| Year |
Citation |
Score |
| 2023 |
Götz J, Jackl MK, Jindakun C, Marziale AN, André J, Gosling DJ, Springer C, Palmieri M, Reck M, Luneau A, Brocklehurst CE, Bode JW. High-throughput synthesis provides data for predicting molecular properties and reaction success. Science Advances. 9: eadj2314. PMID 37889964 DOI: 10.1126/sciadv.adj2314 |
0.308 |
|
| 2022 |
Kumarswamyreddy N, Nakagawa A, Endo H, Shimotohno A, Torii KU, Bode JW, Oishi S. Chemical synthesis of the EPF-family of plant cysteine-rich proteins and late-stage dye attachment by chemoselective amide-forming ligations. Rsc Chemical Biology. 3: 1422-1431. PMID 36544577 DOI: 10.1039/d2cb00155a |
0.787 |
|
| 2022 |
Kumarswamyreddy N, Reddy DN, Robkis DM, Kamiya N, Tsukamoto R, Kanaoka MM, Higashiyama T, Oishi S, Bode JW. Chemical synthesis of plant pollen tube attractant proteins by KAHA ligation. Rsc Chemical Biology. 3: 721-727. PMID 35755195 DOI: 10.1039/d2cb00039c |
0.779 |
|
| 2021 |
Farnung J, Song H, Bode JW. Chemical Protein Synthesis by Chemoselective #x03B1;-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline. Methods in Molecular Biology (Clifton, N.J.). 2355: 151-162. PMID 34386958 DOI: 10.1007/978-1-0716-1617-8_14 |
0.357 |
|
| 2021 |
Fracassi A, Ray A, Nakatsuka N, Passiu C, Tanriver M, Schauenburg D, Scherrer S, Ouald Chaib A, Mandal J, Ramakrishna SN, Bode JW, Spencer ND, Rossi A, Yamakoshi Y. KAT Ligation for Rapid and Facile Covalent Attachment of Biomolecules to Surfaces. Acs Applied Materials & Interfaces. PMID 34105349 DOI: 10.1021/acsami.1c05652 |
0.617 |
|
| 2020 |
Schuhmacher A, Shiro T, Ryan SJ, Bode JW. Synthesis of secondary and tertiary amides without coupling agents from amines and potassium acyltrifluoroborates (KATs). Chemical Science. 11: 7609-7614. PMID 34094137 DOI: 10.1039/d0sc01330g |
0.32 |
|
| 2020 |
Schuhmacher A, Ryab SJ, Bode JW. Catalytic Synthesis of Potassium Acyltrifluoroborates (KATs) from Boronic Acids and the Thioimidate KAT Transfer Reagent. Angewandte Chemie (International Ed. in English). PMID 33231353 DOI: 10.1002/anie.202014581 |
0.307 |
|
| 2020 |
Wu D, Taguchi J, Tanriver M, Bode JW. Synthesis of Acylboron Compounds. Angewandte Chemie (International Ed. in English). PMID 32510826 DOI: 10.1002/Anie.202005050 |
0.646 |
|
| 2020 |
Neumann K, Farnung J, Baldauf S, Bode JW. Prevention of aspartimide formation during peptide synthesis using cyanosulfurylides as carboxylic acid-protecting groups. Nature Communications. 11: 982. PMID 32080186 DOI: 10.1038/S41467-020-14755-6 |
0.395 |
|
| 2020 |
Murar CE, Ninomiya M, Shimura S, Karakus U, Boyman O, Bode JW. Chemical Synthesis of Interleukin-2 and Disulfide Stabilizing Analogues. Angewandte Chemie (International Ed. in English). PMID 32032465 DOI: 10.1002/Anie.201916053 |
0.322 |
|
| 2020 |
Schuhmacher A, Shiro T, Ryan SJ, Bode JW. Synthesis of secondary and tertiary amides without coupling agents from amines and potassium acyltrifluoroborates (KATs) Chemical Science. 11: 7609-7614. DOI: 10.1039/D0Sc01330G |
0.453 |
|
| 2019 |
Baldauf S, Ogunkoya AO, Boross GN, Bode JW. Aspartic Acid Forming α-Ketoacid-Hydroxylamine (KAHA) Ligations with (S)-4,4-difluoro-5-oxaproline. The Journal of Organic Chemistry. PMID 31840512 DOI: 10.1021/Acs.Joc.9B02271 |
0.369 |
|
| 2019 |
Zhang Y, Hirota T, Kuwata K, Oishi S, Gramani SG, Bode JW. Chemical Synthesis of Atomically Tailored SUMO E2 Conjugating Enzymes for the Formation of Covalently Linked SUMO-E2-E3 Ligase Ternary Complexes. Journal of the American Chemical Society. PMID 31436980 DOI: 10.1021/Jacs.9B06820 |
0.314 |
|
| 2019 |
Baldauf S, Schauenburg D, Bode JW. A threonine-forming oxazetidine amino acid for the chemical synthesis of proteins with the KAHA ligation. Angewandte Chemie (International Ed. in English). PMID 31260175 DOI: 10.1002/Anie.201906486 |
0.41 |
|
| 2019 |
Wang YY, Bode JW. Olefin Amine (OLA) Reagents for the Synthesis of Bridged Bicyclic and Spirocyclic Saturated N-Heterocycles by Catalytic HAT Reactions. Journal of the American Chemical Society. PMID 31117673 DOI: 10.1021/Jacs.9B05074 |
0.488 |
|
| 2019 |
Osuna Gálvez A, Bode JW. Traceless Templated Amide-Forming Ligations. Journal of the American Chemical Society. PMID 31117658 DOI: 10.1021/Jacs.9B03597 |
0.374 |
|
| 2019 |
Wu D, Fohn NA, Bode JW. Catalytic Synthesis of Potassium Acyltrifluoroborates (KATs) by Chemoselective Cross-Coupling with a Bifunctional Reagent. Angewandte Chemie (International Ed. in English). PMID 31070291 DOI: 10.1002/Anie.201904576 |
0.688 |
|
| 2019 |
Stepek IA, Cao T, Koetemann A, Shimura S, Wollscheid B, Bode JW. Antibiotic discovery with synthetic fermentation: library assembly, phenotypic screening, and mechanism of action of beta-peptides targeting penicillin-binding proteins. Acs Chemical Biology. PMID 30990649 DOI: 10.1021/Acschembio.9B00227 |
0.303 |
|
| 2019 |
Saito F, Trapp N, Bode JW. Iterative Assembly of Polycyclic Saturated Heterocycles from Monomeric Building Blocks. Journal of the American Chemical Society. PMID 30845799 DOI: 10.1021/Jacs.9B01537 |
0.345 |
|
| 2019 |
Neumann K, Farnung J, Baldauf S, Bode J. Cyanosulfurylides (CSY): Carboxylic Acid Protecting Groups That Prevent Aspartimide Formation During Peptide Synthesis Chemrxiv. DOI: 10.26434/Chemrxiv.9767027.V1 |
0.368 |
|
| 2019 |
Luescher MU, Bode JW. Evidence for a Radical Mechanism in Cu(II)-Promoted SnAP Reactions Synlett. 30: 464-470. DOI: 10.1055/S-0037-1611670 |
0.388 |
|
| 2019 |
Baldauf S, Bode J. Synthesis and Evaluation of Cyclic Acetals of Serine Hydroxylamine for Amide-Forming KAHA Ligations Synthesis. 51: 1273-1283. DOI: 10.1055/S-0037-1611635 |
0.431 |
|
| 2019 |
Baldauf S, Schauenburg D, Bode JW. Eine Threonin‐bildende Oxazetidinaminosäure für die chemische Synthese von Proteinen mittels KAHA‐Ligation Angewandte Chemie. 131: 12729-12733. DOI: 10.1002/Ange.201906486 |
0.324 |
|
| 2019 |
Wu D, Fohn NA, Bode JW. Katalytische Synthese von Kaliumacyltrifluoroboraten mithilfe chemoselektiver Kreuzkupplung eines bifunktionalen Reagenzes Angewandte Chemie. 131: 11174-11178. DOI: 10.1002/Ange.201904576 |
0.633 |
|
| 2018 |
Schauenburg D, Osuna Gálvez A, Bode JW. Covalently functionalized amide cross-linked hydrogels from primary amines and polyethylene glycol acyltrifluoroborates (PEG-KATs). Journal of Materials Chemistry. B. 6: 4775-4782. PMID 32254304 DOI: 10.1039/C8Tb01028E |
0.398 |
|
| 2018 |
Boross GN, Shimura S, Besenius M, Tennagels N, Rossen K, Wagner M, Bode JW. Facile folding of insulin variants bearing a prosthetic C-peptide prepared by α-ketoacid-hydroxylamine (KAHA) ligation. Chemical Science. 9: 8388-8395. PMID 30542587 DOI: 10.1039/C8Sc03738H |
0.342 |
|
| 2018 |
Vagstad AL, Kuranaga T, Püntener S, Pattabiraman VR, Bode JW, Piel J. Introduction of D-Amino Acids in Minimalistic Peptide Substrates by an S-Adenosyl-L-Methionine Radical Epimerase. Angewandte Chemie (International Ed. in English). PMID 30521081 DOI: 10.1002/Anie.201809508 |
0.344 |
|
| 2018 |
Shiro T, Schuhmacher A, Jackl MK, Bode JW. Facile synthesis of α-aminoboronic acids from amines and potassium acyltrifluoroborates (KATs) trifluoroborate-iminiums (TIMs). Chemical Science. 9: 5191-5196. PMID 29997873 DOI: 10.1039/C8Sc01486H |
0.405 |
|
| 2018 |
Jackl MK, Schuhmacher A, Shiro T, Bode JW. Synthesis of N, N-Alkylated α-Tertiary Amines by Coupling of α-Aminoalkyltrifluoroborates and Grignard Reagents. Organic Letters. PMID 29938515 DOI: 10.1021/Acs.Orglett.8B01613 |
0.472 |
|
| 2018 |
Hubert JG, Stepek IA, Noda H, Bode JW. Synthetic fermentation of β-peptide macrocycles by thiadiazole-forming ring-closing reactions. Chemical Science. 9: 2159-2167. PMID 29719689 DOI: 10.1039/C7Sc05057G |
0.44 |
|
| 2018 |
Liu SM, Wu D, Bode JW. One-Step Synthesis of Aliphatic Potassium Acyltrifluoroborates (KATs) from Organocuprates. Organic Letters. PMID 29620901 DOI: 10.1021/Acs.Orglett.8B00720 |
0.687 |
|
| 2018 |
Jindakun C, Hsieh SY, Bode JW. Iridium-catalyzed Synthesis of Saturated N-Heterocycles from Aldehydes and SnAP Reagents with Continuous Flow Photochemistry. Organic Letters. PMID 29558148 DOI: 10.1021/Acs.Orglett.8B00611 |
0.441 |
|
| 2018 |
White CJ, Bode JW. PEGylation and Dimerization of Expressed Proteins under Near Equimolar Conditions with Potassium 2-Pyridyl Acyltrifluoroborates. Acs Central Science. 4: 197-206. PMID 29532019 DOI: 10.1021/Acscentsci.7B00432 |
0.373 |
|
| 2018 |
Luescher MU, Jindakun C, Bode JW. Preparation of Tributyl(iodomethyl)stannane Organic Syntheses. 95: 345-356. DOI: 10.15227/Orgsyn.095.0345 |
0.323 |
|
| 2018 |
Rohrbacher F, Zwicky A, Bode JW. Facile Synthesis of Internal and C-Terminal Peptide α
-Ketoamides with Fmoc-Solid Phase Peptide Synthesis Helvetica Chimica Acta. 101: e1800039. DOI: 10.1002/Hlca.201800039 |
0.367 |
|
| 2018 |
Luescher MU, Jindakun C, Bode JW. Stannylamine Protocol (SnAP) Reagents for the Synthesis of C–Substituted Morpholines from Aldehydes Organic Syntheses. 95: 357-373. DOI: 10.1002/0471264229.Os095.25 |
0.455 |
|
| 2018 |
Murar CE, Harmand TJ, Takano H, Bode JW, Timmerman JC, Huang Y, Wood JL. Preparation of (S)-N-Boc-5-oxaproline Organic Syntheses. 95: 157-176. DOI: 10.1002/0471264229.Os095.11 |
0.332 |
|
| 2018 |
Harmand TJ, Murar CE, Takano H, Bode JW, Timmerman JC, Huang Y, Wood JL. Enantioselective Synthesis of ( S )‐Ethyl 2‐(( tert ‐butoxycarbonyl)(( tert ‐butyldimethylsilyl)oxy)amino)‐4‐oxobutanoate Organic Syntheses. 95: 142-156. DOI: 10.1002/0471264229.Os095.10 |
0.439 |
|
| 2017 |
Taguchi J, Ikeda T, Takahashi R, Sasaki I, Ogasawara Y, Dairi T, Kato N, Yamamoto Y, Bode JW, Ito H. Synthesis of Acylborons by Ozonolysis of Alkenylboronates: Preparation of an Enantioenriched Amino Acid Acylboronate. Angewandte Chemie (International Ed. in English). PMID 28905460 DOI: 10.1002/Anie.201707933 |
0.471 |
|
| 2017 |
Bode JW. Chemical Protein Synthesis with the α-Ketoacid-Hydroxylamine Ligation. Accounts of Chemical Research. PMID 28849903 DOI: 10.1021/Acs.Accounts.7B00277 |
0.446 |
|
| 2017 |
Harmand TJ, Pattabiraman VR, Bode JW. Chemical Synthesis of the Highly Hydrophobic Antiviral Membrane Associated Protein IFITM3 and Modified Variants. Angewandte Chemie (International Ed. in English). PMID 28834009 DOI: 10.1002/Anie.201707554 |
0.324 |
|
| 2017 |
Jackl MK, Legnani L, Morandi B, Bode JW. Continuous Flow Synthesis of Morpholines and Oxazepanes with Silicon Amine Protocol (SLAP) Reagents and Lewis Acid Facilitated Photoredox Catalysis. Organic Letters. PMID 28813158 DOI: 10.1021/Acs.Orglett.7B02395 |
0.646 |
|
| 2017 |
Murar CE, Harmand TJ, Bode JW. Improved synthesis of (S)-N-Boc-5-oxaproline for protein synthesis with the α-ketoacid-hydroxylamine (KAHA) ligation. Bioorganic & Medicinal Chemistry. PMID 28662960 DOI: 10.1016/J.Bmc.2017.06.019 |
0.487 |
|
| 2017 |
Rohrbacher F, Zwicky A, Bode JW. Chemical synthesis of a homoserine-mutant of the antibacterial, head-to-tail cyclized protein AS-48 by α-ketoacid-hydroxylamine (KAHA) ligation. Chemical Science. 8: 4051-4055. PMID 28580120 DOI: 10.1039/C7Sc00789B |
0.367 |
|
| 2017 |
Saito F, Bode JW. Synthesis and stabilities of peptide-based [1]rotaxanes: molecular grafting onto lasso peptide scaffolds. Chemical Science. 8: 2878-2884. PMID 28553526 DOI: 10.1039/C7Sc00021A |
0.316 |
|
| 2017 |
Hsieh SY, Bode JW. Lewis Acid Induced Toggle from Ir(II) to Ir(IV) Pathways in Photocatalytic Reactions: Synthesis of Thiomorpholines and Thiazepanes from Aldehydes and SLAP Reagents. Acs Central Science. 3: 66-72. PMID 28149955 DOI: 10.1021/Acscentsci.6B00334 |
0.427 |
|
| 2017 |
Oriana S, Cai Y, Bode JW, Yamakoshi Y. Synthesis of tri-functionalized MMP2 FRET probes using a chemo-selective and late-stage modification of unprotected peptides. Organic & Biomolecular Chemistry. PMID 28139803 DOI: 10.1039/C7Ob00150A |
0.67 |
|
| 2017 |
Gálvez AO, Schaack CP, Noda H, Bode JW. Chemoselective acylation of primary amines and amides with potassium acyltrifluoroborates under acidic conditions. Journal of the American Chemical Society. PMID 28118000 DOI: 10.1021/Jacs.7B00059 |
0.392 |
|
| 2017 |
Rohrbacher F, Baldauf S, Wucherpfennig TG, Bode JW. Product Selectivity in KAHA Ligations: Ester vs. Amide Formation with Cyclic Hydroxylamines Synlett. 28: 1929-1933. DOI: 10.1055/S-0036-1588480 |
0.418 |
|
| 2017 |
Luescher MU, Songsichan T, Hsieh S, Bode JW. Copper Promoted Oxidative Coupling of SnAP Hydrazines and Aldehydes to Form Chiral 1,4,5‐Oxadiazepanes and 1,2,5‐Triazepanes Helvetica Chimica Acta. 100: e1700199. DOI: 10.1002/Hlca.201700199 |
0.404 |
|
| 2017 |
Mazunin D, Bode JW. Potassium Acyltrifluoroborate (KAT) Ligations are Orthogonal to Thiol-Michaeland SPAAC Reactions: Covalent Dual Immobilization of Proteins onto Synthetic PEG Hydrogels Helvetica Chimica Acta. 100: e1600311. DOI: 10.1002/Hlca.201600311 |
0.39 |
|
| 2016 |
Kreituss I, Bode JW. Catalytic Kinetic Resolution of Saturated N-Heterocycles by Enantioselective Amidation with Chiral Hydroxamic Acids. Accounts of Chemical Research. PMID 27936682 DOI: 10.1021/Acs.Accounts.6B00461 |
0.494 |
|
| 2016 |
Liu SM, Mazunin D, Pattabiraman VR, Bode JW. Synthesis of Bifunctional Potassium Acyltrifluoroborates. Organic Letters. PMID 27709962 DOI: 10.1021/Acs.Orglett.6B02652 |
0.448 |
|
| 2016 |
Trindade AF, Bode JW. Irreversible Conjugation of Aldehydes in Water To Form Stable 1,2,4-Oxadiazinan-5-ones. Organic Letters. PMID 27541010 DOI: 10.1021/Acs.Orglett.6B01889 |
0.409 |
|
| 2016 |
Thuaud F, Rohrbacher F, Zwicky A, Bode JW. Incorporation of Acid-Labile Masking Groups for the Traceless Synthesis of C-Terminal Peptide α-Ketoacids. Organic Letters. PMID 27439001 DOI: 10.1021/Acs.Orglett.6B01692 |
0.428 |
|
| 2016 |
Harmand TJ, Murar CE, Bode JW. Protein chemical synthesis by α-ketoacid-hydroxylamine ligation. Nature Protocols. 11: 1130-47. PMID 27227514 DOI: 10.1038/Nprot.2016.052 |
0.441 |
|
| 2016 |
Luescher MU, Bode JW. SnAP-eX Reagents for the Synthesis of Exocyclic 3-Amino- and 3-Alkoxypyrrolidines and Piperidines from Aldehydes. Organic Letters. PMID 27192447 DOI: 10.1021/Acs.Orglett.6B01099 |
0.483 |
|
| 2016 |
Hsieh SY, Bode JW. Silicon Amine Reagents for the Photocatalytic Synthesis of Piperazines from Aldehydes and Ketones. Organic Letters. PMID 27101157 DOI: 10.1021/Acs.Orglett.6B00722 |
0.493 |
|
| 2016 |
Jackl MK, Kreituss I, Bode JW. Synthesis of Tetrahydronaphthyridines from Aldehydes and HARP Reagents via Radical Pictet-Spengler Reactions. Organic Letters. PMID 27026179 DOI: 10.1021/Acs.Orglett.6B00523 |
0.45 |
|
| 2016 |
Kreituss I, Bode JW. Flow chemistry and polymer-supported pseudoenantiomeric acylating agents enable parallel kinetic resolution of chiral saturated N-heterocycles Nature Chemistry. 9: 446-452. DOI: 10.1038/Nchem.2681 |
0.4 |
|
| 2016 |
Thuaud F, Rohrbacher F, Zwicky A, Bode JW. Photoprotected Peptideα-Ketoacids and Hydroxylamines for Iterative and One-Pot KAHA Ligations: Synthesis of NEDD8 Helvetica Chimica Acta. 99: 868-894. DOI: 10.1002/Hlca.201600264 |
0.459 |
|
| 2015 |
Rohrbacher F, Deniau G, Luther A, Bode JW. Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation. Chemical Science. 6: 4889-4896. PMID 29142720 DOI: 10.1039/C5Sc01774B |
0.419 |
|
| 2015 |
Kreituss I, Chen KY, Eitel SH, Adam JM, Wuitschik G, Fettes A, Bode JW. A Robust, Recyclable Resin for Decagram Scale Resolution of (±)-Mefloquine and Other Chiral N-Heterocycles. Angewandte Chemie (International Ed. in English). PMID 26663345 DOI: 10.1002/Anie.201509256 |
0.388 |
|
| 2015 |
Noda H, Bode JW. Synthesis and reactivities of monofluoro acylboronates in chemoselective amide bond forming ligation with hydroxylamines. Organic & Biomolecular Chemistry. PMID 26566143 DOI: 10.1039/C5Ob02118A |
0.436 |
|
| 2015 |
He C, Kulkarni SS, Thuaud F, Bode JW. Chemical Synthesis of the 20 kDa Heme Protein Nitrophorin 4 by α-Ketoacid-Hydroxylamine (KAHA) Ligation. Angewandte Chemie (International Ed. in English). PMID 26346606 DOI: 10.1002/Anie.201505379 |
0.38 |
|
| 2015 |
Wanner B, Kreituss I, Gutierrez O, Kozlowski MC, Bode JW. Catalytic Kinetic Resolution of Disubstituted Piperidines by Enantioselective Acylation: Synthetic Utility and Mechanistic Insights. Journal of the American Chemical Society. 137: 11491-7. PMID 26308097 DOI: 10.1021/Jacs.5B07201 |
0.424 |
|
| 2015 |
Luescher MU, Bode JW. Catalytic Synthesis of N-Unprotected Piperazines, Morpholines, and Thiomorpholines from Aldehydes and SnAP Reagents. Angewandte Chemie (International Ed. in English). 54: 10884-8. PMID 26212589 DOI: 10.1002/Anie.201505167 |
0.495 |
|
| 2015 |
Pusterla I, Bode JW. An oxazetidine amino acid for chemical protein synthesis by rapid, serine-forming ligations. Nature Chemistry. 7: 668-72. PMID 26201744 DOI: 10.1038/Nchem.2282 |
0.473 |
|
| 2015 |
Geoghegan K, Bode JW. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic Letters. 17: 1934-7. PMID 25822736 DOI: 10.1021/Acs.Orglett.5B00618 |
0.484 |
|
| 2015 |
Rohrbacher F, Wucherpfennig TG, Bode JW. Chemical Protein Synthesis with the KAHA Ligation. Topics in Current Chemistry. 363: 1-31. PMID 25761549 DOI: 10.1007/128_2014_597 |
0.445 |
|
| 2015 |
Noda H, Bode JW. Synthesis of chemically and configurationally stable monofluoro acylboronates: effect of ligand structure on their formation, properties, and reactivities. Journal of the American Chemical Society. 137: 3958-66. PMID 25723308 DOI: 10.1021/Jacs.5B00822 |
0.358 |
|
| 2015 |
Saito F, Noda H, Bode JW. Critical evaluation and rate constants of chemoselective ligation reactions for stoichiometric conjugations in water. Acs Chemical Biology. 10: 1026-33. PMID 25572124 DOI: 10.1021/Cb5006728 |
0.429 |
|
| 2015 |
Schäfer G, Leu L, Bode JW. Synthesis of unsymmetrical, gem-disubstituted bisamides Heterocycles. 90: 1375-1386. DOI: 10.3987/Com-14-S(K)89 |
0.527 |
|
| 2015 |
Geoghegan K, Bode JW. Bespoke SnAP reagents for the synthesis of c-substituted spirocyclic and bicyclic saturated N-heterocycles Organic Letters. 17: 1934-1937. DOI: 10.1021/acs.orglett.5b00618 |
0.354 |
|
| 2015 |
Harmand TJ, Kulkarni SS, Bode JW. Optimized synthesis of a cyanosulfurylide linker for Fmoc-SPPS of C-terminal peptide α-ketoacids Tetrahedron Letters. 56: 3477-3480. DOI: 10.1016/J.Tetlet.2015.01.048 |
0.371 |
|
| 2015 |
Luescher MU, Geoghegan K, Nichols PL, Bode JW. SnAP reagents for a cross-coupling approach to the one-step synthesis of saturated N-heterocycles Aldrichimica Acta. 48: 43-48. |
0.304 |
|
| 2014 |
Siau WY, Bode JW. One-step synthesis of saturated spirocyclic N-heterocycles with stannyl amine protocol (SnAP) reagents and ketones. Journal of the American Chemical Society. 136: 17726-9. PMID 25482378 DOI: 10.1021/Ja511232B |
0.515 |
|
| 2014 |
Murar CE, Thuaud F, Bode JW. KAHA ligations that form aspartyl aldehyde residues as synthetic handles for protein modification and purification. Journal of the American Chemical Society. 136: 18140-8. PMID 25474323 DOI: 10.1021/Ja511231F |
0.418 |
|
| 2014 |
Harmand TJR, Murar CE, Bode JW. New chemistries for chemoselective peptide ligations and the total synthesis of proteins Current Opinion in Chemical Biology. 22: 115-121. PMID 25299573 DOI: 10.1016/J.Cbpa.2014.09.032 |
0.47 |
|
| 2014 |
Wucherpfennig TG, Pattabiraman VR, Limberg FRP, Ruiz-Rodríguez J, Bode JW. Traceless preparation of C-terminal α-Ketoacids for chemical protein synthesis by α-Ketoacid-hydroxylamine ligation: Synthesis of SUMO2/3 Angewandte Chemie - International Edition. 53: 12248-12252. PMID 25244549 DOI: 10.1002/Anie.201407014 |
0.413 |
|
| 2014 |
Wucherpfennig TG, Rohrbacher F, Pattabiraman VR, Bode JW. Formation and rearrangement of homoserine depsipeptides and depsiproteins in the α-ketoacid-hydroxylamine ligation with 5-oxaproline Angewandte Chemie - International Edition. 53: 12244-12247. PMID 25243600 DOI: 10.1002/Anie.201406097 |
0.409 |
|
| 2014 |
Allen SE, Hsieh SY, Gutierrez O, Bode JW, Kozlowski MC. Concerted amidation of activated esters: reaction path and origins of selectivity in the kinetic resolution of cyclic amines via N-heterocyclic carbenes and hydroxamic acid cocatalyzed acyl transfer. Journal of the American Chemical Society. 136: 11783-91. PMID 25050843 DOI: 10.1021/Ja505784W |
0.438 |
|
| 2014 |
Schäfer G, Bode JW. The synthesis of sterically hindered amides. Chimia. 68: 252-5. PMID 24983609 DOI: 10.2533/Chimia.2014.252 |
0.462 |
|
| 2014 |
Erős G, Kushida Y, Bode JW. A reagent for the one-step preparation of potassium acyltrifluoroborates (KATs) from aryl- and heteroarylhalides. Angewandte Chemie (International Ed. in English). 53: 7604-7. PMID 24888578 DOI: 10.1002/Anie.201403931 |
0.448 |
|
| 2014 |
Hsieh SY, Wanner B, Wheeler P, Beauchemin AM, Rovis T, Bode JW. Stereoelectronic basis for the kinetic resolution of N-heterocycles with chiral acylating reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 7228-31. PMID 24839065 DOI: 10.1002/Chem.201402818 |
0.41 |
|
| 2014 |
Noda H, Er?s G, Bode JW. Rapid ligations with equimolar reactants in water with the potassium acyltrifluoroborate (KAT) amide formation. Journal of the American Chemical Society. 136: 5611-4. PMID 24684235 DOI: 10.1021/Ja5018442 |
0.397 |
|
| 2014 |
Vo CV, Luescher MU, Bode JW. SnAP reagents for the one-step synthesis of medium-ring saturated N-heterocycles from aldehydes. Nature Chemistry. 6: 310-4. PMID 24651197 DOI: 10.1038/Nchem.1878 |
0.46 |
|
| 2014 |
Vo CV, Bode JW. Synthesis of saturated N-heterocycles. The Journal of Organic Chemistry. 79: 2809-15. PMID 24617516 DOI: 10.1021/Jo5001252 |
0.437 |
|
| 2014 |
Schäfer G, Bode JW. Synthesis of sterically hindered N-acylated amino acids from N-carboxyanhydrides. Organic Letters. 16: 1526-9. PMID 24571309 DOI: 10.1021/Ol500523N |
0.465 |
|
| 2014 |
Luescher MU, Vo CV, Bode JW. SnAP reagents for the synthesis of piperazines and morpholines. Organic Letters. 16: 1236-9. PMID 24502436 DOI: 10.1021/Ol500210Z |
0.477 |
|
| 2014 |
Mahatthananchai J, Bode JW. On the mechanism of N-heterocyclic carbene-catalyzed reactions involving acyl azoliums. Accounts of Chemical Research. 47: 696-707. PMID 24410291 DOI: 10.1021/Ar400239V |
0.469 |
|
| 2014 |
Noda H, Bode JW. Synthesis and chemoselective ligations of MIDA acylboronates with O-Me hydroxylamines Chemical Science. 5: 4328-4332. DOI: 10.1039/C4Sc00971A |
0.354 |
|
| 2014 |
Vo CVT, Luescher MU, Bode JW. SnAP reagents for the one-step synthesis of medium-ring saturated N-heterocycles from aldehydes Nature Chemistry. 6: 310-314. DOI: 10.1038/nchem.1878 |
0.37 |
|
| 2014 |
Luescher MU, Vo CVT, Bode JW. SnAP reagents for the synthesis of piperazines and morpholines Organic Letters. 16: 1236-1239. DOI: 10.1021/ol500210z |
0.374 |
|
| 2014 |
Vo CVT, Bode JW. Synthesis of saturated N-heterocycles Journal of Organic Chemistry. 79: 2809-2815. DOI: 10.1021/jo5001252 |
0.337 |
|
| 2014 |
Siau WY, Bode JW. One-step synthesis of saturated spirocyclic N-heterocycles with stannyl amine protocol (SnAP) reagents and ketones Journal of the American Chemical Society. 136: 17726-17729. DOI: 10.1021/ja511232b |
0.409 |
|
| 2014 |
Mahatthananchai J, Bode JW. On the mechanism of N-heterocyclic carbene-catalyzed reactions involving acyl azoliums Accounts of Chemical Research. 47: 696-707. DOI: 10.1021/ar400239v |
0.337 |
|
| 2014 |
Erös G, Kushida Y, Bode JW. A reagent for the one-step preparation of potassium acyltrifluoroborates (KATs) from aryl- and heteroarylhalides Angewandte Chemie - International Edition. 53: 7604-7607. DOI: 10.1002/anie.201403931 |
0.345 |
|
| 2014 |
Wucherpfennig TG, Pattabiraman VR, Limberg FRP, Ruiz-Rodríguez J, Bode JW. Spurlose Herstellung C-terminaler α-Ketosäuren zur chemischen Proteinsynthese mittels α-Ketoäure-Hydroxylamin-Ligation: Synthese von SUMO2/3 Angewandte Chemie. 126: 12445-12449. DOI: 10.1002/Ange.201407014 |
0.324 |
|
| 2014 |
Ogunkoya AO, Pattabiraman VR, Bode JW. Berichtigung: Sequentielle α-Ketosäurehydroxylamin(KAHA)-Ligationen: Synthese C-terminaler Varianten des Modifikationsproteins UFM1 Angewandte Chemie. 126: 12200-12200. DOI: 10.1002/Ange.201406882 |
0.305 |
|
| 2014 |
Pattabiraman VR, Ogunkoya AO, Bode JW. Berichtigung: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline Angewandte Chemie. 126: 12200-12200. DOI: 10.1002/Ange.201406880 |
0.4 |
|
| 2014 |
Wucherpfennig TG, Rohrbacher F, Pattabiraman VR, Bode JW. Bildung und Umlagerung von Homoserin-Depsipeptiden und -proteinen durch α-Ketosäure-Hydroxylamin-Ligation mit 5-Oxaprolin Angewandte Chemie. 126: 12441-12444. DOI: 10.1002/Ange.201406097 |
0.311 |
|
| 2013 |
Bode JW. Carbene catalysis: An internal affair Nature Chemistry. 5: 813-815. PMID 24056335 DOI: 10.1038/Nchem.1766 |
0.454 |
|
| 2013 |
Teichert JF, Mazunin D, Bode JW. Chemical sensing of polyols with shapeshifting boronic acids as a self-contained sensor array. Journal of the American Chemical Society. 135: 11314-21. PMID 23802800 DOI: 10.1021/Ja404981Q |
0.673 |
|
| 2013 |
Vo CVT, Mikutis G, Bode JW. SnAP reagents for the transformation of aldehydes into substituted thiomorpholines - An alternative to cross-coupling with saturated heterocycles Angewandte Chemie - International Edition. 52: 1705-1708. PMID 23281159 DOI: 10.1002/Anie.201208064 |
0.351 |
|
| 2013 |
He M, Bode JW. E pluribus unum: Isolation, structure determination, network analysis and DFT studies of a single metastable structure from a shapeshifting mixture of 852 bullvalene structural isomers Organic and Biomolecular Chemistry. 11: 1306-1317. PMID 23188211 DOI: 10.1039/C2Ob26954F |
0.464 |
|
| 2013 |
Gondo CA, Bode JW. Catalytic redox amidations of aldehydes with a polymer-supported peptide-N-heterocyclic carbene multifunctional catalyst Synlett. 24: 1205-1210. DOI: 10.1055/S-0033-1338956 |
0.478 |
|
| 2013 |
Teichert JF, Mazunin D, Bode JW. Chemical sensing of polyols with shapeshifting boronic acids as a self-contained sensor array Journal of the American Chemical Society. 135: 11314-11321. DOI: 10.1021/ja404981q |
0.62 |
|
| 2013 |
Chiang P, Bode JW. ChemInform Abstract: N-Heterocyclic Carbene Catalyzed Reactions of α-Functionalized Aldehydes Cheminform. 44: no-no. DOI: 10.1002/chin.201307232 |
0.373 |
|
| 2012 |
Lyngvi E, Bode JW, Schoenebeck F. A Computational Study of the Origin of Stereoinduction in NHC-Catalyzed Annulation Reactions of α,β-Unsaturated Acyl Azoliums. Chemical Science (Royal Society of Chemistry : 2010). 3: 2346-2350. PMID 23687566 DOI: 10.1039/C2Sc20331F |
0.436 |
|
| 2012 |
Mahatthananchai J, Bode JW. The effect of the N-mesityl group in NHC-catalyzed reactions. Chemical Science (Royal Society of Chemistry : 2010). 3: 192-197. PMID 23687565 DOI: 10.1039/C1Sc00397F |
0.499 |
|
| 2012 |
Bode JW, Mahatthananchai J, Dumas AM. Catalytic selective synthesis Angewandte Chemie - International Edition. 51: 10954-10990. PMID 23011639 DOI: 10.1002/Anie.201201787 |
0.379 |
|
| 2012 |
Kreituss I, Murakami Y, Binanzer M, Bode JW. Kinetic resolution of nitrogen heterocycles with a reusable polymer-supported reagent. Angewandte Chemie (International Ed. in English). 51: 10660-3. PMID 22991265 DOI: 10.1002/Anie.201204991 |
0.314 |
|
| 2012 |
Ogunkoya AO, Pattabiraman VR, Bode JW. Sequential α-ketoacid-hydroxylamine (KAHA) ligations: Synthesis of C-terminal variants of the modifier protein UFM1 Angewandte Chemie - International Edition. 51: 9693-9697. PMID 22915333 DOI: 10.1002/Anie.201204144 |
0.375 |
|
| 2012 |
Kravina AG, Mahatthananchai J, Bode JW. Enantioselective, NHC-catalyzed annulations of trisubstituted enals and cyclic N-sulfonylimines via α,β-unsaturated acyl azoliums. Angewandte Chemie (International Ed. in English). 51: 9433-6. PMID 22907817 DOI: 10.1002/Anie.201204145 |
0.426 |
|
| 2012 |
Schäfer G, Matthey C, Bode JW. Facile synthesis of sterically hindered and electron-deficient secondary amides from isocyanates. Angewandte Chemie (International Ed. in English). 51: 9173-5. PMID 22890627 DOI: 10.1002/Anie.201204481 |
0.399 |
|
| 2012 |
Hsieh SY, Binanzer M, Kreituss I, Bode JW. Expanded substrate scope and catalyst optimization for the catalytic kinetic resolution of N-heterocycles Chemical Communications. 48: 8892-8894. PMID 22842709 DOI: 10.1039/C2Cc34907H |
0.439 |
|
| 2012 |
Allen SE, Mahatthananchai J, Bode JW, Kozlowski MC. Oxyanion steering and CH-Ï€ interactions as key elements in an N-heterocyclic carbene-catalyzed [4 + 2] cycloaddition. Journal of the American Chemical Society. 134: 12098-103. PMID 22765294 DOI: 10.1021/Ja302761D |
0.423 |
|
| 2012 |
Dumas AM, Molander GA, Bode JW. Amide-forming ligation of acyltrifluoroborates and hydroxylamines in water. Angewandte Chemie (International Ed. in English). 51: 5683-6. PMID 22539274 DOI: 10.1002/Anie.201201077 |
0.448 |
|
| 2012 |
Dumas AM, Bode JW. Synthesis of acyltrifluoroborates. Organic Letters. 14: 2138-41. PMID 22475226 DOI: 10.1021/Ol300668M |
0.416 |
|
| 2012 |
Mahatthananchai J, Kaeobamrung J, Bode JW. Chiral N-Heterocyclic Carbene Catalyzed Annulations of Enals and Ynals with Stable Enols: A Highly Enantioselective Coates-Claisen Rearrangement. Acs Catalysis. 2: 494-503. PMID 22468232 DOI: 10.1021/Cs300020T |
0.809 |
|
| 2012 |
Fukuzumi T, Ju L, Bode JW. Chemoselective cyclization of unprotected linear peptides by α-ketoacid-hydroxylamine amide-ligation Organic and Biomolecular Chemistry. 10: 5837-5844. PMID 22426859 DOI: 10.1039/C2Ob25129A |
0.629 |
|
| 2012 |
Pattabiraman VR, Ogunkoya AO, Bode JW. Chemical protein synthesis by chemoselective α-ketoacid-hydroxylamine (KAHA) ligations with 5-oxaproline Angewandte Chemie - International Edition. 51: 5114-5118. PMID 22419525 DOI: 10.1002/Anie.201200907 |
0.4 |
|
| 2012 |
Pusterla I, Bode JW. The mechanism of the α-ketoacid-hydroxylamine amide-forming ligation Angewandte Chemie - International Edition. 51: 513-516. PMID 22125261 DOI: 10.1002/Anie.201107198 |
0.391 |
|
| 2012 |
He M, Rommel M, Bode JW. Formal synthesis of (±)-clausenamide by nhc-catalyzed γ-lactam formation Heterocycles. 86: 1689-1696. DOI: 10.3987/Com-12-S(N)128 |
0.509 |
|
| 2012 |
Huang YL, Frey R, Juarez-Garcia ME, Bode JW. Synthesis of aza-surfactin and 3-epi-aza-surfactin Heterocycles. 84: 1179-1191. DOI: 10.3987/Com-11-S(P)100 |
0.457 |
|
| 2012 |
Larson KK, He M, Teichert JF, Naganawa A, Bode JW. Chemical sensing with shapeshifting organic molecules Chemical Science. 3: 1825-1828. DOI: 10.1039/C2Sc20238G |
0.652 |
|
| 2012 |
Mahatthananchai J, Bode JW. The effect of the N-mesityl group in NHC-catalyzed reactions Chemical Science. 3: 192-197. DOI: 10.1039/c1sc00397f |
0.302 |
|
| 2012 |
Gerfaud T, Chiang YL, Kreituss I, Russak JA, Bode JW. Enantioselective, chromatography-free synthesis of β 3-Amino acids with natural and unnatural side chains Organic Process Research and Development. 16: 687-696. DOI: 10.1021/Op300069N |
0.788 |
|
| 2012 |
Dumas AM, Bode JW. Synthesis of acyltrifluoroborates Organic Letters. 14: 2138-2141. DOI: 10.1021/ol300668m |
0.336 |
|
| 2012 |
Mahatthananchai J, Kaeobamrung J, Bode JW. Chiral N-heterocyclic carbene-catalyzed annulations of enals and ynals with stable enols: A highly enantioselective Coates-Claisen rearrangement Acs Catalysis. 2: 494-503. DOI: 10.1021/cs300020t |
0.773 |
|
| 2012 |
Chiang YL, Russak JA, Carrillo N, Bode JW. Synthesis of enantiomerically pure isoxazolidine monomers for the preparation of β3-oligopeptides by iterative α-keto acidhydroxylamine (KAHA) ligations Helvetica Chimica Acta. 95: 2481-2501. DOI: 10.1002/Hlca.201200484 |
0.809 |
|
| 2012 |
Kravina AG, Mahatthananchai J, Bode JW. Enantioselective, NHC-catalyzed annulations of trisubstituted enals and cyclic n-sulfonylimines via α,β-unsaturated acyl azoliums Angewandte Chemie - International Edition. 51: 9433-9436. DOI: 10.1002/anie.201204145 |
0.313 |
|
| 2012 |
Pattabiraman VR, Ogunkoya AO, Bode JW. Cover Picture: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. Int. Ed. 21/2012) Angewandte Chemie International Edition. 51: 5015-5015. DOI: 10.1002/Anie.201202064 |
0.393 |
|
| 2012 |
Kravina AG, Mahatthananchai J, Bode JW. Enantioselektive NHC-katalysierte Anellierung von trisubstituierten Enalen und cyclischen N-Sulfonyliminen über α,β-ungesättigte Acylazoliumionen† Angewandte Chemie. 124: 9568-9572. DOI: 10.1002/Ange.201204145 |
0.336 |
|
| 2012 |
Ogunkoya AO, Pattabiraman VR, Bode JW. Sequentielle α-Ketosäurehydroxylamin(KAHA)-Ligationen: Synthese C-terminaler Varianten des Modifikationsproteins UFM1 Angewandte Chemie. 124: 9831-9835. DOI: 10.1002/Ange.201204144 |
0.305 |
|
| 2012 |
Pattabiraman VR, Ogunkoya AO, Bode JW. Titelbild: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. 21/2012) Angewandte Chemie. 124: 5101-5101. DOI: 10.1002/Ange.201202064 |
0.4 |
|
| 2012 |
Mahatthananchai J, Dumas AM, Bode JW. Katalytische selektive Synthese Angewandte Chemie. 124: 11114-11152. DOI: 10.1002/Ange.201201787 |
0.364 |
|
| 2011 |
Pattabiraman VR, Bode JW. Rethinking amide bond synthesis Nature. 480: 471-479. PMID 22193101 DOI: 10.1038/Nature10702 |
0.43 |
|
| 2011 |
Binanzer M, Hsieh SY, Bode JW. Catalytic kinetic resolution of cyclic secondary amines Journal of the American Chemical Society. 133: 19698-19701. PMID 22082205 DOI: 10.1021/Ja209472H |
0.48 |
|
| 2011 |
Wanner B, Mahatthananchai J, Bode JW. Enantioselective synthesis of dihydropyridinones via NHC-Catalyzed Aza-Claisen reaction Organic Letters. 13: 5378-5381. PMID 21905682 DOI: 10.1021/Ol202272T |
0.519 |
|
| 2011 |
He M, Bode JW. Racemization as a stereochemical measure of dynamics and robustness in shape-shifting organic molecules. Proceedings of the National Academy of Sciences of the United States of America. 108: 14752-6. PMID 21873220 DOI: 10.1073/Pnas.1108170108 |
0.469 |
|
| 2011 |
Vo CV, Mitchell TA, Bode JW. Expanded substrate scope and improved reactivity of ether-forming cross-coupling reactions of organotrifluoroborates and acetals. Journal of the American Chemical Society. 133: 14082-9. PMID 21776986 DOI: 10.1021/Ja205174C |
0.447 |
|
| 2011 |
Bode JW. Organic synthesis without stoichiometric reagents: A guiding principle for reaction development Chimia. 65: 150-156. PMID 21528650 DOI: 10.2533/Chimia.2011.150 |
0.45 |
|
| 2011 |
Chiang PC, Bode JW. On the role of CO2 in NHC-catalyzed oxidation of aldehydes Organic Letters. 13: 2422-2425. PMID 21486084 DOI: 10.1021/Ol2006538 |
0.552 |
|
| 2011 |
Mahatthananchai J, Zheng P, Bode JW. α,β-Unsaturated acyl azoliums from N-heterocyclic carbene catalyzed reactions: Observation and mechanistic investigation Angewandte Chemie - International Edition. 50: 1673-1677. PMID 21308930 DOI: 10.1002/Anie.201005352 |
0.446 |
|
| 2011 |
Zheng P, Gondo CA, Bode JW. Late-stage diversification of chiral N-heterocyclic-carbene precatalysts for enantioselective homoenolate additions. Chemistry, An Asian Journal. 6: 614-20. PMID 21254434 DOI: 10.1002/Asia.201000617 |
0.523 |
|
| 2011 |
Wu J, Ruiz-Rodríguez J, Comstock JM, Dong JZ, Bode JW. Synthesis of human GLP-1 (7-36) by chemoselective α-ketoacid- hydroxylamine peptide ligation of unprotected fragments Chemical Science. 2: 1976-1979. DOI: 10.1039/C1Sc00398D |
0.408 |
|
| 2011 |
Struble JR, Bode JW. Synthesis of a N‐Mesityl Substituted Aminoindanol‐Derived Triazolium Salt Organic Syntheses. 362-376. DOI: 10.1002/0471264229.Os087.38 |
0.34 |
|
| 2011 |
Ju L, Bode JW. Amide Formation by Decarboxylative Condensation of Hydroxylamines and α‐Ketoacids: N‐[(1S)‐1 Phenylethyl]‐Benzeneacetamide Organic Syntheses. 87: 218-225. DOI: 10.1002/0471264229.Os087.24 |
0.6 |
|
| 2010 |
Juarez-Garcia ME, Yu S, Bode JW. Asymmetric synthesis of enantiopure isoxazolidinone monomers for the synthesis of β-oligopeptides by chemoselective amide ligation. Tetrahedron. 66: 4841-4853. PMID 21499500 DOI: 10.1016/J.Tet.2010.04.016 |
0.724 |
|
| 2010 |
Ju L, Bode JW, Toma T, Fukuyama T. AMIDE FORMATION BY DECARBOXYLATIVE CONDENSATION OF HYDROXYLAMINES AND α-KETOACIDS: N-[(1S)-1 PHENYLETHYL]-BENZENEACETAMIDE. Organic Syntheses; An Annual Publication of Satisfactory Methods For the Preparation of Organic Chemicals. 87: 218-225. PMID 21188289 |
0.577 |
|
| 2010 |
Kaeobamrung J, Kozlowski MC, Bode JW. Chiral N-heterocyclic carbene-catalyzed generation of ester enolate equivalents from {alpha},{beta}-unsaturated aldehydes for enantioselective Diels-Alder reactions. Proceedings of the National Academy of Sciences of the United States of America. 107: 20661-5. PMID 20974930 DOI: 10.1073/Pnas.1007469107 |
0.814 |
|
| 2010 |
Lippert AR, Naganawa A, Keleshian VL, Bode JW. Synthesis of phototrappable shape-shifting molecules for adaptive guest binding Journal of the American Chemical Society. 132: 15790-15799. PMID 20945902 DOI: 10.1021/Ja107314P |
0.644 |
|
| 2010 |
Medina SI, Wu J, Bode JW. Nitrone protecting groups for enantiopure N-hydroxyamino acids: Synthesis of N-terminal peptide hydroxylamines for chemoselective ligations Organic and Biomolecular Chemistry. 8: 3405-3417. PMID 20567784 DOI: 10.1039/C004490C |
0.58 |
|
| 2010 |
Kaeobamrung J, Mahatthananchai J, Zheng P, Bode JW. An enantioselective claisen rearrangement catalyzed by N-heterocyclic carbenes Journal of the American Chemical Society. 132: 8810-8812. PMID 20550127 DOI: 10.1021/Ja103631U |
0.814 |
|
| 2010 |
Flores MA, Bode JW. Chemoselective protection of alpha-ketoacids by direct annulations with oximes. Organic Letters. 12: 1924-7. PMID 20356071 DOI: 10.1021/Ol100467T |
0.325 |
|
| 2010 |
Narumi T, Bode JW. α,α-dichloroisoxazolidinones for the synthesis and chemoselective peptide ligation of α-peptide α-ketoacids Heterocycles. 82: 1515-1525. DOI: 10.3987/Com-10-S(E)106 |
0.338 |
|
| 2010 |
Bode J, Kaeobamrung J, Mahatthananchai J, Zheng P. N-Heterocyclic Carbene Catalyzed Enantioselective Claisen Rearrangement Synfacts. 2010: 1071-1071. DOI: 10.1055/S-0030-1257962 |
0.796 |
|
| 2010 |
Yu S, Ishida H, Juarez-Garcia ME, Bode JW. Unified synthesis of enantiopure β2h, β3h and β2,3-amino acids Chemical Science. 1: 637-641. DOI: 10.1039/C0Sc00317D |
0.671 |
|
| 2010 |
Juarez-Garcia ME, Yu S, Bode JW. Asymmetric synthesis of enantiopure isoxazolidinone monomers for the synthesis of β3-oligopeptides by chemoselective amide ligation Tetrahedron. 66: 4841-4853. DOI: 10.1016/j.tet.2010.04.016 |
0.663 |
|
| 2010 |
Bode JW, Fraefel N, Muri D, Carreira EM. ChemInform Abstract: A General Solution to the Modular Synthesis of Polyketide Building Blocks by Kanemasa Hydroxy-Directed Nitrile Oxide Cycloadditions. Cheminform. 32: no-no. DOI: 10.1002/chin.200137134 |
0.393 |
|
| 2010 |
Struble JR, Bode JW, Lian Y, Davies HML. Synthesis of A A-mesityl substituted aminoindanol-derived triazolium salt: [(5aS,10bR)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H,6H-indeno[2,1-b]-1,2, 4-triazolo[4,3-d]-1,4-oxazinium chloride] Organic Syntheses. 87: 362-376. |
0.75 |
|
| 2009 |
Struble JR, Bode JW. Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization. Tetrahedron. 65: 4957-4967. PMID 20606761 DOI: 10.1016/J.Tet.2009.03.103 |
0.828 |
|
| 2009 |
Ishida H, Carrillo N, Bode JW. Synthesis of an enantiopure isoxazolidine monomer for β-aspartic acid in chemoselective β-oligopeptide synthesis. Tetrahedron Letters. 50: 3258-3260. PMID 20161312 DOI: 10.1016/J.Tetlet.2009.02.045 |
0.395 |
|
| 2009 |
Mitchell TA, Bode JW. Synthesis of dialkyl ethers from organotrifluoroborates and acetals Journal of the American Chemical Society. 131: 18057-18059. PMID 20000858 DOI: 10.1021/Ja906514S |
0.43 |
|
| 2009 |
Chiang PC, Kim Y, Bode JW. Catalytic amide formation with α′-hydroxyenones as acylating reagents Chemical Communications. 4566-4568. PMID 19617985 DOI: 10.1039/B909360E |
0.657 |
|
| 2009 |
Chiang PC, Rommel M, Bode JW. Alpha'-hydroxyenones as mechanistic probes and scope-expanding surrogates for alpha,beta-unsaturated aldehydes in N-heterocyclic carbene-catalyzed reactions. Journal of the American Chemical Society. 131: 8714-8. PMID 19530737 DOI: 10.1021/Ja902143W |
0.654 |
|
| 2009 |
Ju L, Bode JW. A general strategy for the preparation of C-terminal peptide α-ketoacids by solid phase peptide synthesis Organic and Biomolecular Chemistry. 7: 2259-2264. PMID 19462032 DOI: 10.1039/B901198F |
0.608 |
|
| 2009 |
Valenta P, Drucker NA, Bode JW, Walsh PJ. Simple one-pot conversion of aldehydes and ketones to enals. Organic Letters. 11: 2117-9. PMID 19419211 DOI: 10.1021/Ol9005757 |
0.429 |
|
| 2009 |
Lippert AR, Keleshian VL, Bode JW. Dynamic supramolecular complexation by shapeshifting organic molecules Organic and Biomolecular Chemistry. 7: 1529-1532. PMID 19343237 DOI: 10.1039/B822585K |
0.64 |
|
| 2009 |
Fukuzumi T, Bode JW. A reagent for the convenient, solid-phase synthesis of N-Terminal peptide hydroxylamines for chemoselective ligations Journal of the American Chemical Society. 131: 3864-3865. PMID 19256487 DOI: 10.1021/Ja900601C |
0.457 |
|
| 2009 |
Kaeobamrung J, Bode JW. Stereodivergency of triazolium and imidazolium-derived NHcs for catalytic, enantioselective cyclopentane synthesis Organic Letters. 11: 677-680. PMID 19175349 DOI: 10.1021/Ol802739D |
0.797 |
|
| 2009 |
Chiang P-, Kim Y, Bode JW. NHC-Catalyzed Redox Amidation of α-Hydroxyenones Synfacts. 2009: 1042-1042. DOI: 10.1055/S-0029-1217782 |
0.385 |
|
| 2009 |
Rommel M, Fukuzumi T, Bode JW. NHC-Catalyzed Annulation of Enals to Cyclic Ketimines Synfacts. 2009: 216-216. DOI: 10.1055/S-0028-1087585 |
0.483 |
|
| 2009 |
Chiang PC, Rommel M, Bode JW. α′-Hydroxyenones as mechanistic probes and scope-expanding surrogates for α,β-unsaturated aldehydes in N-heterocyclic carbene-catalyzed reactions Journal of the American Chemical Society. 131: 8714-8718. DOI: 10.1021/ja902143w |
0.628 |
|
| 2009 |
Struble JR, Bode JW. Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization Tetrahedron. 65: 4957-4967. DOI: 10.1016/j.tet.2009.03.103 |
0.828 |
|
| 2008 |
Rommel M, Fukuzumi T, Bode JW. Cyclic ketimines as superior electrophiles for NHC-catalyzed homoenolate additions with broad ScoDe and low catalvst loadinas Journal of the American Chemical Society. 130: 17266-17267. PMID 19053399 DOI: 10.1021/Ja807937M |
0.479 |
|
| 2008 |
He M, Beahm BJ, Bode JW. Chiral NHC-catalyzed oxodiene Diels-Alder reactions with α-chloroaldehyde bisulfite salts Organic Letters. 10: 3817-3820. PMID 18656948 DOI: 10.1021/Ol801502H |
0.601 |
|
| 2008 |
Ju L, Lippert AR, Bode JW. Stereoretentive synthesis and chemoselective amide-forming ligations of C-terminal peptide α-ketoacids Journal of the American Chemical Society. 130: 4253-4255. PMID 18335941 DOI: 10.1021/Ja800053T |
0.757 |
|
| 2008 |
Struble JR, Kaeobamrung J, Bode JW. Synthesis of an N-mesityl substituted chiral imidazolium salt for NHC-catalyzed reactions. Organic Letters. 10: 957-60. PMID 18266380 DOI: 10.1021/Ol800006M |
0.831 |
|
| 2008 |
He M, Bode JW. Enantioselective, NHC-catalyzed bicyclo-β-lactam formation via direct annulations of enals and unsaturated N-sulfonyl ketimines Journal of the American Chemical Society. 130: 418-419. PMID 18092785 DOI: 10.1021/Ja0778592 |
0.578 |
|
| 2008 |
Struble JR, Kaeobamrung J, Bode JW. A New Chiral Carbene Catalyst Synfacts. 2008: 645-645. DOI: 10.1055/S-2007-1072755 |
0.334 |
|
| 2008 |
Struble JR, Kaeobamrung J, Bode JW. Synthesis of an n-mesityl substituted chiral imidazolium salt for NHC-catalyzed reactions Organic Letters. 10: 957-960. DOI: 10.1021/ol800006m |
0.832 |
|
| 2008 |
Struble JR, Bode JW. A modular synthesis of chiral aminoindanol-derived imidazolium salts Tetrahedron. 64: 6961-6972. DOI: 10.1016/J.Tet.2008.03.072 |
0.829 |
|
| 2007 |
Bode JW, Sohn SS. N-heterocyclic carbene-catalyzed redox amidations of α-functionalized aldehydes with amines Journal of the American Chemical Society. 129: 13798-13799. PMID 17956104 DOI: 10.1021/Ja0768136 |
0.793 |
|
| 2007 |
Suzuki K, Takikawa H, Hachisu Y, Bode JW. Isoxazole-directed pinacol rearrangement: Stereocontrolled approach to angular stereogenic centers Angewandte Chemie - International Edition. 46: 3252-3254. PMID 17385784 DOI: 10.1002/Anie.200605138 |
0.433 |
|
| 2007 |
Chiang PC, Kaeobamrung J, Bode JW. Enantioselective, cyclopentene-forming annulations via NHC-catalyzed benzoin-oxy-Cope reactions Journal of the American Chemical Society. 129: 3520-3521. PMID 17335218 DOI: 10.1021/Ja0705543 |
0.832 |
|
| 2007 |
Bode J, He M, Uc G. Chiral N-Heterocyclic Carbene Catalyzed Oxodiene Diels-Alder Reactions Synfacts. 2007: 0100-0100. DOI: 10.1055/S-2006-955663 |
0.492 |
|
| 2006 |
He M, Uc GJ, Bode JW. Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene diels-alder reactions with low catalyst loadings Journal of the American Chemical Society. 128: 15088-15089. PMID 17117850 DOI: 10.1021/Ja066380R |
0.615 |
|
| 2006 |
Lippert AR, Kaeobamrung J, Bode JW. Synthesis of oligosubstituted bullvalones: shapeshifting molecules under basic conditions. Journal of the American Chemical Society. 128: 14738-9. PMID 17105247 DOI: 10.1021/Ja063900+ |
0.792 |
|
| 2006 |
Sohn SS, Bode JW. N-heterocyclic carbene catalyzed C-C bond cleavage in redox esterifications of chiral formylcyclopropanes Angewandte Chemie - International Edition. 45: 6021-6024. PMID 16871609 DOI: 10.1002/Anie.200601919 |
0.719 |
|
| 2006 |
He M, Struble JR, Bode JW. Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes. Journal of the American Chemical Society. 128: 8418-20. PMID 16802805 DOI: 10.1021/Ja062707C |
0.835 |
|
| 2006 |
Takikawa H, Hachisu Y, Bode JW, Suzuki K. Catalytic enantioselective crossed aldehyde-ketone benzoin cyclization. Angewandte Chemie (International Ed. in English). 45: 3492-4. PMID 16637094 DOI: 10.1002/Anie.200600268 |
0.56 |
|
| 2006 |
Carrillo N, Davalos EA, Russak JA, Bode JW. Iterative, aqueous synthesis of beta3-oligopeptides without coupling reagents. Journal of the American Chemical Society. 128: 1452-3. PMID 16448107 DOI: 10.1021/Ja057706J |
0.793 |
|
| 2006 |
Bode JW, Fox RM, Baucom KD. Chemoselective amide ligations by decarboxylative condensations of N-alkylhydroxylamines and alpha-ketoacids. Angewandte Chemie (International Ed. in English). 45: 1248-52. PMID 16416482 DOI: 10.1002/Anie.200503991 |
0.328 |
|
| 2006 |
Bode J, He M, Struble J. NHC-Catalyzed Azadiene Diels-Alder Reaction Synfacts. 2006: 0840-0840. DOI: 10.1055/s-2006-942031 |
0.797 |
|
| 2006 |
Suzuki K, Takikawa H, Hachisu Y, Bode J. Asymmetric Intramolecular Crossed Aldehyde-Ketone Benzoin Cyclization Synfacts. 2006: 0725-0725. DOI: 10.1055/S-2006-941910 |
0.553 |
|
| 2006 |
Lippert AR, Kaeobamrung J, Bode JW. Synthesis of oligosubstituted bullvalones: Shapeshifting molecules under basic conditions Journal of the American Chemical Society. 128: 14738-14739. DOI: 10.1021/ja063900+ |
0.785 |
|
| 2005 |
Sohn SS, Bode JW. Catalytic generation of activated carboxylates from enals: a product-determining role for the base. Organic Letters. 7: 3873-6. PMID 16119920 DOI: 10.1021/Ol051269W |
0.729 |
|
| 2005 |
He M, Bode JW. Catalytic Synthesis of gamma-Lactams via direct annulations of enals and N-sulfonylimines. Organic Letters. 7: 3131-4. PMID 15987223 DOI: 10.1021/Ol051234W |
0.591 |
|
| 2004 |
Sohn SS, Rosen EL, Bode JW. N-heterocyclic carbene-catalyzed generation of homoenolates: gamma-butyrolactones by direct annulations of enals and aldehydes. Journal of the American Chemical Society. 126: 14370-1. PMID 15521753 DOI: 10.1021/Ja044714B |
0.77 |
|
| 2004 |
Chow KY, Bode JW. Catalytic generation of activated carboxylates: direct, stereoselective synthesis of beta-hydroxyesters from epoxyaldehydes. Journal of the American Chemical Society. 126: 8126-7. PMID 15225048 DOI: 10.1021/Ja047407E |
0.466 |
|
| 2004 |
Hachisu Y, Bode JW, Suzuki K. Thiazolium ylide-catalyzed intramolecular aldehyde-ketone benzoin-forming reactions: Substrate scope Advanced Synthesis and Catalysis. 346: 1097-1100. DOI: 10.1002/Adsc.200404092 |
0.576 |
|
| 2003 |
Hachisu Y, Bode JW, Suzuki K. Catalytic intramolecular crossed aldehyde--ketone benzoin reactions: a novel synthesis of functionalized preanthraquinones. Journal of the American Chemical Society. 125: 8432-3. PMID 12848538 DOI: 10.1021/Ja035308F |
0.592 |
|
| 2003 |
Bode JW, Uesuka H, Suzuki K. Isoxazole --> benzisoxazole rearrangement promoted cascade reactions affording stereodefined polycycles. Organic Letters. 5: 395-8. PMID 12583727 DOI: 10.1021/Ol0272848 |
0.563 |
|
| 2003 |
Bode JW, Hachisu Y, Matsuura T, Suzuki K. Facile construction and divergent transformation of polycyclic isoxazoles: direct access to polyketide architectures. Organic Letters. 5: 391-4. PMID 12583726 DOI: 10.1021/Ol027283F |
0.579 |
|
| 2003 |
Matsuura T, Bode JW, Hachisu Y, Suzuki K. Molecular sieve (MS 4A) promoted cyclocondensation of hindered, aromatic nitrile oxides and cyclic diketones under mild conditions Synlett. 1746-1748. DOI: 10.1055/S-2003-41436 |
0.417 |
|
| 2003 |
Bode JW, Suzuki K. Corrigendum to: “Structural incongruities of coleophomone natural products: insights by total synthesis of a semi-synthetic derivative” Tetrahedron Letters. 44: 5557. DOI: 10.1016/S0040-4039(03)01283-8 |
0.512 |
|
| 2003 |
Bode JW, Suzuki K. Structural incongruities of coleophomone natural products: Insights by total synthesis of a semi-synthetic derivative Tetrahedron Letters. 44: 3559-3563. DOI: 10.1016/S0040-4039(03)00615-4 |
0.481 |
|
| 2003 |
Bode JW, Hachisu Y, Matsuura T, Suzuki K. Amine-promoted cyclocondensation of highly substituted aromatic nitrile oxides with diketones Tetrahedron Letters. 44: 3555-3558. DOI: 10.1016/S0040-4039(03)00614-2 |
0.576 |
|
| 2001 |
Bode JW, Fraefel N, Muri D, Carreira EM. A General Solution to the Modular Synthesis of Polyketide Building Blocks by Kanemasa Hydroxy-Directed Nitrile Oxide Cycloadditions. Angewandte Chemie (International Ed. in English). 40: 2082-2085. PMID 29712193 DOI: 10.1002/1521-3773(20010601)40:11<2082::Aid-Anie2082>3.0.Co;2-1 |
0.536 |
|
| 2001 |
Bode JW, Carreira EM. Stereoselective syntheses of epothilones A and B via nitrile oxide cycloadditions and related studies. The Journal of Organic Chemistry. 66: 6410-24. PMID 11559194 DOI: 10.1021/Jo015791H |
0.466 |
|
| 2001 |
Bode JW, Carreira EM. Stereoselective syntheses of epothilones A and B via directed nitrile oxide cycloaddition. Journal of the American Chemical Society. 123: 3611-2. PMID 11472140 DOI: 10.1021/Ja0155635 |
0.431 |
|
| 2001 |
Bode JW, Fraefel N, Muri D, Carreira EM. A General Solution to the Modular Synthesis of Polyketide Building Blocks by Kanemasa Hydroxy-Directed Nitrile Oxide Cycloadditions This work was supported by the ETH-Zürich, Hoffmann-LaRoche, Merck, and Novartis. J.W.B. thanks the National Science Foundation (USA) for a predoctoral fellowship. We are grateful to Boehringer-Ingelheim for a generous gift of (R)-3-buten-2-ol. Angewandte Chemie (International Ed. in English). 40: 2082-2085. PMID 11433450 DOI: 10.1002/1521-3773(20010601)40:11<2082::AID-ANIE2082>3.0.CO;2-1 |
0.345 |
|
| 2001 |
Bode JW, Carreira EM. A mild and chemoselective method for the reduction of conjugated isoxazolines to beta-hydroxy ketones. Organic Letters. 3: 1587-90. PMID 11388873 DOI: 10.1021/Ol015885D |
0.462 |
|
| 2001 |
Bode JW, Gauthier J, Carreira EM. Facile enantioselective synthesis of a key homoallylic alcohol building block for polyketide synthesis: TiF4-BINOL catalyzed allylsilylation with allyl trimethylsilane Chemical Communications. 2560-2561. DOI: 10.1039/B107995F |
0.578 |
|
| 2001 |
Bode JW, Fraefel N, Muri D, Carreira EM. Ein allgemeiner Ansatz für die modulare Synthese von Polyketid-Bausteinen durch die Hydroxy-gesteuerte Nitriloxid-Cycloaddition nach Kanemasa Angewandte Chemie. 113: 2128-2131. DOI: 10.1002/1521-3757(20010601)113:11<2128::Aid-Ange2128>3.0.Co;2-K |
0.507 |
|
| 2000 |
Muri D, Bode JW, Carreira EM. A novel, general method for the synthesis of nitrile oxides: dehydration of O-silylated hydroxamic acids Organic Letters. 2: 539-41. PMID 10814371 DOI: 10.1021/Ol991396Q |
0.405 |
|
| 1996 |
Bode JW, Doyle MP, Protopopova MN, Zhou QL. Intramolecular regioselective insertion into unactivated prochiral carbon-hydrogen bonds with diazoacetates of primary alcohols catalyzed by chiral dirhodium(II) carboxamidates. Highly enantioselective total synthesis of natural lignan lactones Journal of Organic Chemistry. 61: 9146-9155. DOI: 10.1021/Jo961607U |
0.567 |
|
| 1995 |
Doyle MP, Protopopova MN, Zhou QL, Bode JW, Simonsen SH, Lynch V. Optimization of enantiocontrol for carbon-hydrogen insertion with chiral dirhodium(II) carboxamidates. Synthesis of natural dibenzylbutyrolactone lignans from 3-aryl-1-propyl diazoacetates in high optical purity Journal of Organic Chemistry. 60: 6654-6655. DOI: 10.1021/Jo00126A002 |
0.47 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2014 |
Huang YL, Bode JW. Synthetic fermentation of bioactive non-ribosomal peptides without organisms, enzymes or reagents. Nature Chemistry. 6: 877-84. PMID 25242482 DOI: 10.1038/Nchem.2048 |
0.299 |
|
| 2016 |
Hofmann R, Bode JW. A radical approach to posttranslational mutagenesis. Science (New York, N.Y.). 354: 553-554. PMID 27811256 DOI: 10.1126/Science.Aai8788 |
0.295 |
|
| 2015 |
Mazunin D, Broguiere N, Zenobi-Wong M, Bode JW. Synthesis of Biocompatible PEG Hydrogels by pH-Sensitive Potassium Acyltrifluoroborate (KAT) Amide Ligations Acs Biomaterials Science & Engineering. 1: 456-462. DOI: 10.1021/Acsbiomaterials.5B00145 |
0.291 |
|
| 2006 |
Bode JW. Emerging methods in amide- and peptide-bond formation Current Opinion in Drug Discovery and Development. 9: 765-775. PMID 17117685 |
0.291 |
|
| 2016 |
Wucherpfennig TG, Müller S, Wolfrum C, Bode JW. Chemical Synthesis of the 12 kDa Human Myokine Irisin by α‐Ketoacid‐Hydroxylamine (KAHA) Ligation Helvetica Chimica Acta. 99: 897-907. DOI: 10.1002/Hlca.201600160 |
0.289 |
|
| 2020 |
Schauenburg D, Divandari M, Neumann K, Spiegel CA, Hackett T, Dzeng YC, Spencer ND, Bode JW. Synthesis of polymers containing potassium acyltrifluoroborates (KATs) and post-polymerization ligation and conjugation. Angewandte Chemie (International Ed. in English). PMID 32378308 DOI: 10.1002/Anie.202006273 |
0.286 |
|
| 2020 |
Hofmann R, Akimoto G, Wucherpfennig TG, Zeymer C, Bode JW. Lysine acylation using conjugating enzymes for site-specific modification and ubiquitination of recombinant proteins. Nature Chemistry. PMID 32929246 DOI: 10.1038/S41557-020-0528-Y |
0.286 |
|
| 2013 |
Mahatthananchai J, Bode JW. Enantioselective Annulations with Chiral N-Mesityl N-Heterocyclic Carbenes Asymmetric Synthesis Ii: More Methods and Applications. 67-77. DOI: 10.1002/9783527652235.ch10 |
0.283 |
|
| 2021 |
Jiang T, Bordi S, McMillan AE, Chen KY, Saito F, Nichols PL, Wanner BM, Bode JW. An integrated console for capsule-based, automated organic synthesis. Chemical Science. 12: 6977-6982. PMID 34123325 DOI: 10.1039/d1sc01048d |
0.28 |
|
| 2018 |
Stepek IA, Bode JW. Synthetic fermentation of bioactive molecules. Current Opinion in Chemical Biology. 46: 18-24. PMID 29627458 DOI: 10.1016/J.Cbpa.2018.03.014 |
0.28 |
|
| 2021 |
Tung P, Schuhmacher A, Schilling PE, Bode JW, Mankad N. Preparation of Potassium Acyltrifluoroborates (KATs) from Carboxylic Acids by Copper-Catalyzed Borylation of Mixed Anhydrides. Angewandte Chemie (International Ed. in English). PMID 34913236 DOI: 10.1002/anie.202114513 |
0.278 |
|
| 2011 |
Zheng P, Gondo CA, Bode JW. Late-stage diversification of chiral N-heterocyclic-carbene precatalysts for enantioselective homoenolate additions Chemistry - An Asian Journal. 6: 614-620. DOI: 10.1002/asia.201000617 |
0.278 |
|
| 2016 |
Saito F, Bode JW. Macrocyclic peptides: Tying up loose ends. Nature Chemistry. 8: 1085-1086. PMID 27874868 DOI: 10.1038/Nchem.2683 |
0.274 |
|
| 2023 |
Coin G, Jiang T, Bordi S, Nichols PL, Bode JW, Wanner BM. Automated, Capsule-Based Suzuki-Miyaura Cross Couplings. Organic Letters. PMID 37126221 DOI: 10.1021/acs.orglett.3c01057 |
0.274 |
|
| 2022 |
Škopić MK, Losch F, McMillan AE, Willeke N, Malenica M, Bering L, Bode J, Brunschweiger A. Reagent-Based Scaffold Diversity for DNA-Encoded Library Design: Solid Phase Synthesis of DNA-Tagged sp-Rich Heterocycles by SnAP Chemistry. Organic Letters. PMID 35113572 DOI: 10.1021/acs.orglett.2c00228 |
0.273 |
|
| 2012 |
Lyngvi E, Bode JW, Schoenebeck F. A computational study of the origin of stereoinduction in NHC-catalyzed annulation reactions of α,β-unsaturated acyl azoliums Chemical Science. 3: 2346-2350. DOI: 10.1039/c2sc20331f |
0.273 |
|
| 2012 |
Schäfer G, Matthey C, Bode JW. Eine einfache Synthese von sterisch gehinderten und elektronenarmen, sekundären Amiden aus Isocyanaten Angewandte Chemie. 124: 9307-9310. DOI: 10.1002/Ange.201204481 |
0.269 |
|
| 2020 |
Broguiere N, Lüchtefeld I, Trachsel L, Mazunin D, Rizzo R, Bode JW, Lutolf MP, Zenobi-Wong M. Morphogenesis Guided by 3D Patterning of Growth Factors in Biological Matrices. Advanced Materials (Deerfield Beach, Fla.). e1908299. PMID 32390195 DOI: 10.1002/Adma.201908299 |
0.267 |
|
| 2011 |
Schäfer G, Bode JW. Friedel-Crafts benzylation of activated and deactivated arenes. Angewandte Chemie (International Ed. in English). 50: 10913-6. PMID 21954140 DOI: 10.1002/Anie.201105380 |
0.264 |
|
| 2009 |
Ishida H, Carrillo N, Bode JW. Synthesis of an enantiopure isoxazolidine monomer for β3-aspartic acid in chemoselective β-oligopeptide synthesis Tetrahedron Letters. 50: 3258-3260. DOI: 10.1016/j.tetlet.2009.02.045 |
0.262 |
|
| 2010 |
Ju L, Bode JW, Toma T, Fukuyama T. Amide formation by decarboxylative condensation of hydroxylamines and α-ketoacids: N-[(1.S)-1 phenylethyl]-benzeneacetamide Organic Syntheses. 87: 218-225. |
0.261 |
|
| 2021 |
Müller M, Gräbnitz F, Barandun N, Shen Y, Wendt F, Steiner SN, Severin Y, Vetterli SU, Mondal M, Prudent JR, Hofmann R, van Oostrum M, Sarott RC, Nesvizhskii AI, Carreira EM, ... Bode JW, et al. Light-mediated discovery of surfaceome nanoscale organization and intercellular receptor interaction networks. Nature Communications. 12: 7036. PMID 34857745 DOI: 10.1038/s41467-021-27280-x |
0.254 |
|
| 2019 |
Chiotellis A, Ahmed H, Betzel T, Tanriver M, White CJ, Song H, Da Ros S, Schibli R, Bode JW, Ametamey SM. Chemoselective F-incorporation into pyridyl acyltrifluoroborates for rapid radiolabelling of peptides and proteins at room temperature. Chemical Communications (Cambridge, England). PMID 31840690 DOI: 10.1039/C9Cc08645E |
0.249 |
|
| 2018 |
Gu Y, Schauenburg D, Bode JW, Johnson JA. Leaving Groups as Traceless Topological Modifiers for the Synthesis of Topologically Isomeric Polymer Networks. Journal of the American Chemical Society. PMID 30335993 DOI: 10.1021/Jacs.8B07967 |
0.24 |
|
| 2015 |
Rohrbacher F, Wucherpfennig TG, Bode JW. Chemical protein synthesis with the KAHA ligation Topics in Current Chemistry. 363. DOI: 10.1007/128_2014_597 |
0.235 |
|
| 2018 |
Boross GN, Schauenburg D, Bode JW. Chemoselective Derivatization of Folded Synthetic Insulin Variants with Potassium Acyltrifluoroborates (KATs) Helvetica Chimica Acta. 102. DOI: 10.1002/Hlca.201800214 |
0.224 |
|
| 2023 |
Neumann K, Vujinovic A, Kamara S, Zwicky A, Baldauf S, Bode JW. Synthesis of multi-module low density lipoprotein receptor class A domains with acid labile cyanopyridiniumylides (CyPY) as aspartic acid masking groups. Rsc Chemical Biology. 4: 292-299. PMID 37034404 DOI: 10.1039/d2cb00234e |
0.223 |
|
| 2022 |
Tolmachova KA, Farnung J, Liang JR, Corn JE, Bode JW. Facile Preparation of UFMylation Activity-Based Probes by Chemoselective Installation of Electrophiles at the C-Terminus of Recombinant UFM1. Acs Central Science. 8: 756-762. PMID 35756382 DOI: 10.1021/acscentsci.2c00203 |
0.221 |
|
| 2015 |
Luescher MU, Nichols PL, Bode JW, Geoghegan K. Access saturated N-heterocycles in a SnAP Aldrichimica Acta. 48: 42. |
0.216 |
|
| 2016 |
Kreituss I, Chen K, Eitel SH, Adam J, Wuitschik G, Fettes A, Bode JW. Ein robustes und wiedergewinnbares Polymer für die Dekagramm‐Racematspaltung von (±)‐Mefloquin und anderen, chiralen N‐Heterocyclen Angewandte Chemie. 128: 1579-1582. DOI: 10.1002/Ange.201509256 |
0.214 |
|
| 2010 |
Chiang PC, Bode JW. Chapter 14: N-heterocyclic carbenes as organic catalysts Rsc Catalysis Series. 399-435. |
0.213 |
|
| 2011 |
Hackenberger CPR, Bode JW, Schwarzer D. Chemoselective Peptide Ligation: A Privileged Tool for Protein Synthesis Amino Acids, Peptides and Proteins in Organic Chemistry. 3: 445-493. DOI: 10.1002/9783527631803.ch13 |
0.21 |
|
| 2019 |
Stepek IA, Hofmann R, Nichols PL, Aschwanden A, Eckard C, Aschwanden P, Bode JW. Make a Molecule: A Synthetic Organic and Medicinal Chemistry Workshop Program for High School Students Journal of Chemical Education. 97: 402-413. DOI: 10.1021/Acs.Jchemed.9B00812 |
0.202 |
|
| 2021 |
Matabaro E, Kaspar H, Dahlin P, Bader DLV, Murar CE, Staubli F, Field CM, Bode JW, Künzler M. Identification, heterologous production and bioactivity of lentinulin A and dendrothelin A, two natural variants of backbone N-methylated peptide macrocycle omphalotin A. Scientific Reports. 11: 3541. PMID 33574430 DOI: 10.1038/s41598-021-83106-2 |
0.202 |
|
| 2022 |
Farnung J, Tolmachova KA, Bode JW. Installation of electrophiles onto the C-terminus of recombinant ubiquitin and ubiquitin-like proteins. Chemical Science. 14: 121-129. PMID 36605735 DOI: 10.1039/d2sc04279g |
0.199 |
|
| 2017 |
Harmand TJ, Pattabiraman VR, Bode JW. Chemical Synthesis of the Highly Hydrophobic Antiviral Membrane-Associated Protein IFITM3 and Modified Variants. Angewandte Chemie (Weinheim An Der Bergstrasse, Germany). 129: 12813-12817. PMID 32313320 DOI: 10.1002/ange.201707554 |
0.19 |
|
| 2004 |
Bode JW. Reactor ChemAxon Ltd., Maramaros koz 2/a, Budapest, 1037 Hungary. www.chemaxon.com. Contact ChemAxon for pricing information. Journal of the American Chemical Society. 126: 15317-15317. DOI: 10.1021/Ja040968L |
0.188 |
|
| 2022 |
McMillan AE, Wu WWX, Nichols PL, Wanner BM, Bode JW. A vending machine for drug-like molecules - automated synthesis of virtual screening hits. Chemical Science. 13: 14292-14299. PMID 36545137 DOI: 10.1039/d2sc05182f |
0.183 |
|
| 2021 |
Matabaro E, Kaspar H, Dahlin P, Bader DLV, Murar CE, Staubli F, Field CM, Bode JW, Künzler M. Author Correction: Identifcation, heterologous production and bioactivity of lentinulin A and dendrothelin A, two natural variants of backbone N-methylated peptide macrocycle omphalotin A. Scientific Reports. 11: 12656. PMID 34112888 DOI: 10.1038/s41598-021-91767-2 |
0.183 |
|
| 2020 |
Broguiere N, Lüchtefeld I, Trachsel L, Mazunin D, Rizzo R, Bode JW, Lutolf MP, Zenobi‐Wong M. Tissue Engineering: Morphogenesis Guided by 3D Patterning of Growth Factors in Biological Matrices (Adv. Mater. 25/2020) Advanced Materials. 32: 2070193. DOI: 10.1002/Adma.202070193 |
0.18 |
|
| 2022 |
Matabaro E, Kaspar H, Dahlin P, Bader DLV, Murar CE, Staubli F, Field CM, Bode JW, Künzler M. Author Correction: Identification, heterologous production and bioactivity of lentinulin A and dendrothelin A, two natural variants of backbone N-methylated peptide macrocycle omphalotin A. Scientific Reports. 12: 17021. PMID 36220874 DOI: 10.1038/s41598-022-21642-1 |
0.179 |
|
| 2012 |
Kreituss I, Murakami Y, Binanzer M, Bode JW. Kinetische Racematspaltung von Stickstoffheterocyclen durch ein wiederverwendbares polymergebundenes Reagens Angewandte Chemie. 124: 10815-10819. DOI: 10.1002/Ange.201204991 |
0.178 |
|
| 2023 |
Mikami T, Majima S, Song H, Bode JW. Biocompatible Lysine Protecting Groups for the Chemoenzymatic Synthesis of K48/K63 Heterotypic and Branched Ubiquitin Chains. Acs Central Science. 9: 1633-1641. PMID 37637747 DOI: 10.1021/acscentsci.3c00389 |
0.178 |
|
| 2014 |
Murar CE, Thuaud F, Bode JW. KAHA ligations that form aspartyl aldehyde residues as synthetic handles for protein modification and purification Journal of the American Chemical Society. 136: 18140-18148. DOI: 10.1021/ja511231f |
0.177 |
|
| 2022 |
Levasseur MD, Hofmann R, Edwardson T, Hehn S, Thanaburakorn M, Bode J, Hilvert D. Post-assembly modification of protein cages by Ubc9-mediated lysine acylation. Chembiochem : a European Journal of Chemical Biology. PMID 35951442 DOI: 10.1002/cbic.202200332 |
0.162 |
|
| 2015 |
Mazunin D, Broguiere N, Zenobi-Wong M, Bode JW. Synthesis of Biocompatible PEG Hydrogels by pH-Sensitive Potassium Acyltrifluoroborate (KAT) Amide Ligations. Acs Biomaterials Science & Engineering. 1: 456-462. PMID 33445248 DOI: 10.1021/acsbiomaterials.5b00145 |
0.152 |
|
| 2023 |
Farnung J, Muhar M, Liang JR, Tolmachova KA, Benoit RM, Corn JE, Bode JW. Semisynthetic LC3 Probes for Autophagy Pathways Reveal a Noncanonical LC3 Interacting Region Motif Crucial for the Enzymatic Activity of Human ATG3. Acs Central Science. 9: 1025-1034. PMID 37252361 DOI: 10.1021/acscentsci.3c00009 |
0.149 |
|
| 2016 |
Bode J, Copéret C. 100th Anniversary of Helvetica Helvetica Chimica Acta. 99: 819-819. DOI: 10.1002/Hlca.201670073 |
0.149 |
|
| 2021 |
Tanriver M, Dzeng YC, Da Ros S, Lam E, Bode JW. Mechanism-Based Design of Quinoline Potassium Acyltrifluoroborates for Rapid Amide-Forming Ligations at Physiological pH. Journal of the American Chemical Society. PMID 34647724 DOI: 10.1021/jacs.1c07354 |
0.132 |
|
| 2015 |
Rohrbacher F, Deniau G, Luther A, Bode JW. Spontaneous head-to-tail cyclization of unprotected linear peptides with the KAHA ligation Chemical Science. 6: 4889-4896. DOI: 10.1039/c5sc01774b |
0.126 |
|
| 2024 |
Gazzi T, Heinke M, Landolt F, Bode JW. Chemical Synthesis of Secretoglobin 3A2 Covalent Homodimer and Photocaged Monomeric Variants. Angewandte Chemie (International Ed. in English). e202404992. PMID 38635000 DOI: 10.1002/anie.202404992 |
0.12 |
|
| 2022 |
Akimoto G, Fernandes AP, Bode JW. Site-Specific Protein Ubiquitylation Using an Engineered, Chimeric E1 Activating Enzyme and E2 SUMO Conjugating Enzyme Ubc9. Acs Central Science. 8: 275-281. PMID 35237717 DOI: 10.1021/acscentsci.1c01490 |
0.117 |
|
| 2012 |
Kreituss I, Murakami Y, Binanzer M, Bode JW. Kinetic resolution of nitrogen heterocycles with a reusable polymer-supported reagent Angewandte Chemie - International Edition. 51: 10660-10663. DOI: 10.1002/anie.201204991 |
0.116 |
|
| 2024 |
Tanriver M, Müller M, Levasseur MD, Richards D, Majima S, DeMello A, Yamauchi Y, Bode JW. Peptide-Directed Attachment of Hydroxylamines to Specific Lysines of IgG Antibodies for Bioconjugations with Acylboronates. Angewandte Chemie (International Ed. in English). e202401080. PMID 38421342 DOI: 10.1002/anie.202401080 |
0.11 |
|
| 2013 |
Bode JW. Reinventing amide bond formation Topics in Organometallic Chemistry. 44: 13-34. DOI: 10.1007/3418-2012-41 |
0.108 |
|
| 2021 |
Bhatt PR, Scaiola A, Loughran G, Leibundgut M, Kratzel A, Meurs R, Dreos R, O'Connor KM, McMillan A, Bode JW, Thiel V, Gatfield D, Atkins JF, Ban N. Structural basis of ribosomal frameshifting during translation of the SARS-CoV-2 RNA genome. Science (New York, N.Y.). PMID 34029205 DOI: 10.1126/science.abf3546 |
0.083 |
|
| 2008 |
Ahn JM, Bode JW. A bright future for peptide science!! Biopolymers - Peptide Science Section. 90: 480. PMID 18561308 DOI: 10.1002/bip.21027 |
0.078 |
|
| 2013 |
Bode J, Wennemers H. Peptide science in Switzerland - a revival. Chimia. 67: 841. PMID 24594323 |
0.077 |
|
| 2020 |
Weidner P, Söhn M, Schroeder T, Helm L, Hauber V, Gutting T, Betge J, Röcken C, Rohrbacher FN, Pattabiraman VR, Bode JW, Seger R, Saar D, Nunes-Alves A, Wade RC, et al. Myotubularin-related protein 7 activates peroxisome proliferator-activated receptor-gamma. Oncogenesis. 9: 59. PMID 32522977 DOI: 10.1038/s41389-020-0238-8 |
0.074 |
|
| 2011 |
He M, Bode JW. Racemization as a stereochemical measure of dynamics and robustness in shape-shifting organic molecules Proceedings of the National Academy of Sciences of the United States of America. 108: 14752-14756. DOI: 10.1073/pnas.1108170108 |
0.074 |
|
| 2022 |
Nakamuro T, Kamei K, Sun K, Bode JW, Harano K, Nakamura E. Time-Resolved Atomistic Imaging and Statistical Analysis of Daptomycin Oligomers with and without Calcium Ions. Journal of the American Chemical Society. 144: 13612-13622. PMID 35857028 DOI: 10.1021/jacs.2c03949 |
0.073 |
|
| 2023 |
Beyer D, Vaccarin C, Deupi X, Mapanao AK, Cohrs S, Sozzi-Guo F, Grundler PV, van der Meulen NP, Wang J, Tanriver M, Bode JW, Schibli R, Müller C. A tool for nuclear imaging of the SARS-CoV-2 entry receptor: molecular model and preclinical development of ACE2-selective radiopeptides. Ejnmmi Research. 13: 32. PMID 37074529 DOI: 10.1186/s13550-023-00979-2 |
0.042 |
|
| 1998 |
Phylipsen GJM, Bode JW, Blok K, Merkus H, Metz B. A Triptych sectoral approach to burden differentiation; GHG emissions in the European bubble Energy Policy. 26: 929-943. DOI: 10.1016/S0301-4215(98)00036-6 |
0.034 |
|
| 2002 |
Phylipsen GJM(, Blok K, Bode JW. Industrial energy efficiency in the climate change debate: comparing the US and major developing countries Energy For Sustainable Development. 6: 30-44. DOI: 10.1016/S0973-0826(08)60445-7 |
0.034 |
|
| 2024 |
Weidner P, Saar D, Söhn M, Schroeder T, Yu Y, Zöllner FG, Ponelies N, Zhou X, Zwicky A, Rohrbacher FN, Pattabiraman VR, Tanriver M, Bauer A, Ahmed H, Ametamey SM, ... ... Bode JW, et al. Myotubularin-related-protein-7 inhibits mutant (G12V) K-RAS by direct interaction. Cancer Letters. 216783. PMID 38462034 DOI: 10.1016/j.canlet.2024.216783 |
0.03 |
|
| 2015 |
Bode J, Davey S. Public libraries. Nature Chemistry. 6: 846-7. PMID 25242469 DOI: 10.1038/nchem.2070 |
0.022 |
|
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