Year |
Citation |
Score |
2021 |
Lubriks D, Zogota R, Sarpe VA, Matsushita T, Sati GC, Haldimann K, Gysin M, Böttger EC, Vasella A, Suna E, Hobbie SN, Crich D. Synthesis and Antibacterial Activity of Propylamycin Derivatives Functionalized at the 5''- and Other Positions with a View to Overcoming Resistance Due to Aminoglycoside Modifying Enzymes. Acs Infectious Diseases. PMID 34114793 DOI: 10.1021/acsinfecdis.1c00158 |
0.737 |
|
2021 |
Jana S, Sarpe VA, Kulkarni SS. Total Synthesis and Structure Revision of a Fungal Glycolipid Fusaroside. Organic Letters. 23: 1664-1668. PMID 33591200 DOI: 10.1021/acs.orglett.1c00077 |
0.73 |
|
2020 |
Ogasahara R, Abdullayev S, Sarpe VA, Mandhapati AR, Crich D. Influence of protecting groups on O- and C-glycosylation with neuraminyl and ulosonyl dibutylphosphates. Carbohydrate Research. 496: 108100. PMID 32755675 DOI: 10.1016/J.Carres.2020.108100 |
0.485 |
|
2020 |
Dadhich R, Mishra M, Ning S, Jana S, Sarpe VA, Mahato J, Duan M, Kulkarni SS, Kapoor S. A Virulence-associated glycolipid with distinct conformational attributes: Impact on lateral organization of host plasma membrane, autophagy and signaling. Acs Chemical Biology. PMID 32078292 DOI: 10.1021/Acschembio.9B00991 |
0.682 |
|
2019 |
Quirke JCK, Rajasekaran P, Sarpe VA, Sonousi A, Osinnii I, Gysin M, Haldimann K, Fang QJ, Shcherbakov D, Hobbie SN, Sha SH, Schacht J, Vasella A, Böttger EC, Crich D. Apralogs: Apramycin 5-O-Glycosides and Ethers with Improved Antibacterial Activity and Ribosomal Selectivity and Reduced Susceptibility to the Aminoacyltranserferase (3)-IV Resistance Determinant. Journal of the American Chemical Society. PMID 31790244 DOI: 10.1021/Jacs.9B11601 |
0.504 |
|
2019 |
Sati GC, Sarpe VA, Furukawa T, Mondal S, Mantovani M, Hobbie SN, Vasella A, Böttger EC, Crich D. Modification at the 2'-Position of the 4,5-Series of 2-Deoxystreptamine Aminoglycoside Antibiotics to Resist Aminoglycoside Modifying Enzymes and Increase Ribosomal Target Selectivity. Acs Infectious Diseases. PMID 31436080 DOI: 10.1021/Acsinfecdis.9B00128 |
0.733 |
|
2019 |
Sarpe VA, Pirrone MG, Haldimann K, Hobbie SN, Vasella A, Crich D. Synthesis of saccharocin from apramycin and evaluation of its ribosomal selectivity. Medchemcomm. 10: 554-558. PMID 31057735 DOI: 10.1039/C9Md00093C |
0.49 |
|
2018 |
Jana S, Sarpe VA, Kulkarni SS. Total Synthesis of Emmyguyacins A and B, Potential Fusion Inhibitors of Influenza Virus. Organic Letters. PMID 30350678 DOI: 10.1021/Acs.Orglett.8B03073 |
0.695 |
|
2018 |
Sonousi A, Sarpe VA, Brilkova M, Schacht J, Vasella A, Böttger EC, Crich D. Effects of the 1-N-(4-Amino-2S-hydroxybutyryl) and 6'-N-(2-Hydroxyethyl) Substituents on Ribosomal Selectivity, Cochleotoxicity and Antibacterial Activity in the Sisomicin Class of Aminoglycoside Antibiotics. Acs Infectious Diseases. PMID 29708331 DOI: 10.1021/Acsinfecdis.8B00052 |
0.428 |
|
2016 |
Chaube MA, Sarpe VA, Jana S, Kulkarni SS. First total synthesis of trehalose containing tetrasaccharides from Mycobacterium smegmatis. Organic & Biomolecular Chemistry. PMID 27035801 DOI: 10.1039/C6Ob00412A |
0.641 |
|
2015 |
Sarpe VA, Jana S, Kulkarni SS. Synthesis of Mycobacterium tuberculosis Sulfolipid-3 Analogues and Total Synthesis of the Tetraacylated Trehaloglycolipid of Mycobacterium paraffinicum. Organic Letters. PMID 26652194 DOI: 10.1021/Acs.Orglett.5B03300 |
0.736 |
|
2014 |
Sarpe VA, Kulkarni SS. Expeditious synthesis of Mycobacterium tuberculosis sulfolipids SL-1 and Ac2SGL analogues. Organic Letters. 16: 5732-5. PMID 25322198 DOI: 10.1021/ol5027987 |
0.656 |
|
2013 |
Sarpe VA, Kulkarni SS. Desymmetrization of trehalose via regioselective DIBAL reductive ring opening of benzylidene and substituted benzylidene acetals. Organic & Biomolecular Chemistry. 11: 6460-5. PMID 23982734 DOI: 10.1039/c3ob41389f |
0.612 |
|
2011 |
Sarpe VA, Kulkarni SS. Synthesis of maradolipid. The Journal of Organic Chemistry. 76: 6866-70. PMID 21739985 DOI: 10.1021/jo200979n |
0.652 |
|
1979 |
Sarpe VA, Crich D. Oxidative deamination of amino sugars: recent advances. Carbohydrate Chemistry. 72: 312-314. PMID 34290849 DOI: 10.1016/s0008-6215(00)83957-9 |
0.432 |
|
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