Year |
Citation |
Score |
2023 |
Xie Y, Luo D, Wiener J, Tang S, Chepyshev S, Schafmeister C. Correction to "Development of Fmoc-Protected Bis-Amino Acids toward Automated Synthesis of Highly Functionalized Spiroligomers". Organic Letters. PMID 36744827 DOI: 10.1021/acs.orglett.3c00270 |
0.639 |
|
2022 |
Xie Y, Luo D, Wiener J, Tang S, Chepyshev S, Schafmeister C. Development of Fmoc-Protected Bis-Amino Acids toward Automated Synthesis of Highly Functionalized Spiroligomers. Organic Letters. PMID 35499925 DOI: 10.1021/acs.orglett.2c01295 |
0.658 |
|
2021 |
Northrup JD, Wiener JA, Hurley MFD, Hou CD, Keller TM, Baxter RHG, Zdilla MJ, Voelz VA, Schafmeister CE. Metal-Binding Q-Proline Macrocycles. The Journal of Organic Chemistry. PMID 33635647 DOI: 10.1021/acs.joc.1c00116 |
0.558 |
|
2018 |
Pfeiffer CT, Northrup JD, Cheong JE, Pham MA, Parker MFL, Schafmeister CE. Utilization of the p-nitrobenzyloxycarbonyl (pNZ) amine protecting group and pentafluorophenyl (Pfp) esters for the solid phase synthesis of spiroligomers Tetrahedron Letters. 59: 2884-2888. DOI: 10.1016/J.Tetlet.2018.05.041 |
0.377 |
|
2017 |
Northrup JD, Mancini G, Purcell CR, Schafmeister CE. Development of Spiroligomer-Peptoid Hybrids. The Journal of Organic Chemistry. PMID 29161507 DOI: 10.1021/Acs.Joc.7B01956 |
0.345 |
|
2016 |
Northrup JD, Purcell CR, Schafmeister CE. One-Pot Synthesis of Chiral, Spirocyclic 4-Hydantoin-Proline Derivatives for Incorporation into Spiroligomer-Based Macromolecules. The Journal of Organic Chemistry. PMID 27690253 DOI: 10.1021/Acs.Joc.6B01773 |
0.36 |
|
2016 |
Cheong JE, Pfeiffer CT, Northrup JD, Parker MF, Schafmeister CE. An improved, scalable synthesis of bis-amino acids Tetrahedron Letters. 57: 4882-4884. DOI: 10.1016/J.Tetlet.2016.09.032 |
0.386 |
|
2015 |
Zhao Q, Schafmeister CE. Synthesis of Spiroligomer-Containing Macrocycles. The Journal of Organic Chemistry. 80: 8968-78. PMID 26296148 DOI: 10.1021/Acs.Joc.5B01109 |
0.52 |
|
2015 |
Zhao Q, Schafmeister CE. Synthesis of Spiroligomer-Containing Macrocycles Journal of Organic Chemistry. 80: 8968-8978. DOI: 10.1021/acs.joc.5b01109 |
0.443 |
|
2014 |
Flanigan PM, Shi F, Perez JJ, Karki S, Pfeiffer C, Schafmeister C, Levis RJ. Determination of internal energy distributions of laser electrospray mass spectrometry using thermometer ions and other biomolecules. Journal of the American Society For Mass Spectrometry. 25: 1572-82. PMID 25012513 DOI: 10.1007/S13361-014-0936-6 |
0.504 |
|
2014 |
Parker MF, Osuna S, Bollot G, Vaddypally S, Zdilla MJ, Houk KN, Schafmeister CE. Acceleration of an aromatic Claisen rearrangement via a designed spiroligozyme catalyst that mimics the ketosteroid isomerase catalytic dyad. Journal of the American Chemical Society. 136: 3817-27. PMID 24456160 DOI: 10.1021/Ja409214C |
0.666 |
|
2013 |
Vaddypally S, Xu C, Zhao S, Fan Y, Schafmeister CE, Zdilla MJ. Architectural spiroligomers designed for binuclear metal complex templating. Inorganic Chemistry. 52: 6457-63. PMID 23668771 DOI: 10.1021/Ic4003498 |
0.665 |
|
2012 |
Kheirabadi M, Çelebi-Ölçüm N, Parker MF, Zhao Q, Kiss G, Houk KN, Schafmeister CE. Spiroligozymes for transesterifications: design and relationship of structure to activity. Journal of the American Chemical Society. 134: 18345-53. PMID 22992057 DOI: 10.1021/Ja3069648 |
0.512 |
|
2012 |
Pfeiffer CT, Schafmeister CE. Solid phase synthesis of a functionalized bis-peptide using "safety catch" methodology. Journal of Visualized Experiments : Jove. e4112. PMID 22635107 DOI: 10.3791/4112 |
0.388 |
|
2012 |
Zhao Q, Lam YH, Kheirabadi M, Xu C, Houk KN, Schafmeister CE. Hydrophobic substituent effects on proline catalysis of aldol reactions in water. The Journal of Organic Chemistry. 77: 4784-92. PMID 22500641 DOI: 10.1021/Jo300569C |
0.499 |
|
2011 |
Brown ZZ, Alleva J, Schafmeister CE. Solid-phase synthesis of functionalized bis-peptides. Biopolymers. 96: 578-85. PMID 22180905 DOI: 10.1002/Bip.21591 |
0.384 |
|
2010 |
Brown ZZ, Schafmeister CE. Synthesis of hexa- and pentasubstituted diketopiperazines from sterically hindered amino acids. Organic Letters. 12: 1436-9. PMID 20218644 DOI: 10.1021/Ol100048G |
0.364 |
|
2009 |
Gupta S, Schafmeister CE. Synthesis of a carboxylate functionalized bis-amino acid monomer. The Journal of Organic Chemistry. 74: 3652-8. PMID 19391596 DOI: 10.1021/Jo802679N |
0.419 |
|
2008 |
Bird GH, Pornsuwan S, Saxena S, Schafmeister CE. Distance distributions of end-labeled curved bispeptide oligomers by electron spin resonance. Acs Nano. 2: 1857-64. PMID 19206425 DOI: 10.1021/Nn800327G |
0.308 |
|
2008 |
Brown ZZ, Schafmeister CE. Exploiting an inherent neighboring group effect of alpha-amino acids to synthesize extremely hindered dipeptides. Journal of the American Chemical Society. 130: 14382-3. PMID 18841897 DOI: 10.1021/Ja806063K |
0.377 |
|
2008 |
Schafmeister CE, Brown ZZ, Gupta S. Shape-programmable macromolecules. Accounts of Chemical Research. 41: 1387-98. PMID 18662022 DOI: 10.1021/Ar700283Y |
0.431 |
|
2006 |
Gupta S, Macala M, Schafmeister CE. Synthesis of structurally diverse bis-peptide oligomers. The Journal of Organic Chemistry. 71: 8691-5. PMID 17080995 DOI: 10.1021/Jo0609125 |
0.359 |
|
2006 |
Levins CG, Brown ZZ, Schafmeister CE. Maximizing the stereochemical diversity of spiro-ladder oligomers. Organic Letters. 8: 2807-10. PMID 16774262 DOI: 10.1021/Ol060902Q |
0.385 |
|
2006 |
Pornsuwan S, Bird G, Schafmeister CE, Saxena S. Flexibility and lengths of bis-peptide nanostructures by electron spin resonance. Journal of the American Chemical Society. 128: 3876-7. PMID 16551072 DOI: 10.1021/Ja058143E |
0.329 |
|
2005 |
Levins CG, Schafmeister CE. The synthesis of curved and linear structures from a minimal set of monomers. The Journal of Organic Chemistry. 70: 9002-8. PMID 16238339 DOI: 10.1021/Jo051639U |
0.374 |
|
2005 |
Gupta S, Das BC, Schafmeister CE. Synthesis of a pipecolic acid-based bis-amino acid and its assembly into a spiro ladder oligomer. Organic Letters. 7: 2861-4. PMID 15987155 DOI: 10.1021/Ol0507672 |
0.409 |
|
2004 |
Habay SA, Schafmeister CE. Synthesis of a bis-amino acid that creates a sharp turn. Organic Letters. 6: 3369-71. PMID 15355054 DOI: 10.1021/Ol048585F |
0.447 |
|
2003 |
Levins CG, Schafmeister CE. The synthesis of functionalized nanoscale molecular rods of defined length. Journal of the American Chemical Society. 125: 4702-3. PMID 12696876 DOI: 10.1021/Ja0293958 |
0.335 |
|
1998 |
Schafmeister CE, Stroud RM. Helical protein design. Current Opinion in Biotechnology. 9: 350-3. PMID 9720261 DOI: 10.1016/S0958-1669(98)80006-2 |
0.453 |
|
1997 |
Schafmeister CE, LaPorte SL, Miercke LJ, Stroud RM. A designed four helix bundle protein with native-like structure. Nature Structural Biology. 4: 1039-46. PMID 9406555 DOI: 10.1038/Nsb1297-1039 |
0.527 |
|
1996 |
Finer-Moore JS, Liu L, Schafmeister CE, Birdsall DL, Mau T, Santi DV, Stroud RM. Partitioning roles of side chains in affinity, orientation, and catalysis with structures for mutant complexes: asparagine-229 in thymidylate synthase. Biochemistry. 35: 5125-36. PMID 8611496 DOI: 10.1021/Bi952751X |
0.492 |
|
1993 |
Schafmeister CE, Miercke LJ, Stroud RM. Structure at 2.5 A of a designed peptide that maintains solubility of membrane proteins. Science (New York, N.Y.). 262: 734-8. PMID 8235592 DOI: 10.1126/Science.8235592 |
0.494 |
|
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