Year |
Citation |
Score |
2022 |
Karipal Padinjare Veedu D, Connal L, Malins L. Tunable Electrochemical Peptide Modifications: Unlocking New Levels of Orthogonality for Side-Chain Functionalization. Angewandte Chemie (International Ed. in English). PMID 36336657 DOI: 10.1002/anie.202215470 |
0.384 |
|
2022 |
Bell HJ, Malins LR. Peptide macrocyclisation late-stage reductive amination. Organic & Biomolecular Chemistry. PMID 35621075 DOI: 10.1039/d2ob00782g |
0.452 |
|
2022 |
Milewska KD, Malins LR. Synthesis of Amino Acid α-Thioethers and Late-Stage Incorporation into Peptides. Organic Letters. 24: 3680-3685. PMID 35575402 DOI: 10.1021/acs.orglett.2c01297 |
0.395 |
|
2022 |
White AM, Palombi IR, Malins LR. Umpolung strategies for the functionalization of peptides and proteins. Chemical Science. 13: 2809-2823. PMID 35382479 DOI: 10.1039/d1sc06133j |
0.417 |
|
2022 |
Schwartz BD, Smyth AP, Nashar PE, Gardiner MG, Malins LR. Investigating Bicyclobutane-Triazolinedione Cycloadditions as a Tool for Peptide Modification. Organic Letters. PMID 35014844 DOI: 10.1021/acs.orglett.1c04071 |
0.764 |
|
2021 |
Mackay AS, Payne RJ, Malins LR. Electrochemistry for the Chemoselective Modification of Peptides and Proteins. Journal of the American Chemical Society. PMID 34968405 DOI: 10.1021/jacs.1c11185 |
0.568 |
|
2021 |
Lin Y, Malins LR. Electrochemically Enabled C-Terminal Peptide Modifications. Methods in Molecular Biology (Clifton, N.J.). 2355: 131-139. PMID 34386956 DOI: 10.1007/978-1-0716-1617-8_12 |
0.43 |
|
2021 |
Lin Y, Malins LR. An Electrochemical Approach to Designer Peptide α-Amides Inspired by α-Amidating Monooxygenase Enzymes. Journal of the American Chemical Society. PMID 34288681 DOI: 10.1021/jacs.1c05718 |
0.402 |
|
2021 |
Vo Y, Schwartz BD, Onagi H, Ward JS, Gardiner MG, Banwell MG, Nelms K, Malins L. A Rapid and Mild Sulfation Strategy Reveals Conformational Preferences in Therapeutically Relevant Sulfated Xylooligosaccharides. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33880824 DOI: 10.1002/chem.202100527 |
0.693 |
|
2020 |
Lin Y, Malins LR. Total synthesis of biseokeaniamides A-C and late-stage electrochemically-enabled peptide analogue synthesis. Chemical Science. 11: 10752-10758. PMID 34094328 DOI: 10.1039/d0sc03701j |
0.445 |
|
2020 |
Zhang MY, Malins LR. Decarboxylative Couplings for Late-Stage Peptide Modifications. Methods in Molecular Biology (Clifton, N.J.). 2103: 275-285. PMID 31879933 DOI: 10.1007/978-1-0716-0227-0_19 |
0.473 |
|
2019 |
Malins L, Schwartz BD, Zhang MY, Attard RH, Gardiner M. Structurally Diverse Acyl Bicyclobutanes: Valuable Strained Electrophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31823414 DOI: 10.1002/Chem.201905539 |
0.718 |
|
2019 |
Gopalakrishnan R, Noisier AFM, Johansson MJ, Knerr L, Hayes MA, Drury WJ, Valeur E, Malins LR. Late-Stage Functionalization of Histidine in Unprotected Peptides. Angewandte Chemie (International Ed. in English). PMID 31609503 DOI: 10.1002/Anie.201910888 |
0.4 |
|
2019 |
Qin T, Malins LR, Edwards JT, Merchant RR, Novak AJE, Zhong JZ, Mills RB, Yan M, Yuan C, Eastgate MD, Baran PS. Corrigendum: Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms. Angewandte Chemie (International Ed. in English). 58: 1866. PMID 30714686 DOI: 10.1002/Anie.201812580 |
0.47 |
|
2018 |
Malins LR. Peptide modification and cyclization via transition-metal catalysis. Current Opinion in Chemical Biology. 46: 25-32. PMID 29656180 DOI: 10.1016/j.cbpa.2018.03.019 |
0.395 |
|
2018 |
Malins LR. Decarboxylative couplings as versatile tools for late-stage peptide modifications Peptide Science. 110: e24049. DOI: 10.1002/pep2.24049 |
0.316 |
|
2017 |
deGruyter JN, Malins LR, Wimmer L, Clay KJ, Lopez-Ogalla J, Qin T, Cornella J, Liu Z, Che G, Bao D, Stevens JM, Qiao JX, Allen MP, Poss MA, Baran PS. CITU: A Peptide and Decarboxylative Coupling Reagent. Organic Letters. PMID 29115835 DOI: 10.1021/Acs.Orglett.7B03121 |
0.716 |
|
2017 |
deGruyter JN, Malins LR, Baran PS. Residue-Specific Peptide Modification: A Chemist's Guide. Biochemistry. PMID 28653834 DOI: 10.1021/Acs.Biochem.7B00536 |
0.561 |
|
2017 |
Smith JM, Qin T, Merchant RR, Edwards JT, Malins LR, Liu Z, Che G, Shen Z, Shaw SA, Eastgate MD, Baran PS. Decarboxylative Alkynylation. Angewandte Chemie (International Ed. in English). PMID 28636185 DOI: 10.1002/anie.201705107 |
0.663 |
|
2017 |
Edwards JT, Merchant RR, McClymont KS, Knouse KW, Qin T, Malins LR, Vokits B, Shaw SA, Bao DH, Wei FL, Zhou T, Eastgate MD, Baran PS. Decarboxylative alkenylation. Nature. PMID 28424520 DOI: 10.1038/nature22307 |
0.555 |
|
2017 |
Malins LR, deGruyter JN, Robbins KJ, Scola PM, Eastgate M, Ghadiri MR, Baran PS. Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products. Journal of the American Chemical Society. PMID 28326777 DOI: 10.1021/Jacs.7B01624 |
0.588 |
|
2017 |
Lopchuk JM, Fjelbye K, Kawamata Y, Malins LR, Pan CM, Gianatassio R, Wang J, Prieto L, Bradow J, Brandt TA, Collins MR, Elleraas J, Ewanicki J, Farrell W, Fadeyi OO, et al. Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity. Journal of the American Chemical Society. PMID 28140573 DOI: 10.1021/Jacs.6B13229 |
0.748 |
|
2016 |
Qin T, Malins LR, Edwards JT, Merchant RR, Novak AJ, Zhong JZ, Mills RB, Yan M, Yuan C, Eastgate MD, Baran PS. Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms. Angewandte Chemie (International Ed. in English). PMID 27981703 DOI: 10.1002/Anie.201609662 |
0.553 |
|
2016 |
Payne RJ, Mitchell N, Kulkarni S, Wang S, Malins L. One-Pot Ligation-Oxidative Deselenization at Selenocysteine and Selenocystine. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27859731 DOI: 10.1002/Chem.201604709 |
0.563 |
|
2016 |
Isahak N, Gody G, Malins LR, Mitchell NJ, Payne RJ, Perrier S. Single addition of an allylamine monomer enables access to end-functionalized RAFT polymers for native chemical ligation. Chemical Communications (Cambridge, England). PMID 27722654 DOI: 10.1039/C6Cc06010B |
0.434 |
|
2016 |
Qin T, Cornella J, Li C, Malins LR, Edwards JT, Kawamura S, Maxwell BD, Eastgate MD, Baran PS. A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents. Science (New York, N.Y.). PMID 27103669 DOI: 10.1126/Science.Aaf6123 |
0.695 |
|
2016 |
Gianatassio R, Lopchuk JM, Wang J, Pan CM, Malins LR, Prieto L, Brandt TA, Collins MR, Gallego GM, Sach NW, Spangler JE, Zhu H, Zhu J, Baran PS. Strain-release amination. Science (New York, N.Y.). 351: 241-246. PMID 26816372 DOI: 10.1126/Science.Aad6252 |
0.744 |
|
2015 |
Mitchell NJ, Malins LR, Liu X, Thompson RE, Chan B, Radom L, Payne RJ. Rapid Additive-Free Selenocystine-Selenoester Peptide Ligation. Journal of the American Chemical Society. 137: 14011-4. PMID 26487084 DOI: 10.1021/Jacs.5B07237 |
0.712 |
|
2015 |
Sayers J, Thompson RE, Perry KJ, Malins LR, Payne RJ. Thiazolidine-Protected β-Thiol Asparagine: Applications in One-Pot Ligation-Desulfurization Chemistry. Organic Letters. 17: 4902-5. PMID 26398220 DOI: 10.1021/Acs.Orglett.5B02468 |
0.617 |
|
2015 |
Malins LR, Mitchell NJ, McGowan S, Payne RJ. Oxidative Deselenization of Selenocysteine: Applications for Programmed Ligation at Serine. Angewandte Chemie (International Ed. in English). 54: 12716-21. PMID 26384718 DOI: 10.1002/Anie.201504639 |
0.681 |
|
2015 |
Malins LR, Giltrap AM, Dowman LJ, Payne RJ. Synthesis of β-Thiol Phenylalanine for Applications in One-Pot Ligation-Desulfurization Chemistry. Organic Letters. 17: 2070-3. PMID 25860301 DOI: 10.1021/Acs.Orglett.5B00597 |
0.782 |
|
2015 |
Malins LR, Payne RJ. Modern extensions of native chemical ligation for chemical protein synthesis. Topics in Current Chemistry. 362: 27-87. PMID 25518971 DOI: 10.1007/128_2014_584 |
0.588 |
|
2015 |
Malins LR, Payne RJ. Synthetic amino acids for applications in peptide ligation-desulfurization chemistry Australian Journal of Chemistry. 68: 521-537. DOI: 10.1071/Ch14568 |
0.618 |
|
2015 |
Malins LR, Giltrap AM, Dowman LJ, Payne RJ. Synthesis of β-Thiol Phenylalanine for Applications in One-Pot Ligation-Desulfurization Chemistry Organic Letters. 17: 2070-2073. DOI: 10.1021/acs.orglett.5b00597 |
0.743 |
|
2015 |
Malins LR, Payne RJ. Modern extensions of native chemical ligation for chemical protein synthesis Topics in Current Chemistry. 362: 27-88. DOI: 10.1007/128_2014_584 |
0.466 |
|
2014 |
Malins LR, Payne RJ. Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins. Current Opinion in Chemical Biology. 22: 70-8. PMID 25285753 DOI: 10.1016/J.Cbpa.2014.09.021 |
0.573 |
|
2014 |
Liu X, Malins LR, Roche M, Sterjovski J, Duncan R, Garcia ML, Barnes NC, Anderson DA, Stone MJ, Gorry PR, Payne RJ. Site-selective solid-phase synthesis of a CCR5 sulfopeptide library to interrogate HIV binding and entry. Acs Chemical Biology. 9: 2074-81. PMID 24963694 DOI: 10.1021/Cb500337R |
0.419 |
|
2014 |
Cergol KM, Thompson RE, Malins LR, Turner P, Payne RJ. One-pot peptide ligation-desulfurization at glutamate. Organic Letters. 16: 290-3. PMID 24294973 DOI: 10.1021/Ol403288N |
0.577 |
|
2014 |
Malins LR, Mitchell NJ, Payne RJ. Peptide ligation chemistry at selenol amino acids. Journal of Peptide Science : An Official Publication of the European Peptide Society. 20: 64-77. PMID 24285588 DOI: 10.1002/Psc.2581 |
0.721 |
|
2014 |
Malins LR, Cergol KM, Payne RJ. Chemoselective sulfenylation and peptide ligation at tryptophan Chemical Science. 5: 260-266. DOI: 10.1039/C3Sc51497H |
0.622 |
|
2014 |
Malins LR, Payne RJ. Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins Current Opinion in Plant Biology. 22: 70-78. DOI: 10.1016/j.cbpa.2014.09.021 |
0.573 |
|
2013 |
Malins LR, Cergol KM, Payne RJ. Peptide ligation-desulfurization chemistry at arginine. Chembiochem : a European Journal of Chemical Biology. 14: 559-63. PMID 23426906 DOI: 10.1002/Cbic.201300049 |
0.591 |
|
2012 |
Malins LR, Payne RJ. Synthesis and utility of β-selenol-phenylalanine for native chemical ligation-deselenization chemistry. Organic Letters. 14: 3142-5. PMID 22642500 DOI: 10.1021/Ol3012265 |
0.635 |
|
2011 |
Wilkinson BL, Day S, Malins LR, Apostolopoulos V, Payne RJ. Self-adjuvanting multicomponent cancer vaccine candidates combining per-glycosylated MUC1 glycopeptides and the Toll-like receptor 2 agonist Pam3CysSer. Angewandte Chemie (International Ed. in English). 50: 1635-9. PMID 21308921 DOI: 10.1002/Anie.201006115 |
0.312 |
|
2010 |
Wilkinson BL, Malins LR, Chun CK, Payne RJ. Synthesis of MUC1-lipopeptide chimeras. Chemical Communications (Cambridge, England). 46: 6249-51. PMID 20664875 DOI: 10.1039/C0Cc01360A |
0.418 |
|
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