| Year |
Citation |
Score |
| 2022 |
Liu R, Marshall K, Ma R, Lien Thi Pham K, Shetye G, Liu Z, Cho S, Jeong H, Franzblau SG, Moraski GC, Miller MJ. Syntheses and studies of deuterated Imdiazo[1,2-a]pyridine-3-carboxamides with potent anti-tuberculosis activity and improved metabolic properties. Bioorganic Chemistry. 128: 106074. PMID 35987188 DOI: 10.1016/j.bioorg.2022.106074 |
0.695 |
|
| 2021 |
Hopfner SM, Lee BS, Kalia NP, Miller MJ, Pethe K, Moraski GC. Syntheses and Structure-Activity Relationships of -Phenethyl-Quinazolin-4-yl-Amines as Potent Inhibitors of Cytochrome Oxidase in . Applied Sciences (Basel, Switzerland). 11. PMID 36698770 DOI: 10.3390/app11199092 |
0.704 |
|
| 2021 |
Hopfner SM, Lee BS, Kalia NP, Miller MJ, Pethe K, Moraski GC. Structure guided generation of thieno[3,2-]pyrimidin-4-amine oxidase inhibitors. Rsc Medicinal Chemistry. 12: 73-77. PMID 34046599 DOI: 10.1039/d0md00398k |
0.695 |
|
| 2021 |
Liu R, Markley L, Miller PA, Franzblau S, Shetye G, Ma R, Savková K, Mikušová K, Lee BS, Pethe K, Moraski GC, Miller MJ. Hydride-induced Meisenheimer complex formation reflects activity of nitro aromatic anti-tuberculosis compounds. Rsc Medicinal Chemistry. 12: 62-72. PMID 34046598 DOI: 10.1039/d0md00390e |
0.705 |
|
| 2021 |
Bolger J, Miller M. Diaryl Ether Containing N-Hydroxycarbamates from Nitroso Cycloadducts. Tetrahedron Letters. 52: 2268-2271. PMID 21479112 DOI: 10.1016/j.tetlet.2011.02.016 |
0.825 |
|
| 2020 |
Lee BS, Hards K, Engelhart CA, Hasenoehrl EJ, Kalia NP, Mackenzie JS, Sviriaeva E, Chong SMS, Manimekalai MSS, Koh VH, Chan J, Xu J, Alonso S, Miller MJ, Steyn AJC, et al. Dual inhibition of the terminal oxidases eradicates antibiotic-tolerant Mycobacterium tuberculosis. Embo Molecular Medicine. e13207. PMID 33283973 DOI: 10.15252/emmm.202013207 |
0.67 |
|
| 2020 |
Moraski GC, Deboosère N, Marshall KL, Weaver HA, Vandeputte A, Hastings C, Woolhiser L, Lenaerts AJ, Brodin P, Miller MJ. Intracellular and in vivo evaluation of imidazo[2,1-b]thiazole-5-carboxamide anti-tuberculosis compounds. Plos One. 15: e0227224. PMID 31905374 DOI: 10.1371/Journal.Pone.0227224 |
0.716 |
|
| 2019 |
Ghosh M, Miller PA, Miller MJ. Antibiotic repurposing: bis-catechol- and mixed ligand (bis-catechol-mono-hydroxamate)-teicoplanin conjugates are active against multidrug resistant Acinetobacter baumannii. The Journal of Antibiotics. PMID 31836835 DOI: 10.1038/S41429-019-0268-7 |
0.307 |
|
| 2019 |
Liu R, Krchnak V, Brown SN, Miller MJ. Deuteration of BTZ043 Extends the Lifetime of Meisenheimer Intermediates to the Antituberculosis Nitroso Oxidation State. Acs Medicinal Chemistry Letters. 10: 1462-1466. PMID 31620234 DOI: 10.1021/Acsmedchemlett.9B00308 |
0.351 |
|
| 2019 |
Kalia NP, Shi Lee B, Ab Rahman NB, Moraski GC, Miller MJ, Pethe K. Carbon metabolism modulates the efficacy of drugs targeting the cytochrome bc:aa in Mycobacterium tuberculosis. Scientific Reports. 9: 8608. PMID 31197236 DOI: 10.1038/S41598-019-44887-9 |
0.689 |
|
| 2019 |
Lin YM, Ghosh M, Miller PA, Möllmann U, Miller MJ. Synthetic sideromycins (skepticism and optimism): selective generation of either broad or narrow spectrum Gram-negative antibiotics. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. PMID 30919118 DOI: 10.1007/S10534-019-00192-6 |
0.553 |
|
| 2018 |
Scherr N, Bieri R, Thomas SS, Chauffour A, Kalia NP, Schneide P, Ruf MT, Lamelas A, Manimekalai MSS, Grüber G, Ishii N, Suzuki K, Tanner M, Moraski GC, Miller MJ, et al. Targeting the Mycobacterium ulcerans cytochrome bc:aa for the treatment of Buruli ulcer. Nature Communications. 9: 5370. PMID 30560872 DOI: 10.1038/S41467-018-07804-8 |
0.69 |
|
| 2018 |
Ghosh M, Lin YM, Miller PA, Möllmann U, Boggess W, Miller MJ. Siderophore Conjugates of Daptomycin are Potent Inhibitors of Carbapenem Resistant Strains of Acinetobacter baumannii. Acs Infectious Diseases. PMID 30043609 DOI: 10.1021/Acsinfecdis.8B00150 |
0.506 |
|
| 2018 |
O'Malley T, Alling T, Early JV, Wescott HA, Kumar A, Moraski GC, Miller MJ, Masquelin T, Hipskind PA, Parish T. Imidazopyridine compounds inhibit mycobacterial growth by depleting ATP levels. Antimicrobial Agents and Chemotherapy. PMID 29632008 DOI: 10.1128/Aac.02439-17 |
0.712 |
|
| 2018 |
Liu R, Miller PA, Vakulenko SB, Stewart NK, Boggess WC, Miller MJ. A Synthetic Dual Drug Sideromycin Induces Gram-Negative Bacteria to Commit Suicide with a Gram-Positive Antibiotic. Journal of Medicinal Chemistry. PMID 29554424 DOI: 10.1021/Acs.Jmedchem.8B00218 |
0.307 |
|
| 2017 |
Carosso S, Liu R, Miller PA, Hecker SJ, Glinka T, Miller MJ. Methodology for Monobactam Diversification: Syntheses and Studies of 4-Thiomethyl Substituted β-Lactams with Activity Against Gram-Negative Bacteria, Including Carbapenemase Producing Acinetobacter baumannii. Journal of Medicinal Chemistry. PMID 28994597 DOI: 10.1021/Acs.Jmedchem.7B01164 |
0.382 |
|
| 2017 |
Moraski GC, Bristol R, Seeger N, Boshoff HI, Tsang PS, Miller MJ. Preparation and Evaluation of Potent Pentafluorosulfanyl-Substituted Anti-Tuberculosis Compounds. Chemmedchem. PMID 28654200 DOI: 10.1002/Cmdc.201700170 |
0.725 |
|
| 2017 |
Ghosh M, Miller PA, Möllmann U, Claypool WD, Schroeder VA, Wolter WR, Suckow M, Yu H, Li S, Huang W, Zajicek J, Miller MJ. Targeted Antibiotic Delivery: Selective Siderophore Conjugation with Daptomycin Confers Potent Activity Against Multi-Drug Resistant Acinetobacter baumannii Both in vitro and in vivo. Journal of Medicinal Chemistry. PMID 28287735 DOI: 10.1021/Acs.Jmedchem.7B00102 |
0.516 |
|
| 2017 |
Moraski GC, Bristol R, Seeger N, Boshoff HI, Tsang PS, Miller MJ. Cover Picture: Preparation and Evaluation of Potent Pentafluorosulfanyl-Substituted Anti-Tuberculosis Compounds (ChemMedChem 14/2017) Chemmedchem. 12: 1102-1102. DOI: 10.1002/Cmdc.201700398 |
0.724 |
|
| 2016 |
Majewski MW, Miller PA, Miller MJ. Studies at the ionizable position of cephalosporins and penicillins: hydroxamates as substitutes for the traditional carboxylate group. The Journal of Antibiotics. PMID 27999444 DOI: 10.1038/Ja.2016.149 |
0.355 |
|
| 2016 |
Krupkova S, Aguete GP, Kocmanova L, Volna T, Grepl M, Novakova L, Miller MJ, Hlavac J. Solid-Phase Synthesis of ɤ-Lactone and 1,2-Oxazine Derivatives and Their Efficient Chiral Analysis. Plos One. 11: e0166558. PMID 27893812 DOI: 10.1371/Journal.Pone.0166558 |
0.43 |
|
| 2016 |
Brulíková L, Harrison A, Miller MJ, Hlaváč J. Stereo- and regioselectivity of the hetero-Diels-Alder reaction of nitroso derivatives with conjugated dienes. Beilstein Journal of Organic Chemistry. 12: 1949-1980. PMID 27829901 DOI: 10.3762/Bjoc.12.184 |
0.396 |
|
| 2016 |
Moraski GC, Seeger N, Miller PA, Oliver AG, Boshoff HI, Cho S, Mulugeta S, Anderson JR, Franzblau SG, Miller MJ. Arrival of Imidazo[2,1-b]thiazole-5-carboxamides: Potent Anti-tuberculosis Agents That Target QcrB. Acs Infectious Diseases. 2: 393-398. PMID 27627627 DOI: 10.1021/Acsinfecdis.5B00154 |
0.727 |
|
| 2016 |
Moraski GC, Cheng Y, Cho S, Cramer JW, Godfrey A, Masquelin T, Franzblau SG, Miller MJ, Schorey J. Imidazo[1,2-a]pyridine-3-carboxamides are Active Antimicrobial Agents of Mycobacterium avium Infection In Vivo. Antimicrobial Agents and Chemotherapy. PMID 27216051 DOI: 10.1128/Aac.00618-16 |
0.699 |
|
| 2016 |
Tiwari R, Miller PA, Chiarelli LR, Mori G, Šarkan M, Centárová I, Cho S, Mikušová K, Franzblau SG, Oliver AG, Miller MJ. Design, Syntheses, and Anti-TB Activity of 1,3-Benzothiazinone Azide and Click Chemistry Products Inspired by BTZ043. Acs Medicinal Chemistry Letters. 7: 266-70. PMID 26985313 DOI: 10.1021/Acsmedchemlett.5B00424 |
0.382 |
|
| 2016 |
Majewski MW, Tiwari R, Miller PA, Cho S, Franzblau SG, Miller MJ. Design, syntheses, and anti-tuberculosis activities of conjugates of piperazino-1,3-benzothiazin-4-ones (pBTZs) with 2,7-dimethylimidazo [1,2-a]pyridine-3-carboxylic acids and 7-phenylacetyl cephalosporins. Bioorganic & Medicinal Chemistry Letters. PMID 26951749 DOI: 10.1016/J.Bmcl.2016.02.076 |
0.348 |
|
| 2016 |
Majewski MW, Watson KD, Cho S, Miller PA, Franzblau SG, Miller MJ. Syntheses and Biological Evaluations of Highly Functionalized Hydroxamate Containing and N-Methylthio Monobactams as Anti-Tuberculosis and β-Lactamase Inhibitory Agents. Medchemcomm. 7: 141-147. PMID 26918106 DOI: 10.1039/C5Md00340G |
0.653 |
|
| 2016 |
Majewski MW, Watson KD, Cho S, Miller PA, Franzblau SG, Miller MJ. Syntheses and biological evaluations of highly functionalized hydroxamate containing and N-methylthio monobactams as anti-tuberculosis and β-lactamase inhibitory agents Medchemcomm. 7: 141-147. DOI: 10.1039/C5Md90052B |
0.653 |
|
| 2015 |
Carosso S, Miller MJ. Syntheses and studies of new forms of N-sulfonyloxy β-lactams as potential antibacterial agents and β-lactamase inhibitors. Bioorganic & Medicinal Chemistry. 23: 6138-47. PMID 26321604 DOI: 10.1016/J.Bmc.2015.08.005 |
0.337 |
|
| 2015 |
Ji C, Miller PA, Miller MJ. Syntheses and Antibacterial Activity of N-Acylated Ciprofloxacin Derivatives Based on the Trimethyl Lock. Acs Medicinal Chemistry Letters. 6: 707-10. PMID 26101578 DOI: 10.1021/Acsmedchemlett.5B00146 |
0.542 |
|
| 2015 |
Majewski MW, Cho S, Miller PA, Franzblau SG, Miller MJ. Syntheses and evaluation of substituted aromatic hydroxamates and hydroxamic acids that target Mycobacterium tuberculosis. Bioorganic & Medicinal Chemistry Letters. PMID 26037320 DOI: 10.1016/J.Bmcl.2015.04.099 |
0.379 |
|
| 2015 |
Moraski GC, Miller PA, Bailey MA, Ollinger J, Parish T, Boshoff HI, Cho S, Anderson JR, Mulugeta S, Franzblau SG, Miller MJ. Putting Tuberculosis (TB) To Rest: Transformation of the Sleep Aid, Ambien, and "Anagrams" Generated Potent Antituberculosis Agents. Acs Infectious Diseases. 1: 85-90. PMID 25984566 DOI: 10.1021/Id500008T |
0.706 |
|
| 2015 |
Tiwari R, Miller PA, Cho S, Franzblau SG, Miller MJ. Syntheses and Antituberculosis Activity of 1,3-Benzothiazinone Sulfoxide and Sulfone Derived from BTZ043. Acs Medicinal Chemistry Letters. 6: 128-33. PMID 25699139 DOI: 10.1021/Ml5003458 |
0.34 |
|
| 2015 |
Ji C, Miller MJ. Siderophore-fluoroquinolone conjugates containing potential reduction-triggered linkers for drug release: synthesis and antibacterial activity. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 28: 541-51. PMID 25663417 DOI: 10.1007/S10534-015-9830-3 |
0.497 |
|
| 2015 |
Lambert LJ, Miller MJ, Huber PW. Tetrahydrofuranyl and tetrahydropyranyl protection of amino acid side-chains enables synthesis of a hydroxamate-containing aminoacylated tRNA. Organic & Biomolecular Chemistry. 13: 2341-9. PMID 25562392 DOI: 10.1039/C4Ob02212B |
0.341 |
|
| 2015 |
Jobbins MO, Majewski MW, Oliver AG, Miller MJ. Diastereoselective synthesis of a hydroxamate containing bicyclo-[3.2.0] β-lactam aminal via ruthenium alkene isomerization and Pd(II)-catalyzed oxidative amidation Tetrahedron Letters. 56: 3141-3143. DOI: 10.1016/J.Tetlet.2014.12.072 |
0.372 |
|
| 2014 |
Carosso S, Miller MJ. Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products. Organic & Biomolecular Chemistry. 12: 7445-68. PMID 25119424 DOI: 10.1039/C4Ob01033G |
0.366 |
|
| 2014 |
Moraski GC, Oliver AG, Markley LD, Cho S, Franzblau SG, Miller MJ. Scaffold-switching: an exploration of 5,6-fused bicyclic heteroaromatics systems to afford antituberculosis activity akin to the imidazo[1,2-a]pyridine-3-carboxylates. Bioorganic & Medicinal Chemistry Letters. 24: 3493-8. PMID 24909079 DOI: 10.1016/J.Bmcl.2014.05.062 |
0.736 |
|
| 2014 |
Tiwari R, Möllmann U, Cho S, Franzblau SG, Miller PA, Miller MJ. Design and Syntheses of Anti-Tuberculosis Agents Inspired by BTZ043 Using a Scaffold Simplification Strategy. Acs Medicinal Chemistry Letters. 5: 587-91. PMID 24900885 DOI: 10.1021/Ml500039G |
0.355 |
|
| 2014 |
Cheng Y, Moraski GC, Cramer J, Miller MJ, Schorey JS. Bactericidal activity of an imidazo[1, 2-a]pyridine using a mouse M. tuberculosis infection model. Plos One. 9: e87483. PMID 24498115 DOI: 10.1371/Journal.Pone.0087483 |
0.707 |
|
| 2014 |
Jobbins MO, Miller MJ. Syntheses of hydroxamic acid-containing bicyclic β-lactams via palladium-catalyzed oxidative amidation of alkenes. The Journal of Organic Chemistry. 79: 1620-5. PMID 24483144 DOI: 10.1021/Jo402544P |
0.357 |
|
| 2013 |
Moraski GC, Markley LD, Cramer J, Hipskind PA, Boshoff H, Bailey M, Alling T, Ollinger J, Parish T, Miller MJ. Advancement of Imidazo[1,2-a]pyridines with Improved Pharmacokinetics and Nanomolar Activity Against Mycobacterium tuberculosis. Acs Medicinal Chemistry Letters. 4: 675-679. PMID 23930153 DOI: 10.1021/Ml400088Y |
0.725 |
|
| 2013 |
Wencewicz TA, Miller MJ. Biscatecholate-monohydroxamate mixed ligand siderophore-carbacephalosporin conjugates are selective sideromycin antibiotics that target Acinetobacter baumannii. Journal of Medicinal Chemistry. 56: 4044-52. PMID 23614627 DOI: 10.1021/Jm400265K |
0.695 |
|
| 2013 |
Ollinger J, Bailey MA, Moraski GC, Casey A, Florio S, Alling T, Miller MJ, Parish T. A dual read-out assay to evaluate the potency of compounds active against Mycobacterium tuberculosis. Plos One. 8: e60531. PMID 23593234 DOI: 10.1371/Journal.Pone.0060531 |
0.703 |
|
| 2013 |
Tiwari R, Moraski GC, Krch?ák V, Miller PA, Colon-Martinez M, Herrero E, Oliver AG, Miller MJ. Thiolates chemically induce redox activation of BTZ043 and related potent nitroaromatic anti-tuberculosis agents. Journal of the American Chemical Society. 135: 3539-49. PMID 23402278 DOI: 10.1021/Ja311058Q |
0.742 |
|
| 2013 |
Wencewicz TA, Long TE, Möllmann U, Miller MJ. Trihydroxamate siderophore-fluoroquinolone conjugates are selective sideromycin antibiotics that target Staphylococcus aureus. Bioconjugate Chemistry. 24: 473-86. PMID 23350642 DOI: 10.1021/Bc300610F |
0.7 |
|
| 2013 |
Watson KD, Carosso S, Miller MJ. New and concise syntheses of the bicyclic oxamazin core using an intramolecular nitroso Diels-Alder reaction and ring-closing olefin metathesis. Organic Letters. 15: 358-61. PMID 23276301 DOI: 10.1021/Ol303305U |
0.667 |
|
| 2013 |
Krchňáková A, Miller PA, Miller MJ, Krchňák V. Teaching old dogs (Fmoc-amine, azodicarboxylate, and phosphine) new tricks (triazolinones) Tetrahedron Letters. 54: 4749-4752. DOI: 10.1016/J.Tetlet.2013.06.115 |
0.351 |
|
| 2012 |
Juárez-Hernández RE, Miller PA, Miller MJ. Syntheses of Siderophore-Drug Conjugates Using a Convergent Thiol-Maleimide System. Acs Medicinal Chemistry Letters. 3: 799-803. PMID 23264853 DOI: 10.1021/Ml300150Y |
0.387 |
|
| 2012 |
Wencewicz TA, Oliver AG, Miller MJ. Iron(III)-templated macrolactonization of trihydroxamate siderophores. Organic Letters. 14: 4390-3. PMID 22906163 DOI: 10.1021/Ol301869X |
0.695 |
|
| 2012 |
Juárez-Hernández RE, Franzblau SG, Miller MJ. Syntheses of mycobactin analogs as potent and selective inhibitors of Mycobacterium tuberculosis. Organic & Biomolecular Chemistry. 10: 7584-93. PMID 22895786 DOI: 10.1039/C2Ob26077H |
0.349 |
|
| 2012 |
Ji C, Miller PA, Miller MJ. Iron transport-mediated drug delivery: practical syntheses and in vitro antibacterial studies of tris-catecholate siderophore-aminopenicillin conjugates reveals selectively potent antipseudomonal activity. Journal of the American Chemical Society. 134: 9898-901. PMID 22656303 DOI: 10.1021/Ja303446W |
0.515 |
|
| 2012 |
Ji C, Miller MJ. Chemical syntheses and in vitro antibacterial activity of two desferrioxamine B-ciprofloxacin conjugates with potential esterase and phosphatase triggered drug release linkers. Bioorganic & Medicinal Chemistry. 20: 3828-36. PMID 22608921 DOI: 10.1016/J.Bmc.2012.04.034 |
0.499 |
|
| 2012 |
Ji C, Lin W, Moraski GC, Thanassi JA, Pucci MJ, Franzblau SG, Möllmann U, Miller MJ. Syntheses and biological studies of novel spiropiperazinyl oxazolidinone antibacterial agents using a spirocyclic diene derived acylnitroso Diels-Alder reaction. Bioorganic & Medicinal Chemistry. 20: 3422-8. PMID 22560837 DOI: 10.1016/J.Bmc.2012.04.026 |
0.801 |
|
| 2012 |
Ji C, Juárez-Hernández RE, Miller MJ. Exploiting bacterial iron acquisition: siderophore conjugates. Future Medicinal Chemistry. 4: 297-313. PMID 22393938 DOI: 10.4155/Fmc.11.191 |
0.484 |
|
| 2012 |
Moraski GC, Markley LD, Chang M, Cho S, Franzblau SG, Hwang CH, Boshoff H, Miller MJ. Generation and exploration of new classes of antitubercular agents: The optimization of oxazolines, oxazoles, thiazolines, thiazoles to imidazo[1,2-a]pyridines and isomeric 5,6-fused scaffolds. Bioorganic & Medicinal Chemistry. 20: 2214-20. PMID 22391032 DOI: 10.1016/J.Bmc.2012.02.025 |
0.726 |
|
| 2011 |
Krchňák V, Zajíček J, Miller PA, Miller MJ. Selective molecular sequestration with concurrent natural product functionalization and derivatization: from crude natural product extracts to a single natural product derivative in one step. The Journal of Organic Chemistry. 76: 10249-53. PMID 22059469 DOI: 10.1021/Jo201361S |
0.312 |
|
| 2011 |
Wencewicz TA, Yang B, Rudloff JR, Oliver AG, Miller MJ. N-O chemistry for antibiotics: discovery of N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds as selective antibacterial agents using nitroso Diels-Alder and ene chemistry. Journal of Medicinal Chemistry. 54: 6843-58. PMID 21859126 DOI: 10.1021/Jm200794R |
0.796 |
|
| 2011 |
Moraski GC, Thanassi JA, Podos SD, Pucci MJ, Miller MJ. One-step syntheses of nitrofuranyl benzimidazoles that are active against multidrug-resistant bacteria. The Journal of Antibiotics. 64: 667-671. PMID 21811261 DOI: 10.1038/Ja.2011.67 |
0.706 |
|
| 2011 |
Moraski GC, Markley LD, Hipskind PA, Boshoff H, Cho S, Franzblau SG, Miller MJ. Advent of Imidazo[1,2-a]pyridine-3-carboxamides with Potent Multi- and Extended Drug Resistant Antituberculosis Activity. Acs Medicinal Chemistry Letters. 2: 466-470. PMID 21691438 DOI: 10.1021/Ml200036R |
0.721 |
|
| 2011 |
Bodnar BS, Miller MJ. The nitrosocarbonyl hetero-Diels-Alder reaction as a useful tool for organic syntheses. Angewandte Chemie (International Ed. in English). 50: 5630-47. PMID 21520360 DOI: 10.1002/Anie.201005764 |
0.793 |
|
| 2011 |
Tardibono LP, Miller MJ, Balzarini J. Enantioselective syntheses of carbocyclic nuleosides 5'-homocarbovir, epi-4'-homocarbovir and their cyclopropylamine analogs using facially selective Pd-mediated allylations. Tetrahedron. 67: 825-829. PMID 21399715 DOI: 10.1016/J.Tet.2010.11.097 |
0.793 |
|
| 2011 |
Bolger JK, Tian W, Wolter WR, Cho W, Suckow MA, Miller MJ. Synthesis and evaluation of 5-lipoxygenase translocation inhibitors from acylnitroso hetero-Diels-Alder cycloadducts. Organic & Biomolecular Chemistry. 9: 2999-3010. PMID 21365098 DOI: 10.1039/C0Ob00714E |
0.806 |
|
| 2011 |
Wu C, Miller PA, Miller MJ. Syntheses and studies of amamistatin B analogs reveals that anticancer activity is relatively independent of stereochemistry, ester or amide linkage and select replacement of one of the metal chelating groups. Bioorganic & Medicinal Chemistry Letters. 21: 2611-5. PMID 21315591 DOI: 10.1016/J.Bmcl.2011.01.084 |
0.369 |
|
| 2011 |
Miller MJ, Walz AJ, Zhu H, Wu C, Moraski G, Möllmann U, Tristani EM, Crumbliss AL, Ferdig MT, Checkley L, Edwards RL, Boshoff HI. Design, synthesis, and study of a mycobactin-artemisinin conjugate that has selective and potent activity against tuberculosis and malaria. Journal of the American Chemical Society. 133: 2076-9. PMID 21275374 DOI: 10.1021/Ja109665T |
0.728 |
|
| 2011 |
Bolger J, Miller M. Diaryl ether containing N-hydroxycarbamates from nitroso cycloadducts Tetrahedron Letters. 52: 2268-2271. DOI: 10.1016/J.Tetlet.2011.02.016 |
0.825 |
|
| 2011 |
Bodnar BS, Miller MJ. Hetero-Diels-Alder-Reaktionen von Nitrosocarbonylverbindungen als nützliches Verfahren in der organischen Synthese Angewandte Chemie. 123: 5746-5764. DOI: 10.1002/Ange.201005764 |
0.772 |
|
| 2010 |
Yan S, Miller MJ, Wencewicz TA, Möollmann U. Syntheses and biological evaluation of new cephalosporin-oxazolidinone conjugates. Medchemcomm. 1: 145-148. PMID 27087912 DOI: 10.1039/C0Md00015A |
0.711 |
|
| 2010 |
Moraski GC, Franzblau SG, Miller MJ. UTILIZTION OF THE SUZUKI COUPLING TO ENHANCE THE ANTITUBERCULOSIS ACTIVITY OF ARYL OXAZOLES. Heterocycles. 80: 977-988. PMID 22003265 DOI: 10.3987/Com-09-S(S)69 |
0.751 |
|
| 2010 |
Cesario C, Tardibono LP, Miller MJ. Syntheses of carbocyclic aminonucleosides and (-)-epi-4'-carbocyclic puromycin: Application of palladium(0)/indium iodide-allylations and tethered aminohydroxylations. Tetrahedron Letters. 51: 3053-3056. PMID 20640052 DOI: 10.1016/J.Tetlet.2010.04.006 |
0.788 |
|
| 2010 |
Ji C, Miller MJ. Cyclopropanation of nitroso Diels-Alder cycloadducts and application to the synthesis of a 2',3'-methano carbocyclic nucleoside. Tetrahedron Letters. 51: 3789-3791. PMID 20607121 DOI: 10.1016/J.Tetlet.2010.05.062 |
0.546 |
|
| 2010 |
Yang B, Zhu ZC, Goodson HV, Miller MJ. Syntheses and biological evaluation of ring-C modified colchicine analogs. Bioorganic & Medicinal Chemistry Letters. 20: 3831-3. PMID 20529690 DOI: 10.1016/J.Bmcl.2010.03.056 |
0.596 |
|
| 2010 |
Cesario C, Miller MJ. Palladium(0)/indium iodide-mediated allylations of electrophiles generated from the hydrolysis of Eschenmoser's salt: One-pot preparation of diverse carbocyclic scaffolds. Tetrahedron Letters. 51: 3050-3052. PMID 20526464 DOI: 10.1016/J.Tetlet.2010.04.007 |
0.791 |
|
| 2010 |
Stefely JA, Palchaudhuri R, Miller PA, Peterson RJ, Moraski GC, Hergenrother PJ, Miller MJ. N-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)arylamide as a new scaffold that provides rapid access to antimicrotubule agents: synthesis and evaluation of antiproliferative activity against select cancer cell lines. Journal of Medicinal Chemistry. 53: 3389-95. PMID 20334421 DOI: 10.1021/Jm1000979 |
0.731 |
|
| 2010 |
Yang B, Miller MJ. Regio- and stereochemically controlled formation of hydroxamic acids from indium triflate-mediated nucleophilic ring-opening reactions with acylnitroso-Diels-Alder adducts. Tetrahedron Letters. 51: 889-891. PMID 20209116 DOI: 10.1016/J.Tetlet.2009.12.006 |
0.592 |
|
| 2010 |
Yang B, Miller MJ. Iminonitroso ene reactions: experimental studies on reactivity, regioselectivity and enantioselectivity. Tetrahedron Letters. 51: 328-331. PMID 20161491 DOI: 10.1016/J.Tetlet.2009.11.015 |
0.569 |
|
| 2010 |
Moraski GC, Chang M, Villegas-Estrada A, Franzblau SG, Möllmann U, Miller MJ. Structure-activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters. European Journal of Medicinal Chemistry. 45: 1703-16. PMID 20116900 DOI: 10.1016/J.Ejmech.2009.12.074 |
0.744 |
|
| 2010 |
Patterson LD, Miller MJ. Enzymatic deprotection of the cephalosporin 3'-acetoxy group using Candida antarctica lipase B. The Journal of Organic Chemistry. 75: 1289-92. PMID 20099862 DOI: 10.1021/Jo902406B |
0.739 |
|
| 2010 |
Yang B, Zöllner T, Gebhardt P, Möllmann U, Miller MJ. Preparation and biological evaluation of novel leucomycin analogs derived from nitroso Diels-Alder reactions. Organic & Biomolecular Chemistry. 8: 691-7. PMID 20090988 DOI: 10.1039/B922450E |
0.612 |
|
| 2010 |
Yan S, Miller MJ, Wencewicz TA, Möllmann U. Syntheses and antibacterial activity studies of new oxazolidinones from nitroso Diels-Alder chemistry. Bioorganic & Medicinal Chemistry Letters. 20: 1302-5. PMID 20031407 DOI: 10.1016/J.Bmcl.2009.10.018 |
0.739 |
|
| 2010 |
Yang B, Miller MJ. Indium triflate-assisted nucleophilic aromatic substitution reactions of nitrosobezene-derived cycloadducts with alcohols. Organic Letters. 12: 392-5. PMID 20000806 DOI: 10.1021/Ol9027607 |
0.572 |
|
| 2010 |
Yan S, Miller MJ, Wencewicz TA, Möllmann U. Syntheses and biological evaluation of new cephalosporin-oxazolidinone conjugates Medchemcomm. 1: 145-148. DOI: 10.1039/c0md00015a |
0.668 |
|
| 2010 |
Surman MD, Mulvihill MJ, Miller MJ. ChemInform Abstract: Novel 1,4-Benzodiazepines from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts. Cheminform. 33: no-no. DOI: 10.1002/chin.200222158 |
0.754 |
|
| 2010 |
Surman MD, Mulvihill MJ, Miller MJ. ChemInform Abstract: Novel α-Substituted β-Amino Diesters from Acylnitroso-Derived Hetero-Diels-Alder Cycloadducts. Cheminform. 33: no-no. DOI: 10.1002/chin.200221148 |
0.734 |
|
| 2010 |
MULVIHILL MJ, SURMAN MD, MILLER MJ. ChemInform Abstract: Regio- and Stereoselective Fe(III)- and Pd(0)-Mediated Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems. Cheminform. 29: no-no. DOI: 10.1002/chin.199850089 |
0.726 |
|
| 2010 |
RITTER AR, MILLER MJ. ChemInform Abstract: Amino Acid Derived Chiral Acyl Nitroso Compounds: Diastereoselectivity in Intermolecular Hetero Diels-Alder Reactions. Cheminform. 26: no-no. DOI: 10.1002/chin.199506216 |
0.303 |
|
| 2009 |
Yang B, Lin W, Krchnak V, Miller MJ. Retro iminonitroso Diels-Alder reactions: interconversion of nitroso cycloadducts. Tetrahedron Letters. 50: 5879-5883. PMID 20161032 DOI: 10.1016/J.Tetlet.2009.07.121 |
0.713 |
|
| 2009 |
Bodnar BS, Miller MJ. Brønsted acid-mediated opening of nitroso cycloadducts under anhydrous conditions. Tetrahedron Letters. 50: 796-798. PMID 20160837 DOI: 10.1016/J.Tetlet.2008.11.120 |
0.779 |
|
| 2009 |
Yang B, Miller MJ. Regio- and stereoselective indium triflate-mediated nucleophilic ring-opening reactions of 3-aza-2-oxabicyclo[2.2.1]hept-5-ene and -[2.2.2]oct-5-ene systems. The Journal of Organic Chemistry. 74: 7990-3. PMID 19754105 DOI: 10.1021/Jo9016343 |
0.571 |
|
| 2009 |
Tardibono LP, Patzner J, Cesario C, Miller MJ. Palladium-catalyzed decarboxylative rearrangements of allyl 2,2,2-trifluoroethyl malonates: direct access to homoallylic esters. Organic Letters. 11: 4076-9. PMID 19694457 DOI: 10.1021/Ol901518G |
0.795 |
|
| 2009 |
Young DC, Kasmar A, Moraski G, Cheng TY, Walz AJ, Hu J, Xu Y, Endres GW, Uzieblo A, Zajonc D, Costello CE, Miller MJ, Moody DB. Synthesis of dideoxymycobactin antigens presented by CD1a reveals T cell fine specificity for natural lipopeptide structures. The Journal of Biological Chemistry. 284: 25087-96. PMID 19605355 DOI: 10.1074/Jbc.M109.000802 |
0.688 |
|
| 2009 |
Lin W, Virga KG, Kim KH, Zajicek J, Mendel D, Miller MJ. Diastereoselective synthesis of a spironoraristeromycin using an acylnitroso Diels-Alder reaction. The Journal of Organic Chemistry. 74: 5941-6. PMID 19601571 DOI: 10.1021/Jo900877B |
0.81 |
|
| 2009 |
Yang B, Miller PA, Möllmann U, Miller MJ. Syntheses and biological activity studies of novel sterol analogs from nitroso Diels-Alder reactions of ergosterol. Organic Letters. 11: 2828-31. PMID 19552465 DOI: 10.1021/Ol900997T |
0.617 |
|
| 2009 |
Cesario C, Miller MJ. Syntheses of carbocyclic uracil polyoxin C analogs: application of Pd(0)/InI-allylation of 4-acetoxy-2-azetidinone. The Journal of Organic Chemistry. 74: 5730-3. PMID 19514728 DOI: 10.1021/Jo900861X |
0.781 |
|
| 2009 |
Tardibono LP, Miller MJ. Synthesis and anticancer activity of new hydroxamic acid containing 1,4-benzodiazepines. Organic Letters. 11: 1575-8. PMID 19320504 DOI: 10.1021/Ol900210H |
0.817 |
|
| 2009 |
Wencewicz TA, Möllmann U, Long TE, Miller MJ. Is drug release necessary for antimicrobial activity of siderophore-drug conjugates? Syntheses and biological studies of the naturally occurring salmycin "Trojan Horse" antibiotics and synthetic desferridanoxamine-antibiotic conjugates. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 22: 633-48. PMID 19221879 DOI: 10.1007/S10534-009-9218-3 |
0.69 |
|
| 2009 |
Cesario C, Miller MJ. Pd(0)/InI-mediated allylic additions to 4-acetoxy-2-azetidinone: new route to highly functionalized carbocyclic scaffolds. Organic Letters. 11: 1293-5. PMID 19216521 DOI: 10.1021/Ol9000685 |
0.791 |
|
| 2009 |
Miller MJ, Li H, Foss CA. Novel antisense oligonucleotides containing hydroxamate linkages: targeted iron-triggered chemical nucleases. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 22: 491-510. PMID 19184459 DOI: 10.1007/S10534-009-9206-7 |
0.311 |
|
| 2009 |
Miller MJ, Zhu H, Xu Y, Wu C, Walz AJ, Vergne A, Roosenberg JM, Moraski G, Minnick AA, McKee-Dolence J, Hu J, Fennell K, Kurt Dolence E, Dong L, Franzblau S, et al. Utilization of microbial iron assimilation processes for the development of new antibiotics and inspiration for the design of new anticancer agents. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 22: 61-75. PMID 19130268 DOI: 10.1007/S10534-008-9185-0 |
0.767 |
|
| 2009 |
Lin W, Gupta A, Kim KH, Mendel D, Miller MJ. Syntheses of new spirocarbocyclic nucleoside analogs using iminonitroso Diels-Alder reactions. Organic Letters. 11: 449-52. PMID 19072701 DOI: 10.1021/Ol802553G |
0.818 |
|
| 2009 |
Cesario C, Tardibono LP, Miller MJ. Titanocene(III) chloride-mediated reductions of oxazines, hydroxamic acids, and N-hydroxy carbamates. The Journal of Organic Chemistry. 74: 448-51. PMID 19053586 DOI: 10.1021/Jo802184Y |
0.789 |
|
| 2008 |
Ding P, Schous CE, Miller MJ. Design and synthesis of a novel protected mixed ligand siderophore. Tetrahedron Letters. 49: 2306-2310. PMID 21915156 DOI: 10.1016/J.Tetlet.2008.02.007 |
0.38 |
|
| 2008 |
Huang W, Miller MJ. Concise syntheses of enantiomerically pure protected 4-hydroxypyroglutamic acid and 4-hydroxyproline from a nitroso-cyclopentadiene cycloadduct. Tetrahedron, Asymmetry. 19: 2835-2838. PMID 20011098 DOI: 10.1016/J.Tetasy.2008.12.013 |
0.526 |
|
| 2008 |
Krchnák V, Waring KR, Noll BC, Moellmann U, Dahse HM, Miller MJ. Evolution of natural product scaffolds by acyl- and arylnitroso hetero-diels-alder reactions: new chemistry on piperine. The Journal of Organic Chemistry. 73: 4559-67. PMID 18489157 DOI: 10.1021/Jo8004827 |
0.381 |
|
| 2008 |
Fennell KA, Möllmann U, Miller MJ. Syntheses and biological activity of amamistatin B and analogs. The Journal of Organic Chemistry. 73: 1018-24. PMID 18173285 DOI: 10.1021/Jo7020532 |
0.774 |
|
| 2008 |
Krchnák V, Moellmann U, Dahse HM, Miller MJ. Solid-supported nitroso hetero-Diels-Alder reactions. 3. Acid-mediated transformation of cycloadducts by scission of the oxazine C-O bonds. Journal of Combinatorial Chemistry. 10: 112-7. PMID 18067270 DOI: 10.1021/Cc700142D |
0.385 |
|
| 2008 |
Krchnák V, Moellmann U, Dahse HM, Miller MJ. Solid-supported nitroso hetero diels-alder reactions. 2. Arylnitroso dienophiles: scope and limitations. Journal of Combinatorial Chemistry. 10: 104-11. PMID 18062671 DOI: 10.1021/Cc7001414 |
0.347 |
|
| 2008 |
Gebhardt P, Crumbliss AL, Miller MJ, Möllmann U. Synthesis and biological activity of saccharide based lipophilic siderophore mimetics as potential growth promoters for mycobacteria. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 21: 41-51. PMID 17390213 DOI: 10.1007/S10534-007-9091-X |
0.324 |
|
| 2007 |
Liu XS, Patterson LD, Miller MJ, Theil EC. Peptides selected for the protein nanocage pores change the rate of iron recovery from the ferritin mineral. The Journal of Biological Chemistry. 282: 31821-5. PMID 17785467 DOI: 10.1074/Jbc.C700153200 |
0.697 |
|
| 2007 |
Li F, Yang B, Miller MJ, Zajicek J, Noll BC, Möllmann U, Dahse HM, Miller PA. Iminonitroso Diels-Alder reactions for efficient derivatization and functionalization of complex diene-containing natural products. Organic Letters. 9: 2923-6. PMID 17602642 DOI: 10.1021/Ol071322B |
0.655 |
|
| 2007 |
Walz AJ, Möllmann U, Miller MJ. Synthesis and studies of catechol-containing mycobactin S and T analogs. Organic & Biomolecular Chemistry. 5: 1621-8. PMID 17571193 DOI: 10.1039/B703116E |
0.301 |
|
| 2007 |
Bodnar BS, Miller MJ. Reactions of nitroso hetero-Diels-Alder cycloadducts with azides: stereoselective formation of triazolines and aziridines. The Journal of Organic Chemistry. 72: 3929-32. PMID 17429998 DOI: 10.1021/Jo0701987 |
0.797 |
|
| 2007 |
Huang W, Miller MJ, De Clercq E, Balzarini J. Syntheses and anti-HIV activities of (+/-)-norcarbovir and (+/-)-norabacavir. Organic & Biomolecular Chemistry. 5: 1164-6. PMID 17406712 DOI: 10.1039/B700321H |
0.455 |
|
| 2007 |
Fennell KA, Miller MJ. Syntheses of amamistatin fragments and determination of their HDAC and antitumor activity. Organic Letters. 9: 1683-5. PMID 17397173 DOI: 10.1021/Ol070382E |
0.789 |
|
| 2007 |
Ding P, Helquist P, Miller MJ. Design, synthesis and pharmacological activity of novel enantiomerically pure phosphonic acid-based NAALADase inhibitors. Organic & Biomolecular Chemistry. 5: 826-31. PMID 17315070 DOI: 10.1039/B615603G |
0.33 |
|
| 2007 |
Walz AJ, Miller MJ. β-Lactams in synthesis: short syntheses of cobactin analogs Tetrahedron Letters. 48: 5103-5105. DOI: 10.1016/J.Tetlet.2007.05.085 |
0.434 |
|
| 2006 |
Miller MJ, Zhao G, Vakulenko S, Franzblau S, Möllmann U. New C-3' hydroxamate-substituted and more lipophilic cyclic hydroxamate cephalosporin derivatives as a potential new generation of selective antimicrobial agents. Organic & Biomolecular Chemistry. 4: 4178-85. PMID 17312974 DOI: 10.1039/B612475E |
0.387 |
|
| 2006 |
Zhao G, Miller MJ, Franzblau S, Wan B, Möllmann U. Syntheses and studies of quinolone-cephalosporins as potential anti-tuberculosis agents. Bioorganic & Medicinal Chemistry Letters. 16: 5534-7. PMID 16945530 DOI: 10.1016/J.Bmcl.2006.08.045 |
0.332 |
|
| 2006 |
Li F, Miller MJ. Stereoselective total synthesis of (+)-streptazolin by using a temporary silicon-tethered RCM strategy. The Journal of Organic Chemistry. 71: 5221-7. PMID 16808509 DOI: 10.1021/Jo060555Y |
0.542 |
|
| 2006 |
Nora GP, Miller MJ, Möllmann U. The synthesis and in vitro testing of structurally novel antibiotics derived from acylnitroso Diels-Alder adducts. Bioorganic & Medicinal Chemistry Letters. 16: 3966-70. PMID 16730172 DOI: 10.1016/J.Bmcl.2006.05.021 |
0.35 |
|
| 2006 |
Jiang MX, Jin B, Gage JL, Priour A, Savela G, Miller MJ. Substrate-dependent dihydroxylation of substituted cyclopentenes: toward the syntheses of carbocyclic sinefungin and noraristeromycin. The Journal of Organic Chemistry. 71: 4164-9. PMID 16709056 DOI: 10.1021/Jo060224L |
0.445 |
|
| 2005 |
Jiang MX, Warshakoon NC, Miller MJ. Chemoenzymatic asymmetric total synthesis of phosphodiesterase inhibitors: preparation of a polycyclic pyrazolo[3,4-d]pyrimidine from an acylnitroso Diels-Alder cycloadduct-derived aminocyclopentenol. The Journal of Organic Chemistry. 70: 2824-7. PMID 15787579 DOI: 10.1021/Jo0484070 |
0.395 |
|
| 2005 |
Bernier G, Girijavallabhan V, Murray A, Niyaz N, Ding P, Miller MJ, Malouin F. Desketoneoenactin-siderophore conjugates for Candida: evidence of iron transport-dependent species selectivity. Antimicrobial Agents and Chemotherapy. 49: 241-8. PMID 15616301 DOI: 10.1128/Aac.49.1.241-248.2005 |
0.746 |
|
| 2004 |
Li F, Warshakoon NC, Miller MJ. Synthetic application of acylnitroso Diels-Alder derived aminocyclopentenols: total synthesis of (+)-streptazolin. The Journal of Organic Chemistry. 69: 8836-41. PMID 15575765 DOI: 10.1021/Jo048606J |
0.588 |
|
| 2004 |
Li F, Brogan JB, Gage JL, Zhang D, Miller MJ. Chemoenzymatic synthesis and synthetic application of enantiopure aminocyclopentenols: total synthesis of carbocyclic (+)-uracil polyoxin C and its alpha-epimer. The Journal of Organic Chemistry. 69: 4538-40. PMID 15202916 DOI: 10.1021/Jo0496796 |
0.551 |
|
| 2004 |
Lee W, Miller MJ. concise synthesis of 4-acylamino analogues of 2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acids (LY354740) from an acylnitroso Diels-Alder cycloadduct. The Journal of Organic Chemistry. 69: 4516-9. PMID 15202910 DOI: 10.1021/Jo0495034 |
0.449 |
|
| 2004 |
Ding P, Miller MJ, Chen Y, Helquist P, Oliver AJ, Wiest O. Syntheses of conformationally constricted molecules as potential NAALADase/PSMA inhibitors. Organic Letters. 6: 1805-8. PMID 15151419 DOI: 10.1021/Ol049473R |
0.347 |
|
| 2004 |
Dong L, Miller MJ, Möllmann U. Microbial growth promotion studies of exochelin MN and analogues thereof. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 17: 99-104. PMID 15088934 DOI: 10.1023/B:Biom.0000018348.89904.60 |
0.437 |
|
| 2003 |
Mineno T, Miller MJ. Stereoselective total synthesis of racemic BCX-1812 (RWJ-270201) for the development of neuraminidase inhibitors as anti-influenza agents. The Journal of Organic Chemistry. 68: 6591-6. PMID 12919021 DOI: 10.1021/Jo034316B |
0.396 |
|
| 2003 |
Dhungana S, Miller MJ, Dong L, Ratledge C, Crumbliss AL. Iron chelation properties of an extracellular siderophore exochelin MN. Journal of the American Chemical Society. 125: 7654-63. PMID 12812507 DOI: 10.1021/Ja029578U |
0.405 |
|
| 2003 |
Murray AP, Miller MJ. The preparation of a fully differentiated "multiwarhead" siderophore precursor. The Journal of Organic Chemistry. 68: 191-4. PMID 12515482 DOI: 10.1021/Jo026391C |
0.651 |
|
| 2003 |
Lee W, Kim KH, Surman MD, Miller MJ. Stereo- and regioselectivity of Pd(0)/InI-mediated allylic additions to aldehydes and ketones. In situ generation of allylindium(III) intermediates from N-acylnitroso Diels-Alder cycloadducts and 1-amino-4-acetoxycyclopentenes. The Journal of Organic Chemistry. 68: 139-49. PMID 12515472 DOI: 10.1021/Jo026488Z |
0.777 |
|
| 2003 |
Durham TB, Miller MJ. An enantioselective synthesis of differentially protected erythro-alpha,beta-diamino acids and its application to the synthesis of an analogue of rhodopeptin B5. The Journal of Organic Chemistry. 68: 35-42. PMID 12515458 DOI: 10.1021/Jo016276M |
0.708 |
|
| 2003 |
Durham TB, Miller MJ. Enantioselective synthesis of alpha-amino acids from N-tosyloxy beta-lactams derived from beta-keto esters. The Journal of Organic Chemistry. 68: 27-34. PMID 12515457 DOI: 10.1021/Jo0162437 |
0.71 |
|
| 2003 |
Kim K, Miller MJ. An enantioselective synthesis of the cyclopentene fragment of nucleoside Q Tetrahedron Letters. 44: 4571-4573. DOI: 10.1016/S0040-4039(03)00973-0 |
0.304 |
|
| 2003 |
Durham TB, Miller MJ. Enantioselective Synthesis of α-Amino Acids from N-Tosyloxy β-Lactams Derived from β-Keto Esters. Cheminform. 34. DOI: 10.1002/chin.200321080 |
0.69 |
|
| 2003 |
Mickel SJ, Hsiao S, Miller MJ. Synthesis of a Key β-Lactam Intermediate by a [2 + 2] Cycloaddition Route: 4-Acetoxyazetidin-2-One Organic Syntheses. 135-135. DOI: 10.1002/0471264180.Os065.17 |
0.35 |
|
| 2002 |
Dong L, Roosenberg JM, Miller MJ. Total synthesis of desferrisalmycin B. Journal of the American Chemical Society. 124: 15001-5. PMID 12475343 DOI: 10.1021/Ja028386W |
0.802 |
|
| 2002 |
Dong L, Miller MJ. Total synthesis of exochelin MN and analogues. The Journal of Organic Chemistry. 67: 4759-70. PMID 12098286 DOI: 10.1021/Jo0256078 |
0.539 |
|
| 2002 |
Surman MD, Mulvihill MJ, Miller MJ. Regio- and stereoselective ring openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene systems with copper catalyst-modified grignard reagents: application to the synthesis of an inhibitor of 5-lipoxygenase. The Journal of Organic Chemistry. 67: 4115-21. PMID 12054945 DOI: 10.1021/Jo016275U |
0.779 |
|
| 2002 |
Walz AJ, Miller MJ. Synthesis and biological activity of hydroxamic acid-derived vasopeptidase inhibitor analogues. Organic Letters. 4: 2047-50. PMID 12049514 DOI: 10.1021/Ol025896M |
0.383 |
|
| 2002 |
Surman MD, Mulvihill MJ, Miller MJ. Novel 1,4-benzodiazepines from acylnitroso-derived hetero-Diels-Alder cycloadducts. Organic Letters. 4: 139-41. PMID 11772110 DOI: 10.1021/ol017036w |
0.774 |
|
| 2002 |
Durham TB, Miller MJ. Conversion of glucuronic acid glycosides to novel bicyclic beta-lactams. Organic Letters. 4: 135-8. PMID 11772109 DOI: 10.1021/Ol017026V |
0.716 |
|
| 2002 |
Durham TB, Miller MJ. Conversion of glucuronic acid glycosides to novel bicyclic β-lactams Organic Letters. 4: 135-138. DOI: 10.1021/ol017026v |
0.672 |
|
| 2002 |
Surman MD, Mulvihill MJ, Miller MJ. Novel α-substituted β-amino diesters from acylnitroso-derived hetero-Diels-Alder cycloadducts Tetrahedron Letters. 43: 1131-1134. DOI: 10.1016/S0040-4039(01)02353-X |
0.761 |
|
| 2001 |
Lin YM, Miller MJ. Oxidation of primary amines to oxaziridines using molecular oxygen (O2) as the ultimate oxidant. The Journal of Organic Chemistry. 66: 8282-5. PMID 11722243 DOI: 10.1021/Jo010965G |
0.453 |
|
| 2001 |
Shireman BT, Miller MJ, Jonas M, Wiest O. Conformational study and enantioselective, regiospecific syntheses of novel aminoxy trans-proline analogues derived from an acylnitroso Diels-Alder cycloaddition. The Journal of Organic Chemistry. 66: 6046-56. PMID 11529730 DOI: 10.1021/Jo010284L |
0.752 |
|
| 2001 |
Lin YM, Miller MJ, Möllmann U. The remarkable hydrophobic effect of a fatty acid side chain on the microbial growth promoting activity of a synthetic siderophore. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 14: 153-7. PMID 11508848 DOI: 10.1023/A:1016666414848 |
0.541 |
|
| 2001 |
Shireman BT, Miller MJ. Synthesis of enantiomerically and diastereomerically pure 2(S)-amino-6(R)-hydroxy-1,7-heptanedioic acid dimethyl ester hydrochloride from cycloheptadiene. The Journal of Organic Chemistry. 66: 4809-13. PMID 11442409 DOI: 10.1021/Jo015544D |
0.744 |
|
| 2001 |
Surman MD, Miller MJ. Regio- and stereochemically controlled formation of hydroxamic acid containing anti- or syn-1,4-cycloalkenols from acylnitroso-derived Diels-Alder adducts. The Journal of Organic Chemistry. 66: 2466-9. PMID 11281789 DOI: 10.1021/Jo010094A |
0.769 |
|
| 2001 |
Surman MD, Miller MJ. Synthesis of a conformationally restricted substrate analogue of siderophore biosynthetases. Organic Letters. 3: 519-21. PMID 11178814 DOI: 10.1021/Ol006813+ |
0.786 |
|
| 2001 |
Shireman BT, Miller MJ. ChemInform Abstract: Rapid Syntheses of Either Enantiomer of Important Carbocyclic Nucleoside Precursors. Cheminform. 32: no-no. DOI: 10.1002/chin.200110234 |
0.725 |
|
| 2000 |
Roosenberg JM, Miller MJ. Total synthesis of the siderophore danoxamine. The Journal of Organic Chemistry. 65: 4833-8. PMID 10956460 DOI: 10.1021/Jo000050M |
0.809 |
|
| 2000 |
Roosenberg JM, Lin YM, Lu Y, Miller MJ. Studies and syntheses of siderophores, microbial iron chelators, and analogs as potential drug delivery agents. Current Medicinal Chemistry. 7: 159-97. PMID 10637361 DOI: 10.2174/0929867003375353 |
0.782 |
|
| 2000 |
Shireman BT, Miller MJ. Rapid syntheses of either enantiomer of important carbocyclic nucleoside precursors Tetrahedron Letters. 41: 9537-9540. DOI: 10.1016/S0040-4039(00)01668-3 |
0.744 |
|
| 2000 |
Bulychev A, Bellettini JR, O'Brien M, Crocker PJ, Samama J, Miller MJ, Mobashery S. N-Sulfonyloxy-β-lactam Inhibitors for β-Lactamases Tetrahedron. 56: 5719-5728. DOI: 10.1016/S0040-4020(00)00427-0 |
0.307 |
|
| 1999 |
Lu Y, Miller MJ. Syntheses and studies of multiwarhead siderophore-5-fluorouridine conjugates. Bioorganic & Medicinal Chemistry. 7: 3025-3038. PMID 10658609 DOI: 10.1016/S0968-0896(99)00248-5 |
0.33 |
|
| 1999 |
Ghosh A, Miller MJ, De Clercq E, Balzarini J. Synthesis and biological evaluation of a carbocyclic azanoraristeromycin siderophore conjugate. Nucleosides & Nucleotides. 18: 217-25. PMID 10067274 DOI: 10.1080/15257779908043069 |
0.393 |
|
| 1999 |
Li H, Miller MJ. Syntheses of 5‘-Deoxy-5‘-N-hydroxylaminopyrimidine and Purine Nucleosides: Building Blocks for Novel Antisense Oligonucleosides with Hydroxamate Linkages The Journal of Organic Chemistry. 64: 9289-9293. DOI: 10.1021/Jo991153B |
0.336 |
|
| 1999 |
Lin Y, Miller MJ. Practical Synthesis of Hydroxamate-Derived Siderophore Components by an Indirect Oxidation Method and Syntheses of a DIG−Siderophore Conjugate and a Biotin−Siderophore Conjugate The Journal of Organic Chemistry. 64: 7451-7458. DOI: 10.1021/Jo990769Y |
0.56 |
|
| 1999 |
Swarén P, Massova I, Bellettini JR, Bulychev A, Maveyraud L, Kotra LP, Miller MJ, Mobashery S, Samama J. Elucidation of Mechanism of Inhibition and X-ray Structure of the TEM-1 β-Lactamase fromEscherichia coliInhibited by aN-Sulfonyloxy-β-lactam Journal of the American Chemical Society. 121: 5353-5359. DOI: 10.1021/Ja990400Q |
0.323 |
|
| 1998 |
Zhang D, Süling C, Miller MJ. The Hetero Diels-Alder Reactions between D-Mannose-Derived Halonitroso Compounds and Cyclopentadiene: Scope and Limitations. The Journal of Organic Chemistry. 63: 885-888. PMID 11672089 DOI: 10.1021/Jo971696Q |
0.357 |
|
| 1998 |
Zhang D, Miller MJ. Total Synthesis of (+/-) Carbocyclic Polyoxin C and Its alpha-Epimer. The Journal of Organic Chemistry. 63: 755-759. PMID 11672070 DOI: 10.1021/Jo971711R |
0.379 |
|
| 1998 |
Möllmann U, Ghosh A, Dolence EK, Dolence JA, Ghosh M, Miller MJ, Reissbrodt R. Selective growth promotion and growth inhibition of gram-negative and gram-positive bacteria by synthetic siderophore-beta-lactam conjugates. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 11: 1-12. PMID 9450313 DOI: 10.1023/A:1009266705308 |
0.328 |
|
| 1998 |
Mulvihill MJ, Surman MD, Miller MJ. Regio- and Stereoselective Fe(III)- and Pd(0)-Mediated Ring Openings of 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene Systems The Journal of Organic Chemistry. 63: 4874-4875. DOI: 10.1021/Jo980950R |
0.739 |
|
| 1998 |
Xu Y, Miller MJ. Total Syntheses of Mycobactin Analogues as Potent Antimycobacterial Agents Using a Minimal Protecting Group Strategy The Journal of Organic Chemistry. 63: 4314-4322. DOI: 10.1021/Jo980063O |
0.403 |
|
| 1998 |
Mulvihill MJ, Gage JL, Miller MJ. Enzymatic Resolution of Aminocyclopentenols as Precursors tod- andl-Carbocyclic Nucleosides The Journal of Organic Chemistry. 63: 3357-3363. DOI: 10.1021/Jo972265A |
0.3 |
|
| 1998 |
Stocksdale MG, Ramurthy S, Miller MJ. Asymmetric Total Synthesis of an Important 3-(Hydroxymethyl)carbacephalosporin The Journal of Organic Chemistry. 63: 1221-1225. DOI: 10.1021/Jo971772P |
0.406 |
|
| 1998 |
Mulvihill MJ, Miller MJ. Syntheses of novel hydroxylamine carbanucleosides Tetrahedron. 54: 6605-6626. DOI: 10.1016/S0040-4020(98)00359-7 |
0.446 |
|
| 1998 |
Vogt PF, Miller MJ. Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions Tetrahedron. 54: 1317-1348. DOI: 10.1016/S0040-4020(97)10072-2 |
0.371 |
|
| 1997 |
Ghosh A, Ghosh M, Niu C, Malouin F, Moellmann U, Miller MJ. Iron transport-mediated drug delivery using mixed-ligand siderophore-beta-lactam conjugates. Chemistry & Biology. 3: 1011-9. PMID 9000006 DOI: 10.1016/S1074-5521(96)90167-2 |
0.309 |
|
| 1997 |
Hu J, Miller MJ. Total Synthesis of a Mycobactin S, a Siderophore and Growth Promoter ofMycobacterium Smegmatis, and Determination of its Growth Inhibitory Activity againstMycobacterium tuberculosis Journal of the American Chemical Society. 119: 3462-3468. DOI: 10.1021/Ja963968X |
0.36 |
|
| 1997 |
Vogt PF, Hansel J, Miller MJ. Asymmetric synthesis of an important precursor to 5′-nor carbocyclic nucleosides Tetrahedron Letters. 38: 2803-2804. DOI: 10.1016/S0040-4039(97)00511-X |
0.412 |
|
| 1997 |
Bellettini JR, Miller MJ. A short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitors Tetrahedron Letters. 38: 167-168. DOI: 10.1016/S0040-4039(96)02264-2 |
0.369 |
|
| 1996 |
Ramurthy S, Miller MJ. Framework-Reactive Siderophore Analogs as Potential Cell-Selective Drugs. Design and Syntheses of Trimelamol-Based Iron Chelators. The Journal of Organic Chemistry. 61: 4120-4124. PMID 11667292 DOI: 10.1021/Jo9600621 |
0.39 |
|
| 1996 |
Lu C, Buyer JS, Okonya JF, Miller MJ. Synthesis of optically pure chrysobactin and immunoassay development. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 9: 377-83. PMID 8837459 DOI: 10.1007/Bf00140607 |
0.302 |
|
| 1996 |
Brickman TJ, Hansel JG, Miller MJ, Armstrong SK. Purification, spectroscopic analysis and biological activity of the macrocyclic dihydroxamate siderophore alcaligin produced by Bordetella pertussis and Bordetella bronchiseptica Biometals. 9: 191-203. PMID 8744901 DOI: 10.1007/Bf00144625 |
0.3 |
|
| 1996 |
Ghosh M, Miller MJ. Synthesis and in vitro antibacterial activity of spermidine-based mixed catechol- and hydroxamate-containing siderophore-vancomycin conjugates Bioorganic and Medicinal Chemistry. 4: 43-48. PMID 8689237 DOI: 10.1016/0968-0896(95)00161-1 |
0.379 |
|
| 1996 |
Niu C, Pettersson T, Miller MJ. Enantioselective total syntheses of [6R,7R] and [6S,7S] tricyclic β-lactams Journal of Organic Chemistry. 61: 1014-1022. DOI: 10.1021/Jo951651U |
0.351 |
|
| 1996 |
Zhang D, Ghosh A, Süling C, Miller MJ. Efficient functionalization of acylnitroso cycloadducts: Application to the syntheses of carbocyclic nucleoside precursors Tetrahedron Letters. 37: 3799-3802. DOI: 10.1016/0040-4039(96)00692-2 |
0.434 |
|
| 1996 |
Ghosh M, Miller MJ. Synthesis of a bicyclic oxamazin. A novel heteroatom activated β-lactam Tetrahedron. 52: 4225-4238. DOI: 10.1016/0040-4020(96)00080-4 |
0.396 |
|
| 1995 |
Ghosh M, Miller MJ. Design, synthesis, and biological evaluation of isocyanurate-based antifungal and macrolide antibiotic conjugates: Iron transport-mediated drug delivery Bioorganic and Medicinal Chemistry. 3: 1519-1525. PMID 8634832 DOI: 10.1016/0968-0896(95)00134-3 |
0.364 |
|
| 1995 |
Ghosh A, Ritter AR, Miller MJ. Synthesis of enantiomerically pure 5'-aza-noraristeromycin analogs The Journal of Organic Chemistry. 60: 5808-5813. DOI: 10.1021/Jo00123A015 |
0.378 |
|
| 1995 |
Ghosh M, Lambert LJ, Huber PW, Miller MJ. Synthesis, bioactivity, and DNA-cleaving ability of desferrioxamine B-nalidixic acid and anthraquinone carboxylic acid conjugates Bioorganic and Medicinal Chemistry Letters. 5: 2337-2340. DOI: 10.1016/0960-894X(95)00412-M |
0.345 |
|
| 1995 |
Ghosh A, Miller MJ. Synthesis of novel hydantoin analogs of 5′-nor carbocyclic nucleosides: Versatility of a chiral acylnitroso cycloaddition Tetrahedron Letters. 36: 6399-6402. DOI: 10.1016/0040-4039(95)01323-A |
0.454 |
|
| 1995 |
Hu J, Miller MJ. An efficient synthesis of cobactin T, a key component of the mycobactin class of siderophores Tetrahedron Letters. 36: 6379-6382. DOI: 10.1016/0040-4039(95)01318-C |
0.342 |
|
| 1995 |
Hansel J, O'Hogan S, Lensky S, Ritter AR, Miller MJ. Oxazoline formation via a palladium-catalyzed cyclization: A direct, stereoselective approach to cis-5-amino-2-cyclopenten-1-ol derivatives Tetrahedron Letters. 36: 2913-2916. DOI: 10.1016/0040-4039(95)00465-O |
0.414 |
|
| 1995 |
Li X, Niu C, Miller MJ. Rearrangement of 3-amido-1-hydroxyazetidin-2-ones Tetrahedron Letters. 36: 1617-1620. DOI: 10.1016/0040-4039(95)00115-S |
0.348 |
|
| 1995 |
Niu C, Miller MJ. Asymmetric syntheses of β-lactams and determination of their absolute configuration Tetrahedron Letters. 36: 497-500. DOI: 10.1016/0040-4039(94)02294-L |
0.352 |
|
| 1994 |
Guzzo PR, Miller MJ. Catalytic, Asymmetric Synthesis of the Carbacephem Framework The Journal of Organic Chemistry. 59: 4862-4867. DOI: 10.1021/Jo00096A031 |
0.376 |
|
| 1994 |
Hu J, Miller MJ. A New Method for the Synthesis ofN.epsilon.-Acetyl-N.epsilon.-hydroxy-L-lysine, the Iron-Binding Constituent of Several Important Siderophores The Journal of Organic Chemistry. 59: 4858-4861. DOI: 10.1021/Jo00096A030 |
0.347 |
|
| 1994 |
Ritter AR, Miller MJ. Amino Acid-Derived Chiral Acyl Nitroso Compounds: Diastereoselectivity in Intermolecular Hetero Diels-Alder Reactions The Journal of Organic Chemistry. 59: 4602-4611. DOI: 10.1021/Jo00095A040 |
0.425 |
|
| 1994 |
Ghosh M, Miller MJ. Iron Transport-Mediated Drug Delivery: Synthesis and Biological Evaluation of Cyanuric Acid-Based Siderophore Analogs and .beta.-Lactam Conjugates The Journal of Organic Chemistry. 59: 1020-1026. DOI: 10.1021/Jo00084A018 |
0.373 |
|
| 1994 |
Darwish IS, Miller MJ. Synthesis of the Antifungal Agent Neoenactin A and Its N-Deshydroxy Derivative The Journal of Organic Chemistry. 59: 451-454. DOI: 10.1021/Jo00081A027 |
0.433 |
|
| 1994 |
Ritter AR, Miller MJ. Asymmetric syntheses of novel amino acids and peptides from acylnitroso-derived cycloadducts Tetrahedron Letters. 35: 9379-9382. DOI: 10.1016/S0040-4039(00)78547-9 |
0.335 |
|
| 1993 |
Ghosh A, Miller MJ. Synthesis of novel citrate-based siderophores and siderophore-.beta.-lactam conjugates. Iron transport-mediated drug delivery systems The Journal of Organic Chemistry. 58: 7652-7659. DOI: 10.1021/Jo00079A007 |
0.397 |
|
| 1993 |
Darwish IS, Patel C, Miller MJ. Synthesis of the antifungal agent norneoenactin A The Journal of Organic Chemistry. 58: 6072-6075. DOI: 10.1021/Jo00074A038 |
0.342 |
|
| 1993 |
Lotz BT, Miller MJ. Diastereoselective synthesis of the carbacephem framework The Journal of Organic Chemistry. 58: 618-625. DOI: 10.1021/Jo00055A013 |
0.381 |
|
| 1993 |
Teng M, Miller MJ. Diastereoselective addition of nucleophiles to the C3 position of N-(tosyloxy)-β-lactams Journal of the American Chemical Society. 115: 548-554. DOI: 10.1021/Ja00055A026 |
0.344 |
|
| 1993 |
Miller MJ, Malouin F. Microbial iron chelators as drug delivery agents: the rational design and synthesis of siderophore-drug conjugates Accounts of Chemical Research. 26: 241-249. DOI: 10.1021/Ar00029A003 |
0.306 |
|
| 1993 |
Teng M, Gasparski CM, Williams MA, Miller MJ. A combined electrophilic diazo and nucleophilic azide transfer reaction for the efficient conversion of an N-hydroxy-β-lactam to a carbacephem precursor Bioorganic and Medicinal Chemistry Letters. 3: 2431-2436. DOI: 10.1016/S0960-894X(01)80971-9 |
0.372 |
|
| 1993 |
Farouz-Grant F, Miller MJ. Syntheses of novel 1-aminocyclopropane-1-carboxylic acid (ACC)-containing β-lactams Bioorganic & Medicinal Chemistry Letters. 3: 2423-2428. DOI: 10.1016/S0960-894X(01)80969-0 |
0.374 |
|
| 1993 |
Ghosh A, Miller MJ. Mn(III) promoted N-O bond reduction of N-hydroxy-2-azetidinones Tetrahedron Letters. 34: 83-86. DOI: 10.1016/S0040-4039(00)60063-1 |
0.303 |
|
| 1992 |
Minnick AA, McKee JA, Dolence EK, Miller MJ. Iron transport-mediated antibacterial activity of and development of resistance to hydroxamate and catechol siderophore-carbacephalosporin conjugates. Antimicrobial Agents and Chemotherapy. 36: 840-50. PMID 1503447 DOI: 10.1128/Aac.36.4.840 |
0.398 |
|
| 1992 |
Gasparski CM, Ghosh A, Miller MJ. Titanium(III)-mediated synthesis of a 1,2,3-tricarbonyl moiety from an .alpha.-oximido-.beta.-keto ester: application to the synthesis of the carbacephem nucleus The Journal of Organic Chemistry. 57: 3546-3550. DOI: 10.1021/Jo00039A009 |
0.328 |
|
| 1992 |
Gasparski CM, Teng M, Miller MJ. Functionalization of the β-lactam ring: Diastereoselective azide transfer and N-O bond reduction on C4-substituted N-hydroxy β-lactams in one step Journal of the American Chemical Society. 114: 2741-2743. DOI: 10.1021/Ja00033A072 |
0.333 |
|
| 1991 |
Minnick AA, Eizember LE, McKee JA, Dolence EK, Miller MJ. Bioassay for siderophore utilization by Candida albicans. Analytical Biochemistry. 194: 223-9. PMID 1907814 DOI: 10.1016/0003-2697(91)90171-O |
0.315 |
|
| 1991 |
McKee JA, Sharma SK, Miller MJ. Iron transport mediated drug delivery systems: synthesis and antibacterial activity of spermidine- and lysine-based siderophore-beta-lactam conjugates. Bioconjugate Chemistry. 2: 281-91. PMID 1837735 DOI: 10.1021/Bc00010A013 |
0.322 |
|
| 1991 |
Dolence EK, Minnick AA, Lin CE, Miller MJ, Payne SM. Synthesis and siderophore and antibacterial activity of N5-acetyl-N5-hydroxy-L-ornithine-derived siderophore-beta-lactam conjugates: iron-transport-mediated drug delivery. Journal of Medicinal Chemistry. 34: 968-78. PMID 1825850 DOI: 10.1021/Jm00107A014 |
0.35 |
|
| 1991 |
Dolence EK, Lin CE, Miller MJ, Payne SM. Synthesis and siderophore activity of albomycin-like peptides derived from N5-acetyl-N5-hydroxy-L-ornithine. Journal of Medicinal Chemistry. 34: 956-68. PMID 1825849 DOI: 10.1021/Jm00107A013 |
0.346 |
|
| 1991 |
Williams MA, Hsiao CN, Miller MJ. Direct conversion of N-alkoxy .beta.-lactams to carbapenams: application to the synthesis of the bicyclic PS-5 keto ester The Journal of Organic Chemistry. 56: 2688-2694. DOI: 10.1021/Jo00008A022 |
0.406 |
|
| 1991 |
Williams MA, Miller MJ, Rath NP. Hemiketal formation and subsequent intramolecular acylation of an N-hydroxy .beta.-lactam The Journal of Organic Chemistry. 56: 1293-1296. DOI: 10.1021/Jo00003A066 |
0.333 |
|
| 1991 |
McKee JA, Miller MJ. Synthesis, siderophore, and antimicrobial evaluation of a spermidine-based tricatecholate siderophore and carbacephalosporin conjugate Bioorganic and Medicinal Chemistry Letters. 1: 513-518. DOI: 10.1016/S0960-894X(01)80456-X |
0.401 |
|
| 1991 |
Farouz F, Miller MJ. Facile syntheses and rearrangements of peptide derived β-lactams Tetrahedron Letters. 32: 3305-3308. DOI: 10.1016/S0040-4039(00)92692-3 |
0.322 |
|
| 1991 |
Ma C, Miller MJ. Asymmetric synthesis of α-hydroxyethyl β-lactam derivatives: an approach to thienamycin Tetrahedron Letters. 32: 2577-2580. DOI: 10.1016/S0040-4039(00)78789-2 |
0.336 |
|
| 1991 |
Gasparski CM, Miller MJ. Synthesis of β-hydroxy-α-amino acids by aldol condensation using a chiral phase transfer catalyst Tetrahedron. 47: 5367-5378. DOI: 10.1016/S0040-4020(01)80971-6 |
0.333 |
|
| 1990 |
Lotz BT, Gasparski CM, Peterson K, Miller MJ. Substrate specificity studies of aldolase enzymes for use in organic synthesis Journal of the Chemical Society, Chemical Communications. 1107-1109. DOI: 10.1039/C39900001107 |
0.335 |
|
| 1990 |
Kolasa T, Miller MJ. 1-Hydroxy-3-amino-2-piperidone (.delta.-N-hydroxycycloornithine) derivatives: key intermediates for the synthesis of hydroxamate-based siderophores The Journal of Organic Chemistry. 55: 1711-1721. DOI: 10.1021/Jo00293A010 |
0.395 |
|
| 1990 |
Williams MA, Miller MJ. Synthesis of the carbapenam ring system via carbene mediated rearrangement of an n-benzyloxy-β-lactam Tetrahedron Letters. 31: 1807-1810. DOI: 10.1016/S0040-4039(00)98791-4 |
0.374 |
|
| 1990 |
Reno DS, Lotz BT, Miller MJ. Asymmetric aldol reactions using boron enolates of chiral oxazinones, synthesis of L-allo-threonine Tetrahedron Letters. 31: 827-830. DOI: 10.1016/S0040-4039(00)94638-0 |
0.349 |
|
| 1990 |
Huang NZ, Kalish VJ, Miller MJ. Double cyclization of aminophosphonoacetate derived β- hydroxyacids to bicyclic β-lactams Tetrahedron. 46: 8067-8074. DOI: 10.1016/S0040-4020(01)81463-0 |
0.312 |
|
| 1990 |
ZERCHER CK, MILLER MJ. ChemInform Abstract: Novel Palladium(II)-Mediated Reactions of N-Hydroxy β-Lactams. Cheminform. 21. DOI: 10.1002/chin.199030164 |
0.649 |
|
| 1989 |
Sharma SK, Miller MJ, Payne SM. Spermexatin and spermexatol: New synthetic spermidine-based siderophore analogues Journal of Medicinal Chemistry. 32: 357-367. PMID 2521517 DOI: 10.1021/Jm00122A013 |
0.388 |
|
| 1989 |
Zercher CK, Miller MJ. Novel palladium (II) mediated reactions of N-hydroxy-β-lactams Tetrahedron Letters. 30: 7009-7012. DOI: 10.1016/S0040-4039(01)93410-0 |
0.689 |
|
| 1988 |
Kolasa T, Miller MJ. Oxidations of some α-amino acids under mitsunobu reaction conditions Tetrahedron Letters. 29: 4661-4664. DOI: 10.1016/S0040-4039(00)80574-2 |
0.326 |
|
| 1988 |
Kolasa T, Sharma SK, Miller MJ. α-n-hydroxyamino acid derivatives Tetrahedron. 44: 5431-5440. DOI: 10.1016/S0040-4020(01)86049-X |
0.384 |
|
| 1987 |
Boyd DB, Eigenbrot C, Indelicato JM, Miller MJ, Pasini CE, Woulfe SR. Heteroatom-activated beta-lactam antibiotics: considerations of differences in the biological activity of [[3(S)-(acylamino)-2-oxo-1-azetidinyl]oxy]acetic acids (oxamazins) and the corresponding sulfur analogues (thiamazins). Journal of Medicinal Chemistry. 30: 528-36. PMID 3820225 DOI: 10.1021/Jm00386A015 |
0.339 |
|
| 1987 |
Kolasa T, Miller MJ. Reactions of .alpha.-hydroxy carbonyl compounds with azodicarboxylates and triphenylphosphine: synthesis of .alpha.-N-hydroxy amino acid derivatives The Journal of Organic Chemistry. 52: 4978-4984. DOI: 10.1021/Jo00231A026 |
0.359 |
|
| 1987 |
Rajendra G, Miller MJ. Intramolecular electrophilic additions to olefins in organic syntheses. Stereoselective synthesis of 3,4-substituted .beta.-lactams by bromine-induced oxidative cyclization of O-acyl .beta.,.gamma.-unsaturated hydroxamic acid derivatives The Journal of Organic Chemistry. 52: 4471-4477. DOI: 10.1021/Jo00229A009 |
0.348 |
|
| 1987 |
Kolasa T, Sharma S, Miller MJ. Reactions of organometallics with oximes. Synthesis of α-N-hydroxy amino acids Tetrahedron Letters. 28: 4973-4976. DOI: 10.1016/S0040-4039(00)96673-5 |
0.411 |
|
| 1987 |
Kolasa T, Miller MJ. Synthesis of substituted 3-hydroxy-4-alkoxycarbonyl-2-azetidinones Tetrahedron Letters. 28: 1861-1863. DOI: 10.1016/S0040-4039(00)95994-X |
0.366 |
|
| 1986 |
Liu L, Tanke RS, Miller MJ. Electrophilic sulfur transfer reactions in organic synthesis. Preparation of a diastereomer of the key macrocyclic component of griseoviridin The Journal of Organic Chemistry. 51: 5332-5337. DOI: 10.1021/Jo00376A052 |
0.338 |
|
| 1986 |
Woulfe SR, Miller MJ. The synthesis of substituted [[3(S)-(acylamino)-2-oxo-1-azetidinyl]thio]acetic acids The Journal of Organic Chemistry. 51: 3133-3139. DOI: 10.1021/Jo00366A010 |
0.307 |
|
| 1986 |
Lee BH, Biswas A, Miller MJ. [1,2]-Anionic rearrangements of substituted N-hydroxy-2-azetidinones and applications to the synthesis of bicyclic .beta.-lactams The Journal of Organic Chemistry. 51: 106-109. DOI: 10.1021/Jo00351A026 |
0.354 |
|
| 1986 |
Iwagami H, Woulfe SR, Miller MJ. Reactions of (2-oxo-1-azetidinyl)-thiophthalimides with nucleophiles Tetrahedron Letters. 27: 3095-3098. DOI: 10.1016/S0040-4039(00)84724-3 |
0.378 |
|
| 1986 |
Biswas A, Eigenbrot C, Miller MJ. Rearrangement of N-hydroxy β-lactams Tetrahedron. 42: 6421-6428. DOI: 10.1016/S0040-4020(01)88103-5 |
0.364 |
|
| 1986 |
MILLER MJ. ChemInform Abstract: Hydroxamate Approach to the Synthesis of β-Lactam Antibiotics Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198631362 |
0.309 |
|
| 1986 |
LEE BH, BISWAS A, MILLER MJ. ChemInform Abstract: [1,2]Anionic Rearrangements of Substituted N-Hydroxy-2-azetidinones and Applications to the Synthesis of Bicyclic β-Lactams. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198626169 |
0.372 |
|
| 1985 |
Woulfe SR, Miller MJ. Synthesis and biological activity of substituted [[3(S)-(acylamino)-2-oxo-1-azetidinyl]oxy]acetic acids. A new class of heteroatom-activated beta-lactam antibiotics. Journal of Medicinal Chemistry. 28: 1447-53. PMID 4045920 DOI: 10.1021/Jm00148A013 |
0.443 |
|
| 1985 |
Lee BH, Miller MJ, Prody CA, Neilands JB. Artificial siderophores. 2. Syntheses of trihydroxamate analogues of rhodotorulic acid and their biological iron transport capabilities in Escherichia coli. Journal of Medicinal Chemistry. 28: 323-7. PMID 3156249 DOI: 10.1002/Chin.198532237 |
0.364 |
|
| 1985 |
Lee BH, Miller MJ, Prody CA, Neilands JB. Artificial siderophores. 1. Synthesis and microbial iron transport capabilities. Journal of Medicinal Chemistry. 28: 317-23. PMID 3156248 DOI: 10.1002/Chin.198532123 |
0.406 |
|
| 1985 |
Woulfe SR, Iwagami H, Miller MJ. Efficient N-sulfenylation of 2-azetidinones using S-substituted thiophthalimides Tetrahedron Letters. 26: 3891-3894. DOI: 10.1016/S0040-4039(00)98680-5 |
0.353 |
|
| 1985 |
Jung M, Miller MJ. The application of highly stereoselective aldol condensations to the synthesis of β-lactam antibiotics. Tetrahedron Letters. 26: 977-980. DOI: 10.1016/S0040-4039(00)98490-9 |
0.334 |
|
| 1985 |
Rajendra G, Miller MJ. Oxidative cyclization of β,γ-unsaturated O-acyl hydroxamates to β-lactams Tetrahedron Letters. 26: 5385-5388. DOI: 10.1016/S0040-4039(00)98214-5 |
0.322 |
|
| 1985 |
Chi-Nung H, Ashburn SP, Miller MJ. Enantioselective aldol reaction of chiral acyl thiazolidine thione derived boron enolates Tetrahedron Letters. 26: 4855-4858. DOI: 10.1016/S0040-4039(00)94969-4 |
0.379 |
|
| 1984 |
Lee BH, Gerfen GJ, Miller MJ. Constituents of microbial iron chelators. Alternate syntheses of .delta.-N-hydroxy-L-ornithine derivatives and applications to the synthesis of rhodotorulic acid The Journal of Organic Chemistry. 49: 2418-2423. DOI: 10.1021/Jo00187A023 |
0.341 |
|
| 1984 |
Woulfe SR, Miller MJ. Heteroatom activated β-lactam antibiotics: Synthesis of biologically active substituted N-oxy-3-amino-2-azetidinones (oxamazins) Tetrahedron Letters. 25: 3293-3296. DOI: 10.1016/S0040-4039(01)81367-8 |
0.379 |
|
| 1984 |
Hyun Lee B, Miller MJ. Constituents of microbial iron chelators. The synthesis of optically active derivatives of δ-N-hydroxy-L-ornithine. Tetrahedron Letters. 25: 927-930. DOI: 10.1016/S0040-4039(01)80064-2 |
0.371 |
|
| 1984 |
MATTINGLY PG, MILLER MJ, COOPER RDG, DAUGHERTY BW. ChemInform Abstract: CHIRAL SYNTHESIS OF PROTECTED 3-AMINO-4-(ALKOXYCARBONYL)-2-AZETIDINONES FROM β-HYDROXYASPARTIC ACID Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198413149 |
0.336 |
|
| 1983 |
Mattingly PG, Miller MJ, Cooper RDG, Daughtery BW. Chiral synthesis of protected 3-amino-4-(alkoxycarbonyl)-2-azetidinones from .beta.-hydroxyaspartic acid The Journal of Organic Chemistry. 48: 3556-3559. DOI: 10.1021/Jo00168A038 |
0.319 |
|
| 1983 |
Capecchi JT, Miller MJ, Loudon GM. Critical examination of a method for the analysis of .alpha. and .omega. linkages in peptides containing aspartic acid and glutamic acid The Journal of Organic Chemistry. 48: 2014-2021. DOI: 10.1021/Jo00160A015 |
0.612 |
|
| 1983 |
Bajwa JS, Miller MJ. Preparation of chiral substituted succinic acids The Journal of Organic Chemistry. 48: 1114-1116. DOI: 10.1021/Jo00155A042 |
0.349 |
|
| 1983 |
Lee BH, Miller MJ. Natural ferric ionophores: total synthesis of schizokinen, schizokinen A, and arthrobactin The Journal of Organic Chemistry. 48: 24-31. DOI: 10.1021/Jo00149A005 |
0.344 |
|
| 1983 |
Miller MJ, Biswas A, Krook MA. Practical synthetic approaches to intermediates for the preparation of the novel O-sulfonated-N-hydroxy-2-azetidinone antibiotics Tetrahedron. 39: 2571-2575. DOI: 10.1016/S0040-4020(01)92150-7 |
0.379 |
|
| 1983 |
Miller M, Mattingly P. The direct chemical conversion of peptides to β-lactams Tetrahedron. 39: 2563-2570. DOI: 10.1016/S0040-4020(01)92149-0 |
0.353 |
|
| 1982 |
Miller MJ, Bajwa JS, Mattingly PG, Peterson K. Enantioselective syntheses of 3-substituted 4-(alkoxycarbonyl)-2-azetidinones from malic acid The Journal of Organic Chemistry. 47: 4928-4933. DOI: 10.1021/Jo00146A020 |
0.375 |
|
| 1982 |
Maurer PJ, Miller MJ. Microbial iron chelators: total synthesis of aerobactin and its constituent amino acid, N6-acetyl-N6-hydroxylysine Journal of the American Chemical Society. 104: 3096-3101. DOI: 10.1021/Ja00375A025 |
0.352 |
|
| 1981 |
Mattingly PG, Miller MJ. Synthesis of 2-azetidinones from serinehydroxamates: approaches to the synthesis of 3-aminonocardicinic acid The Journal of Organic Chemistry. 46: 1557-1564. DOI: 10.1021/Jo00321A007 |
0.351 |
|
| 1981 |
Miller M, Mattingly P, Morrison M, Kerwin, Jr. J. Additions and Corrections - Synthesis of β-Lactams from Substituted Hydroxamic Acids Journal of the American Chemical Society. 103: 2909-2909. DOI: 10.1021/Ja00400A601 |
0.351 |
|
| 1980 |
Mattingly PG, Miller MJ. Titanium trichloride reduction of substituted N-hydroxy-2-azetidinones and other hydroxamic acids The Journal of Organic Chemistry. 45: 410-415. DOI: 10.1021/Jo01291A007 |
0.359 |
|
| 1980 |
Miller MJ, Mattingly PG, Morrison MA, Kerwin JF. Synthesis of .beta.-lactams from substituted hydroxamic acids Journal of the American Chemical Society. 102: 7026-7032. DOI: 10.1021/Ja00543A021 |
0.332 |
|
| 1979 |
Mattingly PG, Kerwin JF, Miller MJ. A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesis Journal of the American Chemical Society. 101: 3983-3985. DOI: 10.1021/Ja00508A056 |
0.359 |
|
| 1977 |
Miller MJ, DeBons FE, Loudon GM. The chemistry of a method for the determination of carboxyl-terminal residues in peptides. The Journal of Organic Chemistry. 42: 1750-61. PMID 853324 DOI: 10.1002/Chin.197742366 |
0.602 |
|
| 1977 |
Miller MJ, Rapoport H. Porphyrin-protein bond of cytochrome c558 from Euglena gracilis. Journal of the American Chemical Society. 99: 3479-85. PMID 192772 DOI: 10.1002/Chin.197733339 |
0.411 |
|
| 1975 |
Miller MJ, Loudon GM. Letter: Carboxyl-terminal amino acid residue analysis of peptides. A new method. Journal of the American Chemical Society. 97: 5295-7. PMID 1165365 DOI: 10.1021/Ja00851A055 |
0.622 |
|
| 1975 |
Miller MJ, Loudon GM. Convenient, high-yield conversion of aldehydes to nitriles The Journal of Organic Chemistry. 40: 126-127. DOI: 10.1021/Jo00889A034 |
0.32 |
|
| Show low-probability matches. |
