Year |
Citation |
Score |
2016 |
Li Y, Ma L, Gaddam V, Gallazzi F, Hennkens HM, Harmata M, Lewis MR, Deakyne CA, Jurisson SS. Synthesis, Characterization, and In Vitro Evaluation of New (99m)Tc/Re(V)-Cyclized Octreotide Analogues: An Experimental and Computational Approach. Inorganic Chemistry. PMID 26789775 DOI: 10.1021/Acs.Inorgchem.5B02306 |
0.494 |
|
2015 |
Rotsch D, Brossard T, Bihmidine S, Ying W, Gaddam V, Harmata M, Robertson JD, Swyers M, Jurisson SS, Braun DM. Radiosynthesis of 6'-Deoxy-6'[18F]Fluorosucrose via Automated Synthesis and Its Utility to Study In Vivo Sucrose Transport in Maize (Zea mays) Leaves. Plos One. 10: e0128989. PMID 26024520 DOI: 10.1371/Journal.Pone.0128989 |
0.6 |
|
2014 |
Gao X, Gaddam V, Harmata M. A synthesis of 6-deoxy-6-fluorosucrose suitable for PET applications. Carbohydrate Research. 400: 14-18. PMID 25318025 DOI: 10.1016/J.Carres.2014.08.015 |
0.511 |
|
2014 |
Gao X, Gaddam V, Harmata M. A synthesis of 6-deoxy-6-fluorosucrose suitable for PET applications Carbohydrate Research. 400: 14-18. DOI: 10.1016/j.carres.2014.08.015 |
0.427 |
|
2013 |
Ying W, Gaddam V, Harmata M. Chemical synthesis of 1′-deoxy-1′-fluorosucrose Organic Letters. 15: 2723-2725. PMID 23742267 DOI: 10.1021/Ol401044H |
0.64 |
|
2013 |
Gaddam V, Harmata M. Synthesis of 6′-deoxy-6′-fluorosucrose Carbohydrate Research. 369: 38-41. PMID 23391562 DOI: 10.1016/J.Carres.2012.12.001 |
0.54 |
|
2012 |
Gao X, Gaddam V, Altenhofer E, Tata RR, Cai Z, Yongpruksa N, Garimallaprabhakaran AK, Harmata M. C-H activation in S-alkenyl sulfoximines: an endo 1,5-hydrogen migration. Angewandte Chemie (International Ed. in English). 51: 7016-9. PMID 22730316 DOI: 10.1002/Anie.201203258 |
0.728 |
|
2012 |
Gao X, Gaddam V, Altenhofer E, Tata RR, Cai Z, Yongpruksa N, Garimallaprabhakaran AK, Harmata M. Addition: CH Activation in S-Alkenyl Sulfoximines: An Endo 1,5-Hydrogen Migration Angewandte Chemie International Edition. 51: 10437-10437. DOI: 10.1002/Anie.201206823 |
0.755 |
|
2012 |
Gao X, Gaddam V, Altenhofer E, Tata RR, Cai Z, Yongpruksa N, Garimallaprabhakaran AK, Harmata M. Inside Cover: CH Activation in S-Alkenyl Sulfoximines: An Endo 1,5-Hydrogen Migration (Angew. Chem. Int. Ed. 28/2012) Angewandte Chemie International Edition. 51: 6796-6796. DOI: 10.1002/Anie.201204561 |
0.75 |
|
2012 |
Gao X, Gaddam V, Altenhofer E, Tata RR, Cai Z, Yongpruksa N, Garimallaprabhakaran AK, Harmata M. C-H activation in S-alkenyl sulfoximines: An endo 1,5-hydrogen migration Angewandte Chemie - International Edition. 51: 7016-7019. DOI: 10.1002/anie.201203258 |
0.743 |
|
2012 |
Gao X, Gaddam V, Altenhofer E, Tata RR, Cai Z, Yongpruksa N, Garimallaprabhakaran AK, Harmata M. Innentitelbild: CH Activation in S-Alkenyl Sulfoximines: An Endo 1,5-Hydrogen Migration (Angew. Chem. 28/2012) Angewandte Chemie. 124: 6902-6902. DOI: 10.1002/Ange.201204561 |
0.754 |
|
2010 |
Ramesh S, Gaddam V, Nagarajan R. A flexible approach to the chromenoquinolines under copper/lewis acid catalysis Synlett. 757-760. DOI: 10.1055/S-0029-1219364 |
0.673 |
|
2010 |
Gaddam V, Ramesh S, Nagarajan R. CuI/La(OTf)3 catalyzed, one-pot synthesis of isomeric ellipticine derivatives in ionic liquid Tetrahedron. 66: 4218-4222. DOI: 10.1016/J.Tet.2010.03.095 |
0.692 |
|
2009 |
Gaddam V, Nagarajan R. A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction Tetrahedron Letters. 50: 1243-1248. DOI: 10.1016/J.Tetlet.2009.01.020 |
0.411 |
|
2008 |
Gaddam V, Nagarajan R. An Efficient, one-pot synthesis of isomeric ellipticine derivatives through intramolecular imino-Diels-Alder reaction. Organic Letters. 10: 1975-8. PMID 18412351 DOI: 10.1021/Ol800497U |
0.537 |
|
2007 |
Gaddam V, Nagarajan R. A new entry to polycyclic indole derivatives via intramolecular imino Diels-Alder reaction: observation of unexpected reaction. The Journal of Organic Chemistry. 72: 3573-6. PMID 17408284 DOI: 10.1021/Jo062321K |
0.531 |
|
2007 |
Gaddam V, Meesala R, Nagarajan R. A rapid intramolecular imino Diels-Alder reaction of aminoanthraquinones with citronellal or prenylated salicylaldehydes: Substituent effect on changing the reaction pathway from Diels-Alder to ene-type cyclization Synthesis. 2503-2512. DOI: 10.1055/S-2007-983790 |
0.338 |
|
2007 |
Gaddam V, Nagarajan R. Highly diastereoselective synthesis of new indolopyrroloquinolines through intramolecular imino Diels-Alder reactions Tetrahedron Letters. 48: 7335-7338. DOI: 10.1016/J.Tetlet.2007.08.016 |
0.398 |
|
2006 |
Gaddam V, Sreenivas DK, Nagarajan R. Highly diastereoselective synthesis of new chromenylaminoanthraquinones through a one-pot, three-component hetero Diels-Alder reaction Tetrahedron Letters. 47: 9291-9295. DOI: 10.1016/J.Tetlet.2006.10.104 |
0.388 |
|
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