing metathesis: Biological studies towards in vitro anticancer activity. Steroids. 188: 109119. PMID 36202314 DOI: 10.1016/j.steroids.2022.109119 |
0.451 |
|
2022 |
Kotha S, Gupta NK, Ansari S. One-pot thiol-free synthetic approach to sulfides, and sulfoxides selectively. Rsc Advances. 12: 25154-25162. PMID 36199306 DOI: 10.1039/d2ra04872h |
0.379 |
|
2022 |
Kotha S, Ansari S, Gupta NK. Annulation Tactics of cis-syn-cis Triquinanes by Allylsilanes: Application of Hosomi-Sakurai Reaction Conditions. Chemistry, An Asian Journal. e202200497. PMID 35796548 DOI: 10.1002/asia.202200497 |
0.295 |
|
2022 |
Kotha S, Agrawal A, Tangella Y. Synthesis of mixed musks Eschenmoser-Tanabe fragmentation, enyne metathesis and Diels-Alder reaction as key steps. Rsc Advances. 12: 14278-14281. PMID 35558836 DOI: 10.1039/d2ra01458k |
0.46 |
|
2022 |
Kotha S, Solanke BU. Modular Approach to Benzofurans, 2H-Chromenes and Benzoxepines via Claisen Rearrangement and Ring-Closing Metathesis: Access to Phenylpropanoids. Chemistry, An Asian Journal. 17: e202200084. PMID 35218606 DOI: 10.1002/asia.202200084 |
0.424 |
|
2021 |
Kotha S, Gupta NK, Ansari S. 5-[(1,3-Dimethyl-5-oxo-2-sulfanylideneimidazolidin-4-yl-idene)amino]-2-methyl-isoindoline-1,3-dione. Iucrdata. 6: x210322. PMID 36339107 DOI: 10.1107/S2414314621003229 |
0.336 |
|
2021 |
Kotha S, Fatma A, Ansari S. 2,3-Di-hydro-1-cyclo-penta-[]naphthalene-4,9-dione. Iucrdata. 6: x210167. PMID 36338857 DOI: 10.1107/S241431462100167X |
0.264 |
|
2021 |
Kotha S, Ansari S, Gupta NK. -(2a,2a ,3a,3a ,5a,6a)-2a-Allyl-2,4-di-chloro-2a,2a,3a,5a,6,6a-hexa-hydro-3a-3-oxadi-cyclo-penta-[,]penta-len-3a-ol. Iucrdata. 6: x211260. PMID 36337590 DOI: 10.1107/S2414314621012608 |
0.228 |
|
2021 |
Kotha S, Keesari RR. A Modular Approach to Angularly Fused Polyquinanes via Ring-Rearrangement Metathesis: Synthetic Access to Cameroonanol Analogues and the Basic Core of Subergorgic Acid and Crinipellin. The Journal of Organic Chemistry. PMID 34788028 DOI: 10.1021/acs.joc.1c02258 |
0.493 |
|
2021 |
Kotha S, Gupta NK, Sreevani G, Panguluri NR. Design, Synthesis and Late-Stage Modification of Indane-Based Peptides via [2+2+2] Cyclotrimerization. Chemistry, An Asian Journal. PMID 34510767 DOI: 10.1002/asia.202100825 |
0.417 |
|
2020 |
Kotha S, Gupta NK, Ansari S. ()-3-Thia-1,5(1,3)-dibenzena-cyclo-undeca-phan-8-ene-6,11-dione 3,3-dioxide. Iucrdata. 5: x201464. PMID 36340018 DOI: 10.1107/S2414314620014649 |
0.294 |
|
2020 |
Kotha S, Ansari S, Cheekatla SR. 7-Meth-oxy-penta-cyclo-[5.4.0.0.0.0]undec-ane-8,11-dione. Iucrdata. 5: x201380. PMID 36339030 DOI: 10.1107/S2414314620013802 |
0.356 |
|
2020 |
Kotha S, Cheekatla SR. A new skeletal rearrangement of 1,7-dimethyl Cookson's cage dione catalyzed by a Lewis acid. Organic & Biomolecular Chemistry. PMID 31998915 DOI: 10.1039/C9Ob02298H |
0.509 |
|
2020 |
Kotha S, Pulletikurti S. Lewis Acid Mediated Synthesis of Indolizidine Derivatives Heterocycles. 101: 717. DOI: 10.3987/com-19-s(f)50 |
0.423 |
|
2020 |
Kotha S, Cheekatla SR. Design, synthesis, and rearrangement studies of gem-dimethyl containing cage systems Tetrahedron. 76: 130898. DOI: 10.1016/J.Tet.2019.130898 |
0.515 |
|
2020 |
Kotha S, Ansari S, Cheekatla SR, Dipak MK. Synthesis of oxa-cage compounds by ketalization and ring-closing metathesis Tetrahedron. 76: 130856. DOI: 10.1016/J.Tet.2019.130856 |
0.505 |
|
2020 |
Kotha S, Fatma A. Construction of [5/7/5] Fused Tricyclic Sulfones via Ring‐Rearrangement Metathesis Chemistryselect. 5: 1929-1931. DOI: 10.1002/slct.201904381 |
0.309 |
|
2020 |
Kotha S, Gupta NK, Ansari S. Facile Synthetic Route to [3.n]Thiacyclophanes through Ring‐Closing Metathesis and their Structural Studies European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.202000697 |
0.372 |
|
2019 |
Kotha S, Chavan AS, Goyal D. Diversity-Oriented Approaches to Polycycles and Heterocycles via Enyne Metathesis and Diels-Alder Reaction as Key Steps. Acs Omega. 4: 22261-22273. PMID 31909309 DOI: 10.1021/acsomega.9b03020 |
0.429 |
|
2019 |
Kotha S, Sreevani G, Dzhemileva LU, Yunusbaeva MM, Dzhemilev UM, D'yakonov VA. Diversity-oriented synthesis of spirothiazolidinediones and their biological evaluation. Beilstein Journal of Organic Chemistry. 15: 2774-2781. PMID 31807211 DOI: 10.3762/Bjoc.15.269 |
0.47 |
|
2019 |
Kotha S, Keesari RR, Fatma A, Gunta R. Synthetic Strategies to Diverse Polyquinanes via Olefin Metathesis: Access to the Basic Core of Crinipellin, Presilphiperfolanol and Cucumin. The Journal of Organic Chemistry. PMID 31802663 DOI: 10.1021/Acs.Joc.9B02829 |
0.526 |
|
2019 |
Kotha S, Cheekatla SR, Fatma A. Synthetic Approach to the ABCD Ring System of Anticancer Agent Fredericamycin A via Claisen Rearrangement and Ring-Closing Metathesis as Key Steps. Acs Omega. 4: 17109-17116. PMID 31656883 DOI: 10.1021/acsomega.9b01178 |
0.474 |
|
2019 |
Kotha S, Meshram M. Development of New Synthetic Strategies, Tactics and their Applications. Chemical Record (New York, N.Y.). PMID 31631498 DOI: 10.1002/Tcr.201900041 |
0.49 |
|
2019 |
Kotha S, Gupta NK, Aswar VR. Multicomponent Approach to Hydantoins and Thiohydantoins Involving a Deep Eutectic Solvent. Chemistry, An Asian Journal. PMID 31386259 DOI: 10.1002/Asia.201900744 |
0.474 |
|
2019 |
Kotha S, Todeti S. Synthesis of -symmetric star-shaped molecules containing α-amino acids and dipeptides via Negishi coupling as a key step. Beilstein Journal of Organic Chemistry. 15: 371-377. PMID 30800186 DOI: 10.3762/Bjoc.15.33 |
0.527 |
|
2019 |
Kotha S, Meshram M, Panguluri NR, Shah VR, Todeti S, Shirbhate ME. Synthetic Approaches to Star-Shaped Molecules with 1,3,5-Trisubstituted Aromatic Cores. Chemistry, An Asian Journal. PMID 30762307 DOI: 10.1002/Asia.201801912 |
0.482 |
|
2019 |
Kotha S, Pulletikurti S, Dommaraju Y. Ring-Opening Metathesis of N-Alkenyl β-Lactams Heterocycles. 98: 79. DOI: 10.3987/Com-18-S(F)81 |
0.408 |
|
2019 |
Kotha S, Gunta R. Synthesis of Alkenyl Sulfones Containing Norbornene Moiety Heterocycles. 98: 271. DOI: 10.3987/Com-18-S(F)80 |
0.527 |
|
2019 |
Kotha S, Pulletikurti S. A Metathetic Approach to [5/5/6] Aza-Tricyclic Core of Dendrobine, Kopsanone, and Lycopalhine A Type of Alkaloids Synthesis. 51: 3981-3988. DOI: 10.1055/S-0039-1690620 |
0.555 |
|
2019 |
Kotha S, Keesari RR, Ansari S. Synthesis of Aza-polyquinanes via Fischer Indolization and Ring-Rearrangement Metathesis as Key Steps Synthesis. 51: 3989-3997. DOI: 10.1055/S-0039-1690179 |
0.552 |
|
2019 |
Kotha S, Meshram M, Panguluri N. Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions Synthesis. 51: e1-e1. DOI: 10.1055/S-0037-1610876 |
0.456 |
|
2019 |
Kotha S, Meshram M, Aswar VR. Application of ring-rearrangement metathesis in organic synthesis: A grand design Tetrahedron Letters. 60: 151337. DOI: 10.1016/J.Tetlet.2019.151337 |
0.539 |
|
2019 |
Kotha S, Khedkar P, Dommaraju Y. Synthetic applications of rongalite: A green tool in the service of Diels–Alder chemistry and beyond Tetrahedron Letters. 60: 631-648. DOI: 10.1016/J.Tetlet.2019.01.031 |
0.445 |
|
2019 |
Kotha S, Todeti S. Synthesis of C3-Symmetric star-shaped molecules containing 1,3-azoles via hetero-aryl Heck coupling Tetrahedron. 75: 1359-1363. DOI: 10.1016/J.Tet.2019.01.044 |
0.467 |
|
2019 |
Kotha S, Cheekatla SR. Synthesis of functionalized cage propellanes and D3-Trishomocubanes via the ring-closing metathesis and acid-promoted rearrangement Tetrahedron. 75: 84-93. DOI: 10.1016/J.Tet.2018.11.027 |
0.524 |
|
2019 |
Kotha S, Ali R. A simple synthetic strategy to
$$\pi $$
π
-conjugated spirofluorenes Journal of Chemical Sciences. 131. DOI: 10.1007/S12039-019-1637-2 |
0.554 |
|
2019 |
Kotha S, Cheekatla SR. Synthesis and Acid Catalyzed Rearrangement of Cage Propellanes Chemistryselect. 4: 13440-13445. DOI: 10.1002/slct.201903441 |
0.436 |
|
2019 |
Kotha S, Cheekatla SR, Meshram M, Bandi V, Seema V. Realization of Photo‐Thermal Metathesis Under Microwave Irradiation Conditions: An Entry to Triquinane Frameworks Asian Journal of Organic Chemistry. 8: 2097-2104. DOI: 10.1002/Ajoc.201900432 |
0.363 |
|
2019 |
Kotha S, Aswar VR, Ansari S. Selectivity in Ring‐Closing Metathesis: Synthesis of Propellanes and Angular Aza‐tricycles Advanced Synthesis & Catalysis. 361: 1376-1382. DOI: 10.1002/Adsc.201801123 |
0.446 |
|
2018 |
Kotha S, Pulletikurti S. Synthesis of propellanes containing a bicyclo[2.2.2]octene unit the Diels-Alder reaction and ring-closing metathesis as key steps. Rsc Advances. 8: 14906-14915. PMID 35541332 DOI: 10.1039/c8ra02687d |
0.515 |
|
2018 |
Kotha S, Sreevani G. [2 + 2 + 2] Cyclotrimerization with Propargyl Halides as Copartners: Formal Total Synthesis of the Antitumor Hsp90 Inhibitor AT13387. Acs Omega. 3: 1850-1855. PMID 31458497 DOI: 10.1021/acsomega.7b01976 |
0.276 |
|
2018 |
Kotha S, Todeti S, Aswar VR. Design and synthesis of -symmetric molecules bearing propellane moieties via cyclotrimerization and a ring-closing metathesis sequence. Beilstein Journal of Organic Chemistry. 14: 2537-2544. PMID 30410614 DOI: 10.3762/Bjoc.14.230 |
0.548 |
|
2018 |
Kotha S, Meshram M, Chakkapalli C. Synergistic approach to polycycles through Suzuki-Miyaura cross coupling and metathesis as key steps. Beilstein Journal of Organic Chemistry. 14: 2468-2481. PMID 30344770 DOI: 10.3762/Bjoc.14.223 |
0.48 |
|
2018 |
Kotha S, Meshram M. Application of Claisen Rearrangement and Olefin Metathesis in Organic Synthesis. Chemistry, An Asian Journal. PMID 29956880 DOI: 10.1002/Asia.201800613 |
0.539 |
|
2018 |
Kotha S, Meshram M, Dommaraju Y. Design and Synthesis of Polycycles, Heterocycles, and Macrocycles via Strategic Utilization of Ring-Closing Metathesis. Chemical Record (New York, N.Y.). PMID 29920922 DOI: 10.1002/Tcr.201800025 |
0.578 |
|
2018 |
Kotha S, Cheekatla SR. Molecular acrobatics in polycyclic frames: Synthesis of functionalized D3-trishomocubanes via rearrangement approach. The Journal of Organic Chemistry. PMID 29768916 DOI: 10.1021/Acs.Joc.8B00449 |
0.496 |
|
2018 |
Kotha S, Rao Cheekatla S, Meshram M. Synthetic Approach to Oxa-Cage Systems via Ring-Closing Metathesis Heterocycles. 97: 1008. DOI: 10.3987/Com-18-S(T)83 |
0.455 |
|
2018 |
Kotha S, Gunta R, Cheekatla SR, Mhatre DS. Spiro[cyclopentane-1,11′-hexacyclo[7.6.0.01,6.06,13.08,12.010,14]pentadecane]-7′,15′-dione Iucrdata. 3. DOI: 10.1107/S2414314618015900 |
0.479 |
|
2018 |
Kotha S, Cheekatla SR, Gunta R. Hexacyclo[6.5.1.01,5.05,12.07,11.09,13]tetradecane-4,6,14-trione Iucrdata. 3. DOI: 10.1107/S2414314618008520 |
0.444 |
|
2018 |
Kotha S, Cheekatla SR, Gunta R. 7-Hydroxyhexacyclo[7.5.1.01,7.06,13.08,12.010,14]pentadecan-15-one-11-spirocyclopentane Iucrdata. 3. DOI: 10.1107/S2414314618000901 |
0.492 |
|
2018 |
Kotha S, Sreevani G. Synthesis of Spiro Barbiturates and Meldrum’s Acid Derivatives via a [2+2+2] Cyclotrimerization Synthesis. 50: 4883-4888. DOI: 10.1055/S-0037-1610238 |
0.545 |
|
2018 |
Kotha S, Lahiri K, Sreevani G. Design and Synthesis of Aromatics through [2+2+2] Cyclotrimerization Synlett. 29: 2342-2361. DOI: 10.1055/S-0037-1609584 |
0.554 |
|
2018 |
Kotha S, Pulletikurti S. Synthesis of propellanes containing a bicyclo[2.2.2]octene unit via the Diels–Alder reaction and ring-closing metathesis as key steps Rsc Advances. 8: 14906-14915. DOI: 10.1039/C8Ra02687D |
0.557 |
|
2018 |
Kotha S, Ali R, Panguluri NR, Datta A, Kannaujiya KK. Synthesis and photophysical properties of star-shaped blue green emitting π-conjugated spirotruxenes Tetrahedron Letters. 59: 4080-4085. DOI: 10.1016/J.Tetlet.2018.10.005 |
0.401 |
|
2018 |
Kotha S, Todeti S, Das T, Datta A. Synthesis of star-shaped pyrrole-based C3-symmetric molecules via ring-closing metathesis, Buchwald–Hartwig cross-coupling and Clauson–Kaas pyrrole synthesis as key steps Tetrahedron Letters. 59: 1023-1027. DOI: 10.1016/J.Tetlet.2018.01.084 |
0.525 |
|
2018 |
Kotha S, Meshram M. Application of organometallics in organic synthesis Journal of Organometallic Chemistry. 874: 13-25. DOI: 10.1016/J.Jorganchem.2018.08.008 |
0.481 |
|
2018 |
Kotha S, Cheekatla SR. Synthesis of cage [4.4.2]propellanes and
$${D_{3}}$$
D
3
-trishomocubanes bearing spiro linkage Journal of Chemical Sciences. 130. DOI: 10.1007/S12039-018-1569-2 |
0.359 |
|
2018 |
Kotha S, Todeti S, Das T, Datta A. Synthesis and Photophysical Properties of C3
-Symmetric Star-Shaped Molecules Containing Heterocycles: A New Tactics for Multiple Fischer Indolization Chemistryselect. 3: 136-141. DOI: 10.1002/slct.201702675 |
0.346 |
|
2018 |
Kotha S, Sreevani G. Diversity-Oriented Approach to Spirorhodanines via a [2+2+2] Cyclotrimerization European Journal of Organic Chemistry. 2018: 5935-5941. DOI: 10.1002/Ejoc.201800775 |
0.36 |
|
2017 |
Kotha S, Todeti S, Gopal MB, Datta A. Synthesis and Photophysical Properties of -Symmetric Star-Shaped Molecules Containing Heterocycles Such as Furan, Thiophene, and Oxazole. Acs Omega. 2: 6291-6297. PMID 31457237 DOI: 10.1021/acsomega.7b00941 |
0.425 |
|
2017 |
Kotha S, Gunta R. Synthesis of Intricate Fused N-Heterocycles via Ring-Rearrangement Metathesis. The Journal of Organic Chemistry. PMID 28721727 DOI: 10.1021/Acs.Joc.7B01299 |
0.455 |
|
2017 |
Kotha S, Chakkapalli C. Application of Fischer Indolization under Green Conditions using Deep Eutectic Solvents. Chemical Record (New York, N.Y.). PMID 28378920 DOI: 10.1002/Tcr.201600138 |
0.468 |
|
2017 |
Kotha S, Cheekatla S, Mhatre D. Ring-Closing Metathesis Approach to Cage Propellanes Containing Oxepane and Tetrahydrofuran Hybrid System Synthesis. 49: 5339-5350. DOI: 10.1055/S-0036-1591726 |
0.526 |
|
2017 |
Kotha S, Aswar VR, Chinnam AK. One-pot synthesis of carbazoles from indoles via a metal free benzannulation Tetrahedron Letters. 58: 4360-4362. DOI: 10.1016/J.Tetlet.2017.10.002 |
0.779 |
|
2017 |
Kotha S, Rao NN, Ravikumar O, Sreevani G. Isomerization and functionalization of 2:1 Diels–Alder adducts of cyclopentadiene and p -benzoquinone: Applications to polycycles via ring-closing metathesis and ring-opening metathesis as key steps Tetrahedron Letters. 58: 1283-1286. DOI: 10.1016/J.Tetlet.2017.02.039 |
0.504 |
|
2017 |
Kotha S, Aswar VR, Singhal G. Synthesis of tricyclic units of indole alkaloids: Application of Fischer indolization and olefin metathesis Tetrahedron. 73: 6436-6442. DOI: 10.1016/J.Tet.2017.09.039 |
0.579 |
|
2017 |
Kotha S, Sreevani G. A Short Synthetic Route to Benzosultine-sulfone using Rongalite and [2+2+2]-Cyclotrimerization Chemistryselect. 2: 10804-10808. DOI: 10.1002/slct.201702348 |
0.308 |
|
2017 |
Kotha S, Cheekatla SR. A New Synthetic Approach toC2-Symmetric Octacyclic Cage Diol via Claisen Rearrangement and Ring-Closing Metathesis as Key Steps Chemistryselect. 2: 6877-6881. DOI: 10.1002/slct.201701633 |
0.444 |
|
2017 |
Kotha S, Rao Cheekatla S, Mandal B. Synthesis and Rearrangement of Cage [4.3.2]Propellanes that Contain a Spiro Linkage European Journal of Organic Chemistry. 2017: 4277-4282. DOI: 10.1002/Ejoc.201700617 |
0.545 |
|
2017 |
Kotha S, Panguluri NR, Ali R. Design and Synthesis of Spirocycles European Journal of Organic Chemistry. 2017: 5316-5342. DOI: 10.1002/Ejoc.201700439 |
0.557 |
|
2016 |
Kotha S, Gunta R. Bridgehead vicinal diallylation of norbornene derivatives and extension to propellane derivatives via ring-closing metathesis. Beilstein Journal of Organic Chemistry. 12: 1877-1883. PMID 27829894 DOI: 10.3762/Bjoc.12.177 |
0.472 |
|
2016 |
Kotha S, Saifuddin M, Aswar VR. A diversity-oriented approach to indolocarbazoles via Fischer indolization and olefin metathesis: total synthesis of tjipanazole D and I. Organic & Biomolecular Chemistry. PMID 27714197 DOI: 10.1039/C6Ob01679K |
0.531 |
|
2016 |
Kotha S, Aswar VR. Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes. Organic Letters. PMID 27050839 DOI: 10.1021/Acs.Orglett.6B00537 |
0.491 |
|
2016 |
Kotha S, Misra S, Gopal Krishna N, Bandi V, Saifuddin M, Devunuri N. Diversity-Oriented Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives Heterocycles. 93: 185. DOI: 10.3987/Com-15-S(T)16 |
0.453 |
|
2016 |
Kotha S, Bandi V, Gunta R, Gaddamedi S. Hexacyclo[7.5.1.01,6.06,13.08,12.010,14]pentadecane-7,15-dione Iucrdata. 1. DOI: 10.1107/S2414314616011731 |
0.404 |
|
2016 |
Kotha S, Cheekatla SR, Chinnam AK, Jain T. Design and synthesis of polycyclic bisindoles via Fischer indolization and ring-closing metathesis as key steps Tetrahedron Letters. 57: 5605-5607. DOI: 10.1016/J.Tetlet.2016.10.112 |
0.795 |
|
2016 |
Kotha S, Gunta R. A new synthetic strategy to 2,3-diallyl-1,4-quinones via one-pot double Claisen rearrangement and retro Diels–Alder reaction Tetrahedron Letters. 57: 3021-3023. DOI: 10.1016/J.Tetlet.2016.05.101 |
0.502 |
|
2016 |
Kotha S, Ravikumar O. Synthesis of fused azacycle via Overman rearrangement and ring-rearrangement metathesis as key steps Tetrahedron Letters. 57: 1994-1996. DOI: 10.1016/J.Tetlet.2016.03.087 |
0.551 |
|
2016 |
Kotha SS, Sharma N, Sekar G. Stable and reusable platinum nanocatalyst: An efficient chemoselective reduction of nitroarenes in water Tetrahedron Letters. 57: 1410-1413. DOI: 10.1016/j.tetlet.2016.01.111 |
0.237 |
|
2016 |
Kotha S, Ravikumar O, Sreevani G. Design and synthesis of oxacycles from norbornene derivatives via ring-opening metathesis and ring-rearrangement metathesis Tetrahedron. 72: 6611-6615. DOI: 10.1016/J.Tet.2016.08.073 |
0.515 |
|
2016 |
Kotha S, Aswar VR, Manchoju A. A four-step route to synthetic equivalents of ortho-xylylenes: Dötz benzannulation, desilylation, bromo-dehydroxylation, and sultine formation. A concise approach to oxygenated linearly fused polycyclic aromatics Tetrahedron. 72: 2306-2315. DOI: 10.1016/J.Tet.2016.03.047 |
0.534 |
|
2016 |
Wentzell S, Nesbitt RS, Macione J, Kotha S. Measurement of lacunar bone strains and crack formation during tensile loading by digital volume correlation of second harmonic generation images Journal of the Mechanical Behavior of Biomedical Materials. 60: 148-156. DOI: 10.1016/j.jmbbm.2015.12.027 |
0.186 |
|
2016 |
Wadhwa A, Phelps C, Kotha S. Corporate venture capital portfolios and firm innovation Journal of Business Venturing. 31: 95-112. DOI: 10.1016/J.Jbusvent.2015.04.006 |
0.185 |
|
2016 |
Kotha SR, Bindi D, Cotton F. Partially non-ergodic region specific GMPE for Europe and Middle-East Bulletin of Earthquake Engineering. 14: 1245-1263. DOI: 10.1007/s10518-016-9875-x |
0.173 |
|
2016 |
Kotha S, Ravikumar O. Ring-Rearrangement-Metathesis Approach to Polycycles: Substrate-Controlled Stereochemical Outcome During Grignard Addition European Journal of Organic Chemistry. 2016: 3900-3906. DOI: 10.1002/Ejoc.201600596 |
0.433 |
|
2016 |
Kotha S, Gunta R. ChemInform Abstract: A New Synthetic Strategy to 2,3-Diallyl-1,4-quinones via One-Pot Double Claisen Rearrangement and Retro Diels-Alder Reaction. Cheminform. 47. DOI: 10.1002/chin.201643079 |
0.422 |
|
2016 |
Kotha S, Aswar VR, Manchoju A. ChemInform Abstract: A Four-Step Route to Synthetic Equivalents of ortho-Xylylenes: Doetz Benzannulation, Desilylation, Bromo-Dehydroxylation, and Sultine Formation. A Concise Approach to Oxygenated Linearly Fused Polycyclic Aromatics. Cheminform. 47. DOI: 10.1002/chin.201632105 |
0.379 |
|
2016 |
Kotha S, Chavan AS, Waghule GT. ChemInform Abstract: Synthetic Approaches to Cyclophanes via Claisen Rearrangement and Ring-Closing Metathesis as Key Steps. Cheminform. 47: no-no. DOI: 10.1002/chin.201610057 |
0.449 |
|
2015 |
Azam A, Manchanda S, Thotapalli S, Kotha SB. Botox Therapy in Dentistry: A Review. Journal of International Oral Health : Jioh. 7: 103-5. PMID 26668495 |
0.165 |
|
2015 |
Kotha S, Meshram M, Khedkar P, Banerjee S, Deodhar D. Recent applications of ring-rearrangement metathesis in organic synthesis. Beilstein Journal of Organic Chemistry. 11: 1833-1864. PMID 26664603 DOI: 10.3762/Bjoc.11.199 |
0.478 |
|
2015 |
Kotha S, Gunta R. Design and synthesis of propellane derivatives and oxa-bowls via ring-rearrangement metathesis as a key step. Beilstein Journal of Organic Chemistry. 11: 1727-31. PMID 26664592 DOI: 10.3762/Bjoc.11.188 |
0.536 |
|
2015 |
Kotha S, Chinnam AK, Shirbhate ME. Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps. Beilstein Journal of Organic Chemistry. 11: 1514-9. PMID 26425209 DOI: 10.3762/Bjoc.11.165 |
0.813 |
|
2015 |
Kotha S, Ravikumar O, Majhi J. Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps. Beilstein Journal of Organic Chemistry. 11: 1503-8. PMID 26425207 DOI: 10.3762/Bjoc.11.163 |
0.537 |
|
2015 |
Kotha S, Gunta R. Design and synthesis of polycyclic sulfones via Diels-Alder reaction and ring-rearrangement metathesis as key steps. Beilstein Journal of Organic Chemistry. 11: 1373-8. PMID 26425192 DOI: 10.3762/Bjoc.11.148 |
0.548 |
|
2015 |
Kotha S, Saifuddin M, Ali R, Sreevani G. Spiro annulation of cage polycycles via Grignard reaction and ring-closing metathesis as key steps. Beilstein Journal of Organic Chemistry. 11: 1367-72. PMID 26425191 DOI: 10.3762/Bjoc.11.147 |
0.54 |
|
2015 |
Kotha S, Shirbhate ME, Waghule GT. Selected synthetic strategies to cyclophanes. Beilstein Journal of Organic Chemistry. 11: 1274-331. PMID 26425186 DOI: 10.3762/Bjoc.11.142 |
0.448 |
|
2015 |
Kotha S, Ravikumar O. Design and synthesis of fused polycycles via Diels-Alder reaction and ring-rearrangement metathesis as key steps. Beilstein Journal of Organic Chemistry. 11: 1259-64. PMID 26425184 DOI: 10.3762/Bjoc.11.140 |
0.552 |
|
2015 |
Kotha S, Chinnam AK, Shirbhate ME. Diversity-Oriented Approach to Cyclophanes via Fischer Indolization and Ring-Closing Metathesis: Substrate-Controlled Stereochemical Outcome in RCM. The Journal of Organic Chemistry. 80: 9141-6. PMID 26317873 DOI: 10.1021/Acs.Joc.5B01433 |
0.793 |
|
2015 |
Macione J, Long D, Nesbitt S, Wentzell S, Yokota H, Pandit V, Kotha S. Stimulation of osteoblast differentiation with guided ultrasound waves. Journal of Therapeutic Ultrasound. 3: 12. PMID 26246899 DOI: 10.1186/S40349-015-0034-7 |
0.187 |
|
2015 |
Heisler DB, Kudryashova E, Grinevich DO, Suarez C, Winkelman JD, Birukov KG, Kotha SR, Parinandi NL, Vavylonis D, Kovar DR, Kudryashov DS. ACTIN-DIRECTED TOXIN. ACD toxin-produced actin oligomers poison formin-controlled actin polymerization. Science (New York, N.Y.). 349: 535-9. PMID 26228148 DOI: 10.1126/Science.Aab4090 |
0.21 |
|
2015 |
Kotha S, Chinnam AK, Ali R. Hybrid macrocycle formation and spiro annulation on cis-syn-cis-tricyclo[6.3.0.0(2,6)]undeca-3,11-dione and its congeners via ring-closing metathesis. Beilstein Journal of Organic Chemistry. 11: 1123-8. PMID 26199668 DOI: 10.3762/Bjoc.11.126 |
0.762 |
|
2015 |
Yeoman AD, Kotha S, Heneghan MA. Reply to "The role of corticosteroids in acute-severe autoimmune hepatitis is still highly debatable". Journal of Hepatology. 63: 1043. PMID 26163987 DOI: 10.1016/j.jhep.2015.06.029 |
0.178 |
|
2015 |
Kotha S, Chavan AS, Goyal D. Diversity-Oriented Approaches to Polycyclics and Bioinspired Molecules via the Diels-Alder Strategy: Green Chemistry, Synthetic Economy, and Beyond. Acs Combinatorial Science. 17: 253-302. PMID 25875156 DOI: 10.1021/Co500146U |
0.538 |
|
2015 |
Marcu R, Kotha S, Zhi Z, Qin W, Neeley CK, Wang RK, Zheng Y, Hawkins BJ. The mitochondrial permeability transition pore regulates endothelial bioenergetics and angiogenesis. Circulation Research. 116: 1336-45. PMID 25722455 DOI: 10.1161/Circresaha.116.304881 |
0.176 |
|
2015 |
Pandit V, Watson A, Ren L, Mixon A, Kotha SP. Multilayered Nanoparticles for Gene Delivery Used to Reprogram Human Foreskin Fibroblasts to Neurospheres. Tissue Engineering. Part C, Methods. PMID 25687130 DOI: 10.1089/Ten.Tec.2014.0482 |
0.239 |
|
2015 |
Pandit V, Nesbitt SR, Kim DY, Mixon A, Kotha SP. Combinatorial therapy using negative pressure and varying lithium dosage for accelerated wound healing. Journal of the Mechanical Behavior of Biomedical Materials. 44: 173-8. PMID 25658877 DOI: 10.1016/J.Jmbbm.2015.01.012 |
0.188 |
|
2015 |
Guha S, Rajeshkumar V, Kotha SS, Sekar G. A versatile and one-pot strategy to synthesize α-amino ketones from benzylic secondary alcohols using N -bromosuccinimide Organic Letters. 17: 406-409. PMID 25633934 DOI: 10.1021/ol503683q |
0.388 |
|
2015 |
Harvey BM, Eschbach M, Glynn EA, Kotha S, Darre M, Adams DJ, Ramanathan R, Mancini R, Govoni KE. Effect of daily lithium chloride administration on bone mass and strength in growing broiler chickens,1. Poultry Science. 94: 296-301. PMID 25609690 DOI: 10.3382/Ps/Peu079 |
0.22 |
|
2015 |
Badam RB, Kanth S, Raju S, Kotha SK, Rao M, Chandra KLP. Current concepts of salivary gland tumors Journal of Orofacial Sciences. 7: 76-79. DOI: 10.4103/0975-8844.169751 |
0.166 |
|
2015 |
Kotha S, Bandi V. Diversity oriented approach to phenylalanine derivatives via the dielsalder reaction involving sulfolene intermediates Heterocycles. 90: 226-237. DOI: 10.3987/Com-14-S(K)9 |
0.498 |
|
2015 |
Kotha S, Waghule GT. New approach to cyclophanes containing ethyleneoxy bridge by glaser-eglinton coupling Heterocycles. 90: 1289-1298. DOI: 10.3987/Com-14-S(K)37 |
0.405 |
|
2015 |
Kotha S, Chinnam AK. Design of aza-polyquinanes via fischer indole cyclization under green conditions Heterocycles. 90: 690-697. DOI: 10.3987/Com-14-S(K)35 |
0.741 |
|
2015 |
Kotha S, Meshram M. Design and synthesis of conformationally constrained bicyclo[2.2.2]octane-based unusual α-amino acid derivatives via the diels-alder reaction Heterocycles. 90: 357-371. DOI: 10.3987/Com-14-S(K)26 |
0.53 |
|
2015 |
Kotha S, Ali R. Diversity oriented approach to oxepine derivatives: further expansion via diels?Alder reaction Heterocycles. 90: 645-658. DOI: 10.3987/Com-14-S(K)21 |
0.489 |
|
2015 |
Kotha S, Ali R. A simple approach to bis-spirocycles and spiroindole derivatives via green methods such as Fischer indolization, ring-closing metathesis, and Suzuki-Miyaura cross-coupling Turkish Journal of Chemistry. 39: 1190-1198. DOI: 10.3906/kim-1502-116 |
0.418 |
|
2015 |
Nesbitt S, Scott W, Macione J, Kotha S. Collagen fibrils in skin orient in the direction of applied uniaxial load in proportion to stress while exhibiting differential strains around hair follicles Materials. 8: 1841-1857. DOI: 10.3390/ma8041841 |
0.19 |
|
2015 |
Kotha S, Adimulam YB, Reddi KK. Computer-aided virtual screening of Telmisartan analogues as possible CDK cell cycle inhibitors International Journal of Computational Biology and Drug Design. 8: 359-382. DOI: 10.1504/IJCBDD.2015.073681 |
0.199 |
|
2015 |
Kotha SR, Singhvi A, Sahoo SK. A new approach for high performance RNS-FIR filter using the moduli set {2k-1, 2k, 2k-1-1} Iscaie 2014 - 2014 Ieee Symposium On Computer Applications and Industrial Electronics. 136-140. DOI: 10.1109/ISCAIE.2014.7010225 |
0.192 |
|
2015 |
Sharma N, Kotha SS, Lahiri N, Sekar G. Copper-catalyzed one-pot synthesis of α-ketoamides from 1-arylethanols Synthesis (Germany). 46. DOI: 10.1055/s-0034-1379975 |
0.364 |
|
2015 |
Dutta S, Kotha SS, Sekar G. Metal free one-pot synthesis of α-ketoamides from terminal alkenes Rsc Advances. 5: 47265-47269. DOI: 10.1039/c5ra05671c |
0.318 |
|
2015 |
Kotha S, Chavan AS, Goyal D. Diversity-oriented approaches to polycyclics and bioinspired molecules via the diels-alder strategy: Green chemistry, synthetic economy, and beyond Acs Combinatorial Science. 17: 253-302. DOI: 10.1021/co500146u |
0.323 |
|
2015 |
Ren L, Ozisik R, Kotha SP, Underhill PT. Highly efficient fabrication of polymer nanofiber assembly by centrifugal jet spinning: Process and characterization Macromolecules. 48: 2593-2602. DOI: 10.1021/Acs.Macromol.5B00292 |
0.209 |
|
2015 |
Kotha SS, Sekar G. Metal free synthesis of α-keto amides from 2-hydroxy acetophenones through domino alcohol oxidation-oxidative amidation reaction Tetrahedron Letters. 56: 6323-6326. DOI: 10.1016/j.tetlet.2015.09.053 |
0.32 |
|
2015 |
Kotha S, Sreevani G. Molybdenum hexacarbonyl: air stable catalyst for microwave assisted intermolecular [2+2+2] co-trimerization involving propargyl halides Tetrahedron Letters. 56: 5903-5908. DOI: 10.1016/J.Tetlet.2015.09.029 |
0.454 |
|
2015 |
Kotha S, Ali R. Diversity-oriented approach to spirooxindoles: Application of a green reagent 'rongalite' Tetrahedron Letters. 56: 3992-3995. DOI: 10.1016/J.Tetlet.2015.04.095 |
0.504 |
|
2015 |
Kotha S, Ali R. Diversity-oriented approach to intricate bis-armed spirocycles involving a two directional [2+2+2] co-trimerization and the [4+2] cycloaddition reaction as key steps Tetrahedron Letters. 56: 2172-2175. DOI: 10.1016/J.Tetlet.2015.03.021 |
0.545 |
|
2015 |
Ganapathy D, Kotha SS, Sekar G. Stable palladium nanoparticles catalyzed synthesis of benzonitriles using K4[Fe(CN)6] Tetrahedron Letters. 56: 172-178. DOI: 10.1016/j.tetlet.2014.11.051 |
0.271 |
|
2015 |
Kotha S, Ali R, Saifuddin M. Diversity-oriented approach to natural product inspired pyrano-carbazole derivatives: strategic utilization of hetero-Diels-Alder reaction, Fischer indolization and the Suzuki-Miyaura cross-coupling reaction Tetrahedron. 71: 9003-9011. DOI: 10.1016/J.Tet.2015.09.044 |
0.527 |
|
2015 |
Kotha S, Ali R. Diversity-oriented approach to novel spirocycles via 1,2,4,5-tetrakis(bromomethyl)benzene under operationally simple reaction conditions Tetrahedron. DOI: 10.1016/J.Tet.2015.07.008 |
0.569 |
|
2015 |
Kotha S, Ali R. Diversity-oriented approach to linearly fused spirocycles via strategic utilization of a [2+2+2] cycloaddition and the Diels-Alder reaction Tetrahedron. 71: 1597-1603. DOI: 10.1016/J.Tet.2015.01.009 |
0.5 |
|
2015 |
Kotha S, Ali R, Srinivas V, Krishna NG. Diversity-oriented approach to spirocycles with indole moiety via Fischer indole cyclization, olefin metathesis and Suzuki-Miyaura cross-coupling reactions Tetrahedron. 71: 129-138. DOI: 10.1016/J.Tet.2014.11.024 |
0.562 |
|
2015 |
Kotha S, Seema V, Banerjee S, Dipak MK. Diversity oriented approach to polycyclics via cross-enyne metathesis and Diels-Alder reaction as key steps Journal of Chemical Sciences. 127: 155-162. DOI: 10.1007/S12039-015-0765-6 |
0.502 |
|
2015 |
Kotha S, Ali R, Dipak MK. ChemInform Abstract: Bidirectional Approach to Symmetrical Spiro-1,3-bisketone via Grignard Reaction and Two Fold Ring-Closing Metathesis as Key Steps. Cheminform. 46: no-no. DOI: 10.1002/chin.201538072 |
0.472 |
|
2015 |
Kotha S, Bandi V. ChemInform Abstract: Diversity Oriented Approach to Phenylalanine Derivatives via the Diels-Alder Reaction Involving Sulfolene Intermediates. Cheminform. 46: no-no. DOI: 10.1002/chin.201521026 |
0.432 |
|
2015 |
Kotha S, Meshram M, Muthusamy G. Synthesis of conformationally constrained α-amino acid derivatives containing bicyclo[2.2.2] unit via the Diels-Alder and Suzuki-Miyaura cross-coupling reactions as key steps Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 54: 505-513. |
0.484 |
|
2015 |
Kotha S, Shirbhate ME. A general synthetic approach to para-cyclophanes via ring-closing metathesis Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 54: 1483-1494. |
0.401 |
|
2014 |
Vaz M, Pereira CM, Kotha S, Oliveira J. Neurological Manifestations in a Patient of Kikuchi's Disease. The Journal of the Association of Physicians of India. 62: 57-61. PMID 26281486 |
0.191 |
|
2014 |
Pereira CM, Vaz M, Kotha S, Santosh NH. Dapsone hypersensitivity syndrome with myocarditis. The Journal of the Association of Physicians of India. 62: 728-31. PMID 25856947 |
0.198 |
|
2014 |
Kotha S, Dipak MK. Design and synthesis of novel bis-annulated caged polycycles via ring-closing metathesis: pushpakenediol. Beilstein Journal of Organic Chemistry. 10: 2664-70. PMID 25550729 DOI: 10.3762/Bjoc.10.280 |
0.534 |
|
2014 |
Kotha S, Gunta R. Crystal structure of 1,3-diallyl-1,3,3a,4,7,7a-hexa-hydro-4,7-methano-2-benzo-thio-phene 2,2-dioxide. Acta Crystallographica. Section E, Structure Reports Online. 70: o1163-4. PMID 25484805 DOI: 10.1107/S1600536814022053 |
0.404 |
|
2014 |
Kotha S, Seema V, Deodhar D, Shaikh M. Crystal structures of 3,6-di-allyl-tetra-cyclo[6.3.0.0(4,11).0(5,9)]undeca-2,7-dione and 1,7-di-allyl-penta-cyclo-[5.4.0.0(2,6). 0(3,10).0(5,9)]undecane-8,11-dione: allyl-ated caged compounds. Acta Crystallographica. Section E, Structure Reports Online. 70: 410-4. PMID 25484760 DOI: 10.1107/S1600536814023149 |
0.447 |
|
2014 |
Kotha S, Sreenivasachary N, Deodhar D, Shaikh M. Crystal structure of the cage derivative penta-cyclo-[5.4.0.0(2,6).0(3,10).0(5,9)]undeca-8,11-dione ethyl-ene di-thio-ketal. Acta Crystallographica. Section E, Structure Reports Online. 70: 246-8. PMID 25484664 DOI: 10.1107/S1600536814020790 |
0.469 |
|
2014 |
Kotha S, Deodhar D, Khedkar P. Diversity-oriented synthesis of medicinally important 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives and higher analogs Organic and Biomolecular Chemistry. 12: 9054-9091. PMID 25299735 DOI: 10.1039/C4Ob01446D |
0.545 |
|
2014 |
Animireddy D, Reddy Bekkem VT, Vallala P, Kotha SB, Ankireddy S, Mohammad N. Evaluation of pH, buffering capacity, viscosity and flow rate levels of saliva in caries-free, minimal caries and nursing caries children: An in vivo study. Contemporary Clinical Dentistry. 5: 324-8. PMID 25191067 DOI: 10.4103/0976-237X.137931 |
0.164 |
|
2014 |
Huang LS, Mathew B, Li H, Zhao Y, Ma SF, Noth I, Reddy SP, Harijith A, Usatyuk PV, Berdyshev EV, Kaminski N, Zhou T, Zhang W, Zhang Y, Rehman J, ... Kotha SR, et al. The mitochondrial cardiolipin remodeling enzyme lysocardiolipin acyltransferase is a novel target in pulmonary fibrosis. American Journal of Respiratory and Critical Care Medicine. 189: 1402-1415. PMID 24779708 DOI: 10.1164/Rccm.201310-1917Oc |
0.599 |
|
2014 |
Ren L, Ozisik R, Kotha SP. Rapid and efficient fabrication of multilevel structured silica micro-/nanofibers by centrifugal jet spinning. Journal of Colloid and Interface Science. 425: 136-42. PMID 24776675 DOI: 10.1016/J.Jcis.2014.03.039 |
0.228 |
|
2014 |
Xu J, Shen Lx, Yan Ch, Hu H, Yang F, Wang L, Kotha SR, Ouyang F, Zhang Ln, Liao Xp, Zhang J, Zhang Js, Shen Xm. Parent-adolescent interaction and risk of adolescent internet addiction: A population-based study in Shanghai Bmc Psychiatry. 14. PMID 24731648 DOI: 10.1186/1471-244X-14-112 |
0.191 |
|
2014 |
Kotha S, Murtomäki L. Virtual pharmacokinetic model of human eye Mathematical Biosciences. 253: 11-18. PMID 24721554 DOI: 10.1016/j.mbs.2014.03.014 |
0.194 |
|
2014 |
Ren L, Kotha SP. Centrifugal Jet Spinning for Highly Efficient and Large-scale Fabrication of Barium Titanate Nanofibers. Materials Letters. 117: 153-157. PMID 24563566 DOI: 10.1016/J.Matlet.2013.11.103 |
0.234 |
|
2014 |
Macione J, Nesbitt RS, Kotha S. Magnitude of loads influences the site of failure of highly curved bones Journal of the Mechanical Behavior of Biomedical Materials. 30: 274-278. PMID 24361931 DOI: 10.1016/J.Jmbbm.2013.11.018 |
0.178 |
|
2014 |
Joshi M, Kotha SR, Malireddy S, Selvaraju V, Satoskar AR, Palesty A, McFadden DW, Parinandi NL, Maulik N. Conundrum of pathogenesis of diabetic cardiomyopathy: role of vascular endothelial dysfunction, reactive oxygen species, and mitochondria. Molecular and Cellular Biochemistry. 386: 233-49. PMID 24307101 DOI: 10.1007/S11010-013-1861-X |
0.18 |
|
2014 |
Kotha S, Ali R. Diversity Oriented Approach to Spirobarbituric Acid Derivatives via a [2+2+2] Cycloaddition and Diels‒Alder Reaction as Key Steps Heterocycles. 88: 789. DOI: 10.3987/Com-13-S(S)48 |
0.54 |
|
2014 |
Kotha S, Dipak MK. Design and synthesis of novel bis-annulated caged polycycles via ring-closing metathesis: Pushpakenediol Beilstein Journal of Organic Chemistry. 10: 2664-2670. DOI: 10.3762/bjoc.10.280 |
0.438 |
|
2014 |
Ren L, Pandit V, Mixon A, James C, Kotha SP. Novel silicone-epoxy composites for dental restorations Journal of Fluid Mechanics. 1621. DOI: 10.1557/Opl.2014.199 |
0.175 |
|
2014 |
Long F, Ozturk MS, Intes X, Kotha S. Dental imaging using laminar optical tomography and micro CT Progress in Biomedical Optics and Imaging - Proceedings of Spie. 8937. DOI: 10.1117/12.2037766 |
0.177 |
|
2014 |
Kotha SR, Bajaj S, Subhendu Kumar S. An RNS based FIR filter design using shift and add approach Midwest Symposium On Circuits and Systems. 707-712. DOI: 10.1109/MWSCAS.2014.6908513 |
0.217 |
|
2014 |
Kotha SR, Bilaye D, Jain U, Kumar SS. An approach for efficient FIR filter design for hearing aid application 18th International Symposium On Vlsi Design and Test, Vdat 2014. DOI: 10.1109/ISVDAT.2014.6881051 |
0.23 |
|
2014 |
Kotha SR, Bajaj S, Kumar SS. An LUT based RNS FIR filter implementation for reconfigurable applications 18th International Symposium On Vlsi Design and Test, Vdat 2014. DOI: 10.1109/ISVDAT.2014.6881047 |
0.185 |
|
2014 |
Kotha SR, Bajaj S, Kumar SS. An RNS based reconfigurable FIR filter design using shift and add approach 2014 9th International Symposium On Communication Systems, Networks and Digital Signal Processing, Csndsp 2014. 640-645. DOI: 10.1109/CSNDSP.2014.6923906 |
0.217 |
|
2014 |
Kotha S, Seema V, Deodhar D, Shaikh M. Crystal structures of 3,6-diallyltetracyclo[6.3.0.04,11.05,9]undeca-2,7-dione and 1,7-diallylpentacyclo[5.4.0.02,6. 03,10.05,9]undecane-8,11-dione: Allylated caged compounds Acta Crystallographica Section E: Structure Reports Online. 70: 410-414. DOI: 10.1107/S1600536814023149 |
0.266 |
|
2014 |
Kotha S, Gunta R. Crystal structure of 1,3-diallyl-1,3,3a,4,7,7a-hexahydro-4,7-methano-2-benzothiophene 2,2-dioxide Acta Crystallographica Section E: Structure Reports Online. 70: o1163-o1164. DOI: 10.1107/S1600536814022053 |
0.195 |
|
2014 |
Kotha S, Sreenivasachary N, Deodhar D, Shaikh M. Crystal structure of the cage derivative pentacyclo[5.4.0.02,6.03,10.05,9]undeca-8,11-dione ethylene dithioketal Acta Crystallographica Section E: Structure Reports Online. 70: 246-248. DOI: 10.1107/S1600536814020790 |
0.244 |
|
2014 |
Kotha S, Ali R, Tiwari A. Design and synthesis of angularly annulated spirocyclics via enyne metathesis and the Diels-Alder reaction as key steps Synthesis (Germany). 46: 2471-2480. DOI: 10.1055/S-0034-1378280 |
0.537 |
|
2014 |
Kotha S, Meshram M. Synthesis of novel fluoranthene-based conformationally constrained α-amino acid derivatives and polycyclic aromatics via the diels-alder reaction Synthesis (Germany). 46: 1525-1531. DOI: 10.1055/S-0033-1341042 |
0.535 |
|
2014 |
Kotha S, Chinnam AK. Anomalous behaviour of cis-bicyclo[33.0]octane-3,7-dione and its derivatives during twofold Fischer indole cyclization using low-melting mixtures Synthesis (Germany). 46: 301-306. DOI: 10.1055/S-0033-1340341 |
0.742 |
|
2014 |
Kotha S, Shirbhate ME. Design of new synthetic strategies to cyclophanes via ring-closing metathesis Tetrahedron Letters. 55: 6972-6975. DOI: 10.1016/J.Tetlet.2014.10.092 |
0.549 |
|
2014 |
Kotha S, Ravikumar O. Design and synthesis of oxa-bowls via Diels-Alder reaction and ring-rearrangement metathesis as key steps Tetrahedron Letters. 55: 5781-5784. DOI: 10.1016/J.Tetlet.2014.08.108 |
0.561 |
|
2014 |
Kotha S, Ali R, Chinnam AK. Diversity-oriented approach to spirocycles via ring-closing metathesis Tetrahedron Letters. 55: 4492-4495. DOI: 10.1016/J.Tetlet.2014.06.049 |
0.793 |
|
2014 |
Kotha S, Waghule GT. Diversity-oriented approach to cyclophanes via Claisen rearrangement and ring-closing metathesis as key steps Tetrahedron Letters. 55: 4264-4268. DOI: 10.1016/J.Tetlet.2014.05.129 |
0.557 |
|
2014 |
Kotha S, Bandarugattu VB, Krishna NG. Diversity-oriented approach to unusual amino acid derivatives and heterocycles via methyl 2-acetamidoacrylate and its congeners Tetrahedron. 5361-5384. DOI: 10.1016/J.Tet.2014.05.056 |
0.45 |
|
2014 |
Ren L, Kotha SP. Centrifugal jet spinning for highly efficient and large-scale fabrication of barium titanate nanofibers Materials Letters. 117: 153-157. DOI: 10.1016/j.matlet.2013.11.103 |
0.202 |
|
2014 |
Ren L, Pashayi K, Fard HR, Kotha SP, Borca-Tasciuc T, Ozisik R. Engineering the coefficient of thermal expansion and thermal conductivity of polymers filled with high aspect ratio silica nanofibers Composites Part B: Engineering. 58: 228-234. DOI: 10.1016/J.Compositesb.2013.10.049 |
0.202 |
|
2014 |
Ren L, Simmons TJ, Lu F, Rahmi O, Kotha SP. Template free and large-scale fabrication of silica nanotubes with centrifugal jet spinning Chemical Engineering Journal. 254: 39-45. DOI: 10.1016/J.Cej.2014.05.077 |
0.208 |
|
2014 |
Fisher G, Kotha S. HomeGrocer.com: Anatomy of a failure Business Horizons. 57: 301-304. DOI: 10.1016/j.bushor.2013.12.003 |
0.171 |
|
2014 |
Kotha S, Banerjee S, Shaikh M. Correlation between carbon-carbon bond length and the ease of retro Diels-Alder reaction Journal of Chemical Sciences. 126: 1369-1371. DOI: 10.1007/S12039-014-0709-6 |
0.408 |
|
2014 |
Kotha SS, Chandrasekar S, Sahu S, Sekar G. Iron-TEMPO-catalyzed domino aerobic alcohol oxidation/oxidative cross-dehydrogenative coupling for the synthesis of α-keto amides European Journal of Organic Chemistry. 2014: 7451-7457. DOI: 10.1002/Ejoc.201402961 |
0.331 |
|
2014 |
Kotha S, Ravikumar O. Diversity-oriented approach to carbocycles and heterocycles through ring-rearrangement metathesis, fischer indole cyclization, and diels-alder reaction as key steps European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201402273 |
0.565 |
|
2014 |
Kotha S, Waghule GT, Shirbhate ME. Diversity-oriented approach to normuscopyridine and its analogues through ring-closing metathesis European Journal of Organic Chemistry. 2014: 984-992. DOI: 10.1002/Ejoc.201301493 |
0.523 |
|
2014 |
Vaz M, Pereira CM, Kotha S, Oliveira J. Neurological manifestations in a patient of kikuchi’s disease Journal of Association of Physicians of India. 62: 57-60. |
0.169 |
|
2014 |
Kotha S, Reddy MS, Makula S. The prospective clinical observational study on assessment and evaluation of serum fucose as biomarker in cervical cancer Research Journal of Pharmaceutical, Biological and Chemical Sciences. 5: 1159-1166. |
0.175 |
|
2014 |
Kotha SR, Vij S, Sahoo SK. A study on strategies and mutant factor in differential evolution algorithm for FIR filter design 2014 International Conference On Signal Processing and Integrated Networks, Spin 2014. 50-55. |
0.194 |
|
2013 |
Malireddy S, Lawson C, Steinhour E, Hart J, Kotha SR, Patel RB, Zhao L, Wilkins JR, Marsh CB, Magalang UJ, Romberger D, Wewers MD, Parinandi NL. Airborne agricultural particulate matter induces inflammatory cytokine secretion by respiratory epithelial cells: mechanisms of regulation by eicosanoid lipid signal mediators. Indian Journal of Biochemistry & Biophysics. 50: 387-401. PMID 24772960 |
0.219 |
|
2013 |
Kotha S, Chinnam AK, Tiwari A. Synthesis of indole-based propellane derivatives via Weiss-Cook condensation, Fischer indole cyclization, and ring-closing metathesis as key steps. Beilstein Journal of Organic Chemistry. 9: 2709-14. PMID 24367436 DOI: 10.3762/Bjoc.9.307 |
0.807 |
|
2013 |
Sherwani SI, Aldana C, Usmani S, Adin C, Kotha S, Khan M, Eubank T, Scherer PE, Parinandi N, Magalang UJ. Intermittent hypoxia exacerbates pancreatic β-cell dysfunction in a mouse model of diabetes mellitus Sleep. 36: 1849-1858. PMID 24293759 DOI: 10.5665/Sleep.3214 |
0.191 |
|
2013 |
Kotha S, Goyal D, Chavan AS. Diversity-oriented approaches to unusual α-amino acids and peptides: Step economy, atom economy, redox economy, and beyond Journal of Organic Chemistry. 78: 12288-12313. PMID 24219241 DOI: 10.1021/Jo4020722 |
0.467 |
|
2013 |
Wentzell S, Sterling Nesbitt R, Macione J, Kotha S. Measuring strain using digital image correlation of second harmonic generation images Journal of Biomechanics. 46: 2032-2038. PMID 23845730 DOI: 10.1016/J.Jbiomech.2013.06.003 |
0.189 |
|
2013 |
Pandit V, Zuidema JM, Venuto KN, Macione J, Dai G, Gilbert RJ, Kotha SP. Evaluation of multifunctional polysaccharide hydrogels with varying stiffness for bone tissue engineering Tissue Engineering - Part A. 19: 2452-2463. PMID 23724786 DOI: 10.1089/Ten.Tea.2012.0644 |
0.206 |
|
2013 |
Usatyuk PV, Kotha SR, Parinandi NL, Natarajan V. Phospholipase D signaling mediates reactive oxygen species-induced lung endothelial barrier dysfunction. Pulmonary Circulation. 3: 108-15. PMID 23662182 DOI: 10.4103/2045-8932.109925 |
0.205 |
|
2013 |
Ren L, Pandit V, Elkin J, Denman T, Cooper JA, Kotha SP. Large-scale and highly efficient synthesis of micro- and nano-fibers with controlled fiber morphology by centrifugal jet spinning for tissue regeneration. Nanoscale. 5: 2337-45. PMID 23392606 DOI: 10.1039/C3Nr33423F |
0.204 |
|
2013 |
Sliman SM, Patel RB, Cruff JP, Kotha SR, Newland CA, Schrader CA, Sherwani SI, Gurney TO, Magalang UJ, Parinandi NL. Adiponectin protects against hyperoxic lung injury and vascular leak. Cell Biochemistry and Biophysics. 67: 399-414. PMID 22183615 DOI: 10.1007/s12013-011-9330-1 |
0.199 |
|
2013 |
Kotha SR, Piper MG, Patel RB, Sliman S, Malireddy S, Zhao L, Baran CP, Nana-Sinkam PS, Wewers MD, Romberger D, Marsh CB, Parinandi NL. Phospholipase A(2) activation by poultry particulate matter is mediated through extracellular signal-regulated kinase in lung epithelial cells: regulation of interleukin-8 release. Cell Biochemistry and Biophysics. 67: 415-29. PMID 22183614 DOI: 10.1007/S12013-011-9329-7 |
0.19 |
|
2013 |
Sherwani SI, Pabon S, Patel RB, Sayyid MM, Hagele T, Kotha SR, Magalang UJ, Maddipati KR, Parinandi NL. Eicosanoid signaling and vascular dysfunction: methylmercury-induced phospholipase D activation in vascular endothelial cells. Cell Biochemistry and Biophysics. 67: 317-29. PMID 22020799 DOI: 10.1007/s12013-011-9304-3 |
0.229 |
|
2013 |
Kotha S, Chinnam AK, Tiwari A. Synthesis of indole-based propellane derivatives via Weiss-Cook condensation, Fischer indole cyclization, and ring-closing metathesis as key steps Beilstein Journal of Organic Chemistry. 9: 2709-2714. DOI: 10.3762/bjoc.9.307 |
0.496 |
|
2013 |
Kotha S, Misra S, Sreevani G, Babu BV. Non-metathetic behaviour of olefin metathesis catalysts Current Organic Chemistry. 17: 2776-2795. DOI: 10.2174/13852728113179990118 |
0.342 |
|
2013 |
Kotha SR, Singhvi A, Sahoo SK. An efficient RNS-FIR filter implementation using the moduli set {2 k - 1, 2k, 2k-1 - 1} Asia Pacific Conference On Postgraduate Research in Microelectronics and Electronics. 191-195. DOI: 10.1109/PrimeAsia.2013.6731203 |
0.181 |
|
2013 |
Watson A, Yocum C, Pandit V, Kotha SP. Optimizing polymeric nanoparticle core designs for gene delivery Proceedings of the Ieee Annual Northeast Bioengineering Conference, Nebec. 1-2. DOI: 10.1109/NEBEC.2013.122 |
0.201 |
|
2013 |
Venuto K, Pandit V, Kotha S. Multifunctional polysaccharide hydrogels capable of mineralization, vascularization, and anti-bacterial efficacy Proceedings of the Ieee Annual Northeast Bioengineering Conference, Nebec. 111-112. DOI: 10.1109/NEBEC.2013.113 |
0.19 |
|
2013 |
Kotha S, Ali R, Tiwari A. Diversity-oriented approach to novel spirocyclics via enyne metathesis, diels-alder reaction, and a [2+2+2] cycloaddition as key steps Synlett. 24: 1921-1926. DOI: 10.1055/S-0033-1339489 |
0.558 |
|
2013 |
Kotha S, Goyal D, Bitra A, Thota N, Kruger G, Anand R. Diversity oriented approach to triazole based peptidomimetics as mammalian sterile 20 kinase inhibitors Rsc Advances. 3: 24447-24454. DOI: 10.1039/C3Ra44318C |
0.364 |
|
2013 |
Kotha S, Banerjee S. Recent developments in the retro-Diels-Alder reaction Rsc Advances. 3: 7642-7666. DOI: 10.1039/C3Ra22762F |
0.469 |
|
2013 |
Kotha S, Srinivas V, Krishna NG. ChemInform Abstract: Diversity Oriented Approach to 9-Aryl-Substituted Naphthoxepine Derivatives via Claisen Rearrangement, Ring-Closing Metathesis and Suzuki-Miyaura Cross-Coupling as Key Steps. Cheminform. 44: no-no. DOI: 10.1002/chin.201318173 |
0.466 |
|
2013 |
Kotha S, Meshram M. Functionalization of anthracene by strategic utilization of the Diels-Alder reaction and the ring-closing metathesis Journal of the Indian Chemical Society. 90: 1789-1794. |
0.439 |
|
2012 |
Xu J, Shen Lx, Yan Ch, Hu H, Yang F, Wang L, Kotha SR, Zhang Ln, Liao Xp, Zhang J, Ouyang Fx, Zhang Js, Shen Xm. Personal characteristics related to the risk of adolescent internet addiction: a survey in Shanghai, China. Bmc Public Health. 12: 1106. PMID 23259906 DOI: 10.1186/1471-2458-12-1106 |
0.185 |
|
2012 |
Hinzey AH, Kline MA, Kotha SR, Sliman SM, Butler ES, Shelton AB, Gurney TR, Parinandi NL. Choice of cyclodextrin for cellular cholesterol depletion for vascular endothelial cell lipid raft studies: cell membrane alterations, cytoskeletal reorganization and cytotoxicity. Indian Journal of Biochemistry & Biophysics. 49: 329-41. PMID 23259319 |
0.205 |
|
2012 |
Kotha SR, Johnson JC, Galea S, Agyei-Baffour P, Nakua E, Asabir K, Kwansah J, Gyakobo M, Dzodzomenyo M, Kruk ME. Lifecourse factors and likelihood of rural practice and emigration: A survey of Ghanaian medical students Rural and Remote Health. 12. PMID 22967220 |
0.179 |
|
2012 |
Kotha S, Waghule GT. Diversity oriented approach to crownophanes by enyne metathesis and Diels-Alder reaction as key steps. The Journal of Organic Chemistry. 77: 6314-8. PMID 22731677 DOI: 10.1021/Jo300766F |
0.526 |
|
2012 |
Kotha S, Goyal née Bansal D, Banerjee S, Datta A. A novel di-triazole based peptide as a highly sensitive and selective fluorescent chemosensor for Zn2+ ions. The Analyst. 137: 2871-5. PMID 22576100 DOI: 10.1039/C2An35222B |
0.362 |
|
2012 |
Patel RB, Kotha SR, Sauers LA, Malireddy S, Gurney TO, Gupta NN, Elton TS, Magalang UJ, Marsh CB, Haley BE, Parinandi NL. Thiol-redox antioxidants protect against lung vascular endothelial cytoskeletal alterations caused by pulmonary fibrosis inducer, bleomycin: comparison between classical thiol-protectant, N-acetyl-L-cysteine, and novel thiol antioxidant, N,N'-bis-2-mercaptoethyl isophthalamide. Toxicology Mechanisms and Methods. 22: 383-96. PMID 22409285 DOI: 10.3109/15376516.2012.673089 |
0.227 |
|
2012 |
Malireddy S, Kotha SR, Secor JD, Gurney TO, Abbott JL, Maulik G, Maddipati KR, Parinandi NL. Phytochemical antioxidants modulate mammalian cellular epigenome: implications in health and disease. Antioxidants & Redox Signaling. 17: 327-39. PMID 22404530 DOI: 10.1089/ars.2012.4600 |
0.217 |
|
2012 |
Macione J, Nesbitt S, Pandit V, Kotha S. Design and analysis of a novel mechanical loading machine for dynamic in vivo axial loading. The Review of Scientific Instruments. 83: 025113. PMID 22380131 DOI: 10.1063/1.3687781 |
0.197 |
|
2012 |
Kotha S, Chavan AS, Shaikh M. Diversity-oriented approach to macrocyclic cyclophane derivatives by Suzuki-Miyaura cross-coupling and olefin metathesis as key steps. The Journal of Organic Chemistry. 77: 482-9. PMID 22129223 DOI: 10.1021/Jo2020714 |
0.544 |
|
2012 |
Kotha S, Khedkar P. Rongalite: a useful green reagent in organic synthesis. Chemical Reviews. 112: 1650-80. PMID 22107104 DOI: 10.1021/Cr100175T |
0.424 |
|
2012 |
Kotha S, Srinivas V, Krishna NG. Diversity oriented approach to 9-aryl-substituted naphthoxepine derivatives via claisen rearrangement, ring-closing metathesis and suzuki-miyaura cross-coupling as key steps Heterocycles. 86: 1555-1563. DOI: 10.3987/Com-12-S(N)89 |
0.539 |
|
2012 |
Pandit V, Kotha SP. Genipin crosslinked polysaccharide hydrogels as rheologically enhanced osteoblast growth substrates 2012 38th Annual Northeast Bioengineering Conference, Nebec 2012. 275-276. DOI: 10.1109/NEBC.2012.6207071 |
0.194 |
|
2012 |
Narayanan R, Kotha S, Lin G, Khan A, Rizvi S, Javed W, Khan H, Khayam SA. Macroflows and microflows: Enabling rapid network innovation through a split SDN data plane Proceedings - European Workshop On Software Defined Networks, Ewsdn 2012. 79-84. DOI: 10.1109/EWSDN.2012.16 |
0.189 |
|
2012 |
Maas R, Kotha SR, Sehr A, Kellermann W. Combined-order hidden Markov models for reverberation-robust speech recognition 2012 3rd International Workshop On Cognitive Information Processing, Cip 2012. DOI: 10.1109/CIP.2012.6232918 |
0.176 |
|
2012 |
Kotha S, Shirbhate ME. Diversity-oriented approach to macrocyclic cyclophane derivatives via ring-closing metathesis Synlett. 23: 2183-2188. DOI: 10.1055/S-0032-1317020 |
0.504 |
|
2012 |
Kotha S, Waghule GT. Diversity oriented approach to crownophanes by enyne metathesis and Diels-Alder reaction as key steps Journal of Organic Chemistry. 77: 6314-6318. DOI: 10.1021/jo300766f |
0.417 |
|
2012 |
Kotha S, Khedkar P. Rongalite: A useful green reagent in organic synthesis Chemical Reviews. 112: 1650-1680. DOI: 10.1021/cr100175t |
0.33 |
|
2012 |
Kotha S, Dipak MK. Strategies and tactics in olefin metathesis Tetrahedron. 68: 397-421. DOI: 10.1016/J.Tet.2011.10.018 |
0.411 |
|
2012 |
Manne S, Kotha SK, Sameen Fatima S. Text categorization with k-nearest neighbor approach Advances in Intelligent and Soft Computing. 132: 413-420. DOI: 10.1007/978-3-642-27443-5-47 |
0.22 |
|
2012 |
Beckman C, Eisenhardt K, Kotha S, Meyer A, Rajagopalan N. Technology entrepreneurship Strategic Entrepreneurship Journal. 6: 89-93. DOI: 10.1002/sej.1134 |
0.164 |
|
2012 |
Kotha S, Misra S, Srinivas V. Diversity oriented approach to polycyclic compounds through the diels-alder reaction and the Suzuki coupling European Journal of Organic Chemistry. 4052-4062. DOI: 10.1002/Ejoc.201200484 |
0.484 |
|
2012 |
Kotha S, Goyal D, Thota N, Srinivas V. Synthesis of modified phenylalanine peptides by cross enyne metathesis and a diels-alder reaction as key steps European Journal of Organic Chemistry. 1843-1850. DOI: 10.1002/Ejoc.201101744 |
0.47 |
|
2012 |
Kotha S, Khedkar P. ChemInform Abstract: Rongalite: A Useful Reagent in Organic Synthesis Cheminform. 43: no-no. DOI: 10.1002/chin.201222220 |
0.338 |
|
2012 |
Faillace S, Kotha SP, Prasetyanti W, Sumantri I, Adriono GA, Adriono GAD, Yudantha AR, Subekti I, Yunir E, Budiman. Helping patients find their way to better diabetic retinopathy care Community Eye Health Journal. 25: 34. |
0.171 |
|
2011 |
Johnson JC, Nakua E, Dzodzomenyo M, Agyei-Baffour P, Gyakobo M, Asabir K, Kwansah J, Kotha SR, Snow RC, Kruk ME. For money or service?: a cross-sectional survey of preference for financial versus non-financial rural practice characteristics among Ghanaian medical students. Bmc Health Services Research. 11: 300. PMID 22050704 DOI: 10.1186/1472-6963-11-300 |
0.188 |
|
2011 |
Secor JD, Kotha SR, Gurney TO, Patel RB, Kefauver NR, Gupta N, Morris AJ, Haley BE, Parinandi NL. Novel lipid-soluble thiol-redox antioxidant and heavy metal chelator, N,N'-bis(2-mercaptoethyl)isophthalamide (NBMI) and phospholipase D-specific inhibitor, 5-fluoro-2-indolyl des-chlorohalopemide (FIPI) attenuate mercury-induced lipid signaling leading to protection against cytotoxicity in aortic endothelial cells. International Journal of Toxicology. 30: 619-38. PMID 21994240 DOI: 10.1177/1091581811422413 |
0.219 |
|
2011 |
Agyei-Baffour P, Kotha SR, Johnson JC, Gyakobo M, Asabir K, Kwansah J, Nakua E, Dzodzomenyo M, Snow RC, Kruk ME. Willingness to work in rural areas and the role of intrinsic versus extrinsic professional motivations - a survey of medical students in Ghana. Bmc Medical Education. 11: 56. PMID 21827698 DOI: 10.1186/1472-6920-11-56 |
0.185 |
|
2011 |
Kotha S, Krishna NG, Halder S, Misra S. A synergistic approach to polycyclics via a strategic utilization of Claisen rearrangement and olefin metathesis. Organic & Biomolecular Chemistry. 9: 5597-624. PMID 21727970 DOI: 10.1039/C1Ob05413A |
0.483 |
|
2011 |
Macione J, Kavukcuoglu NB, Nesbitt RS, Mann AB, Guzelsu N, Kotha SP. Hierarchies of damage induced loss of mechanical properties in calcified bone after in vivo fatigue loading of rat ulnae. Journal of the Mechanical Behavior of Biomedical Materials. 4: 841-8. PMID 21616465 DOI: 10.1016/J.Jmbbm.2011.03.010 |
0.191 |
|
2011 |
Bush KF, Luber G, Kotha SR, Dhaliwal RS, Kapil V, Pascual M, Brown DG, Frumkin H, Dhiman RC, Hess J, Wilson ML, Balakrishnan K, Eisenberg J, Kaur T, Rood R, et al. Impacts of climate change on public health in India: future research directions. Environmental Health Perspectives. 119: 765-70. PMID 21273162 DOI: 10.1289/Ehp.1003000 |
0.2 |
|
2011 |
Patel RB, Kotha SR, Sherwani SI, Sliman SM, Gurney TO, Loar B, Butler SO, Morris AJ, Marsh CB, Parinandi NL. Pulmonary fibrosis inducer, bleomycin, causes redox-sensitive activation of phospholipase D and cytotoxicity through formation of bioactive lipid signal mediator, phosphatidic acid, in lung microvascular endothelial cells. International Journal of Toxicology. 30: 69-90. PMID 21131602 DOI: 10.1177/1091581810388850 |
0.22 |
|
2011 |
Kotha S, Misra S, Mobin SM. A new approach to 3-substituted tetrahydro-β-carboline derivative via diethyl acetamidomalonate. Amino Acids. 41: 933-6. PMID 21061028 DOI: 10.1007/S00726-010-0792-Z |
0.43 |
|
2011 |
Kodavanti UP, Thomas R, Ledbetter AD, Schladweiler MC, Shannahan JH, Wallenborn JG, Lund AK, Campen MJ, Butler EO, Gottipolu RR, Nyska A, Richards JE, Andrews D, Jaskot RH, McKee J, ... Kotha SR, et al. Vascular and cardiac impairments in rats inhaling ozone and diesel exhaust particles. Environmental Health Perspectives. 119: 312-8. PMID 20980218 DOI: 10.1289/Ehp.1002386 |
0.171 |
|
2011 |
Nesbitt RS, MacIone JJ, Wentzell S, Corr DT, Intes X, Kotha SP. Mapping of strains in bundles of skin collagen microfibrils 2011 Ieee 37th Annual Northeast Bioengineering Conference, Nebec 2011. DOI: 10.1109/NEBC.2011.5778667 |
0.173 |
|
2011 |
Wentzell S, Nesbitt RS, Macione J, Knapp R, Kotha SP. Bone strain measurement using 3D digital image correlation of second harmonic generation images 2011 Ieee 37th Annual Northeast Bioengineering Conference, Nebec 2011. DOI: 10.1109/NEBC.2011.5778642 |
0.183 |
|
2011 |
Nesbitt RS, Pandit VA, Karande P, Kotha SP. Relationship between deformation and electrical impedance in mouse skin 2011 Ieee 37th Annual Northeast Bioengineering Conference, Nebec 2011. DOI: 10.1109/NEBC.2011.5778608 |
0.165 |
|
2011 |
Pandit V, Nesbitt RS, Macione J, Kotha SP. Reprogramming of cells using modified mRNA 2011 Ieee 37th Annual Northeast Bioengineering Conference, Nebec 2011. DOI: 10.1109/NEBC.2011.5778580 |
0.188 |
|
2011 |
Kotha S, Basu S. Amazon and eBay: Online Retailers as Market Makers The Market Makers: How Retailers Are Reshaping the Global Economy. DOI: 10.1093/acprof:oso/9780199590179.003.0006 |
0.171 |
|
2011 |
Kotha S, Seema V. Diversity-oriented synthesis of biaryl derivatives using cross-enyne metathesis, diels-alder reaction, and suzuki-miyaura cross-coupling as key steps Synlett. 2329-2334. DOI: 10.1055/S-0030-1260315 |
0.515 |
|
2011 |
Kotha S, Krishna NG, Misra S, Khedkar P. Synthesis of linearly and angularly fused indane-based constrained α-amino acid derivatives Synthesis. 2945-2950. DOI: 10.1055/S-0030-1260145 |
0.484 |
|
2011 |
Kotha S, Seema V, Mobin SM. Synthesis of biaryl derivatives by using ruthenium-mediated [2+2+2] cyclotrimerization and Suzuki-Miyaura cross-coupling as key steps Synthesis. 1581-1586. DOI: 10.1055/S-0030-1260009 |
0.491 |
|
2011 |
Kotha S, Dipak MK, Mobin SM. Serendipitous and acid catalyzed synthesis of spirolactones Tetrahedron. 67: 4616-4619. DOI: 10.1016/J.Tet.2011.04.073 |
0.47 |
|
2011 |
Kotha S, Chavan AS, Dipak MK. Synthetic approach to cis and trans-decalins via Diels - Alder reaction and ring-closing metathesis as key steps: Further extension to dioxapropellane derivative by ring-closing metathesis Tetrahedron. 67: 501-504. DOI: 10.1016/J.Tet.2010.10.080 |
0.534 |
|
2011 |
Kotha S, Bansal D, Singh K, Banerjee S. Synthesis of a new fluorescent macrocyclic α-amino acid derivative via tandem cross-enyne/ring-closing metathesis cascade catalyzed by ruthenium based catalysts Journal of Organometallic Chemistry. 696: 1856-1860. DOI: 10.1016/J.Jorganchem.2011.02.019 |
0.604 |
|
2011 |
Basu S, Phelps C, Kotha S. Towards understanding who makes corporate venture capital investments and why Journal of Business Venturing. 26: 153-171. DOI: 10.1016/J.Jbusvent.2009.07.001 |
0.19 |
|
2011 |
Kotha S, Krishna NG. Synthetic approach to linearly annulated tetralin-based constrained α-amino acid derivatives via Rongalite Current Science. 101: 923-926. |
0.37 |
|
2010 |
Larget BR, Kotha SK, Dewey CN, Ané C. BUCKy: gene tree/species tree reconciliation with Bayesian concordance analysis. Bioinformatics (Oxford, England). 26: 2910-1. PMID 20861028 DOI: 10.1093/Bioinformatics/Btq539 |
0.196 |
|
2010 |
Sansom SE, Nuovo GJ, Martin MM, Kotha SR, Parinandi NL, Elton TS. miR-802 regulates human angiotensin II type 1 receptor expression in intestinal epithelial C2BBe1 cells. American Journal of Physiology. Gastrointestinal and Liver Physiology. 299: G632-42. PMID 20558762 DOI: 10.1152/ajpgi.00120.2010 |
0.174 |
|
2010 |
Kotha S, Chavan AS. Design and synthesis of benzosultine-sulfone as a o-xylylene precursor via cross-enyne metathesis and rongalite: further expansion to polycyclics via regioselective Diels-Alder reaction. The Journal of Organic Chemistry. 75: 4319-22. PMID 20496902 DOI: 10.1021/Jo100655C |
0.496 |
|
2010 |
Kruk ME, Johnson JC, Gyakobo M, Agyei-Baffour P, Asabir K, Kotha SR, Kwansah J, Nakua E, Snow RC, Dzodzomenyo M. Rural practice preferences among medical students in Ghana: a discrete choice experiment. Bulletin of the World Health Organization. 88: 333-41. PMID 20458371 DOI: 10.2471/Blt.09.072892 |
0.178 |
|
2010 |
Macione J, Depaula CA, Guzelsu N, Kotha SP. Correlation between longitudinal, circumferential, and radial moduli in cortical bone: effect of mineral content. Journal of the Mechanical Behavior of Biomedical Materials. 3: 405-13. PMID 20416555 DOI: 10.1016/J.Jmbbm.2010.03.004 |
0.186 |
|
2010 |
Guzelsu N, Wienstien C, Kotha SP. A new streaming potential chamber for zeta potential measurements of particulates. The Review of Scientific Instruments. 81: 015106. PMID 20113128 DOI: 10.1063/1.3284510 |
0.214 |
|
2010 |
Khanna S, Parinandi NL, Kotha SR, Roy S, Rink C, Bibus D, Sen CK. Nanomolar vitamin E alpha-tocotrienol inhibits glutamate-induced activation of phospholipase A2 and causes neuroprotection. Journal of Neurochemistry. 112: 1249-60. PMID 20028458 DOI: 10.1111/j.1471-4159.2009.06550.x |
0.223 |
|
2010 |
Kline MA, O'Connor Butler ES, Hinzey A, Sliman S, Kotha SR, Marsh CB, Uppu RM, Parinandi NL. A simple method for effective and safe removal of membrane cholesterol from lipid rafts in vascular endothelial cells: implications in oxidant-mediated lipid signaling. Methods in Molecular Biology (Clifton, N.J.). 610: 201-11. PMID 20013180 DOI: 10.1007/978-1-60327-029-8_12 |
0.201 |
|
2010 |
Sliman SM, Eubank TD, Kotha SR, Kuppusamy ML, Sherwani SI, Butler ES, Kuppusamy P, Roy S, Marsh CB, Stern DM, Parinandi NL. Hyperglycemic oxoaldehyde, glyoxal, causes barrier dysfunction, cytoskeletal alterations, and inhibition of angiogenesis in vascular endothelial cells: aminoguanidine protection. Molecular and Cellular Biochemistry. 333: 9-26. PMID 19585224 DOI: 10.1007/S11010-009-0199-X |
0.215 |
|
2010 |
Kotha S, Rallapalli S. A simple approach to curved hexaquinane via Weiss–Cook reaction Arkivoc. 2010. DOI: 10.3998/Ark.5550190.0011.408 |
0.456 |
|
2010 |
Kotha S, Meshram M. Synthesis of polycyclic aromatics from a diiodosultine by Suzuki-miyaura cross-coupling and Diels-Alder reaction Heterocycles. 82: 1663-1668. DOI: 10.3987/Com-10-S(E)63 |
0.514 |
|
2010 |
Kotha S, Misra S, Krishna NG, Devunuri N, Hopf H, Keecherikunnel A. Diversity-oriented approach to 1,2,3,4-tetrahydroiso-quinoline-3-carboxylic acid (Tic) derivatives using diethyl acetamidomalonate as a glycine equivalent: Further expansion by Suzuki-Miyaura cross-coupling reaction Heterocycles. 80: 847-854. DOI: 10.3987/Com-09-S(S)103 |
0.566 |
|
2010 |
Kotha S, Halder S. Ethyl isocyanoacetate as a useful glycine equivalent Synlett. 337-354. DOI: 10.1055/S-0029-1219149 |
0.502 |
|
2010 |
Kotha S, Seema V, Singh K, Deodhar KD. Strategic utilization of catalytic metathesis and photo-thermal metathesis in caged polycyclic frames Tetrahedron Letters. 51: 2301-2304. DOI: 10.1016/J.Tetlet.2010.02.131 |
0.56 |
|
2010 |
Kotha S, Brahmachary E. ChemInform Abstract: Synthesis of Constrained Phenylalanine Derivatives via a [2 + 2 +2] Cycloaddition Strategy. Cheminform. 33: no-no. DOI: 10.1002/chin.200238192 |
0.442 |
|
2010 |
Kotha S, Manivannan E. ChemInform Abstract: Synthesis of Functionalized cis-syn-cis Triquinanes. Cheminform. 33: no-no. DOI: 10.1002/chin.200232076 |
0.286 |
|
2010 |
Kotha S, Ghosh AK. ChemInform Abstract: Synthesis of 9,10-Diarylanthracene Derivatives via bis Suzuki-Miyaura Cross-Coupling Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200228130 |
0.448 |
|
2010 |
Kotha S, Halder S, Lahiri K. ChemInform Abstract: Modification of Indan-Based Unusual α-Amino Acid Derivatives via the Suzuki-Miyaura Coupling Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200225179 |
0.436 |
|
2010 |
Kotha S, Stoodley RJ. ChemInform Abstract: Enantioselective Synthesis of (+)-4-Demethoxy-1,4-dimethyldaunomycinone. Cheminform. 33: no-no. DOI: 10.1002/chin.200220214 |
0.426 |
|
2010 |
Kotha S, Sreenivasachary N. ChemInform Abstract: Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches. Cheminform. 33: no-no. DOI: 10.1002/chin.200218137 |
0.452 |
|
2010 |
Kotha S, Sivakumar R, Manivannan E. ChemInform Abstract: Allylation of cis-Bicyclo(3.3.0)octane 3,7-Dione Derivatives via Fragmentation Methodology. Cheminform. 33: no-no. DOI: 10.1002/chin.200216091 |
0.325 |
|
2010 |
Kotha S, Tafesh A, Davenport K, Ortiz P. ChemInform Abstract: Synthesis and Carbonylation of Aryl Acetylenes. Cheminform. 33: no-no. DOI: 10.1002/chin.200213094 |
0.457 |
|
2010 |
Kotha S, Sreenivasachary N, Brahmachary E. ChemInform Abstract: Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels-Alder Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200210164 |
0.43 |
|
2010 |
Kotha S, Lahiri K. ChemInform Abstract: A New Approach for Modification of Phenylalanine Peptides by Suzuki-Miyaura Coupling Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200209185 |
0.37 |
|
2010 |
Kotha S, Lahiri K, Sreenivasachary N. ChemInform Abstract: Synthesis of Useful Benzocyclobutene Building Blocks via the Suzuki-Miyaura Coupling Reaction. Cheminform. 33: no-no. DOI: 10.1002/chin.200206107 |
0.424 |
|
2010 |
Kotha S, Sreenivasachary N. ChemInform Abstract: Catalytic Metathesis Reaction in Organic Synthesis Cheminform. 32: no-no. DOI: 10.1002/chin.200149281 |
0.413 |
|
2010 |
Kotha S, Sreenivasachary N, Brahmachary E. ChemInform Abstract: Synthesis of Benzocycloheptene-Based Amino Acid Derivatives via a [4 + 2] Cycloaddition Reaction as a Key Step. Cheminform. 32: no-no. DOI: 10.1002/chin.200143107 |
0.489 |
|
2010 |
Kotha S, Sreenivasachary N, Mohanraja K, Durani S. ChemInform Abstract: Modification of Constrained Peptides by Ring-Closing Metathesis Reaction. Cheminform. 32: no-no. DOI: 10.1002/chin.200138177 |
0.396 |
|
2010 |
Kotha S, Brahmachary E. ChemInform Abstract: First Synthesis of Indane-Based α-Amino Acid Derivatives with a Crown Ether Side Chain. Cheminform. 32: no-no. DOI: 10.1002/chin.200123162 |
0.403 |
|
2010 |
Kotha S, Sreenivasachary N. ChemInform Abstract: A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via Enyne Metathesis and the Diels-Alder Reaction. Cheminform. 31: no-no. DOI: 10.1002/chin.200027147 |
0.468 |
|
2010 |
Kotha S, Brahmachary E. ChemInform Abstract: Synthesis of Indan-Based Unusual α-Amino Acid Derivatives under Phase-Transfer Catalysis Conditions. Cheminform. 31: no-no. DOI: 10.1002/chin.200023049 |
0.375 |
|
2010 |
Kotha S, Manivannan E, Sreenivasachary N. ChemInform Abstract: Allylation of Caged Diketones via Fragmentation Methodology. Cheminform. 31: no-no. DOI: 10.1002/chin.200004091 |
0.323 |
|
2010 |
Kotha S, Chakraborty K, Brahmachary E. ChemInform Abstract: A General and Simple Method for the Synthesis of Star-Shaped Thiophene Derivatives. Cheminform. 31: no-no. DOI: 10.1002/chin.200002138 |
0.36 |
|
2010 |
Kotha S, Manivannan E, Ganesh T, Sreenivasachary N, Deb A. ChemInform Abstract: Spiro-Annulation via Ring Closing Metathesis Reaction. Cheminform. 31: no-no. DOI: 10.1002/chin.200002102 |
0.454 |
|
2010 |
KOTHA S, BRAHMACHARY E, SREENIVASACHARY N. ChemInform Abstract: Synthesis of Constrained α-Amino Acid Derivatives via Diels-Alder Approach. Cheminform. 29: no-no. DOI: 10.1002/chin.199834242 |
0.423 |
|
2010 |
KOTHA S, SREENIVASACHARY N, BRAHMACHARY E. ChemInform Abstract: Synthesis of Constrained α-Amino Acid Derivatives via Enyne Metathesis Reaction. Cheminform. 29: no-no. DOI: 10.1002/chin.199830112 |
0.459 |
|
2010 |
KOTHA S, SREENIVASACHARY N. ChemInform Abstract: Synthesis of Constrained α-Amino Acid Derivatives via Ring-Closing Olefin Metathesis. Cheminform. 29: no-no. DOI: 10.1002/chin.199825232 |
0.46 |
|
2010 |
KOTHA S, BRAHMACHARY E, KUKI A, LANG K, ANGLOS D, SINGARAM B, CHRISMAN W. ChemInform Abstract: Synthesis of a Novel Constrained α-Amino Acid with Quinoxaline Side Chain: 7-Amino-6,7-dihydro-8H-cyclopenta[g]quinoxaline-7-carboxylic Acid. Cheminform. 29: no-no. DOI: 10.1002/chin.199815202 |
0.355 |
|
2010 |
KOTHA S, BRAHMACHARY E. ChemInform Abstract: Synthesis of Conformationally Constrained α-Amino Acid Derivatives Using Ethyl Isocyanoacetate as Glycine Equivalent. Cheminform. 29: no-no. DOI: 10.1002/chin.199810218 |
0.399 |
|
2010 |
KOTHA S, BRAHMACHARY E, SIVAKUMAR R, JOSEPH A, SREENIVASACHARY N. ChemInform Abstract: A Simple Route to Cyclopentane Annulation. Cheminform. 28: no-no. DOI: 10.1002/chin.199739087 |
0.33 |
|
2010 |
KOTHA S, BRAHMACHARY E. ChemInform Abstract: Synthesis of Unusual α-Amino Acids via a (2 + 2 + 2) Cycloaddition Strategy. Cheminform. 28: no-no. DOI: 10.1002/chin.199735238 |
0.394 |
|
2010 |
KOTHA S. ChemInform Abstract: Opportunities in Asymmetric Synthesis: An Industrial Prospect Cheminform. 25: no-no. DOI: 10.1002/chin.199431312 |
0.346 |
|
2010 |
KOTHA S, BINDRA V, KUKI A. ChemInform Abstract: Synthesis and Reactions of 3,4-Dihydro-2H-1,4-benzoxazine Derivatives. Cheminform. 25: no-no. DOI: 10.1002/chin.199423175 |
0.417 |
|
2010 |
KOTHA S, KUKI A. ChemInform Abstract: Synthesis of a New Rigid Quinone-Amino Acid and Diels-Alder Extension to Higher Quinones. Cheminform. 24: no-no. DOI: 10.1002/chin.199349154 |
0.409 |
|
2010 |
KOTHA S, ANGLOS D, KUKI A. ChemInform Abstract: Friedel-Crafts Approach to Electron Deficient Cyclic α-Amino Acids. Cheminform. 23: no-no. DOI: 10.1002/chin.199240163 |
0.326 |
|
2010 |
KOTHA S, KUKI A. ChemInform Abstract: A Simple Method for the Synthesis of Cyclic α-Amino Acids. Cheminform. 23: no-no. DOI: 10.1002/chin.199240092 |
0.382 |
|
2010 |
KOTHA S, KUKI A. ChemInform Abstract: A New Synthetic Approach to Unusually Electron Rich α-Amino Acids. Cheminform. 23: no-no. DOI: 10.1002/chin.199228189 |
0.336 |
|
2010 |
Kotha S, Lilley DG. Two-room structural fire calculations with the FDS computer code for smoke and heat detector response 48th Aiaa Aerospace Sciences Meeting Including the New Horizons Forum and Aerospace Exposition. |
0.174 |
|
2010 |
Kotha S, Rallapalli S. A simple approach to a curved hexaquinane Arkivoc. 2010: 90-95. |
0.263 |
|
2009 |
Kotha S, Meshram M, Tiwari A. Advanced approach to polycyclics by a synergistic combination of enyne metathesis and Diels-Alder reaction. Chemical Society Reviews. 38: 2065-92. PMID 19551182 DOI: 10.1039/B810094M |
0.52 |
|
2009 |
Peltz A, Sherwani SI, Kotha SR, Mazerik JN, O'Connor Butler ES, Kuppusamy ML, Hagele T, Magalang UJ, Kuppusamy P, Marsh CB, Parinandi NL. Calcium and calmodulin regulate mercury-induced phospholipase D activation in vascular endothelial cells. International Journal of Toxicology. 28: 190-206. PMID 19546257 DOI: 10.1177/1091581809338077 |
0.19 |
|
2009 |
Kotha S, Khedkar P. Differential reactivity pattern of hybrid o-quinodimethane precursors: strategic expansion to annulated benzocycloalkanes via rongalite. The Journal of Organic Chemistry. 74: 5667-70. PMID 19545134 DOI: 10.1021/Jo900658Z |
0.451 |
|
2009 |
Kotha S, Mandal K. A retrospective on the design and synthesis of novel molecules through a strategic consideration of metathesis and Suzuki-Miyaura cross-coupling. Chemistry, An Asian Journal. 4: 354-62. PMID 19065595 DOI: 10.1002/Asia.200800244 |
0.505 |
|
2009 |
Khan M, Mohan IK, Kutala VK, Kotha SR, Parinandi NL, Hamlin RL, Kuppusamy P. Sulfaphenazole protects heart against ischemia-reperfusion injury and cardiac dysfunction by overexpression of iNOS, leading to enhancement of nitric oxide bioavailability and tissue oxygenation. Antioxidants & Redox Signaling. 11: 725-38. PMID 18855521 DOI: 10.1089/Ars.2008.2155 |
0.188 |
|
2009 |
Kotha S, Li C, Schmid S, Mason J. Reinforcement of bone cement using zirconia fibers with and without acrylic coating. Journal of Biomedical Materials Research. Part A. 88: 898-906. PMID 18384160 DOI: 10.1002/Jbm.A.31783 |
0.181 |
|
2009 |
Kotha S, Deb AC, Lahiri K, Manivannan E. Selected synthetic strategies to spirocyclics Synthesis. 165-193. DOI: 10.1055/S-0028-1083300 |
0.487 |
|
2009 |
Macione J, Contreras S, Yang Z, Chiu T, Kotha SP, Fox M. Modeling the point spread function of paired angle multiplicative compounding in ultrasound Ifmbe Proceedings. 25: 857-859. DOI: 10.1007/978-3-642-03879-2-239 |
0.249 |
|
2009 |
Kotha S, Khedkar P. A diversity-oriented approach to diphenylalkanes by strategic utilization of [2+2+2] cyclotrimerization, cross-enyne metathesis and diels-alder reaction European Journal of Organic Chemistry. 730-738. DOI: 10.1002/Ejoc.200800924 |
0.542 |
|
2009 |
Kotha S, Lilley DG. FDS: Application of the Fire Dynamics Simulator code to two-room structural fires with smoke detectors 47th Aiaa Aerospace Sciences Meeting Including the New Horizons Forum and Aerospace Exposition. |
0.172 |
|
2009 |
Kotha S, Kashinath D, Lopus M, Panda D. Synthesis of nano-sized C3-symmetric 2,4,6-triphenyl-l,3,5-s- triazine and 1,3,5triphenylbenzene derivatives via the trimerization followed by Suzuki-Miyaura cross-coupling or O-alkylation reactions and their biological evaluation Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 48: 1766-1770. |
0.389 |
|
2009 |
Chen XP, Yao X, Kotha S. Entrepreneur passion and preparedness in business plan presentations: A persuasion analysis of venture capitalists' funding decisions Academy of Management Journal. 52: 199-214. |
0.179 |
|
2009 |
Kotha S, Bansal D, Kumar RV. Synthesis of symmetrical and unsymmetrical trisubstituted benzene derivatives through ring-closing alkyne metathesis strategy and dcpropargylation with various catalysts Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 48: 225-230. |
0.429 |
|
2008 |
Kotha S, Shah VR. Synthesis of C3-symmetric and C4-symmetric amino acid derivatives via Suzuki-Miyaura cross-coupling reaction. Amino Acids. 35: 83-8. PMID 18235995 DOI: 10.1007/S00726-007-0626-9 |
0.507 |
|
2008 |
Kotha S, Shah VR, Mishra PP, Datta A. Design and synthesis of a novel anthracene-based fluorescent probe through the application of the Suzuki-Miyaura cross-coupling reaction. Amino Acids. 35: 169-73. PMID 17914601 DOI: 10.1007/S00726-007-0592-2 |
0.515 |
|
2008 |
Kumaradhas P, Gupta KR, Kotha S, Brahmachari E, Nirmala KA. Crystal structure of 2,6-diisocyano-1,2,3,5,6,7-hexahydro-s-indacene-2,6-dicarboxylic acid diethylester Analytical Sciences: X-Ray Structure Analysis Online. 24: x65-x66. DOI: 10.2116/Analscix.24.X65 |
0.426 |
|
2008 |
Kotha S, Nasser F. Virtualization-enabled undustrial grade software platforms Ieee Industrial Electronics Magazine. 2: 7-9. DOI: 10.1109/MIE.2008.930357 |
0.172 |
|
2008 |
Kotha S, Khedkar P. Synthesis of a conformationally constrained phenylalanine derivative by a strategic combination of ring-closing enyne metathesis and Diels-Alder reaction Synthesis. 2925-2928. DOI: 10.1055/S-2008-1067237 |
0.585 |
|
2008 |
Kotha S, Kashinath D, Kumar S. Synthesis of liquid crystalline materials based on 1,3,5-triphenylbenzene and 2,4,6-triphenyl-1,3,5-s-triazine Tetrahedron Letters. 49: 5419-5423. DOI: 10.1016/J.Tetlet.2008.07.021 |
0.394 |
|
2008 |
Kotha S, Misra S, Halder S. Benzannulation Tetrahedron. 64: 10775-10790. DOI: 10.1016/j.tet.2008.09.004 |
0.375 |
|
2008 |
Kotha S, Shah VR. Design and synthesis of 1-benzazepine derivatives by strategic utilization of Suzuki-Miyaura cross-coupling, aza-Claisen rearrangement and ring-closing metathesis European Journal of Organic Chemistry. 1054-1064. DOI: 10.1002/Ejoc.200700921 |
0.537 |
|
2008 |
Kotha S, Deb AC. Design and synthesis of spiro-heterocycles by ring-closing metathesis Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 47: 1120-1134. |
0.431 |
|
2007 |
Kotha S, Shah VR, Halder S, Vinodkumar R, Lahiri K. Synthesis of bis-armed amino acid derivatives via the alkylation of ethyl isocyanoacetate and the Suzuki-Miyaura cross-coupling reaction. Amino Acids. 32: 387-94. PMID 17031480 DOI: 10.1007/S00726-006-0402-2 |
0.557 |
|
2007 |
Kotha SP, Guzelsu N. Tensile behavior of cortical bone: dependence of organic matrix material properties on bone mineral content. Journal of Biomechanics. 40: 36-45. PMID 16434048 DOI: 10.1016/J.Jbiomech.2005.11.016 |
0.204 |
|
2007 |
Kotha S, Lahiri K. Synthesis of diverse polycyclic compounds via catalytic metathesis Synlett. 2767-2784. DOI: 10.1055/S-2007-990954 |
0.584 |
|
2007 |
Kotha S, Shah VR. Synthesis of bis- and trisoxazole derivatives via Suzuki-Miyaura cross-coupling reaction and van Leusen oxazole synthesis Synthesis. 3653-3658. DOI: 10.1055/S-2007-990865 |
0.508 |
|
2007 |
Kotha S, Kashinath D, Khedkar P. Synthesis of crown-based sulfones via rongalite: Diversity-oriented approach to annulated benzocrowns by Diels-Alder reactions Synthesis. 3357-3360. DOI: 10.1055/S-2007-990822 |
0.557 |
|
2007 |
Kotha S, Banerjee S. Synthesis of novel 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives through the application of rongalite: A synergistic combination of [2+2+2]- and [4+2]-cycloaddition reactions Synthesis. 1015-1020. DOI: 10.1055/S-2007-965946 |
0.56 |
|
2007 |
Kotha S, Mandal K. Metathesis of a novel dienediyne system: A unique example involving the usage of in situ generated ethylene as cross-enyne metathesis partner Journal of Organometallic Chemistry. 692: 4921-4927. DOI: 10.1016/J.Jorganchem.2007.07.009 |
0.485 |
|
2007 |
Kotha S, Singh K. Cross-enyne and ring-closing metathesis cascade: A building-block approach suitable for diversity-oriented synthesis of densely functionalized macroheterocycles with amino acid scaffolds European Journal of Organic Chemistry. 5909-5916. DOI: 10.1002/Ejoc.200700744 |
0.642 |
|
2007 |
Kotha S, Mandal K, Banerjee S, Mobin SM. Synthesis of novel quinone-amino acid hybrids via cross-enyne metathesis and Diels-Alder reaction as key steps European Journal of Organic Chemistry. 1244-1255. DOI: 10.1002/Ejoc.200600970 |
0.571 |
|
2007 |
Kotha S, Lahiri K. Expanding the diversity of polycyclic aromatics through a Suzuki-Miyaura cross-coupling strategy European Journal of Organic Chemistry. 1221-1236. DOI: 10.1002/Ejoc.200600519 |
0.487 |
|
2007 |
Kotha S, Shah VR, Mandal K. Formation of arenes via diallylarenes: Strategic utilization of Suzuki-Miyaura cross-coupling, Claisen rearrangement and ring-closing metathesis Advanced Synthesis and Catalysis. 349: 1159-1172. DOI: 10.1002/Adsc.200600469 |
0.547 |
|
2007 |
Kotha S, Khedkar P. Synthesis of conformationally constrained elimino acid derivatives via ring-closing metathesis Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 46: 975-979. |
0.476 |
|
2006 |
Kotha S, Mandal K, Tiwari A, Mobin SM. Diversity-oriented approach to biologically relevant molecular frameworks starting with beta-naphthol and using the Claisen rearrangement and olefin metathesis as key steps. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 8024-38. PMID 16983708 DOI: 10.1002/Chem.200600540 |
0.524 |
|
2006 |
Kotha S, Banerjee S, Patil MP, Sunoj RB. Retro Diels-Alder reaction under mild conditions: experimental and theoretical studies. Organic & Biomolecular Chemistry. 4: 1854-6. PMID 16688327 DOI: 10.1039/B604063B |
0.425 |
|
2006 |
Kotha S, Dipak MK. Design and synthesis of novel propellanes by using claisen rearrangement and ring-closing metathesis as the key steps. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4446-50. PMID 16568489 DOI: 10.1002/Chem.200501366 |
0.565 |
|
2006 |
Kotha S, Deb A, Chattopadhyay S. Design and Synthesis of Spirocyclics Via the Diels Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps Letters in Organic Chemistry. 3: 128-134. DOI: 10.2174/157017806775224350 |
0.561 |
|
2006 |
Wereley NM, Chaudhuri A, Yoo JH, John S, Kotha S, Suggs A, Radhakrishnan R, Love BJ, Sudarshan TS. Bidisperse magnetorheological fluids using Fe particles at nanometer and micron scale Journal of Intelligent Material Systems and Structures. 17: 393-401. DOI: 10.1177/1045389X06056953 |
0.302 |
|
2006 |
Kotha S, Mandal K. Suzuki-Miyaura cross-coupling and ring-closing metathesis: A strategic combination for the synthesis of cyclophane derivatives European Journal of Organic Chemistry. 5387-5393. DOI: 10.1002/Ejoc.200600549 |
0.529 |
|
2006 |
Kotha S, Deb AC, Chattopadhyay S. Design and Synthesis of Spirocyclics via the Diels—Alder Reaction and Ring-Opening Cross-Metathesis as Key Steps. Cheminform. 37. DOI: 10.1002/chin.200639116 |
0.475 |
|
2006 |
Kotha S, Ghosh AK. A New and Simple Synthetic Approach to Functionalized Sulfone Derivatives by the Suzuki—Miyaura Cross-Coupling Reaction. Cheminform. 37. DOI: 10.1002/chin.200618103 |
0.41 |
|
2006 |
Kotha S, Brahmachary E, Lahiri K. Transition Metal Catalyzed [2 + 2 + 2] Cycloaddition and Application in Organic Synthesis. Cheminform. 37. DOI: 10.1002/chin.200607256 |
0.297 |
|
2006 |
Kotha S, Behera M. Preparation of functionalised tetraphenylmethane derivatives via the Suzuki-Miyaura cross-coupling reaction Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. 45: 2684-2689. |
0.406 |
|
2005 |
Kotha S, Lahiri K. Post-assembly peptide modifications by chemical methods. Current Medicinal Chemistry. 12: 849-75. PMID 15853715 DOI: 10.2174/0929867053507333 |
0.441 |
|
2005 |
Eick JD, Smith RE, Pinzino CS, Kotha SP, Kostoryz EL, Chappelow CC. Photopolymerization of developmental monomers for dental cationically initiated matrix resins. Dental Materials : Official Publication of the Academy of Dental Materials. 21: 384-90. PMID 15766586 DOI: 10.1016/J.Dental.2004.07.001 |
0.256 |
|
2005 |
Yang W, Lu Y, Kalajzic I, Guo D, Harris MA, Gluhak-Heinrich J, Kotha S, Bonewald LF, Feng JQ, Rowe DW, Turner CH, Robling AG, Harris SE. Dentin matrix protein 1 gene cis-regulation: use in osteocytes to characterize local responses to mechanical loading in vitro and in vivo. The Journal of Biological Chemistry. 280: 20680-90. PMID 15728181 DOI: 10.1074/Jbc.M500104200 |
0.202 |
|
2005 |
Kotha S, Deb AC, Kumar RV. Spiro-annulation of barbituric acid derivatives and its analogs by ring-closing metathesis reaction. Bioorganic & Medicinal Chemistry Letters. 15: 1039-43. PMID 15686908 DOI: 10.1016/J.Bmcl.2004.12.034 |
0.524 |
|
2005 |
Kotha S, Behera M, Shah VR. A Simple Synthetic Approach to Allylated Aromatics via the Suzuki—Miyaura Cross-Coupling Reaction. Cheminform. 36. DOI: 10.1055/S-2005-871569 |
0.496 |
|
2005 |
Kotha S, Behera M, Shah VR. A simple synthetic approach to allylated aromatics via the Suzuki-Miyaura cross-coupling reaction Synlett. 1877-1880. DOI: 10.1055/s-2005-871569 |
0.419 |
|
2005 |
Kotha S, Kashinath D. Synthesis of Functionalized Benzo-18-Crown-6 Compounds via the Suzuki-Miyaura Cross-Coupling Reaction Synthesis. 2005: 971-976. DOI: 10.1055/S-2005-861840 |
0.532 |
|
2005 |
Kotha S, Behera M, Khedkar P. Environmentally Benign Process for the Synthesis of N-Formyl Amino Acid Esters. Cheminform. 36. DOI: 10.1016/J.Tetlet.2004.08.129 |
0.449 |
|
2005 |
Kotha S, Brahmachary E, Lahiri K. Transition Metal Catalyzed [2+2+2] Cycloaddition and Application in Organic Synthesis European Journal of Organic Chemistry. 2005: 4741-4767. DOI: 10.1002/Ejoc.200500411 |
0.545 |
|
2005 |
Kotha S, Khedkar P, Ghosh AK. Synthesis of Symmetrical Sulfones from Rongalite: Expansion to Cyclic Sulfones by Ring-Closing Metathesis European Journal of Organic Chemistry. 2005: 3581-3585. DOI: 10.1002/Ejoc.200500264 |
0.563 |
|
2005 |
Kotha S, Khedkar P, Ghosh AK. Synthesis of Symmetrical Sulfones from Rongalite: Expansion to Cyclic Sulfones by Ring-Closing Metathesis. Cheminform. 36. DOI: 10.1002/chin.200548063 |
0.456 |
|
2005 |
Kotha S, Singh K. N-Alkylation of Diethyl Acetamidomalonate: Synthesis of Constrained Amino Acid Derivatives by Ring-Closing Metathesis. Cheminform. 36. DOI: 10.1002/chin.200517193 |
0.585 |
|
2005 |
Kotha S, Ghosh AK. Cycloaddition Approach to Benzo-Annulated Indan-Based ?-Amino Acid Derivatives. Cheminform. 36. DOI: 10.1002/chin.200515091 |
0.376 |
|
2005 |
Kotha S, Mandal K, Deb AC, Banerjee S. Microwave-Assisted Claisen Rearrangement on a Silica Gel Support. Cheminform. 36. DOI: 10.1002/chin.200515047 |
0.228 |
|
2005 |
Kotha S, Banerjee S, Mandal K. Oxidative Dehydrogenation and the Aromatization of Polycycles Using o-Iodoxybenzoic Acid (IBX). Cheminform. 36. DOI: 10.1002/chin.200503106 |
0.265 |
|
2005 |
Kotha S, Kashinath D, Lahiri K, Sunoj RB. Synthesis of C3-Symmetric Nano-Sized Polyaromatic Compounds by Trimerization and Suzuki?Miyaura Cross-Coupling Reactions. Cheminform. 36. DOI: 10.1002/chin.200502085 |
0.409 |
|
2005 |
Kotha S, Mandal K, Arora K, Pedireddi V. New Synthetic Approach to a [1.1.6] Metapara Cyclophane Derivativevia Suzuki–Miyaura Cross-Coupling and Ring-Closing Metathesis Advanced Synthesis & Catalysis. 347: 1215-1218. DOI: 10.1002/Adsc.200404373 |
0.554 |
|
2004 |
Kotha SP, Li C, Schmid SR, Mason JJ. Fracture toughness of steel-fiber-reinforced bone cement. Journal of Biomedical Materials Research. Part A. 70: 514-21. PMID 15293326 DOI: 10.1002/Jbm.A.30107 |
0.176 |
|
2004 |
Kotha S, Behera M. Synthesis and modification of dibenzylglycine derivatives via the Suzuki-Miyaura cross-coupling reaction. The Journal of Peptide Research : Official Journal of the American Peptide Society. 64: 72-85. PMID 15251033 DOI: 10.1111/J.1399-3011.2004.00171.X |
0.404 |
|
2004 |
Damodharan L, Pattabhi V, Behera M, Kotha S. Conformational switching caused by biphenyl substitution at the Calpha position: ethyl 2-benzyl-2-(formylamino)-3-phenylpropionate and ethyl 3-(1,1'-biphenyl-4-yl)-2-(formylamino)-2-(4-phenylbenzyl)propionate. Acta Crystallographica. Section C, Crystal Structure Communications. 60: o527-30. PMID 15237187 DOI: 10.1107/S0108270104013150 |
0.451 |
|
2004 |
Poddar P, Wilson JL, Srikanth H, Yoo JH, Wereley NM, Kotha S, Barghouty L, Radhakrishnan R. Nanocomposite magneto-rheological fluids with uniformly dispersed Fe nanoparticles. Journal of Nanoscience and Nanotechnology. 4: 192-6. PMID 15112566 DOI: 10.1166/jnn.2004.020 |
0.199 |
|
2004 |
Kotha SP, Hsieh YF, Strigel RM, Müller R, Silva MJ. Experimental and finite element analysis of the rat ulnar loading model-correlations between strain and bone formation following fatigue loading. Journal of Biomechanics. 37: 541-8. PMID 14996566 DOI: 10.1016/J.Jbiomech.2003.08.009 |
0.197 |
|
2004 |
Thallapally PK, Jetti RK, Katz AK, Carrell HL, Singh K, Lahiri K, Kotha S, Boese R, Desiraju GR. Polymorphism of 1,3,5-trinitrobenzene induced by a trisindane additive. Angewandte Chemie (International Ed. in English). 43: 1149-55. PMID 14983460 DOI: 10.1002/Anie.200352253 |
0.5 |
|
2004 |
Kotha S, Sivakumar R. An iterative approach to higher polyquinanes Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.B08 |
0.443 |
|
2004 |
Kotha S, Halder S. Synthesis of macrocyclic cyclophane-based unusual α-amino acid derivatives Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.308 |
0.48 |
|
2004 |
Wilson JL, Poddar P, Frey NA, Srikanth H, Mohomed K, Harmon JP, Kotha S, Wachsmuth J. Synthesis and magnetic properties of polymer nanocomposites with embedded iron nanoparticles Journal of Applied Physics. 95: 1439-1443. DOI: 10.1063/1.1637705 |
0.338 |
|
2004 |
Kotha S, Banerjee S, Mandal K. Oxidative Dehydrogenation and the Aromatization of Polycycles Using o-Iodoxybenzoic Acid (IBX) Synlett. 2004: 2043-2045. DOI: 10.1055/S-2004-829580 |
0.399 |
|
2004 |
Kotha S, Ghosh AK. The Diels—Alder Approach for the Synthesis of Tetralin-Based α-Amino Acid Derivatives and Their Modification by the Suzuki—Miyaura Cross-Coupling Reaction. Cheminform. 35. DOI: 10.1055/S-2004-815987 |
0.534 |
|
2004 |
Kotha S, Ghosh AK, Deodhar KD. Synthesis of Symmetrical and Unsymmetrical 9,10-Diarylanthracene Derivatives via Bis-Suzuki—Miyaura Cross-Coupling Reaction. Cheminform. 35. DOI: 10.1055/S-2004-815981 |
0.525 |
|
2004 |
Kotha S, Singh K. N-Alkylation of diethyl acetamidomalonate: synthesis of constrained amino acid derivatives by ring-closing metathesis Tetrahedron Letters. 45: 9607-9610. DOI: 10.1016/J.Tetlet.2004.11.013 |
0.609 |
|
2004 |
Kotha S, Mandal K, Deb AC, Banerjee S. Microwave-assisted Claisen rearrangement on a silica gel support Tetrahedron Letters. 45: 9603-9605. DOI: 10.1016/J.Tetlet.2004.11.012 |
0.406 |
|
2004 |
Kotha S, Behera M, Khedkar P. Environmentally benign process for the synthesis of N-formyl amino acid esters Tetrahedron Letters. 45: 7589-7590. DOI: 10.1016/j.tetlet.2004.08.129 |
0.352 |
|
2004 |
Kotha S, Ghosh AK. A Diels—Alder Approach for the Synthesis of Highly Functionalized Benzo-annulated Indan-Based α-Amino Acid Derivatives via a Sultine Intermediate. Cheminform. 35. DOI: 10.1016/J.Tetlet.2004.02.060 |
0.495 |
|
2004 |
Kotha S, Ghosh AK. A Diels–Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate Tetrahedron Letters. 45: 2931-2934. DOI: 10.1016/j.tetlet.2004.02.060 |
0.424 |
|
2004 |
Kotha S, Mandal K. A New Protocol for Benzoannulation by Double Claisen Rearrangement and Ring-Closing Metathesis Reactions as Key Steps. Cheminform. 35. DOI: 10.1016/J.Tetlet.2004.01.149 |
0.525 |
|
2004 |
Kotha S, Mandal K. A new protocol for benzoannulation by double Claisen rearrangement and ring-closing metathesis reactions as key steps Tetrahedron Letters. 45: 2585-2588. DOI: 10.1016/j.tetlet.2004.01.149 |
0.462 |
|
2004 |
Kotha S, Mandal K. Metathetic approach to naphthoxepin and spirocyclic molecular frameworks Tetrahedron Letters. 45: 1391-1394. DOI: 10.1016/J.Tetlet.2003.12.075 |
0.537 |
|
2004 |
Kotha S, Ghosh AK. Cycloaddition approach to benzo-annulated indane-based α-amino acid derivatives Tetrahedron. 60: 10833-10841. DOI: 10.1016/J.Tet.2004.09.051 |
0.534 |
|
2004 |
Damodharan L, Pattabhi V, Behera M, Kotha S. Optimization of interactions in crystal packing revealed by crystal structures [ethyl 2-(formylamino)-3-thien-2-yl-2-(thien-2-ylmethyl)propanoate and ethyl 3-(5-bromothien-2-yl)-2-[(5-bromothien-2-yl)methyl]-2-(formylamino) propanoate] Journal of Molecular Structure. 705: 101-106. DOI: 10.1016/J.Molstruc.2004.06.021 |
0.405 |
|
2004 |
Kotha S, Brahmachary E. Synthesis and reactions of silicon containing cyclic α-amino acid derivatives Journal of Organometallic Chemistry. 689: 158-163. DOI: 10.1016/J.Jorganchem.2003.09.044 |
0.546 |
|
2004 |
Kotha S, Kashinath D, Lahiri K, Sunoj R. Synthesis ofC3-Symmetric Nano-Sized Polyaromatic Compounds by Trimerization and Suzuki−Miyaura Cross-Coupling Reactions European Journal of Organic Chemistry. 2004: 4003-4013. DOI: 10.1002/Ejoc.200400257 |
0.495 |
|
2004 |
Kotha S, Behera M. Alkylation of Isonitrile Derivatives with 2,2′-Bis(bromomethyl)-1,1′-biphenyl. Cheminform. 35. DOI: 10.1002/chin.200436084 |
0.371 |
|
2004 |
Kotha S, Sreenivasachary N. Synthetic Approaches to Tetrahydroisoquinoline-3-carboxylic Acid Derivatives Cheminform. 35. DOI: 10.1002/chin.200413245 |
0.383 |
|
2003 |
Kotha S, Lahiri K. Application of the Suzuki-Miyaura cross-coupling reaction for the modification of phenylalanine peptides. Biopolymers. 69: 517-28. PMID 12879497 DOI: 10.1002/Bip.10420 |
0.461 |
|
2003 |
Damodharan L, Pattabhi V, Sivakumar R, Kotha S. Precursors to dodecahedrane. Acta Crystallographica. Section C, Crystal Structure Communications. 59: o373-5. PMID 12855860 DOI: 10.1107/S0108270103010825 |
0.432 |
|
2003 |
Kotha S. The building block approach to unusual alpha-amino acid derivatives and peptides. Accounts of Chemical Research. 36: 342-51. PMID 12755644 DOI: 10.1021/Ar020147Q |
0.518 |
|
2003 |
Damodharan L, Pattabhi V, Behera M, Kotha S. Ethyl 2-formamido-2-(4-iodobenzyl)-3-(4-iodophenyl)propionate and ethyl 2-(3-bromobenzyl)-3-(3-bromophenyl)-2-formamidopropionate. Acta Crystallographica. Section C, Crystal Structure Communications. 59: O216-8. PMID 12682414 DOI: 10.1107/S0108270103005183 |
0.395 |
|
2003 |
Kotha S, Manivannan E. Synthesis of spiro-cyclics via ring-closing metathesis Arkivoc. 2003. DOI: 10.3998/Ark.5550190.0004.308 |
0.519 |
|
2003 |
Damodharan L, Pattabhi V, Behera M, Kotha S. Ethyl 2-formamido-2-(4-iodobenzyl)-3-(4-iodophenyl)propionate and ethyl 2-(3-bromobenzyl)-3-(3-bromophenyl)-2-formamidopropionate Acta Crystallographica Section C: Crystal Structure Communications. 59. DOI: 10.1107/S0108270103005183 |
0.329 |
|
2003 |
Kotha S, Halder S, Brahmachary E. Synthesis of Highly Functionalized Phenylalanine Derivatives via Cross-Enyne Metathesis Reactions. Cheminform. 34. DOI: 10.1016/S0040-4020(02)01178-X |
0.581 |
|
2003 |
Kotha S, Halder S. Synthesis of Optically Active Benzocyclobutene and Biphenylene Based Unusual α-Amino Acid Derivatives. Cheminform. 34. DOI: 10.1002/chin.200332136 |
0.359 |
|
2003 |
Kotha S, Lahiri K, Kashinath D. Recent Applications of the Suzuki—Miyaura Cross-Coupling Reaction in Organic Synthesis Cheminform. 34. DOI: 10.1002/chin.200309228 |
0.386 |
|
2003 |
Kotha S, Ghosh AK, Behera M. Synthesis of Highly Constrained Unusual α-Amino Acid Derivative (III) by the Diels—Alder Approach. Cheminform. 34. DOI: 10.1002/chin.200309082 |
0.404 |
|
2002 |
Damodharan L, Shamaladevi N, Pattabhi V, Behera M, Kotha S. Ethyl 6-acetylamino-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-6-carboxylate. Acta Crystallographica. Section C, Crystal Structure Communications. 58: o266-7. PMID 11983986 DOI: 10.1107/S0108270102004687 |
0.47 |
|
2002 |
Kotha S, Brahmachary E. Synthesis of constrained phenylalanine derivatives via a [2+2+2] cycloaddition strategy. Bioorganic & Medicinal Chemistry. 10: 2291-5. PMID 11983526 DOI: 10.1016/S0968-0896(02)00039-1 |
0.541 |
|
2002 |
Kotha S, Halder S, Damodharan L, Pattabhi V. First and unexpected synthesis of macrocyclic cyclophane-based unusual alpha-amino acid derivatives by phosphazene base without high dilution conditions. Bioorganic & Medicinal Chemistry Letters. 12: 1113-5. PMID 11909729 DOI: 10.1016/S0960-894X(02)00068-9 |
0.477 |
|
2002 |
Kotha S, Stoodley RJ. Enantioselective synthesis of ( + )-4-demethoxy-1,4-dimethyldaunomycinone Bioorganic and Medicinal Chemistry. 10: 621-624. PMID 11814850 DOI: 10.1016/S0968-0896(01)00316-9 |
0.69 |
|
2002 |
Kotha S, Behera M, Kumar RV. Synthesis of highly functionalised dibenzylglycine derivatives via the Suzuki-Miyaura coupling reaction. Bioorganic & Medicinal Chemistry Letters. 12: 105-8. PMID 11738584 DOI: 10.1016/S0960-894X(01)00686-2 |
0.513 |
|
2002 |
Kotha S, Halder S, Sreenivasachary N. Synthesis of dibenzocyclobutenylglycine derivatives Arkivoc. 2002. DOI: 10.3998/Ark.5550190.0003.703 |
0.543 |
|
2002 |
Damodharan L, Ibrahim BS, Pattabhi V, Halder S, Kotha S. anti-2,19-Diethoxycarbonyl-2,19-diformylamino[3.2.3.2]paracyclophane Acta Crystallographica Section E-Structure Reports Online. 58. DOI: 10.1107/S1600536802015313 |
0.378 |
|
2002 |
Kotha S, Ghosh AK. Synthesis of 9,10-Diarylanthracene Derivatives via bis Suzuki-Miyaura Cross-coupling Reaction Synlett. 2002: 0451-0452. DOI: 10.1055/S-2002-20463 |
0.546 |
|
2002 |
Kotha S, Halder S, Lahiri (née Chakraborty) K. Modification of Indane-Based Unusual α-Amino Acid Derivatives via the Suzuki-Miyaura Coupling Reaction Synthesis. 2002: 339-342. DOI: 10.1055/S-2002-20026 |
0.53 |
|
2002 |
Kotha S, Sivakumar R, Damodharan L, Pattabhi V. Synthesis of two new hexaquinanes: advanced C20 precursors to dodecahedrane Tetrahedron Letters. 43: 4523-4525. DOI: 10.1016/S0040-4039(02)00815-8 |
0.5 |
|
2002 |
Kotha S, Lahiri K, Kashinath D. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis Tetrahedron. 58: 9633-9695. DOI: 10.1016/S0040-4020(02)01188-2 |
0.472 |
|
2002 |
Kotha S, Halder S, Brahmachary E. Synthesis of highly functionalized phenylalanine derivatives via cross-enyne metathesis reactions Tetrahedron. 58: 9203-9208. DOI: 10.1016/S0040-4020(02)01178-X |
0.499 |
|
2001 |
Kotha S, Lahiri K. A new approach for modification of phenylalanine peptides by Suzuki-Miyaura coupling reaction. Bioorganic & Medicinal Chemistry Letters. 11: 2887-90. PMID 11597423 DOI: 10.1016/S0960-894X(01)00582-0 |
0.45 |
|
2001 |
Damodharan L, Mohanraja K, Kotha S, Durani S, Pattabhi V. Conformational effects of C(alpha,alpha)-dipropargylglycine as a constrained residue. Biopolymers. 59: 330-8. PMID 11514936 DOI: 10.1002/1097-0282(20011015)59:5<330::Aid-Bip1030>3.0.Co;2-M |
0.345 |
|
2001 |
Kotha S, Sreenivasachary N, Mohanraja K, Durani S. Modification of constrained peptides by ring-closing metathesis reaction. Bioorganic & Medicinal Chemistry Letters. 11: 1421-3. PMID 11378368 DOI: 10.1016/S0960-894X(01)00227-X |
0.387 |
|
2001 |
Knight M, Kotha S. Measurement of Geotextile-Water Characteristic Curves Using a Controlled Outflow Capillary Pressure Cell Geosynthetics International. 8: 271-282. DOI: 10.1680/gein.8.0195 |
0.176 |
|
2001 |
Kotha S, Lahiri (née Chakraborty) K, Sreenivasachary N. Synthesis of Useful Benzocyclobutene Building Blocks via the Suzuki-Miyaura Coupling Reaction Synthesis. 2001: 1932-1934. DOI: 10.1055/S-2001-17698 |
0.516 |
|
2001 |
Kotha S, Manivannan E. Synthesis of spiro-indanes by cycloaddition strategy Journal of the Chemical Society-Perkin Transactions 1. 2543-2547. DOI: 10.1039/B106280H |
0.559 |
|
2001 |
Thallapally PK, Chakraborty K, Katz AK, Carrell HL, Kotha S, Desiraju GR. Matching of molecular and supramolecular symmetry. An exercise in crystal engineering Crystengcomm. 3: 134. DOI: 10.1039/B104431C |
0.335 |
|
2001 |
Kotha S, Sreenivasachary N, Brahmachary E. Synthesis of benzocycloheptene-based amino acid derivatives via a [4+2] cycloaddition reaction as a key step Tetrahedron. 57: 6261-6265. DOI: 10.1016/S0040-4020(01)00575-0 |
0.563 |
|
2001 |
Mehta G, Kotha S. Recent chemistry of benzocyclobutenes Tetrahedron. 57: 625-659. DOI: 10.1016/S0040-4020(00)00958-3 |
0.632 |
|
2001 |
Mehta G, Kotha S. ChemInform Abstract: Recent Chemistry of Benzocyclobutenes Cheminform. 32: no-no. DOI: 10.1002/chin.200118233 |
0.539 |
|
2001 |
Kotha S, Mohanraja K, Durani S. ChemInform Abstract: Constrained Phenylalanyl Peptides via a [2 + 2 + 2]-Cycloaddition Strategy. Cheminform. 32: no-no. DOI: 10.1002/chin.200102190 |
0.259 |
|
2001 |
Kotha S, Chakraborty K. ChemInform Abstract: Protection and Deprotection Sequence in Tetracyclo[6.3.0.04,11.05,9]undeca-2,7-dione System Using Tetrachlorosilane. Cheminform. 32: no-no. DOI: 10.1002/chin.200102086 |
0.249 |
|
2001 |
Kotha S, Sreenivasachary N. Synthesis of 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives by Cycloaddition Approaches European Journal of Organic Chemistry. 2001: 3375. DOI: 10.1002/1099-0690(200109)2001:17<3375::Aid-Ejoc3375>3.0.Co;2-R |
0.591 |
|
2001 |
Kotha S, Sreenivasachary N, Brahmachary E. Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels−Alder Reaction European Journal of Organic Chemistry. 2001: 787-792. DOI: 10.1002/1099-0690(200102)2001:4<787::Aid-Ejoc787>3.0.Co;2-N |
0.565 |
|
2000 |
Foulger SH, Kotha S, Sweryda-Krawiec B, Baughman TW, Ballato JM, Jiang P, Smith DW. Robust polymer colloidal crystal photonic bandgap structures. Optics Letters. 25: 1300-2. PMID 18066199 DOI: 10.1364/Ol.25.001300 |
0.228 |
|
2000 |
Kotha S, Ganesh T, Ghosh AK. Diels-Alder approach to tetralin-based constrained α-amino acid derivatives Bioorganic and Medicinal Chemistry Letters. 10: 1755-1757. PMID 10937741 DOI: 10.1016/S0960-894X(00)00333-4 |
0.497 |
|
2000 |
Kotha S, Sreenivasachary N. A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via a [2 + 2 + 2] cycloaddition reaction. Bioorganic & Medicinal Chemistry Letters. 10: 1413-5. PMID 10888321 DOI: 10.1016/S0960-894X(00)00259-6 |
0.542 |
|
2000 |
Kotha S, Brahmachary E. Synthesis of indan-based unusual alpha-amino acid derivatives under phase-transfer catalysis conditions. The Journal of Organic Chemistry. 65: 1359-65. PMID 10814097 DOI: 10.1021/Jo991387V |
0.425 |
|
2000 |
Kotha S, Halder S, Brahmachary E, Ganesh T. Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction Synlett. 2000: 853-855. DOI: 10.1055/S-2000-6706 |
0.554 |
|
2000 |
Kotha S, Mohanraja K, Durani S. Constrained phenylalanyl peptides via a [2+2+2]-cycloaddition strategy Chemical Communications. 1909-1910. DOI: 10.1039/B005605G |
0.389 |
|
2000 |
Kotha S, Sreenivasachary N. A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via enyne metathesis and the Diels–Alder reaction Chemical Communications. 503-504. DOI: 10.1039/A910217P |
0.544 |
|
2000 |
Thallapally PK, Chakraborty K, Carrell H, Kotha S, Desiraju GR. Shape and Size Effects in the Crystal Structures of Complexes of 1,3,5-Trinitrobenzene with some Trigonal Donors: The Benzene–Thiophene Exchange Rule Tetrahedron. 56: 6721-6728. DOI: 10.1016/S0040-4020(00)00493-2 |
0.388 |
|
2000 |
Kotha S, Ganesh T, Ghosh AK. ChemInform Abstract: Diels-Alder Approach to Tetralin-Based Constrained α-Amino Acid Derivatives. Cheminform. 31: no-no. DOI: 10.1002/chin.200044109 |
0.376 |
|
2000 |
Kotha S, Sreenivasachary N. ChemInform Abstract: A New Synthetic Approach to 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid (Tic) Derivatives via a [2 + 2 + 2] Cycloaddition Reaction. Cheminform. 31: no-no. DOI: 10.1002/chin.200042129 |
0.46 |
|
2000 |
Kotha S, Halder S, Brahmachary E, Ganesh T. ChemInform Abstract: Synthesis of Unusual α-Amino Acid Derivatives via Cross-Enyne Metathesis Reaction. Cheminform. 31: no-no. DOI: 10.1002/chin.200039082 |
0.458 |
|
1999 |
Kotha S, Sreenivasachary N, Halder S. First synthesis of optically active benzocyclobutene and biphenylene-based unusual α-amino acid derivatives Bioorganic and Medicinal Chemistry Letters. 9: 2565-2568. PMID 10498209 DOI: 10.1016/S0960-894X(99)00437-0 |
0.457 |
|
1999 |
Kotha S, Sreenivasachary N. Synthesis of constrained alpha-amino acid derivatives via ring-closing olefin metathesis. Bioorganic & Medicinal Chemistry Letters. 8: 257-60. PMID 9871665 DOI: 10.1016/S0960-894X(98)00002-X |
0.523 |
|
1999 |
Kotha S, Manivannan E, Ganesh T, Sreenivasachary N, Deb A. Spiro-Annulation via Ring Closing Metathesis Reaction Synlett. 1999: 1618-1620. DOI: 10.1055/S-1999-2896 |
0.542 |
|
1999 |
Kotha S, Chakraborty K, Brahmachary E. A General and Simple Method for the Synthesis of Star-Shaped Thiophene Derivatives Synlett. 1999: 1621-1623. DOI: 10.1055/S-1999-2895 |
0.54 |
|
1999 |
Kotha S, Manivannan E, Sreenivasachary N. Allylation of caged diketones via fragmentation methodology Journal of the Chemical Society-Perkin Transactions 1. 2845-2848. DOI: 10.1039/A902629K |
0.538 |
|
1998 |
Kotha S, Brahmachary E, Sreenivasachary N. Synthesis of constrained α-amino acid derivatives via Diels-Alder approach Tetrahedron Letters. 39: 4095-4098. DOI: 10.1016/S0040-4039(98)00562-0 |
0.521 |
|
1998 |
Kotha S, Sreenivasachary N, Brahmachary E. Synthesis of constrained α-amino acid derivatives via enyne metathesis reaction Tetrahedron Letters. 39: 2805-2808. DOI: 10.1016/S0040-4039(98)00251-2 |
0.545 |
|
1997 |
Kotha S, Brahmachary E. Synthesis of conformationally constrained α-amino acid derivatives using ethyl isocyanoacetate as glycine equivalent Bioorganic & Medicinal Chemistry Letters. 7: 2719-2722. DOI: 10.1016/S0960-894X(97)10075-0 |
0.47 |
|
1997 |
Kotha S, Brahmachary E, Kuki A, Lang K, Anglos D, Singaram B, Chrisman W. Synthesis of a novel constrained α-amino acid with quinoxaline side chain: 7-amino-6,7-dihydro-8H-cyclopenta[g]quinoxaline-7-carboxylic acid Tetrahedron Letters. 38: 9031-9034. DOI: 10.1016/S0040-4039(97)10427-0 |
0.569 |
|
1997 |
Kotha S, Brahmachary E, Kuki A, Lang K, Anglos D, Singaram B, Chrisman W. Synthesis of a novel constrained α-amino acid with quinoxaline side chain : 7-Amino-6,7-dihydro-8H-cyclopenta[g]quinoxaline-7-carbox-ylic acid Tetrahedron Letters. 38: 9031-9034. DOI: 10.1016/S0040-4039(97)10427-0 |
0.61 |
|
1997 |
Kotha S, Brahmachary E, Sivakumar R, Joseph A, Sreenivasachary N. A simple route to cyclopentane annulation Tetrahedron Letters. 38: 4497-4500. DOI: 10.1016/S0040-4039(97)00912-X |
0.444 |
|
1997 |
Kotha S, Brahmachary E. Synthesis of unsual α-amino acids via a 2+2+2 cycloaddition strategy Tetrahedron Letters. 38: 3561-3564. DOI: 10.1016/S0040-4039(97)00663-1 |
0.496 |
|
1994 |
Kotha S, Bindra V, Kuki A. Synthesis and Reactions of 3,4-dihydro-2H-1,4-benzoxazine Derivatives Heterocycles. 38: 5. DOI: 10.3987/Com-93-6523 |
0.515 |
|
1994 |
Kotha S. Opportunities in asymmetric synthesis: An industrial prospect Tetrahedron. 50: 3639-3662. DOI: 10.1016/S0040-4020(01)90388-6 |
0.427 |
|
1993 |
Kotha S, Kuki A. Synthesis of a New Rigid Quinone-Amino Acid and Diels-Alder Extension to Higher Quinones Chemistry Letters. 22: 299-302. DOI: 10.1246/Cl.1993.299 |
0.499 |
|
1992 |
Kotha S, Kuki A. A new synthetic approach to unusually electron rich α-amino acids Journal of the Chemical Society, Chemical Communications. 404-406. DOI: 10.1039/C39920000404 |
0.43 |
|
1992 |
Kotha S, Anglos D, Kuki A. Friedel-Crafts Approach to Electron Deficient Cyclic α- Amino Acids Tetrahedron Letters. 33: 1569-1572. DOI: 10.1016/S0040-4039(00)91676-9 |
0.459 |
|
1992 |
Kotha S, Kuki A. A Simple Method for the Synthesis of Cyclic α- Amino Acids Tetrahedron Letters. 33: 1565-1568. DOI: 10.1016/S0040-4039(00)91675-7 |
0.492 |
|
Show low-probability matches. |