Year |
Citation |
Score |
2014 |
Ghosh AK, Xi K. Platensimycin and Platencin Natural Products in Medicinal Chemistry. 271-300. DOI: 10.1002/9783527676545.ch08 |
0.337 |
|
2010 |
Ghosh AK, Xi K. Formal Synthesis of (±)-Platencin Synfacts. 2010: 20-20. DOI: 10.1055/S-0029-1218396 |
0.392 |
|
2009 |
Ghosh AK, Xi K. A symmetry-based concise formal synthesis of platencin, a novel lead against "superbugs". Angewandte Chemie (International Ed. in English). 48: 5372-5. PMID 19572306 DOI: 10.1002/Anie.200902338 |
0.474 |
|
2009 |
Ghosh AK, Xi K. Total synthesis of (-)-platensimycin, a novel antibacterial agent. The Journal of Organic Chemistry. 74: 1163-70. PMID 19123842 DOI: 10.1021/Jo802261F |
0.462 |
|
2007 |
Ghosh AK, Xi K, Johnson ME, Baker SC, Mesecar AD. Progress in Anti-SARS Coronavirus Chemistry, Biology and Chemotherapy. Annual Reports in Medicinal Chemistry. 41: 183-196. PMID 19649165 DOI: 10.1016/S0065-7743(06)41011-3 |
0.457 |
|
2007 |
Ghosh AK, Xi K, Grum-Tokars V, Xu X, Ratia K, Fu W, Houser KV, Baker SC, Johnson ME, Mesecar AD. Structure-based design, synthesis, and biological evaluation of peptidomimetic SARS-CoV 3CLpro inhibitors. Bioorganic & Medicinal Chemistry Letters. 17: 5876-80. PMID 17855091 DOI: 10.1016/J.Bmcl.2007.08.031 |
0.527 |
|
2007 |
Ghosh AK, Xi K. Enantioselective synthesis of (-)-platensimycin oxatetracyclic core by using an intramolecular Diels-Alder reaction. Organic Letters. 9: 4013-6. PMID 17764196 DOI: 10.1021/Ol701783Z |
0.425 |
|
2005 |
Ghosh AK, Xi K, Ratia K, Santarsiero BD, Fu W, Harcourt BH, Rota PA, Baker SC, Johnson ME, Mesecar AD. Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors. Journal of Medicinal Chemistry. 48: 6767-71. PMID 16250632 DOI: 10.1021/Jm050548M |
0.472 |
|
2005 |
Ratia K, Santarsiero B, Xi K, Jukneliene D, Harcourt B, Baker S, Ghosh A, Mesecar A. Kinetic and crystallographic analyses of SARS coronavirus 3CLpro inhibitors Acta Crystallographica Section a Foundations of Crystallography. 61: c236-c236. DOI: 10.1107/S0108767305089944 |
0.382 |
|
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