Year |
Citation |
Score |
2020 |
Rutledge KM, Griesbach C, Mercado BQ, Peczuh MW. Structures of three disubstituted [13]-macro-di-lac-tones reveal effects of substitution on macrocycle conformation. Acta Crystallographica. Section E, Crystallographic Communications. 76: 1617-1623. PMID 33117575 DOI: 10.1107/S2056989020012037 |
0.366 |
|
2020 |
Chen C, Bosko C, McGeough CP, McLean R, Zaino AM, Kyle Hadden M, Peczuh MW. Exploring the physicochemical and antiproliferative properties of biaryl-linked [13]-macrodilactones. Bioorganic & Medicinal Chemistry. 28: 115671. PMID 33069068 DOI: 10.1016/J.Bmc.2020.115671 |
0.321 |
|
2019 |
Cannone Z, Shaqra A, Lorenc C, Henowitz L, Keshipeddy S, Robinson VL, Zweifach A, Wright DL, Peczuh M. Post Glycosylation Diversification (PGD): An Approach for Assembling Collections of Glycosylated Small Molecules. Acs Combinatorial Science. PMID 30607941 DOI: 10.1021/Acscombsci.8B00139 |
0.329 |
|
2019 |
Cannone ZP, Peczuh MW. A method for preparing N-alkylated kanosamines from diacetone d-glucose Tetrahedron Letters. 60: 1830-1833. DOI: 10.1016/J.Tetlet.2019.06.012 |
0.333 |
|
2018 |
Sager CP, Fiege B, Zihlmann P, Vannam R, Rabbani S, Jakob RP, Preston RC, Zalewski A, Maier T, Peczuh MW, Ernst B. The price of flexibility - a case study on septanoses as pyranose mimetics. Chemical Science. 9: 646-654. PMID 29629131 DOI: 10.1039/C7Sc04289B |
0.393 |
|
2017 |
Rutledge KM, Hamlin TA, Baldisseri DM, Bickelhaupt FM, Peczuh MW. Macrocycles All Aflutter: Substitution at an Allylic Center Reveals the Conformational Dynamics of [13]-Macrodilactones. Chemistry, An Asian Journal. PMID 28783877 DOI: 10.1002/Asia.201700997 |
0.378 |
|
2017 |
Vannam R, Pote AR, Peczuh MW. Formation and selective rupture of 1,4-anhydroseptanoses Tetrahedron. 73: 418-425. DOI: 10.1016/J.Tet.2016.12.031 |
0.306 |
|
2016 |
Si D, Peczuh MW. Synthesis and structure of a carbohydrate-fused [15]-macrodilactone. Carbohydrate Research. 434: 113-120. PMID 27639337 DOI: 10.1016/J.Carres.2016.08.010 |
0.39 |
|
2016 |
Vannam R, Peczuh MW. A practical and scalable synthesis of carbohydrate based oxepines. Organic & Biomolecular Chemistry. PMID 27056249 DOI: 10.1039/C6Ob00262E |
0.376 |
|
2016 |
Magpusao AN, Rutledge K, Hamlin TA, Lawrence JM, Mercado BQ, Leadbeater NE, Peczuh MW. Rules of Macrocycle Topology: A [13]-Macrodilactone Case Study. Chemistry (Weinheim An Der Bergstrasse, Germany). 22: 6001-11. PMID 27001347 DOI: 10.1002/Chem.201504684 |
0.345 |
|
2016 |
Vannam R, Peczuh MW. How to Homologate Your Sugar: Synthetic Approaches to Septanosyl Containing Carbohydrates European Journal of Organic Chemistry. 2016: 1800-1812. DOI: 10.1002/Ejoc.201600052 |
0.381 |
|
2015 |
Lorenc C, Saurí J, Moser A, Buevich AV, Williams AJ, Williamson RT, Martin GE, Peczuh MW. Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation. Chemistryopen. 4: 577-80. PMID 26491634 DOI: 10.1002/Open.201500122 |
0.325 |
|
2015 |
Lorenc C, Saurí J, Moser A, Buevich AV, Williams AJ, Williamson RT, Martin GE, Peczuh MW. Cover Picture: Turning Spiroketals Inside Out: A Rearrangement Triggered by an Enol Ether Epoxidation (ChemistryOpen 5/2015). Chemistryopen. 4: 541. PMID 26491627 DOI: 10.1002/Open.201500185 |
0.339 |
|
2015 |
Si D, Peczuh MW. Synthesis, structure and reactivity of [15]-macrodilactones. Organic & Biomolecular Chemistry. 13: 6463-7. PMID 25994512 DOI: 10.1039/C5Ob00809C |
0.362 |
|
2015 |
Magpusao AN, Rutledge K, Mercado BQ, Peczuh MW. Stereogenic α-carbons determine the shape and topology of [13]-macrodilactones. Organic & Biomolecular Chemistry. 13: 5086-9. PMID 25846133 DOI: 10.1039/C5Ob00402K |
0.332 |
|
2014 |
Desmond RT, Magpusao AN, Lorenc C, Alverson JB, Priestley N, Peczuh MW. De novo macrolide-glycolipid macrolactone hybrids: Synthesis, structure and antibiotic activity of carbohydrate-fused macrocycles. Beilstein Journal of Organic Chemistry. 10: 2215-21. PMID 25246980 DOI: 10.3762/Bjoc.10.229 |
0.369 |
|
2014 |
Ma J, Vannam R, Terwilliger DW, Peczuh MW. Synthesis, structure and reactivity of a macrocyclic imine: aza-[13]-macrodiolides Tetrahedron Letters. 55: 4255-4259. DOI: 10.1016/J.Tetlet.2014.05.081 |
0.321 |
|
2013 |
Vannam R, Peczuh MW. Synthesis of C-septanosides from pyranoses via vinyl addition and electrophilic cyclization. Organic Letters. 15: 4122-5. PMID 23906012 DOI: 10.1021/Ol401769K |
0.403 |
|
2012 |
Beck JM, Miller SM, Peczuh MW, Hadad CM. C2 hydroxyl group governs the difference in hydrolysis rates of methyl-α-D-glycero-D-guloseptanoside and methyl-β-D-glycero-D-guloseptanoside. The Journal of Organic Chemistry. 77: 4242-51. PMID 22493940 DOI: 10.1021/Jo202639G |
0.401 |
|
2012 |
Saha J, Lorenc C, Surana B, Peczuh MW. Discovery of a phosphine-mediated cycloisomerization of alkynyl hemiketals: access to spiroketals and dihydropyrazoles via tandem reactions. The Journal of Organic Chemistry. 77: 3846-58. PMID 22428530 DOI: 10.1021/Jo3001854 |
0.339 |
|
2012 |
Saha J, Peczuh MW. Glycosylations with a septanosyl fluoride donor lacking a C2 protecting group Tetrahedron Letters. 53: 5667-5670. DOI: 10.1016/J.Tetlet.2012.08.039 |
0.304 |
|
2011 |
Saha J, Peczuh MW. Synthesis and properties of septanose carbohydrates. Advances in Carbohydrate Chemistry and Biochemistry. 66: 121-86. PMID 22123189 DOI: 10.1016/B978-0-12-385518-3.00003-1 |
0.406 |
|
2011 |
Saha J, Peczuh MW. Expanding the scope of aminosugars: synthesis of 2-amino septanosyl glycoconjugates using septanosyl fluoride donors. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 7357-65. PMID 21567495 DOI: 10.1002/Chem.201003721 |
0.44 |
|
2011 |
Duff MR, Fyvie WS, Markad SD, Frankel AE, Kumar CV, Gascón JA, Peczuh MW. Computational and experimental investigations of mono-septanoside binding by Concanavalin A: correlation of ligand stereochemistry to enthalpies of binding. Organic & Biomolecular Chemistry. 9: 154-64. PMID 21085738 DOI: 10.1039/C0Ob00425A |
0.716 |
|
2010 |
Magpusao AN, Desmond RT, Billings KJ, Fenteany G, Peczuh MW. Synthesis and evaluation of antimigratory and antiproliferative activities of lipid-linked [13]-macro-dilactones. Bioorganic & Medicinal Chemistry Letters. 20: 5472-6. PMID 20709546 DOI: 10.1016/J.Bmcl.2010.07.083 |
0.315 |
|
2010 |
Markad SD, Miller SM, Morton M, Peczuh MW. Hydroxyl group orientation affects hydrolysis rates of methyl α-septanosides Tetrahedron Letters. 51: 1209-1212. DOI: 10.1016/J.Tetlet.2009.12.109 |
0.38 |
|
2009 |
Saha J, Peczuh MW. Access to ring-expanded analogues of 2-amino sugars. Organic Letters. 11: 4482-4. PMID 19722606 DOI: 10.1021/Ol9018387 |
0.443 |
|
2009 |
Castro S, Johnson CS, Surana B, Peczuh MW. An oxepinone route to carbohydrate based oxepines Tetrahedron. 65: 7921-7926. DOI: 10.1016/J.Tet.2009.07.041 |
0.399 |
|
2008 |
Fyvie WS, Peczuh MW. Remote induction of asymmetry in [13]-macro-dilactone topology by a single stereogenic center. Chemical Communications (Cambridge, England). 4028-30. PMID 18758615 DOI: 10.1039/B807562J |
0.722 |
|
2008 |
Markad SD, Xia S, Snyder NL, Surana B, Morton MD, Hadad CM, Peczuh MW. Stereoselectivity in the epoxidation of carbohydrate-based oxepines. The Journal of Organic Chemistry. 73: 6341-54. PMID 18651775 DOI: 10.1021/Jo800979A |
0.714 |
|
2008 |
Fyvie WS, Peczuh MW. Diastereoselectivity in epoxidation of carbohydrate fused [13]-macro-dilactones. The Journal of Organic Chemistry. 73: 3626-9. PMID 18363373 DOI: 10.1021/Jo800027Y |
0.719 |
|
2007 |
Castro S, Cherney EC, Snyder NL, Peczuh MW. Synthesis of substituted septanosyl-1,2,3-triazoles. Carbohydrate Research. 342: 1366-72. PMID 17466290 DOI: 10.1016/J.Carres.2007.03.026 |
0.715 |
|
2006 |
DeMatteo MP, Mei S, Fenton R, Morton M, Baldisseri DM, Hadad CM, Peczuh MW. Conformational analysis of methyl 5-O-methyl septanosides: effect of glycosylation on conformer populations. Carbohydrate Research. 341: 2927-45. PMID 17056019 DOI: 10.1016/J.Carres.2006.09.024 |
0.379 |
|
2006 |
Snyder NL, Haines HM, Peczuh MW. Recent Developments in the Synthesis of Oxepines Cheminform. 37. DOI: 10.1016/J.Tet.2006.07.021 |
0.654 |
|
2006 |
Snyder NL, Haines HM, Peczuh MW. Recent developments in the synthesis of oxepines Tetrahedron. 62: 9301-9320. DOI: 10.1016/j.tet.2006.07.021 |
0.654 |
|
2005 |
Castro S, Duff M, Snyder NL, Morton M, Kumar CV, Peczuh MW. Recognition of septanose carbohydrates by concanavalin A. Organic & Biomolecular Chemistry. 3: 3869-72. PMID 16239999 DOI: 10.1039/B509243D |
0.678 |
|
2005 |
Castro S, Fyvie WS, Hatcher SA, Peczuh MW. Synthesis of alpha-D-idoseptanosyl glycosides using an S-phenyl septanoside donor. Organic Letters. 7: 4709-12. PMID 16209516 DOI: 10.1021/Ol051912E |
0.755 |
|
2005 |
Castro S, Peczuh MW. Sequential cyclization-elimination route to carbohydrate-based oxepines. The Journal of Organic Chemistry. 70: 3312-5. PMID 15823004 DOI: 10.1021/Jo048128C |
0.34 |
|
2005 |
Dematteo MP, Snyder NL, Morton M, Baldisseri DM, Hadad CM, Peczuh MW. Septanose carbohydrates: synthesis and conformational studies of methyl alpha-D-glycero-D-idoseptanoside and methyl beta-D-glycero-D-guloseptanoside. The Journal of Organic Chemistry. 70: 24-38. PMID 15624903 DOI: 10.1021/Jo048932Z |
0.703 |
|
2005 |
DeMatteo MP, Snyder NL, Morton M, Baldisseri DM, Hadad CM, Peczuh MW. Septanose Carbohydrates: Synthesis and Conformational Studies of Methyl α-D-Glycero-D-idoseptanoside (I) and Methyl β-D-Glycero-D-guloseptanoside (II). Cheminform. 36. DOI: 10.1002/chin.200523204 |
0.684 |
|
2004 |
Fyvie WS, Morton M, Peczuh MW. Synthesis of 2-iodo-2-deoxy septanosides from a D-xylose-based oxepine: intramolecular cyclization in the absence of a glycosyl acceptor. Carbohydrate Research. 339: 2363-70. PMID 15388351 DOI: 10.1016/J.Carres.2004.07.009 |
0.755 |
|
2004 |
Peczuh MW, Snyder NL, Sean Fyvie W. Synthesis, crystal structure, and reactivity of a D-xylose based oxepine. Carbohydrate Research. 339: 1163-71. PMID 15063206 DOI: 10.1016/J.Carres.2004.01.022 |
0.725 |
|
2003 |
Peczuh MW, Snyder NL. Carbohydrate-based oxepines: ring expanded glycals for the synthesis of septanose saccharides Tetrahedron Letters. 44: 4057-4061. DOI: 10.1016/S0040-4039(03)00849-9 |
0.678 |
|
2003 |
Peczuh MW, Snyder NL. Carbohydrate-Based Oxepines: Ring Expanded Glycals for the Synthesis of Septanose Saccharides. Cheminform. 34. DOI: 10.1016/S0040-4039(03)00849-9 |
0.699 |
|
2001 |
Losey HC, Peczuh MW, Chen Z, Eggert US, Dong SD, Pelczer I, Kahne D, Walsh CT. Tandem action of glycosyltransferases in the maturation of vancomycin and teicoplanin aglycones: novel glycopeptides. Biochemistry. 40: 4745-55. PMID 11294642 DOI: 10.1021/Bi010050W |
0.323 |
|
2000 |
Peczuh MW, Hamilton AD. Peptide and protein recognition by designed molecules. Chemical Reviews. 100: 2479-94. PMID 11749292 DOI: 10.1021/Cr9900026 |
0.425 |
|
2000 |
Salvatella X, Peczuh MW, Gairí M, Jain RK, Sánchez-Quesada J, Mendoza Jd, Hamilton AD, Giralt E. Side chain elongation causes a change from enthalpy driven to entropy driven binding in the molecular recognition of tetraanionic peptides Chemical Communications. 1399-1400. DOI: 10.1039/B003728L |
0.6 |
|
2000 |
Peczuh MW, Hamilton AD. ChemInform Abstract: Peptide and Protein Recognition by Designed Molecules Cheminform. 31: no-no. DOI: 10.1002/chin.200042260 |
0.356 |
|
1999 |
Haack T, Peczuh MW, Salvatella X, Sánchez-Quesada J, de Mendoza J, Hamilton AD, Giralt E. Surface Recognition and Helix Stabilization of a Tetraaspartate Peptide by Shape and Electrostatic Complementarity of an Artificial Receptor Journal of the American Chemical Society. 121: 11813-11820. DOI: 10.1021/Ja9910154 |
0.432 |
|
1997 |
Albert JS, Peczuh MW, Hamilton AD. Design, synthesis and evaluation of synthetic receptors for the recognition of aspartate pairs in an α-helical confirmation Bioorganic and Medicinal Chemistry. 5: 1455-1467. PMID 9313852 DOI: 10.1016/S0968-0896(97)00086-2 |
0.481 |
|
1997 |
Peczuh MW, Hamilton AD, Sánchez-Quesada J, de Mendoza J, Haack T, Giralt E. Recognition and Stabilization of an α-Helical Peptide by a Synthetic Receptor Journal of the American Chemical Society. 119: 9327-9328. DOI: 10.1021/Ja970951L |
0.439 |
|
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