| Year |
Citation |
Score |
| 2018 |
Pierce MR, Bakas NA, Pirrung MC, Bachmann AS. Thiasyrbactins Induce Cell Death Proteasome Inhibition in Multiple Myeloma Cells. Anticancer Research. 38: 5607-5613. PMID 30275178 DOI: 10.21873/Anticanres.12895 |
0.758 |
|
| 2017 |
Bakas NA, Schultz CR, Yco LP, Roberts CC, Chang CA, Bachmann AS, Pirrung MC. Immunoproteasome inhibition and bioactivity of thiasyrbactins. Bioorganic & Medicinal Chemistry. PMID 29269255 DOI: 10.1016/j.bmc.2017.11.048 |
0.782 |
|
| 2017 |
Pirrung MC, Dorsey A, Howitt N, Liao J. β-Deuterium Isotope Effects on Firefly Luciferase Bioluminescence. Chemistryopen. 6: 697-700. PMID 29226056 DOI: 10.1002/Open.201700136 |
0.586 |
|
| 2017 |
Pirrung M, Bakas N. Homoserine and Threonine Peptide Assembly Synlett. 29: 238-242. DOI: 10.1055/s-0036-1589123 |
0.77 |
|
| 2016 |
Pirrung MC, Schreihans RS. Native Serine Peptide Assembly: Scope and Utility. European Journal of Organic Chemistry. 2016: 5633-5636. PMID 28111523 DOI: 10.1002/Ejoc.201601148 |
0.38 |
|
| 2016 |
Pirrung MC, Zhang F, Ambadi S, Gangadhara Rao Y. Correction: Total synthesis of fellutamides, lipopeptide proteasome inhibitors. More sustainable peptide bond formation. Organic & Biomolecular Chemistry. 14: 9159. PMID 27714303 DOI: 10.1039/c6ob90139e |
0.762 |
|
| 2016 |
Pirrung MC, Zhang F, Ambadi S, Gangadhara Rao Y. Total synthesis of fellutamides, lipopeptide proteasome inhibitors. More sustainable peptide bond formation. Organic & Biomolecular Chemistry. PMID 27533920 DOI: 10.1039/C6Ob01233G |
0.767 |
|
| 2016 |
Bachmann AS, Opoku-Ansah J, Ibarra-Rivera TR, Yco LP, Ambadi S, Roberts CC, Chang CA, Pirrung MC. Syrbactin Structural Analog TIR-199 Blocks Proteasome Activity And Induces Tumor Cell Death. The Journal of Biological Chemistry. PMID 26907687 DOI: 10.1074/Jbc.M115.710053 |
0.758 |
|
| 2014 |
Pirrung MC, Biswas G, De Howitt N, Liao J. Synthesis and bioluminescence of difluoroluciferin. Bioorganic & Medicinal Chemistry Letters. 24: 4881-3. PMID 25239851 DOI: 10.1016/J.Bmcl.2014.08.048 |
0.315 |
|
| 2013 |
Pirrung MC, Nalbandian JN. Catalyzed Claisen rearrangements of O-allyl kojates. Tetrahedron Letters. 54. PMID 24187389 DOI: 10.1016/J.Tetlet.2013.05.002 |
0.758 |
|
| 2012 |
Opoku-Ansah J, Ibarra-Rivera TR, Pirrung MC, Bachmann AS. Syringolin B-inspired proteasome inhibitor analogue TIR-203 exhibits enhanced biological activity in multiple myeloma and neuroblastoma. Pharmaceutical Biology. 50: 25-9. PMID 22196580 DOI: 10.3109/13880209.2011.626784 |
0.305 |
|
| 2012 |
Pirrung MC, Zhang F, Ambadi S, Ibarra-Rivera TR. Reactive esters in amide ligation with β-hydroxyamines European Journal of Organic Chemistry. 4283-4286. DOI: 10.1002/Ejoc.201200624 |
0.77 |
|
| 2011 |
Ibarra-Rivera TR, Opoku-Ansah J, Ambadi S, Bachmann AS, Pirrung MC. Syntheses and cytotoxicity of syringolin B-based proteasome inhibitors Tetrahedron. 67: 9950-9956. DOI: 10.1016/J.Tet.2011.09.048 |
0.779 |
|
| 2010 |
Pirrung MC, Biswas G, Ibarra-Rivera TR. Total synthesis of syringolin A and B. Organic Letters. 12: 2402-5. PMID 20426399 DOI: 10.1021/Ol100761Z |
0.386 |
|
| 2010 |
Surpin M, Zou Y, Xiong C, Raikhel NV, Pirrung MC. Iodine scanning of a phenazine inhibitor of vacuolar sorting. Bioorganic & Medicinal Chemistry Letters. 20: 1496-9. PMID 20153185 DOI: 10.1016/J.Bmcl.2010.01.106 |
0.658 |
|
| 2010 |
Pirrung M, Biswas G, Ibarra‐Rivera T. Syringolin total synthesis F1000research. 1. DOI: 10.7490/F1000Research.418.1 |
0.351 |
|
| 2010 |
Pirrung MC, Roy BG, Gadamsetty S. Structure-reactivity relationships in (2-hydroxyethyl)benzophenone photoremovable protecting Groups Tetrahedron. 66: 3147-3151. DOI: 10.1016/J.Tet.2010.02.087 |
0.375 |
|
| 2009 |
Pirrung MC, Ghorai S, Ibarra-Rivera TR. Multicomponent reactions of convertible isonitriles. The Journal of Organic Chemistry. 74: 4110-7. PMID 19408909 DOI: 10.1021/Jo900414N |
0.386 |
|
| 2009 |
Pirrung MC, Wang J. Multicomponent reactions of cyclobutanones. The Journal of Organic Chemistry. 74: 2958-63. PMID 19354324 DOI: 10.1021/Jo802170K |
0.525 |
|
| 2008 |
Pirrung MC, Das Sarma K, Wang J. Hydrophobicity and mixing effects on select heterogeneous, water-accelerated synthetic reactions. The Journal of Organic Chemistry. 73: 8723-30. PMID 18954111 DOI: 10.1021/Jo801134R |
0.519 |
|
| 2008 |
Pirrung MC, Bleecker AB, Inoue Y, Rodríguez FI, Sugawara N, Wada T, Zou Y, Binder BM. Ethylene receptor antagonists: strained alkenes are necessary but not sufficient. Chemistry & Biology. 15: 313-21. PMID 18420138 DOI: 10.1016/J.Chembiol.2008.02.018 |
0.654 |
|
| 2008 |
Zou Y, Rojas-Pierce M, Raikhel NV, Pirrung MC. Preparation of methyl ester precursors of biologically active agents Biotechniques. 44: 377-384. PMID 18361791 DOI: 10.2144/000112704 |
0.682 |
|
| 2008 |
Xiong X, Pirrung MC. Modular synthesis of candidate indole-based insulin mimics by Claisen rearrangement. Organic Letters. 10: 1151-4. PMID 18303898 DOI: 10.1021/Ol800058D |
0.35 |
|
| 2008 |
Pirrung MC, Deng L, Lin B, Webster NJ. Quinone replacements for small molecule insulin mimics. Chembiochem : a European Journal of Chemical Biology. 9: 360-2. PMID 18232038 DOI: 10.1002/Cbic.200700597 |
0.627 |
|
| 2008 |
Pirrung MC. Book Review of Amino Group Chemistry: From Synthesis to the Life Sciences Amino Group Chemistry: From Synthesis to the Life Sciences . Edited by Alfredo Ricci (Università di Bologna, Italy) . Wiley-VCH Verlag GmbH & Co. KGaA : Weinheim 2008 . xiv +394 pp. $200. ISBN 978-3-527-31741-7 . Journal of the American Chemical Society. 130: 8567-8567. DOI: 10.1021/Ja803747N |
0.308 |
|
| 2007 |
Lin B, Li Z, Park K, Deng L, Pai A, Zhong L, Pirrung MC, Webster NJ. Identification of novel orally available small molecule insulin mimetics. The Journal of Pharmacology and Experimental Therapeutics. 323: 579-85. PMID 17687071 DOI: 10.1124/Jpet.107.126102 |
0.613 |
|
| 2007 |
Pirrung MC, Li Z, Hensley E, Liu Y, Tanksale A, Lin B, Pai A, Webster NJ. Parallel synthesis of indolylquinones and their cell-based insulin mimicry. Journal of Combinatorial Chemistry. 9: 844-54. PMID 17595147 DOI: 10.1021/Cc070062M |
0.388 |
|
| 2007 |
Kim H, Deng L, Xiong X, Hunter WD, Long MC, Pirrung MC. Glyceraldehyde 3-phosphate dehydrogenase is a cellular target of the insulin mimic demethylasterriquinone B1. Journal of Medicinal Chemistry. 50: 3423-6. PMID 17595071 DOI: 10.1021/Jm070437I |
0.589 |
|
| 2007 |
Xiong X, Pirrung MC. Practical synthesis of 7-prenylindole. The Journal of Organic Chemistry. 72: 5832-4. PMID 17580906 DOI: 10.1021/Jo070734V |
0.36 |
|
| 2007 |
Lin B, Pirrung MC, Deng L, Li Z, Liu Y, Webster NJ. Neuroprotection by small molecule activators of the nerve growth factor receptor. The Journal of Pharmacology and Experimental Therapeutics. 322: 59-69. PMID 17468299 DOI: 10.1124/Jpet.106.118034 |
0.61 |
|
| 2006 |
Pirrung MC, Ghorai S. Versatile, fragrant, convertible isonitriles. Journal of the American Chemical Society. 128: 11772-3. PMID 16953613 DOI: 10.1021/Ja0644374 |
0.379 |
|
| 2006 |
Pirrung MC, Ye T, Zhou Z, Simon JD. Mechanistic studies on the photochemical deprotection of 3',5'-dimethoxybenzoin esters. Photochemistry and Photobiology. 82: 1258-64. PMID 16752957 DOI: 10.1562/2006-02-07-Ra-798 |
0.305 |
|
| 2006 |
Mdluli KE, Witte PR, Kline T, Barb AW, Erwin AL, Mansfield BE, McClerren AL, Pirrung MC, Tumey LN, Warrener P, Raetz CR, Stover CK. Molecular validation of LpxC as an antibacterial drug target in Pseudomonas aeruginosa. Antimicrobial Agents and Chemotherapy. 50: 2178-84. PMID 16723580 DOI: 10.1128/Aac.00140-06 |
0.706 |
|
| 2005 |
Pirrung MC, Liu Y, Deng L, Halstead DK, Li Z, May JF, Wedel M, Austin DA, Webster NJ. Methyl scanning: total synthesis of demethylasterriquinone B1 and derivatives for identification of sites of interaction with and isolation of its receptor(s). Journal of the American Chemical Society. 127: 4609-24. PMID 15796526 DOI: 10.1021/Ja044325H |
0.656 |
|
| 2005 |
Pirrung MC, Fujita K, Park K. Organometallic routes to 2,5-dihydroxy-3-(indol-3-yl)benzoquinones. Synthesis of demethylasterriquinone B4. The Journal of Organic Chemistry. 70: 2537-42. PMID 15787540 DOI: 10.1021/Jo048126S |
0.375 |
|
| 2004 |
Pirrung MC, Das Sarma K. β-lactam synthesis by Ugi reaction of β-keto acids in aqueous solution Synlett. 1425-1427. DOI: 10.1055/S-2004-825606 |
0.331 |
|
| 2003 |
Pirrung MC, Pieper WH, Kaliappan KP, Dhananjeyan MR. Combinatorial discovery of two-photon photoremovable protecting groups. Proceedings of the National Academy of Sciences of the United States of America. 100: 12548-53. PMID 14557545 DOI: 10.1073/Pnas.2131115100 |
0.592 |
|
| 2003 |
Sohn J, Kiburz B, Li Z, Deng L, Safi A, Pirrung MC, Rudolph J. Inhibition of Cdc25 phosphatases by indolyldihydroxyquinones. Journal of Medicinal Chemistry. 46: 2580-8. PMID 12801222 DOI: 10.1021/Jm0300835 |
0.644 |
|
| 2003 |
Pirrung MC, Liu H. Modular, parallel synthesis of an illudinoid combinatorial library. Organic Letters. 5: 1983-5. PMID 12762702 DOI: 10.1021/Ol034565M |
0.334 |
|
| 2003 |
Pirrung MC, Tumey LN, McClerren AL, Raetz CR. High-throughput catch-and-release synthesis of oxazoline hydroxamates. Structure-activity relationships in novel inhibitors of Escherichia coli LpxC: in vitro enzyme inhibition and antibacterial properties. Journal of the American Chemical Society. 125: 1575-86. PMID 12568618 DOI: 10.1021/Ja0209114 |
0.743 |
|
| 2002 |
Pirrung MC, Deng L, Li Z, Park K. Synthesis of 2,5-dihydroxy-3-(indol-3-yl)benzoquinones by acid-catalyzed condensation of indoles with 2,5-dichlorobenzoquinone. The Journal of Organic Chemistry. 67: 8374-88. PMID 12444614 DOI: 10.1021/Jo0204597 |
0.68 |
|
| 2002 |
Pirrung MC, Li Z, Park K, Zhu J. Total syntheses of demethylasterriquinone B1, an orally active insulin mimetic, and demethylasterriquinone A1. The Journal of Organic Chemistry. 67: 7919-26. PMID 12423119 DOI: 10.1021/Jo020182A |
0.388 |
|
| 2002 |
Pirrung MC, Tumey LN, Raetz CR, Jackman JE, Snehalatha K, McClerren AL, Fierke CA, Gantt SL, Rusche KM. Inhibition of the antibacterial target UDP-(3-O-acyl)-N-acetylglucosamine deacetylase (LpxC): isoxazoline zinc amidase inhibitors bearing diverse metal binding groups. Journal of Medicinal Chemistry. 45: 4359-70. PMID 12213077 DOI: 10.1021/Jm020183V |
0.728 |
|
| 2002 |
Pirrung MC, Park K, Tumey LN. (19)F-encoded combinatorial libraries: discovery of selective metal binding and catalytic peptoids. Journal of Combinatorial Chemistry. 4: 329-44. PMID 12099851 DOI: 10.1021/Cc010083V |
0.717 |
|
| 2002 |
Pirrung MC, Liu H, Morehead AT. Rhodium chemzymes: Michaelis-Menten kinetics in dirhodium(II) carboxylate-catalyzed carbenoid reactions. Journal of the American Chemical Society. 124: 1014-23. PMID 11829610 DOI: 10.1021/Ja011599L |
0.776 |
|
| 2002 |
Pirrung MC, Wedel M, Zhao Y. 7-Alkyl indole synthesis via a convenient formation/alkylation of lithionitrobenzenes and an improved Bartoli reaction Synlett. 143-145. DOI: 10.1055/S-2002-19346 |
0.367 |
|
| 2002 |
Pirrung MC. Total Synthesis Of (.+‐.)‐Isocomene Cheminform. 11. DOI: 10.1002/Chin.198007332 |
0.35 |
|
| 2001 |
Pirrung MC, Fallon L, Zhu J, Lee YR. Photochemically removable silyl protecting groups. Journal of the American Chemical Society. 123: 3638-43. PMID 11457095 DOI: 10.1021/Ja002370T |
0.344 |
|
| 2001 |
Pirrung MC, Park K, Li Z. Synthesis of 3-indolyl-2,5-dihydroxybenzoquinones. Organic Letters. 3: 365-7. PMID 11428015 DOI: 10.1021/Ol006852L |
0.347 |
|
| 2001 |
Pirrung MC, Wang L, Montague-Smith MP. 3'-nitrophenylpropyloxycarbonyl (NPPOC) protecting groups for high-fidelity automated 5' --> 3' photochemical DNA synthesis. Organic Letters. 3: 1105-8. PMID 11348170 DOI: 10.1021/Ol0069150 |
0.311 |
|
| 2001 |
Pirrung MC, Pansare SV. Trityl isothiocyanate support for solid-phase synthesis. Journal of Combinatorial Chemistry. 3: 90-6. PMID 11148069 DOI: 10.1021/Cc000072M |
0.367 |
|
| 2000 |
Pirrung MC, Tumey LN. Oxazoline synthesis from hydroxyamides by resin capture and ring-forming release. Journal of Combinatorial Chemistry. 2: 675-80. PMID 11126295 |
0.703 |
|
| 2000 |
Pirrung MC, Kaliappan KP. Dipolar cycloaddition of rhodium-generated carbonyl ylides with p-quinones. Organic Letters. 2: 353-5. PMID 10814321 DOI: 10.1021/Ol991300S |
0.617 |
|
| 2000 |
Pirrung MC, Pei T. Synthesis of (+/-)-homohistidine. The Journal of Organic Chemistry. 65: 2229-30. PMID 10774052 DOI: 10.1021/Jo991630Q |
0.361 |
|
| 2000 |
Jackman JE, Fierke CA, Tumey LN, Pirrung M, Uchiyama T, Tahir SH, Hindsgaul O, Raetz CR. Antibacterial agents that target lipid A biosynthesis in gram-negative bacteria. Inhibition of diverse UDP-3-O-(r-3-hydroxymyristoyl)-n-acetylglucosamine deacetylases by substrate analogs containing zinc binding motifs. The Journal of Biological Chemistry. 275: 11002-9. PMID 10753902 DOI: 10.1074/Jbc.275.15.11002 |
0.719 |
|
| 1999 |
Pirrung MC, Lee YR, Park K, Springer JB. Pentadienylnitrobenzyl and Pentadienylnitropiperonyl Photochemically Removable Protecting Groups. The Journal of Organic Chemistry. 64: 5042-5047. PMID 34237832 DOI: 10.1021/jo982383d |
0.518 |
|
| 1999 |
Pirrung MC, Blume F. Rhodium-Mediated Dipolar Cycloaddition of Diazoquinolinediones. The Journal of Organic Chemistry. 64: 3642-3649. PMID 11674492 DOI: 10.1021/Jo982503H |
0.366 |
|
| 1999 |
Pirrung MC, Zhao X. Hybridization properties and polymerase acceptance of nitropiperonyl deoxyriboside. Photochemical DNA backbone cleavage Phosphorus, Sulfur and Silicon and Related Elements. 144: 371-372. DOI: 10.1080/10426509908546258 |
0.318 |
|
| 1999 |
Pirrung MC. Ethylene biosynthesis from 1-aminocyclopropanecarboxylic acid Accounts of Chemical Research. 32: 711-718. DOI: 10.1021/Ar960003+ |
0.301 |
|
| 1998 |
Pirrung MC, Cao J, Chen J. Ethylene biosynthesis: processing of a substrate analog supports a radical mechanism for the ethylene-forming enzyme. Chemistry & Biology. 5: 49-57. PMID 9479479 DOI: 10.1016/S1074-5521(98)90086-2 |
0.331 |
|
| 1998 |
Pirrung MC, Fallon L, McGall G. Proofing of Photolithographic DNA Synthesis with 3′,5′-Dimethoxybenzoinyloxycarbonyl-Protected Deoxynucleoside Phosphoramidites Journal of Organic Chemistry. 63: 241-246. DOI: 10.1021/Jo970872S |
0.351 |
|
| 1996 |
Pirrung MC, Han H, Chen J. O-Alkyl Hydroxamates as Metaphors of Enzyme-Bound Enolate Intermediates in Hydroxy Acid Dehydrogenases. Inhibitors of Isopropylmalate Dehydrogenase, Isocitrate Dehydrogenase, and Tartrate Dehydrogenase(1). The Journal of Organic Chemistry. 61: 4527-4531. PMID 11667376 DOI: 10.1021/Jo952090+ |
0.324 |
|
| 1996 |
Pirrung MC, Chidambaram N. Preparation of thymine dinucleotide methylphosphonate analogs via thymine methylpnosphonofluoridate Journal of Organic Chemistry. 61: 1540-1542. DOI: 10.1021/Jo951395L |
0.311 |
|
| 1996 |
Pirrung MC, Morehead AT. Saturation kinetics in dirhodium(II) carboxylate-catalyzed ons of diazo compounds Journal of the American Chemical Society. 118: 8162-8163. DOI: 10.1021/Ja961806V |
0.307 |
|
| 1996 |
Pirrung MC, Nunn DS. Photochemical rearrangements of quinone monoketals Tetrahedron. 52: 5707-5738. DOI: 10.1016/0040-4020(96)00207-4 |
0.381 |
|
| 1995 |
Pirrung MC, Chau JH, Chen J. Discovery of a novel tetrahydroacridine acetylcholinesterase inhibitor through an indexed combinatorial library. Chemistry & Biology. 2: 621-6. PMID 9383467 DOI: 10.1016/1074-5521(95)90127-2 |
0.356 |
|
| 1995 |
Pirrung MC, Lee YR. Hydroxy direction of the rhodium-mediated dipolar cycloaddition of cyclic carbenoids with vinyl ethers Journal of the Chemical Society, Chemical Communications. 673-674. DOI: 10.1039/C39950000673 |
0.385 |
|
| 1995 |
Pirrung MC, Chau JHL. A convenient procedure for the preparation of amino acid hydroxamates from esters Journal of Organic Chemistry. 60: 8084-8085. DOI: 10.1021/Jo00129A059 |
0.325 |
|
| 1995 |
Pirrung MC, Zhang J, Lackey K, Sternbach DD, Brown F. Reactions of a cyclic rhodium carbenoid with aromatic compounds and vinyl ethers Journal of Organic Chemistry. 60: 2112-2124. DOI: 10.1021/Jo00112A036 |
0.351 |
|
| 1995 |
Pirrung MC, Huang CY. Photochemical deprotection of 3′,5′-dimethoxybenzoin (DMB) carbamates derived from secondary amines Tetrahedron Letters. 36: 5883-5884. DOI: 10.1016/0040-4039(95)01184-J |
0.332 |
|
| 1994 |
Pirrung MC, Shuey SW. Photoremovable protecting groups for phosphorylation of chiral alcohols. Asymmetric synthesis of phosphotriesters of (-)-3′,5′-dimethoxybenzoin Journal of Organic Chemistry. 59: 3890-3897. DOI: 10.1021/Jo00093A021 |
0.405 |
|
| 1994 |
Pirrung MC, Han H, Ludwig RT. Inhibitors of Thermus thermophilus isopropylmalate dehydrogenase Journal of Organic Chemistry. 59: 2430-2436. DOI: 10.1021/Jo00088A026 |
0.379 |
|
| 1994 |
Pirrung MC, Han H, Nunn DS. Kinetic mechanism and reaction pathway of Thermus thermophilus isopropylmalate dehydrogenase Journal of Organic Chemistry. 59: 2423-2429. DOI: 10.1021/Jo00088A025 |
0.329 |
|
| 1994 |
Pirrung MC, Lee YR. Dipolar cycloaddition of rhodium carbenoids with vinyl esters. Total synthesis of pongamol and lanceolatin B Tetrahedron Letters. 35: 6231-6234. DOI: 10.1016/S0040-4039(00)73399-5 |
0.388 |
|
| 1994 |
Pirrung MC, Zhang J, Morehead AT. Dipolar cycloaddition of cyclic rhodium carbenoids to digonal carbon. Synthesis of isoeuparin Tetrahedron Letters. 35: 6229-6230. DOI: 10.1016/S0040-4039(00)73398-3 |
0.348 |
|
| 1993 |
Pirrung MC, Rowley EG, Holmes CP. Methods for the stereoselective synthesis of 2-fluoroalkenoates. Carbonyl condensation reactions of 3,3-bis(methylthio)-2-fluoropropenal, a highly-functionalized fluoroacrylate cation equivalent Journal of Organic Chemistry. 58: 5683-5689. DOI: 10.1021/Jo00073A029 |
0.407 |
|
| 1993 |
Pirrung MC, Krishnamurthy N. Preparation of (R)-phenylalanine analogues by enantioselective destruction using L-amino acid oxidase Journal of Organic Chemistry. 58: 957-958. DOI: 10.1021/Jo00056A033 |
0.307 |
|
| 1993 |
Pirrung MC, Chen J, Rowley EG, McPhail AT. Mechanistic and stereochemical study of phenylpyruvate tautomerase Journal of the American Chemical Society. 115: 7103-7110. DOI: 10.1021/Ja00069A006 |
0.314 |
|
| 1993 |
Pirrung MC, Nunn DS, McPhail AT, Mitchell RE. Synthesis and absolute configuration of hydroxythreonine, a biosynthetic precursor of rhizobitoxine in pseudomonas Bioorganic and Medicinal Chemistry Letters. 3: 2095-2098. DOI: 10.1016/S0960-894X(01)81024-6 |
0.359 |
|
| 1992 |
Pirrung MC, Zhang J. Asymmetric dipolar cycloaddition reactions of diazocompounds mediated by a binaphtholphosphate rhodium catalyst Tetrahedron Letters. 33: 5987-5990. DOI: 10.1016/S0040-4039(00)61107-3 |
0.313 |
|
| 1992 |
Pirrung MC, Nunn DS. Synthesis of quinone monoketals by diol exchange Tetrahedron Letters. 33: 6591-6594. DOI: 10.1016/S0040-4039(00)60993-0 |
0.363 |
|
| 1991 |
Pirrung MC, Zhang J, McPhail AT. Dipolar cycloaddition of cyclic rhodium carbenoids to aromatic heterocycles Journal of Organic Chemistry. 56: 6269-6271. DOI: 10.1021/Jo00022A010 |
0.371 |
|
| 1991 |
Pirrung MC, Brown WL, Rege S, Laughton P. Total synthesis of (+)-griseofulvin Journal of the American Chemical Society. 113: 8561-8562. DOI: 10.1021/Ja00022A075 |
0.35 |
|
| 1990 |
Montgomery SH, Pirrung MC, Heathcock CH. De novo synthesis of carbohydrates by stereoselective aldol reaction: L-cladinose. Carbohydrate Research. 202: 13-32. PMID 2224887 DOI: 10.1016/0008-6215(90)84068-6 |
0.613 |
|
| 1989 |
Pirrung MC, Trinks UP. Ethylene biosynthesis. Aminocyclopropenecarboxylic acid Journal of the Chemical Society, Chemical Communications. 857-859. DOI: 10.1039/C39890000857 |
0.36 |
|
| 1987 |
Pirrung MC, Kenney PM. Synthesis of pederol The Journal of Organic Chemistry. 52: 2335-2336. DOI: 10.1021/Jo00387A053 |
0.361 |
|
| 1986 |
Pirrung MC, McGeehan GM. Ethylene biosynthesis. 6. Synthesis and evaluation of methylaminocyclopropanecarboxylic acid Journal of Organic Chemistry. 51: 2103-2106. DOI: 10.1021/Jo00361A032 |
0.356 |
|
| 1986 |
Pirrung MC, McGeehan GM. Ethylene biosynthesis. 7. Secondary isotope effects Journal of the American Chemical Society. 108: 5647-5648. DOI: 10.1021/Ja00278A059 |
0.326 |
|
| 1984 |
Heathcock CH, Pirrung MC, Young SD, Hagen JP, Jarvi ET, Badertscher U, Märki HP, Montgomery SH. Acyclic stereoselection. 23. Lactaldehyde enolate equivalents Journal of the American Chemical Society. 106: 8161-8174. DOI: 10.1021/Ja00338A027 |
0.596 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of Cram's rule stereoselection in synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy carboxylic acids from chiral aldehydes Journal of Organic Chemistry. 46: 2290-2300. DOI: 10.1021/Jo00324A017 |
0.647 |
|
| 1981 |
Heathcock CH, Hagen JP, Jarvi ET, Pirrung MC, Young SD. Acyclic stereoselection. 14. O-alkyllactic acid esters: reagents for the stereoselective construction of erythro- and threo-.alpha.-methyl-.alpha.,.beta.-dihydroxy carbonyl compounds Journal of the American Chemical Society. 103: 4972-4974. DOI: 10.1021/Ja00406A064 |
0.621 |
|
| 1981 |
Pirrung MC. Total synthesis of (.+-.)-isocomene and related studies Journal of the American Chemical Society. 103: 82-87. DOI: 10.1021/Ja00391A016 |
0.319 |
|
| 1981 |
Heathcock CH, Pirrung MC, Montgomery SH, Lampe J. Acyclic stereoselection-13. Aryl esters: reagents for threo-aldolization Tetrahedron. 37: 4087-4095. DOI: 10.1016/S0040-4020(01)93284-3 |
0.635 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of Cram's rule stereoselection in synthesis of erythro-.alpha.-alkyl-.beta.-hydroxy carboxylic acids from chiral aldehydes Cheminform. 12. DOI: 10.1002/Chin.198142079 |
0.647 |
|
| 1981 |
Heathcock CH, Hagen JP, Jarvi ET, Pirrung MC, Young SD. Acyclic stereoselection. 14. O-alkyllactic acid esters: Reagents for the stereoselective construction of erythro- and threo-α-methyl-α,β-dihydroxy carbonyl compounds Journal of the American Chemical Society. 103: 4972-4974. |
0.598 |
|
| 1981 |
Heathcock CH, Pirrung MC, Lampe J, Buse CT, Young SD. Acyclic stereoselection. 12. Double stereodifferentiation with mutual kinetic resolution. A superior class of reagents for control of cram's rule stereoselection in synthesis of erythro-α-alkyl-β-hydroxy carboxylic acids from chiral aldehydes Journal of Organic Chemistry. 46: 2290-2300. |
0.62 |
|
| 1980 |
Heathcock CH, Young SD, Hagen JP, Pirrung MC, White CT, VanDerveer D. Acyclic stereoselection. 9. Stereochemistry of the addition of lithium enolates to .alpha.-alkoxy aldehydes Journal of Organic Chemistry. 12: 3846-3856. DOI: 10.1021/Jo01307A023 |
0.6 |
|
| 1980 |
Pirrung MC, Heathcock CH. Acyclic stereoselection. 8. A new class of reagents for the highly stereoselective preparation of threo-2-alkyl-3-hydroxycarboxylic acids by the aldol condensation Journal of Organic Chemistry. 45: 1727-1728. DOI: 10.1021/Jo01297A057 |
0.659 |
|
| 1980 |
Heathcock CH, Buse CT, Kleschick WA, Pirrung MC, Sohn JE, Lampe J. Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensation Journal of Organic Chemistry. 45: 1066-1081. DOI: 10.1021/Jo01294A030 |
0.67 |
|
| 1980 |
Heathcock CH, Buse CT, Kleschick WA, Pirrung MC, Sohn JE, Lampe J. Correction. Acyclic Stereoselection. 7. Stereoselective Synthesis of 2-Alkyl-3-hydroxy Carbonyl Compounds by Aldol Condensation Journal of Organic Chemistry. 45: 1066-1081. DOI: 10.1021/Jo00339A601 |
0.668 |
|
| 1980 |
Heathcock CH, Pirrung MC, Buse CT, Hagen JP, Young SD, Sohn JE. Acyclic stereoselection. 6. A reagent for achieving high 1,2-diastereoselection in the aldol conversion of chiral aldehydes into 3-hydroxy-2-methylcarboxylic acids Cheminform. 11. DOI: 10.1002/Chin.198007106 |
0.641 |
|
| 1980 |
Heathcock CH, Young SD, Hagen JP, Pirrung MC, White CT, VanDerveer D. Acyclic stereoselection. 9. Stereochemistry of the addition of lithium enolates to α-alkoxy aldehydes Journal of Organic Chemistry. 45: 3846-3856. |
0.58 |
|
| 1979 |
Heathcock CH, Pirrung MC, Sohn JE. Acyclic stereoselection. 4. Assignment of stereostructure to .beta.-hydroxycarbonyl compounds by carbon-13 nuclear magnetic resonance The Journal of Organic Chemistry. 44: 4294-4299. DOI: 10.1021/Jo01338A015 |
0.576 |
|
| 1979 |
Pirrung MC. Total synthesis of (.+-.)-isocomene Journal of the American Chemical Society. 101: 7130-7131. DOI: 10.1021/Ja00517A087 |
0.351 |
|
| 1979 |
Heathcock CH, Pirrung MC, Buse CT, Hagen JP, Young SD, Sohn JE. Acyclic stereoselection. 6. A reagent for achieving high 1,2-diastereoselection in the aldol conversion of chiral aldehydes into 3-hydroxy-2-methylcarboxylic acids Journal of the American Chemical Society. 101: 7077-7079. DOI: 10.1021/Ja00517A056 |
0.655 |
|
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