Year |
Citation |
Score |
2022 |
Tavakoli A, Dudley GB. Synthesis of Coprinol and Several Alcyopterosin Sesquiterpenes by Regioselective [2 + 2 + 2] Alkyne Cyclotrimerization. The Journal of Organic Chemistry. PMID 36215202 DOI: 10.1021/acs.joc.2c01741 |
0.334 |
|
2022 |
Tavakoli A, Dudley GB. Synthesis of 4,4-Dimethyl-1,6-heptadiyne and Other Neopentylene-Tethered (NPT) 1,6-Diynes. The Journal of Organic Chemistry. 87: 5773-5784. PMID 35427143 DOI: 10.1021/acs.joc.2c00110 |
0.36 |
|
2021 |
Fulo HF, Rueb NJ, Gaston R, Batsomboon P, Ahmed KT, Barrios AM, Dudley GB. Synthesis of illudalic acid and analogous phosphatase inhibitors. Organic & Biomolecular Chemistry. PMID 34847212 DOI: 10.1039/d1ob02106k |
0.743 |
|
2021 |
Martin AC, Rogers JA, Batsomboon P, Morrison AE, Ramsubhag RR, Popp BV, Dudley GB. Benzannulation and Hydrocarboxylation Methods for the Synthesis of a Neopentylene-Fused Analogue of Ibuprofen. Acs Omega. 6: 30108-30114. PMID 34778682 DOI: 10.1021/acsomega.1c04943 |
0.74 |
|
2021 |
Zhang L, Jin T, Guo Y, Martin AC, Sun K, Dudley GB, Yang J. Synthesis of -Dimethylcyclopentane-Fused Arenes with Various Topologies via TBD-Mediated Dehydro-Diels-Alder Reaction. The Journal of Organic Chemistry. PMID 34709035 DOI: 10.1021/acs.joc.1c01957 |
0.527 |
|
2020 |
Gaston R, Geldenhuys WJ, Dudley GB. Synthesis of Illudinine from Dimedone and Identification of Activity as a Monoamine Oxidase Inhibitor. The Journal of Organic Chemistry. PMID 32830978 DOI: 10.1021/Acs.Joc.0C01301 |
0.412 |
|
2020 |
Frasso MA, Stiegman AE, Dudley GB. Microwave-specific acceleration of a retro-Diels-Alder reaction. Chemical Communications (Cambridge, England). PMID 32820765 DOI: 10.1039/D0Cc04584E |
0.373 |
|
2019 |
McCullough BS, Batsomboon P, Hutchinson KB, Dudley GB, Barrios AM. Synthesis and PTP Inhibitory Activity of Illudalic Acid and Its Methyl Ether, with Insights into Selectivity for LAR PTP over Other Tyrosine Phosphatases under Physiologically Relevant Conditions. Journal of Natural Products. PMID 31809044 DOI: 10.1021/Acs.Jnatprod.9B00663 |
0.737 |
|
2019 |
Duangkamol C, Batsomboon P, Stiegman AE, Dudley GB. Microwave heating outperforms conventional heating for a thermal reaction that produces a thermally labile product: Observations consistent with selective microwave heating. Chemistry, An Asian Journal. PMID 31157510 DOI: 10.1002/Asia.201900625 |
0.756 |
|
2019 |
Hayes KE, Batsomboon P, Chen WC, Johnson BD, Becker A, Eschrich S, Yang Y, Robart AR, Dudley GB, Geldenhuys WJ, Hazlehurst LA. Inhibition of the FAD containing ER oxidoreductin 1 (Ero1) protein by EN-460 as a strategy for treatment of multiple myeloma. Bioorganic & Medicinal Chemistry. PMID 30850265 DOI: 10.1016/J.Bmc.2019.02.016 |
0.706 |
|
2019 |
Yang J, Guo Y, Wang J, Dudley GB, Sun K. DFT study on the reaction mechanism and regioselectivity for the [1,2]-anionic rearrangement of 2-benzyloxypyridine derivatives Tetrahedron. 75: 4451-4457. DOI: 10.1016/J.Tet.2019.06.018 |
0.591 |
|
2018 |
El Anwar S, Laila Z, Ramsubhag R, Tlais S, Safa A, Dudley G, Naoufal D. Synthesis and characterization of click-decahydrodecaborate derivatives by the copper(I) catalyzed [3+2] azide-alkyne cycloaddition reaction Journal of Organometallic Chemistry. 865: 89-94. DOI: 10.1016/J.Jorganchem.2018.01.039 |
0.804 |
|
2017 |
Dudley GB, Stiegman AE. Changing Perspectives on the Strategic use of Microwave Heating in Organic Synthesis. Chemical Record (New York, N.Y.). PMID 29044842 DOI: 10.1002/Tcr.201700044 |
0.37 |
|
2017 |
Kramer NJ, Hoang TT, Dudley GB. Reaction Discovery Using Neopentylene-Tethered Coupling Partners: Cycloisomerization/Oxidation of Electron-Deficient Dienynes. Organic Letters. PMID 28832157 DOI: 10.1021/Acs.Orglett.7B02261 |
0.407 |
|
2017 |
Morrison AE, Hoang TT, Birepinte M, Dudley GB. Synthesis of Illudinine from Dimedone. Organic Letters. PMID 28133968 DOI: 10.1021/Acs.Orglett.6B03887 |
0.446 |
|
2016 |
Wu Y, Gagnier J, Dudley GB, Stiegman AE. The "chaperone" effect in microwave-driven reactions. Chemical Communications (Cambridge, England). 52: 11281-11283. PMID 27711277 DOI: 10.1039/C6Cc06032C |
0.317 |
|
2016 |
Hoang TT, Birepinte M, Kramer NJ, Dudley GB. Correction to "Six-Step Synthesis of Alcyopterosin A, a Bioactive Illudalane Sesquiterpene with a gem-Dimethylcyclopentane Ring". Organic Letters. PMID 27575925 DOI: 10.1021/Acs.Orglett.6B02561 |
0.383 |
|
2016 |
Morrison AE, Hrudka JJ, Dudley GB. Thermal Cycloisomerization of Putative Allenylpyridines for the Synthesis of Isoquinoline Derivatives. Organic Letters. PMID 27490496 DOI: 10.1021/Acs.Orglett.6B02034 |
0.354 |
|
2016 |
Hoang TT, Birepinte M, Kramer NM, Dudley GB. Six-Step Synthesis of Alcyopterosin A, a Bioactive Illudalane Sesquiterpene with a gem-Dimethylcyclopentane Ring. Organic Letters. PMID 27359158 DOI: 10.1021/Acs.Orglett.6B01665 |
0.4 |
|
2016 |
Ramsubhag RR, Dudley GB. Orthogonal dual-click diyne for CuAAC and/or SPAAC couplings. Organic & Biomolecular Chemistry. 14: 5028-31. PMID 27193964 DOI: 10.1039/C6Ob00795C |
0.303 |
|
2016 |
Wright AK, Batsomboon P, Dai J, Hung I, Zhou HX, Dudley GB, Cross TA. Differential Binding of Rimantadine Enantiomers to Influenza A M2 Proton Channel. Journal of the American Chemical Society. PMID 26804976 DOI: 10.1021/Jacs.5B13129 |
0.71 |
|
2016 |
Batsomboon P, Dudley GB. Synthesis of C1–C15 of palmerolide A: tactical advances that can lead to better design strategies for polyketide synthesis Tetrahedron Letters. 57: 3757-3759. DOI: 10.1016/J.Tetlet.2016.07.014 |
0.785 |
|
2016 |
Slegeris R, Dudley GB. Alternative synthetic approaches to rac-progesterone by way of the classic Johnson cationic polycyclization strategy Tetrahedron. 72: 3666-3672. DOI: 10.1016/J.Tet.2016.03.041 |
0.308 |
|
2015 |
Dudley GB, Richert R, Stiegman AE. On the existence of and mechanism for microwave-specific reaction rate enhancement. Chemical Science. 6: 2144-2152. PMID 29308138 DOI: 10.1039/C4Sc03372H |
0.374 |
|
2015 |
Ferrari A, Hunt J, Stiegman A, Dudley GB. Microwave-Assisted Superheating and/or Microwave-Specific Superboiling (Nucleation-Limited Boiling) of Liquids Occurs under Certain Conditions but is Mitigated by Stirring. Molecules (Basel, Switzerland). 20: 21672-80. PMID 26690096 DOI: 10.3390/Molecules201219793 |
0.316 |
|
2015 |
Rizkallah R, Batsomboon P, Dudley GB, Hurt MM. Identification of the oncogenic kinase TOPK/PBK as a master mitotic regulator of C2H2 zinc finger proteins. Oncotarget. 6: 1446-61. PMID 25575812 DOI: 10.18632/Oncotarget.2735 |
0.694 |
|
2015 |
Diaz Muñoz G, Dudley GB. Synthesis of 1,2,3,4-tetrahydroquinolines including angustureine and congeneric alkaloids. A review Organic Preparations and Procedures International. 47: 179-206. DOI: 10.1080/00304948.2015.1025012 |
0.339 |
|
2014 |
Chen PK, Rosana MR, Dudley GB, Stiegman AE. Parameters affecting the microwave-specific acceleration of a chemical reaction. The Journal of Organic Chemistry. 79: 7425-36. PMID 25050921 DOI: 10.1021/Jo5011526 |
0.775 |
|
2014 |
Rosana MR, Hunt J, Ferrari A, Southworth TA, Tao Y, Stiegman AE, Dudley GB. Microwave-specific acceleration of a Friedel-Crafts reaction: evidence for selective heating in homogeneous solution. The Journal of Organic Chemistry. 79: 7437-50. PMID 25050855 DOI: 10.1021/Jo501153R |
0.765 |
|
2014 |
Gold B, Batsomboon P, Dudley GB, Alabugin IV. Alkynyl crown ethers as a scaffold for hyperconjugative assistance in noncatalyzed azide-alkyne click reactions: ion sensing through enhanced transition-state stabilization. The Journal of Organic Chemistry. 79: 6221-32. PMID 24927131 DOI: 10.1021/Jo500958N |
0.728 |
|
2014 |
Hoang TT, Dudley GB, Williams LJ. Fragmentation Reactions Comprehensive Organic Synthesis: Second Edition. 6: 842-860. DOI: 10.1016/B978-0-08-097742-3.00630-3 |
0.522 |
|
2013 |
Lisboa MP, Dudley GB. Synthesis of cytotoxic palmerolides. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 16146-68. PMID 24249686 DOI: 10.1002/Chem.201302167 |
0.783 |
|
2013 |
Hoang TT, Dudley GB. Synthesis of high-value 1,6-enynes by tandem fragmentation/olefination. Organic Letters. 15: 4026-9. PMID 23885858 DOI: 10.1021/Ol401839E |
0.416 |
|
2013 |
Dudley GB, Stiegman AE, Rosana MR. Correspondence on microwave effects in organic synthesis. Angewandte Chemie (International Ed. in English). 52: 7918-23. PMID 23824983 DOI: 10.1002/Anie.201301539 |
0.778 |
|
2013 |
Lisboa MP, Jones DM, Dudley GB. Formal synthesis of palmerolide A, featuring alkynogenic fragmentation and syn-selective vinylogous aldol chemistry. Organic Letters. 15: 886-9. PMID 23373594 DOI: 10.1021/Ol400014E |
0.787 |
|
2013 |
Gold B, Dudley GB, Alabugin IV. Moderating strain without sacrificing reactivity: design of fast and tunable noncatalyzed alkyne-azide cycloadditions via stereoelectronically controlled transition state stabilization. Journal of the American Chemical Society. 135: 1558-69. PMID 23272641 DOI: 10.1021/Ja3114196 |
0.334 |
|
2013 |
Tummatorn J, Muñoz GD, Dudley GB. Synthesis of (-)-(R)-angustureine by formal alkynylation of a chiral β-amino ester Tetrahedron Letters. 54: 1312-1314. DOI: 10.1016/J.Tetlet.2012.12.122 |
0.361 |
|
2012 |
Tlais SF, Dudley GB. On the proposed structures and stereocontrolled synthesis of the cephalosporolides. Beilstein Journal of Organic Chemistry. 8: 1287-92. PMID 23019461 DOI: 10.3762/Bjoc.8.146 |
0.79 |
|
2012 |
Tummatorn J, Batsomboon P, Clark RJ, Alabugin IV, Dudley GB. Strain-promoted azide-alkyne cycloadditions of benzocyclononynes. The Journal of Organic Chemistry. 77: 2093-7. PMID 22316100 DOI: 10.1021/Jo300188Y |
0.738 |
|
2012 |
Gold B, Shevchenko NE, Bonus N, Dudley GB, Alabugin IV. Selective transition state stabilization via hyperconjugative and conjugative assistance: stereoelectronic concept for copper-free click chemistry. The Journal of Organic Chemistry. 77: 75-89. PMID 22077877 DOI: 10.1021/Jo201434W |
0.354 |
|
2012 |
Wang TW, Intaranukulkit T, Rosana MR, Slegeris R, Simon J, Dudley GB. Microwave-assisted benzyl-transfer reactions of commercially available 2-benzyloxy-1-methylpyridinium triflate. Organic & Biomolecular Chemistry. 10: 248-50. PMID 22025036 DOI: 10.1039/C1Ob06504A |
0.799 |
|
2012 |
Yang J, Wangweerawong A, Dudley GB. [1,2]-Wittig rearrangement of aromatic heterocycles Heterocycles. 85: 1603-1606. DOI: 10.3987/Com-12-12492 |
0.568 |
|
2012 |
Lisboa MP, Hoang TT, Dudley GB. Tandem nucleophilic addition/fragmentation of vinylogous acyl triflates: 2-methyl-2-(1-oxo-5-heptynyl)-1,3-dithiane Organic Syntheses. 88: 353-363. DOI: 10.15227/orgsyn.088.0353 |
0.759 |
|
2012 |
Batsomboon P, Gold BA, Alabugin IV, Dudley GB. Tandem nucleophilic addition/fragmentation of vinylogous acyl nonaflates for the synthesis of functionalized alkynes, with new mechanistic insight Synthesis (Germany). 44: 1818-1824. DOI: 10.1055/S-0031-1290945 |
0.751 |
|
2012 |
Lisboa MP, Jeong-Im JH, Jones DM, Dudley GB. Toward a new palmerolide assembly strategy: Synthesis of C16-C24 Synlett. 23: 1493-1496. DOI: 10.1055/S-0031-1290675 |
0.79 |
|
2012 |
Rosana MR, Tao Y, Stiegman AE, Dudley GB. On the rational design of microwave-actuated organic reactions Chemical Science. 3: 1240-1244. DOI: 10.1039/C2Sc01003H |
0.785 |
|
2012 |
Yang J, Wangweerawong A, Dudley GB. ChemInform Abstract: [1,2]-Wittig Rearrangement of Aromatic Heterocycles. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201244036 |
0.54 |
|
2012 |
Wang T, Intaranukulkit T, Rosana MR, Slegeris R, Simon J, Dudley GB. ChemInform Abstract: Microwave-Assisted Benzyl-Transfer Reactions of Commercially Available 2-Benzyloxy-1-methylpyridinium Triflate. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201221040 |
0.788 |
|
2012 |
Lisboa MP, Hoang TT, Dudley GB. Tandem Nucleophilic Addition / Fragmentation of Vinylogous Acyl Triflates: 2‐Methyl‐2‐(1‐Oxo‐5‐Heptynyl)‐1,3‐Dithiane Organic Syntheses. 353-363. DOI: 10.1002/0471264229.Os088.32 |
0.775 |
|
2011 |
Tlais SF, Dudley GB. A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals. Beilstein Journal of Organic Chemistry. 7: 570-7. PMID 21647322 DOI: 10.3762/Bjoc.7.66 |
0.803 |
|
2011 |
Yang J, Tummatorn J, Slegeris R, Tlais SF, Dudley GB. Synthesis of the tricyclic core of aldingenin B by oxidative cyclo-ketalization of an alkyne-diol. Organic Letters. 13: 2065-7. PMID 21391664 DOI: 10.1021/Ol200421S |
0.78 |
|
2011 |
Tummatorn J, Dudley GB. Generation of medium-ring cycloalkynes by ring expansion of vinylogous acyl triflates. Organic Letters. 13: 1572-5. PMID 21348490 DOI: 10.1021/Ol2003308 |
0.409 |
|
2011 |
Tummatorn J, Dudley GB. Stereodefined homopropargyl amines by tandem nucleophilic addition/fragmentation of dihydropyridone triflates. Organic Letters. 13: 158-60. PMID 21105673 DOI: 10.1021/Ol102760Q |
0.382 |
|
2010 |
Tlais SF, Dudley GB. Stereocontrol of 5,5-spiroketals in the synthesis of cephalosporolide H epimers. Organic Letters. 12: 4698-701. PMID 20860404 DOI: 10.1021/Ol102201Z |
0.788 |
|
2010 |
Jones DM, Lisboa MP, Kamijo S, Dudley GB. Ring opening of cyclic vinylogous acyl triflates using stabilized carbanion nucleophiles: claisen condensation linked to carbon-carbon bond cleavage. The Journal of Organic Chemistry. 75: 3260-7. PMID 20429608 DOI: 10.1021/Jo100249G |
0.791 |
|
2010 |
Albiniak PA, Dudley GB. New reagents for the synthesis of arylmethyl ethers and esters Synlett. 841-851. DOI: 10.1055/S-0029-1219531 |
0.418 |
|
2010 |
Jones DM, Dudley GB. Synthesis of the C1-C15 region of palmerolide A using refined claisen-type addition-bond cleavage methodology Synlett. 223-226. DOI: 10.1055/S-0029-1218565 |
0.315 |
|
2010 |
Jones DM, Dudley GB. An open-and-shut strategy: Preparation of benzo-fused indanes by ring-opening of a vinylogous acyl triflate and metal-catalyzed Asao-Yamamoto benzannulation Tetrahedron. 66: 4860-4866. DOI: 10.1016/J.Tet.2010.03.014 |
0.434 |
|
2010 |
Engel DA, Dudley GB. ChemInform Abstract: The MeyerâSchuster Rearrangement for the Synthesis of α,β-Unsaturated Carbonyl Compounds Cheminform. 41. DOI: 10.1002/CHIN.201004264 |
0.689 |
|
2010 |
Tan DS, Dudley GB, Danishefsky SJ. ChemInform Abstract: Synthesis of the Functionalized Tricyclic Skeleton of Guanacastepene A (IV): A Tandem Epoxide-Opening β-Elimination/Knoevenagel Cyclization. Cheminform. 33: no-no. DOI: 10.1002/chin.200242195 |
0.545 |
|
2010 |
Dudley GB, Tan DS, Kim G, Tanski JM, Danishefsky SJ. ChemInform Abstract: Remarkable Stereoselectivity in the Alkylation of a Hydroazulenone: Progress Towards the Total Synthesis of Guanacastepene. Cheminform. 32: no-no. DOI: 10.1002/chin.200152185 |
0.598 |
|
2010 |
Yang J, Dudley GB. Pyridine-directed organolithium addition to an enol ether Advanced Synthesis and Catalysis. 352: 3438-3442. DOI: 10.1002/Adsc.201000495 |
0.581 |
|
2009 |
Tlais SF, Clark RJ, Dudley GB. A striking exception to the chelate model for acyclic diastereocontrol: efficient access to a versatile propargyl alcohol for chemical synthesis. Molecules (Basel, Switzerland). 14: 5216-22. PMID 20032887 DOI: 10.3390/Molecules14125216 |
0.795 |
|
2009 |
Engel DA, Dudley GB. The Meyer-Schuster rearrangement for the synthesis of alpha,beta-unsaturated carbonyl compounds. Organic & Biomolecular Chemistry. 7: 4149-58. PMID 19795050 DOI: 10.1039/B912099H |
0.703 |
|
2009 |
Yang J, Dudley GB. [1,2]-Anionic rearrangement of 2-benzyloxypyridine and related pyridyl ethers. The Journal of Organic Chemistry. 74: 7998-8000. PMID 19761204 DOI: 10.1021/Jo901707X |
0.585 |
|
2009 |
Tlais SF, Lam H, House SE, Dudley GB. New strategies for protecting group chemistry: synthesis, reactivity, and indirect oxidative cleavage of para-siletanylbenzyl ethers. The Journal of Organic Chemistry. 74: 1876-85. PMID 19183037 DOI: 10.1021/Jo802229P |
0.795 |
|
2008 |
Lopez SS, Dudley GB. Convenient method for preparing benzyl ethers and esters using 2-benzyloxypyridine. Beilstein Journal of Organic Chemistry. 4: 44. PMID 19104674 DOI: 10.3762/Bjoc.4.44 |
0.441 |
|
2008 |
Tummatorn J, Dudley GB. Ring opening/fragmentation of dihydropyrones for the synthesis of homopropargyl alcohols. Journal of the American Chemical Society. 130: 5050-1. PMID 18357983 DOI: 10.1021/Ja801018R |
0.387 |
|
2008 |
Albiniak PA, Amisial SM, Dudley GB, Hernandez JP, House SE, Matthews ME, Nwoye EO, Reilly MK, Tlais SF. Stable oxypyridinium triflate (OPT) salts for the synthesis of halobenzyl ethers Synthetic Communications. 38: 656-665. DOI: 10.1080/00397910701818362 |
0.8 |
|
2008 |
Kozytska MV, Dudley GB. On the intramolecular pyrone Diels-Alder approach to basiliolide B Tetrahedron Letters. 49: 2899-2901. DOI: 10.1016/J.Tetlet.2008.03.031 |
0.332 |
|
2008 |
Engel DA, Lopez SS, Dudley GB. Lewis acid-catalyzed Meyer-Schuster reactions: methodology for the olefination of aldehydes and ketones Tetrahedron. 64: 6988-6996. DOI: 10.1016/J.Tet.2008.02.030 |
0.716 |
|
2008 |
Yang J, Dudley GB. ChemInform Abstract: Conjugate Addition of Organocopper Reagents in Dichloromethane to α,β-Unsaturated Esters. Cheminform. 39. DOI: 10.1002/CHIN.200807077 |
0.461 |
|
2007 |
Tummatorn J, Albiniak PA, Dudley GB. Synthesis of benzyl esters using 2-benzyloxy-1-methylpyridinium triflate. The Journal of Organic Chemistry. 72: 8962-4. PMID 17935354 DOI: 10.1021/Jo7018625 |
0.406 |
|
2007 |
Dudley GB, Engel DA, Ghiviriga I, Lam H, Poon KW, Singletary JA. Synthesis of +-dihydro-epi-deoxyarteannuin B. Organic Letters. 9: 2839-42. PMID 17583345 DOI: 10.1021/Ol070992E |
0.69 |
|
2007 |
Nwoye EO, Dudley GB. Synthesis of para-methoxybenzyl (PMB) ethers under neutral conditions. Chemical Communications (Cambridge, England). 1436-7. PMID 17389984 DOI: 10.1039/B617926F |
0.361 |
|
2007 |
Lopez SS, Engel DA, Dudley GB. The Meyer-Schuster rearrangement of ethoxyalkynyl carbinols Synlett. 949-953. DOI: 10.1055/S-2007-973885 |
0.715 |
|
2007 |
Albiniak PA, Dudley GB. Thermally generated phenylcarbenium ions: acid-free and self-quenching Friedel-Crafts reactions Tetrahedron Letters. 48: 8097-8100. DOI: 10.1016/J.Tetlet.2007.09.116 |
0.332 |
|
2007 |
Yang J, Dudley GB. Conjugate addition of organocopper reagents in dichloromethane to α,β-unsaturated esters Tetrahedron Letters. 48: 7887-7889. DOI: 10.1016/J.Tetlet.2007.08.105 |
0.569 |
|
2007 |
Poon KWC, Albiniak PA, Dudley GB. Protection of Alcohols Using 2‐Benzyloxy‐1‐Methylpyridinium Trifluoromethanesulfonate: Methyl (R)‐(−)‐3‐Benzyloxy‐2‐Methyl Propanote Organic Syntheses. 295-305. DOI: 10.1002/0471264229.Os084.29 |
0.332 |
|
2006 |
Engel DA, Dudley GB. Olefination of ketones using a gold(III)-catalyzed Meyer-Schuster rearrangement. Organic Letters. 8: 4027-9. PMID 16928065 DOI: 10.1021/Ol0616743 |
0.722 |
|
2006 |
Kamijo S, Dudley GB. Tandem nucleophilic addition/fragmentation reactions and synthetic versatility of vinylogous acyl triflates. Journal of the American Chemical Society. 128: 6499-507. PMID 16683816 DOI: 10.1021/Ja0608085 |
0.453 |
|
2006 |
Poon KW, Dudley GB. Mix-and-heat benzylation of alcohols using a bench-stable pyridinium salt. The Journal of Organic Chemistry. 71: 3923-7. PMID 16674068 DOI: 10.1021/Jo0602773 |
0.349 |
|
2006 |
House SE, Poon KW, Lam H, Dudley GB. p-Siletanylbenzylidene acetal: oxidizable protecting group for diols. The Journal of Organic Chemistry. 71: 420-2. PMID 16388675 DOI: 10.1021/Jo052015R |
0.386 |
|
2006 |
Kamijo S, Dudley GB. Claisen-type condensation of vinylogous acyl triflates. Organic Letters. 8: 175-7. PMID 16381596 DOI: 10.1021/Ol0527781 |
0.407 |
|
2006 |
Jones DM, Kamijo S, Dudley GB. Grignard-triggered fragmentation of vinylogous acyl triflates: Synthesis of (Z)-6-heneicosen-11-one, the Douglas fir tussock moth sex pheromone Synlett. 936-938. DOI: 10.1055/S-2006-939051 |
0.392 |
|
2006 |
Kamijo S, Dudley GB. Cyclic vinylogous triflate hemiacetals as new surrogates for alkynyl aldehydes Tetrahedron Letters. 47: 5629-5632. DOI: 10.1016/J.Tetlet.2006.06.040 |
0.412 |
|
2005 |
Mandal M, Yun H, Dudley GB, Lin S, Tan DS, Danishefsky SJ. Total synthesis of guanacastepene a: a route to enantiomeric control. The Journal of Organic Chemistry. 70: 10619-37. PMID 16355979 DOI: 10.1021/Jo051470K |
0.741 |
|
2005 |
Salamone SG, Dudley GB. A ring-expansion approach to roseophilin. Organic Letters. 7: 4443-5. PMID 16178554 DOI: 10.1021/Ol051730K |
0.414 |
|
2005 |
Kozytska MV, Dudley GB. Siletanylmethyllithium: an ambiphilic organosilane. Chemical Communications (Cambridge, England). 3047-9. PMID 15959580 DOI: 10.1039/B503110A |
0.347 |
|
2005 |
Singletary JA, Lam H, Dudley GB. A succinct method for preparing the Stork-Jung vinylsilane robinson annulation reagent. The Journal of Organic Chemistry. 70: 739-41. PMID 15651834 DOI: 10.1021/Jo0480803 |
0.406 |
|
2005 |
Poon KWC, House SE, Dudley GB. A bench-stable organic salt for the benzylation of alcohols Synlett. 3142-3144. DOI: 10.1055/S-2005-921898 |
0.339 |
|
2005 |
Briggs TF, Dudley GB. Synthesis of the floresolide B hydroquinone lactone core using ring-closing metathesis Tetrahedron Letters. 46: 7793-7796. DOI: 10.1016/J.Tetlet.2005.09.023 |
0.433 |
|
2005 |
Lam H, House SE, Dudley GB. The para-siletanylbenzyl (PSB) ether: A peroxide-cleavable protecting group for alcohols and phenols Tetrahedron Letters. 46: 3283-3285. DOI: 10.1016/J.Tetlet.2005.03.110 |
0.334 |
|
2003 |
Sunderhaus JD, Lam H, Dudley GB. Oxidation of carbon-silicon bonds: the dramatic advantage of strained siletanes. Organic Letters. 5: 4571-3. PMID 14627386 DOI: 10.1021/Ol035695Y |
0.302 |
|
2002 |
Lin S, Dudley GB, Tan DS, Danishefsky SJ. A stereoselective route to guanacastepene A through a surprising epoxidation. Angewandte Chemie (International Ed. in English). 41: 2188-91. PMID 19746640 DOI: 10.1002/1521-3773(20020617)41:12<2188::Aid-Anie2188>3.0.Co;2-J |
0.653 |
|
2002 |
Tan DS, Dudley GB, Danishefsky SJ. Synthesis of the functionalized tricyclic skeleton of guanacastepene A: a tandem epoxide-opening beta-elimination/knoevenagel cyclization. Angewandte Chemie (International Ed. in English). 41: 2185-8. PMID 19746639 DOI: 10.1002/1521-3773(20020617)41:12<2185::Aid-Anie2185>3.0.Co;2-0 |
0.646 |
|
2002 |
Dudley GB, Danishefsky SJ, Sukenick G. On the use of deuterium isotope effects in chemical synthesis Tetrahedron Letters. 43: 5605-5606. DOI: 10.1016/S0040-4039(02)01114-0 |
0.51 |
|
2002 |
Lin S, Dudley GB, Tan DS, Danishefsky SJ. A Stereoselective Route to Guanacastepene A through a Surprising Epoxidation This work was supported by the National Institutes of Health (CA-28824). S.L. is a US Army breast cancer research program postdoctoral fellow (DAMD-17-99-1-9373). G.B.D. is an NIH postdoctoral fellow (1 F32 NS11150-01). D.S.T. is a Damon Runyon Cancer Research Foundation postdoctoral fellow (DRG-1641). We thank Dr. George Sukenick and Sylvi Rusli (NMR Core Facility, CA-02848) for mass spectral analyses. Angewandte Chemie International Edition. 41: 2188. DOI: 10.1002/1521-3773(20020617)41:12<2188::AID-ANIE2188>3.0.CO;2-J |
0.538 |
|
2002 |
Tan DS, Dudley GB, Danishefsky SJ. Synthesis of the Functionalized Tricyclic Skeleton of Guanacastepene A: A Tandem Epoxide-Opening β-Elimination/Knoevenagel Cyclization This work was supported by the National Institutes of Health (HL-25848 and CA-28824). D.S.T. is a Damon Runyon Cancer Research Foundation postdoctoral fellow (DRG-1641). G.B.D. is an NIH postdoctoral fellow (1 F32 NS11150-01). We thank Dr. George Sukenick and Sylvi Rusli (NMR Core Facility, CA-02848) for mass spectral analyses. Angewandte Chemie International Edition. 41: 2185. DOI: 10.1002/1521-3773(20020617)41:12<2185::AID-ANIE2185>3.0.CO;2-0 |
0.566 |
|
2001 |
Dudley GB, Danishefsky SJ. A four-step synthesis of the hydroazulene core of guanacastepene Organic Letters. 3: 2399-2402. PMID 11463326 DOI: 10.1021/Ol016222Z |
0.508 |
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2001 |
Dudley GB, Tan DS, Kim G, Tanski JM, Danishefsky SJ. Remarkable stereoselectivity in the alkylation of a hydroazulenone: Progress towards the total synthesis of guanacastepene Tetrahedron Letters. 42: 6789-6791. DOI: 10.1016/S0040-4039(01)01342-9 |
0.621 |
|
2000 |
Dudley GB, Takaki KS, Cha DD, Danheiser RL. Total synthesis of (-)-ascochlorin via a cyclobutenone-based benzannulation strategy. Organic Letters. 2: 3407-10. PMID 11029223 DOI: 10.1021/Ol006561C |
0.618 |
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