| Year |
Citation |
Score |
| 2021 |
Watson A, Simmermaker C, Aung E, Do S, Hackbusch S, Franz AH. NMR analysis and molecular dynamics conformation of α-1,6-linear and α-1,3-branched isomaltose oligomers as mimetics of α-1,6-linked dextran. Carbohydrate Research. 503: 108296. PMID 33813322 DOI: 10.1016/j.carres.2021.108296 |
0.726 |
|
| 2018 |
Watson A, Hackbusch S, Franz AH. NMR solution geometry of saccharides containing the 6-O-(α-D-glucopyranosyl)-α/β-D-glucopyranose (isomaltose) or 6-O-(α-D-galactopyranosyl)-α/β-D-glucopyranose (melibiose) core. Carbohydrate Research. 473: 18-35. PMID 30599389 DOI: 10.1016/J.Carres.2018.12.012 |
0.725 |
|
| 2018 |
Hackbusch S, Watson A, Franz AH. Synthesis and conformational analysis of d-gluco-pyranosyl-(6,6')-d-gluco-pyranuronate, a model compound for the inter-glycan 6,6'-ester linkage. Carbohydrate Research. 458: 1-12. PMID 29428481 DOI: 10.1016/J.Carres.2018.01.005 |
0.73 |
|
| 2018 |
Watson A, Wallis C, Franz AH. NMR solution structures and MD-simulation of procyanidin B1, B2, and C1 Arkivoc. 2018: 279-301. DOI: 10.24820/Ark.5550190.P010.340 |
0.705 |
|
| 2017 |
Hackbusch S, Watson A, Franz AH. Development of a Karplus equation for 3JCOCH in ester-functionalized glucopyranoses and methylglucuronate. Arkivoc. 2017: 268-292. DOI: 10.24820/Ark.5550190.P010.113 |
0.693 |
|
| 2014 |
Dotsenko IA, Zhao Q, Franz AH, Batoon P, Samoshina NM, Samoshin VV. Convenient synthesis of 1,3-dithiolane-2-thiones: Cyclic trithiocarbonates as conformational locks Arkivoc. 2014: 16-41. DOI: 10.3998/Ark.5550190.P008.671 |
0.338 |
|
| 2014 |
Samoshin AV, Dotsenko IA, Samoshina NM, Franz AH, Samoshin VV. Thio-β-D-glucosides: Synthesis and Evaluation as Glycosidase Inhibitors and Activators International Journal of Carbohydrate Chemistry. 2014: 1-8. DOI: 10.1155/2014/941059 |
0.309 |
|
| 2012 |
Samoshin AV, Visser J, Curtis M, Samoshin VV, Franz AH. The first example of amine-induced reversal of diastereoselectivity in acylation of some trans -2-substituted cyclohexanols Arkivoc. 2012: 27-35. DOI: 10.3998/Ark.5550190.0013.803 |
0.307 |
|
| 2011 |
Jeffery F, La Mattina C, Tuton-Blasingame T, Hsia Y, Gnesa E, Zhao L, Franz A, Vierra C. Microdissection of black widow spider silk-producing glands. Journal of Visualized Experiments : Jove. PMID 21248709 DOI: 10.3791/2382 |
0.359 |
|
| 2011 |
Hsia Y, Gnesa E, Tang S, Jeffery F, Geurts P, Zhao L, Franz A, Vierra C. Identification and synthesis of novel biomaterials based on spider structural silk fibers Applied Physics A. 105: 301-309. DOI: 10.1007/S00339-011-6621-8 |
0.38 |
|
| 2010 |
Geurts P, Zhao L, Hsia Y, Gnesa E, Tang S, Jeffery F, La Mattina C, Franz A, Larkin L, Vierra C. Synthetic spider silk fibers spun from Pyriform Spidroin 2, a glue silk protein discovered in orb-weaving spider attachment discs. Biomacromolecules. 11: 3495-503. PMID 21053953 DOI: 10.1021/Bm101002W |
0.343 |
|
| 2010 |
Liu W, Navarro E, Franz AH, Xue L. Regioselective Bromination of a Thymine–Acridine Conjugate by N-Bromosuccinimide Synthetic Communications. 40: 1192-1201. DOI: 10.1080/00397910903061050 |
0.308 |
|
| 2009 |
Zhao L, Almaraz RT, Xiang F, Hedrick JL, Franz AH. Gas-phase scrambling of disulfide bonds during matrix-assisted laser desorption/ionization mass spectrometry analysis. Journal of the American Society For Mass Spectrometry. 20: 1603-16. PMID 19535267 DOI: 10.1016/J.Jasms.2009.04.021 |
0.368 |
|
| 2009 |
Franz AH, Gross PH, Samoshin VV. Syntheses of small cluster oligosaccharide mimetics Arkivoc. 2008: 231-308. DOI: 10.3998/Ark.5550190.0009.110 |
0.335 |
|
| 2008 |
Bhattacharya S, Franz A, Li X, Jasti B. Synthesis of folate-conjugated amphiphiles for tumor-targeted drug delivery. Journal of Drug Targeting. 16: 780-9. PMID 18985509 DOI: 10.1080/10611860802475639 |
0.309 |
|
| 2008 |
Chindarkar NS, Franz AH. Synthesis and characterization of biotin derivatives as multifunctional oligosaccharide tags Arkivoc. 2008: 21-33. DOI: 10.3998/Ark.5550190.0009.F03 |
0.711 |
|
| 2008 |
Yu H, Murata K, Hedrick JL, Almaraz RT, Xiang F, Franz AH. Corrigendum to "The disulfide bond pattern of salmon egg lectin 24 K from the Chinook salmon Oncorhynchus tshawytscha" [Arch. Biochem. Biophys. 463 (2007) 1-11] (DOI:10.1016/j.abb.2007.02.002) Archives of Biochemistry and Biophysics. 479: 179. DOI: 10.1016/J.Abb.2008.08.017 |
0.484 |
|
| 2007 |
Yu H, Murata K, Hedrick JL, T Almaraz R, Xiang F, Franz AH. The disulfide bond pattern of salmon egg lectin 24K from the Chinook salmon Oncorhynchus tshawytscha. Archives of Biochemistry and Biophysics. 463: 1-11. PMID 17376399 DOI: 10.1016/J.Abb.2007.02.002 |
0.524 |
|
| 2007 |
Nguyen QL, Olmstead L, Bains S, Franz AH. Solution conformations of three small cluster oligosaccharide mimetics (SCOM) from D-glucosamine, D-altrosamine, and (-)-quinic acid Arkivoc. 2007: 235-251. DOI: 10.3998/Ark.5550190.0008.D27 |
0.366 |
|
| 2007 |
Chiu TMK, Sigillo K, Gross PH, Franz AH. Synthesis of Anomerically Pure, Furanose‐Free α‐Benzyl‐2‐amino‐2‐deoxy‐d‐altro‐ andd‐manno‐pyranosides and Some of Their Derivatives Synthetic Communications. 37: 2355-2381. DOI: 10.1080/00397910701410871 |
0.592 |
|
| 2006 |
Hsu J, Chang SJ, Franz AH. MALDI-TOF and ESI-MS analysis of oligosaccharides labeled with a new multifunctional oligosaccharide tag. Journal of the American Society For Mass Spectrometry. 17: 194-204. PMID 16406228 DOI: 10.1016/J.Jasms.2005.10.010 |
0.307 |
|
| 2005 |
Nguyen TTM, Gross PH, Franz AH. Synthesis and NMR-characterization of three quinamide-based disaccharide mimetics with unusual cyclohexane twist- conformation † Arkivoc. 2005: 110-128. DOI: 10.3998/Ark.5550190.0006.409 |
0.419 |
|
| 2003 |
An HJ, Franz AH, Lebrilla CB. Improved capillary electrophoretic separation and mass spectrometric detection of oligosaccharides. Journal of Chromatography. A. 1004: 121-9. PMID 12929968 DOI: 10.1016/S0021-9673(03)00718-0 |
0.58 |
|
| 2003 |
Franz AH, Samoshin VV, Myers C, Hunter AD, Gross PH. C-H-deprotonation mediated by a remote syn-axial acetoxy group--an unprecedented double bond formation upon cyanation of the dimer from L-fucal. Carbohydrate Research. 338: 851-4. PMID 12681909 DOI: 10.1016/S0008-6215(03)00048-X |
0.577 |
|
| 2003 |
Franz AH, Liu R, Song A, Lam KS, Lebrilla CB. High-throughput one-bead-one-compound approach to peptide-encoded combinatorial libraries: MALDI-MS analysis of single TentaGel beads. Journal of Combinatorial Chemistry. 5: 125-37. PMID 12625702 DOI: 10.1021/Cc020083A |
0.467 |
|
| 2002 |
Franz AH, Wei Y, Samoshin VV, Gross PH. Mild synthesis of disaccharidic 2,3-enopyranosyl cyanides and 2-C-2-deoxy pyranosyl cyanides with Hg(CN)(2)/HgBr(2)/TMSCN. The Journal of Organic Chemistry. 67: 7662-9. PMID 12398487 DOI: 10.1021/Jo0111661 |
0.588 |
|
| 2002 |
Stone MM, Franz AH, Lebrilla CB. Non-covalent calixarene-amino acid complexes formed by MALDI-MS. Journal of the American Society For Mass Spectrometry. 13: 964-74. PMID 12216737 DOI: 10.1016/S1044-0305(02)00417-8 |
0.474 |
|
| 2002 |
Franz AH, Lebrilla CB. Evidence for long-range glycosyl transfer reactions in the gas phase. Journal of the American Society For Mass Spectrometry. 13: 325-37. PMID 11951970 DOI: 10.1016/S1044-0305(02)00343-4 |
0.449 |
|
| 2002 |
Liang YZ, Franz AH, Newbury C, Lebrilla CB, Patten TE. Synthesis and end group structure of 2-deoxydextrans prepared via the cationic ring-opening polymerization of an anhydro sugar Macromolecules. 35: 3402-3412. DOI: 10.1021/Ma012033K |
0.475 |
|
| 2001 |
Franz AH, Molinski TF, Lebrilla CB. MALDI-FTMS characterization of oligosaccharides labeled with 9-aminofluorene. Journal of the American Society For Mass Spectrometry. 12: 1254-61. PMID 11766752 DOI: 10.1016/S1044-0305(01)00313-0 |
0.484 |
|
| 1999 |
Franz AH, Zhdankin VV, Samoshin VV, Minch MJ, Young VG, Gross PH. Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution Mendeleev Communications. 9: 45-47. DOI: 10.1070/Mc1999V009N02Abeh001061 |
0.381 |
|
| 1999 |
Zhang K, Franz A, Craig Hill G, Michael McCallum C, Minch MJ. Etoposide: conformational and hydration features Magnetic Resonance in Chemistry. 37: 788-798. DOI: 10.1002/(Sici)1097-458X(199911)37:11<788::Aid-Mrc526>3.0.Co;2-# |
0.321 |
|
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