| Year |
Citation |
Score |
| 2020 |
Shang J, Thombare VJ, Charron CL, Wille U, Hutton CA. Ring expansion of thiolactams via imide intermediates: an amino acid insertion strategy. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33289186 DOI: 10.1002/chem.202005035 |
0.757 |
|
| 2020 |
Shabani S, Hutton CA. Total Synthesis of Seongsanamide B. Organic Letters. PMID 32463242 DOI: 10.1021/Acs.Orglett.0C01642 |
0.319 |
|
| 2019 |
Thombare VJ, Holden JA, Reynolds EC, O'Brien-Simpson NM, Hutton CA. Celogentin mimetics as inhibitors of tubulin polymerization. Journal of Peptide Science : An Official Publication of the European Peptide Society. e3239. PMID 31847053 DOI: 10.1002/Psc.3239 |
0.328 |
|
| 2019 |
Shabani S, White JM, Hutton CA. Synthesis of the C-Terminal Macrocycle of Asperipin-2a. Organic Letters. PMID 30840468 DOI: 10.1021/Acs.Orglett.9B00488 |
0.345 |
|
| 2019 |
Thombare VJ, Hutton CA. Rapid, Traceless, Ag -Promoted Macrocyclization of Peptides Possessing an N-Terminal Thioamide. Angewandte Chemie (International Ed. in English). 58: 4998-5002. PMID 30779282 DOI: 10.1002/Anie.201900243 |
0.361 |
|
| 2019 |
Haskali MB, Denoyer D, Roselt PD, Hicks RJ, Hutton CA. Radiosynthesis and preliminary in vivo evaluation of 18F-labelled glycosylated duramycin peptides for imaging of phosphatidylethanolamine during apoptosis Medchemcomm. 10: 1930-1934. DOI: 10.1039/C9Md00354A |
0.304 |
|
| 2018 |
Xie SC, Gillett DL, Spillman NJ, Tsu C, Luth MR, Ottilie S, Duffy S, Gould A, Hales P, Seager BA, Charron CL, Bruzzese F, Yang X, Zhao X, Huang SC, ... Hutton CA, et al. Target Validation and Identification of Novel Boronate Inhibitors of the Plasmodium falciparum Proteasome. Journal of Medicinal Chemistry. PMID 30373366 DOI: 10.1021/Acs.Jmedchem.8B01161 |
0.726 |
|
| 2018 |
Borges EL, Ignasiak MT, Velichenko Y, Perin G, Hutton CA, Davies MJ, Schiesser CH. Synthesis and antioxidant capacity of novel stable 5-tellurofuranose derivatives. Chemical Communications (Cambridge, England). PMID 29505059 DOI: 10.1039/C8Cc00565F |
0.321 |
|
| 2018 |
Charron CL, Cottam Jones JM, Hutton CA. Are Aminomethyl Thioesters Viable Intermediates in Native Chemical Ligation Type Amide Bond Forming Reactions? Australian Journal of Chemistry. 71: 697. DOI: 10.1071/Ch18198 |
0.749 |
|
| 2018 |
Thombare VJ, Holden JA, Pal S, Reynolds EC, Chattopadhyay A, O'Brien-Simpson NM, Hutton CA. Antimicrobial activity of simplified mimics of celogentin C Tetrahedron. 74: 1288-1293. DOI: 10.1016/J.Tet.2017.12.032 |
0.329 |
|
| 2018 |
Thombare VJ, Hutton CA. Bridged bicyclic peptides: Structure and function Peptide Science. 110: e24057. DOI: 10.1002/Pep2.24057 |
0.322 |
|
| 2017 |
Haskali MB, Roselt PD, Hicks RJ, Hutton CA. Automated Preparation of 2-[(18) F]Fluoropropionate Labelled Peptides using a Flexible, Multi-stage Synthesis Platform (iPHASE Flexlab). Journal of Labelled Compounds & Radiopharmaceuticals. PMID 29143364 DOI: 10.1002/Jlcr.3580 |
0.339 |
|
| 2017 |
Mukherjee S, Kapp EA, Lothian A, Roberts AM, Vasilev Y, Boughton B, Barnham KJ, Kok WM, Hutton CA, Masters CL, Bush A, Beckman JS, Dey SG, Roberts BR. Characterization and identification of dityrosine cross-linked peptides using tandem mass spectrometry. Analytical Chemistry. PMID 28453255 DOI: 10.1021/Acs.Analchem.7B00941 |
0.315 |
|
| 2017 |
Haskali MB, Denoyer D, Noonan W, Cullinane C, Rangger C, Pouliot N, Haubner R, Roselt PD, Hicks RJ, Hutton CA. Sulfonation of Tyrosine as a Method to Improve Biodistribution of Peptide-Based Radiotracers: Novel (18)F-Labelled Cyclic RGD Analogues. Molecular Pharmaceutics. PMID 28191977 DOI: 10.1021/Acs.Molpharmaceut.6B01062 |
0.341 |
|
| 2016 |
Hutton CA, Shang J, Wille U. Synthesis of Peptides by Silver-Promoted Coupling of Carboxylates and Thioamides: Mechanistic Insight from Computational Studies. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26813415 DOI: 10.1002/Chem.201503753 |
0.397 |
|
| 2016 |
Charron CL, Farnsworth AL, Roselt PD, Hicks RJ, Hutton CA. Recent developments in radiolabelled peptides for PET imaging of cancer Tetrahedron Letters. 57: 4119-4127. DOI: 10.1016/J.Tetlet.2016.07.083 |
0.743 |
|
| 2016 |
Brown AL, Fifer NL, Hunter L, Churches QI, Chan PWH, Cohen SB, Hutton CA. Total Synthesis of Ustiloxin D Strategies and Tactics in Organic Synthesis. 12: 169-191. DOI: 10.1016/B978-0-08-100756-3.00006-6 |
0.333 |
|
| 2016 |
Charron CL, Farnsworth AL, Roselt PD, Hicks RJ, Hutton CA. ChemInform Abstract: Recent Developments in Radiolabeled Peptides for PET Imaging of Cancer Cheminform. 47. DOI: 10.1002/CHIN.201642277 |
0.729 |
|
| 2015 |
Brown AL, Churches QI, Hutton CA. Total Synthesis of Ustiloxin D Utilizing an Ammonia-Ugi Reaction. The Journal of Organic Chemistry. PMID 26394038 DOI: 10.1021/Acs.Joc.5B01519 |
0.378 |
|
| 2015 |
Churches QI, Hooper JF, Hutton CA. A general method for interconversion of boronic acid protecting groups: trifluoroborates as common intermediates. The Journal of Organic Chemistry. 80: 5428-35. PMID 25993092 DOI: 10.1021/Acs.Joc.5B00182 |
0.362 |
|
| 2015 |
Shang J, Pourvali A, Cochrane JR, Hutton CA. Steric and Electronic Effects in the Synthesis and Regioselective Hydrolysis of Unsymmetrical Imides Australian Journal of Chemistry. 68: 1854-1858. DOI: 10.1071/Ch15504 |
0.325 |
|
| 2014 |
Pourvali A, Cochrane JR, Hutton CA. A new method for peptide synthesis in the N→C direction: amide assembly through silver-promoted reaction of thioamides. Chemical Communications (Cambridge, England). 50: 15963-6. PMID 25384109 DOI: 10.1039/C4Cc07601J |
0.395 |
|
| 2013 |
Cochrane JR, Schmitt A, Wille U, Hutton CA. Synthesis of cyclic peptide hemicryptophanes: enantioselective recognition of a chiral zwitterionic guest. Chemical Communications (Cambridge, England). 49: 8504-6. PMID 23942591 DOI: 10.1039/C3Cc44784G |
0.377 |
|
| 2013 |
Tirotta I, Fifer NL, Eakins J, Hutton CA. Synthesis of tryptophans by Lewis acid promoted ring-opening of aziridine-2-carboxylates: Optimization of protecting group and Lewis acid Tetrahedron Letters. 54: 618-620. DOI: 10.1016/J.Tetlet.2012.11.139 |
0.379 |
|
| 2012 |
Boughton BA, Dobson RC, Hutton CA. The crystal structure of dihydrodipicolinate synthase from Escherichia coli with bound pyruvate and succinic acid semialdehyde: unambiguous resolution of the stereochemistry of the condensation product. Proteins. 80: 2117-22. PMID 22552955 DOI: 10.1002/Prot.24106 |
0.312 |
|
| 2012 |
Boughton BA, Hor L, Gerrard JA, Hutton CA. 1,3-Phenylene bis(ketoacid) derivatives as inhibitors of Escherichia coli dihydrodipicolinate synthase. Bioorganic & Medicinal Chemistry. 20: 2419-26. PMID 22386717 DOI: 10.1016/J.Bmc.2012.01.045 |
0.315 |
|
| 2011 |
Churches QI, White JM, Hutton CA. Synthesis of β,γ-dihydroxyhomotyrosines by a tandem Petasis-asymmetric dihydroxylation approach. Organic Letters. 13: 2900-3. PMID 21561144 DOI: 10.1021/Ol200917S |
0.394 |
|
| 2011 |
Churches QI, Johnson JK, Fifer NL, Hutton CA. Anomalies in the stereoselectivity of the petasis reaction using styrenyl boronic acids Australian Journal of Chemistry. 64: 62-67. DOI: 10.1071/Ch10341 |
0.387 |
|
| 2010 |
Lam AK, Hutton CA, O'Hair RA. Role of 2-oxo and 2-thioxo modifications on the proton affinity of histidine and fragmentation reactions of protonated histidine. Rapid Communications in Mass Spectrometry : Rcm. 24: 2591-604. PMID 20740535 DOI: 10.1002/Rcm.4671 |
0.3 |
|
| 2010 |
Li BTY, White JM, Hutton CA. Synthesis of the LeuTrp component of the celogentin family of cyclic peptides through a CH activationcross-coupling strategy Australian Journal of Chemistry. 63: 438-444. DOI: 10.1071/Ch10033 |
0.355 |
|
| 2010 |
EASTON CJ, HUTTON CA, MERRETT MC, TIEKINK ERT. ChemInform Abstract: Neighboring Group Effects Promote Substitution Reactions over Elimination and Provide a Stereocontrolled Route to Chloramphenicol. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199637265 |
0.462 |
|
| 2010 |
EASTON CJ, HUTTON CA, ROSELT PD, TIEKINK ERT. ChemInform Abstract: Stereocontrolled Synthesis of β-Hydroxyphenylalanine and β- Hydroxytyrosine Derivatives. Cheminform. 25: no-no. DOI: 10.1002/CHIN.199446227 |
0.441 |
|
| 2010 |
EASTON CJ, HUTTON CA, TAN EW, TIEKINK ERT. ChemInform Abstract: Synthesis of Homochiral Hydroxy α-Amino Acid Derivatives. Cheminform. 23: no-no. DOI: 10.1002/CHIN.199209279 |
0.508 |
|
| 2010 |
EASTON CJ, HUTTON CA, ROSELT PD, TIEKINK ERT. ChemInform Abstract: Synthesis and Molecular Structure of Stable Derivatives of (E)- and (Z) -Dehydrophenylalanine. Cheminform. 22: no-no. DOI: 10.1002/CHIN.199133262 |
0.462 |
|
| 2009 |
Kok WM, Scanlon DB, Karas JA, Miles LA, Tew DJ, Parker MW, Barnham KJ, Hutton CA. Solid-phase synthesis of homodimeric peptides: preparation of covalently-linked dimers of amyloid beta peptide. Chemical Communications (Cambridge, England). 6228-30. PMID 19826677 DOI: 10.1039/B912784D |
0.346 |
|
| 2009 |
Harding M, Bodkin JA, Issa F, Hutton CA, Willis AC, McLeod MD. The asymmetric aminohydroxylation route to GABOB and homoserine derivatives Tetrahedron. 65: 831-843. DOI: 10.1016/J.Tet.2008.11.037 |
0.333 |
|
| 2008 |
Boughton BA, Griffin MD, O'Donnell PA, Dobson RC, Perugini MA, Gerrard JA, Hutton CA. Irreversible inhibition of dihydrodipicolinate synthase by 4-oxo-heptenedioic acid analogues. Bioorganic & Medicinal Chemistry. 16: 9975-83. PMID 18977662 DOI: 10.1016/J.Bmc.2008.10.026 |
0.321 |
|
| 2008 |
Dobson RC, Griffin MD, Devenish SR, Pearce FG, Hutton CA, Gerrard JA, Jameson GB, Perugini MA. Conserved main-chain peptide distortions: a proposed role for Ile203 in catalysis by dihydrodipicolinate synthase. Protein Science : a Publication of the Protein Society. 17: 2080-90. PMID 18787203 DOI: 10.1110/Ps.037440.108 |
0.329 |
|
| 2008 |
Boughton BA, Dobson RC, Gerrard JA, Hutton CA. Conformationally constrained diketopimelic acid analogues as inhibitors of dihydrodipicolinate synthase. Bioorganic & Medicinal Chemistry Letters. 18: 460-3. PMID 18077163 DOI: 10.1016/J.Bmcl.2007.11.108 |
0.332 |
|
| 2008 |
Churches QI, Stewart HE, Cohen SB, Shröder A, Turner P, Hutton CA. Stereoselectivity of the Petasis reaction with various chiral amines and styrenylboronic acids Pure and Applied Chemistry. 80: 687-694. DOI: 10.1351/Pac200880040687 |
0.383 |
|
| 2007 |
Shuter EC, Duong H, Hutton CA, McLeod MD. The enantioselective synthesis of APTO and AETD: polyhydroxylated beta-amino acid constituents of the microsclerodermin cyclic peptides. Organic & Biomolecular Chemistry. 5: 3183-9. PMID 17878977 DOI: 10.1039/B707891A |
0.402 |
|
| 2007 |
Hutton CA, Bartlett PA. Preparation of diazabicyclo[4.3.0]nonene-based peptidomimetics. The Journal of Organic Chemistry. 72: 6865-72. PMID 17685573 DOI: 10.1021/Jo071074X |
0.563 |
|
| 2007 |
Kaiser PF, Churches QI, Hutton CA. Organoboron Reagents in the Preparation of Functionalized ?-Amino Acids Australian Journal of Chemistry. 60: 799. DOI: 10.1071/Ch07103 |
0.405 |
|
| 2006 |
Yuen AKL, Hutton CA. Preparation of Cyclic Peptide Alkaloids Containing Functionalized Tryptophan Residues Natural Product Communications. 1: 1934578X0600101. DOI: 10.1177/1934578X0600101010 |
0.375 |
|
| 2006 |
Yuen AKL, Jolliffe KA, Hutton CA. Preparation of the Central Tryptophan Moiety of the Celogentin/Moroidin Family of Anti-Mitotic Cyclic Peptides Australian Journal of Chemistry. 59: 819. DOI: 10.1071/Ch06324 |
0.339 |
|
| 2006 |
Yuen AKL, Hutton CA. Deprotection of Pinacolyl Boronate Esters via Hydrolysis of Intermediate Potassium Trifluoroborates. Cheminform. 37. DOI: 10.1016/J.Tetlet.2005.09.101 |
0.342 |
|
| 2006 |
Southwood TJ, Curry MC, Hutton CA. Factors affecting the efficiency and stereoselectivity of α-amino acid synthesis by the Petasis reaction Tetrahedron. 62: 236-242. DOI: 10.1016/J.Tet.2005.09.114 |
0.392 |
|
| 2005 |
Skaff O, Jolliffe KA, Hutton CA. Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine. The Journal of Organic Chemistry. 70: 7353-63. PMID 16122259 DOI: 10.1021/Jo051076M |
0.38 |
|
| 2005 |
Harding M, Bodkin JA, Hutton CA, McLeod MD. Substrate control in the asymmetric aminohydroxylation of monosubstituted alkenes: The enantioselective synthesis of GABOB and homoserine derivatives Synlett. 2005: 2829-2831. DOI: 10.1055/S-2005-918939 |
0.352 |
|
| 2004 |
Pennington TE, Kardiman C, Hutton CA. Deprotection of pinacolyl boronate esters by transesterification with polystyrene-boronic acid Tetrahedron Letters. 45: 6657-6660. DOI: 10.1016/J.Tetlet.2004.07.014 |
0.347 |
|
| 2003 |
Hutton CA, Skaff O. A convenient preparation of dityrosine via Miyaura borylation–Suzuki coupling of iodotyrosine derivatives Tetrahedron Letters. 44: 4895-4898. DOI: 10.1016/S0040-4039(03)01081-5 |
0.328 |
|
| 2001 |
Cuzzupe AN, Hutton CA, Lilly MJ, Mann RK, McRae KJ, Zammit SC, Rizzacasa MA. Total synthesis of the epidermal growth factor inhibitor (-)-reveromycin B. The Journal of Organic Chemistry. 66: 2382-93. PMID 11281779 DOI: 10.1021/Jo001646C |
0.301 |
|
| 1999 |
Hutton CA. Synthesis of beta-hydroxy-beta-(fluoronitrophenyl)alanines: vital components in the assembly of biologically active cyclic peptides. Organic Letters. 1: 295-7. PMID 10822566 DOI: 10.1021/Ol9906054 |
0.428 |
|
| 1998 |
Easton CJ, Hutton CA. Recent developments in the use of N-phthaloyl-amino acid derivatives in synthesis Synlett. 457-466. DOI: 10.1055/S-1998-1686 |
0.571 |
|
| 1997 |
Tian ZQ, Brown BB, Mack DP, Hutton CA, Bartlett PA. Potentially Macrocyclic Peptidyl Boronic Acids as Chymotrypsin Inhibitors. The Journal of Organic Chemistry. 62: 514-522. PMID 11671443 DOI: 10.1021/Jo9615007 |
0.569 |
|
| 1997 |
Hutton CA. Substituent effects in the stereoconvergent synthesis of β-hydroxyphenylalanine derivatives Tetrahedron Letters. 38: 5899-5902. DOI: 10.1016/S0040-4039(97)01314-2 |
0.304 |
|
| 1997 |
Hutton CA, White JM. Towards a total synthesis of ustiloxins A & B. Stereocontrolled synthesis of (2S,4S,6S)-4-hydroxy-5-phenylsulfinylnorvaline Tetrahedron Letters. 38: 1643-1646. DOI: 10.1016/S0040-4039(97)00110-X |
0.35 |
|
| 1996 |
Easton CJ, Merrett MC, Hutton CA, Tiekink ERT. Crystal structure of (2S,3S)-3-bromo-N-phthaloyl-p-nitrophenylalanine methyl ester, C18H13BrN2O6 Zeitschrift FüR Kristallographie - Crystalline Materials. 211. DOI: 10.1524/Zkri.1996.211.4.291 |
0.51 |
|
| 1996 |
Easton CJ, Merrett MC, Hutton CA, Tiekink ERT. Crystal structure of (S)-3-hydroxy-N-tert-butyl-Nα-phthaloylvalinamide, C17H22N2O4 Zeitschrift FüR Kristallographie - Crystalline Materials. 211. DOI: 10.1524/Zkri.1996.211.4.289 |
0.502 |
|
| 1996 |
Easton CJ, Merrett MC, Hutton CA, Tiekink ERT. Crystal structure of (2RS, 3RS)-3-bromo-N-tert-butyl-Nα-phthaloyl-p-nitrophenylalaninamide, C21H20BrN3O5 Zeitschrift FüR Kristallographie - Crystalline Materials. 211. DOI: 10.1524/Zkri.1996.211.4.287 |
0.492 |
|
| 1996 |
Easton CJ, Hutton CA, Merrett MC, Tiekink ER. Neighbouring group effects promote substitution reactions over elimination and provide a stereocontrolled route to chloramphenicol Tetrahedron. 52: 7025-7036. DOI: 10.1016/0040-4020(96)00307-9 |
0.565 |
|
| 1995 |
Easton CJ, Hutton CA, Roselt PD, Tiekink ERT. Crystal structure of (Z)-N-phthaloyl-2,3-dehydrophenylalanine methyl ester, C18H13NO4 Zeitschrift FüR Kristallographie. 210: 233-234. DOI: 10.1524/Zkri.1995.210.3.233 |
0.507 |
|
| 1994 |
Easton CJ, Hutton CA. Synthesis of each stereoisomer of [3-2H1]phenylalanine and evaluation of the stereochemical course of the reaction of (R)-phenylalanine with (S)-phenylalanine ammonia-lyase Journal of the Chemical Society-Perkin Transactions 1. 3545-3548. DOI: 10.1039/P19940003545 |
0.519 |
|
| 1994 |
Easton CJ, Hutton CA, Roselt PD, Tiekink ER. Stereocontrolled synthesis of β-hydroxyphenylalanine and β-hydroxytyrosine derivatives Tetrahedron. 50: 7327-7340. DOI: 10.1016/S0040-4020(01)85256-X |
0.57 |
|
| 1993 |
Easton CJ, Hutton CA, Tiekink ERT. Crystal structure of N-phthaloyl-β-phenylserine methylester, C18H15NO5 Zeitschrift FüR Kristallographie - Crystalline Materials. 203. DOI: 10.1524/Zkri.1993.203.Part-2.310 |
0.507 |
|
| 1991 |
Easton C, Hutton C, Roselt P, Tiekink E. Synthesis and Molecular Structure of Stable Derivatives of (E)- and (Z)-Dehydrophenylalanine Australian Journal of Chemistry. 44: 687. DOI: 10.1071/Ch9910687 |
0.517 |
|
| 1991 |
Easton CJ, Hutton CA, Rositano G, Tan EW. Regioselective functionalization of N-phthaloyl-substituted amino acid and peptide derivatives The Journal of Organic Chemistry. 56: 5614-5618. DOI: 10.1021/Jo00019A029 |
0.591 |
|
| 1990 |
Easton CJ, Hutton CA, Eng WT, Tiekink ERT. Synthesis of homochiral hydroxy-α-amino acid derivatives Tetrahedron Letters. 31: 7059-7062. DOI: 10.1016/S0040-4039(00)97242-3 |
0.386 |
|
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