| Year |
Citation |
Score |
| 2024 |
Mi T, Nguyen D, Gao Z, Burgess K. Bioinformatics leading to conveniently accessible, helix enforcing, bicyclic ASX motif mimics (BAMMs). Nature Communications. 15: 4217. PMID 38760359 DOI: 10.1038/s41467-024-48323-z |
0.505 |
|
| 2024 |
Mi T, Gao Z, Mituta Z, Burgess K. Dual-Capped Helical Interface Mimics. Journal of the American Chemical Society. PMID 38573124 DOI: 10.1021/jacs.3c11717 |
0.494 |
|
| 2023 |
Kumarasamy V, Gao Z, Zhao B, Jiang B, Rubin SM, Burgess K, Witkiewicz AK, Knudsen ES. PROTAC-mediated CDK degradation differentially impacts cancer cell cycles due to heterogeneity in kinase dependencies. British Journal of Cancer. PMID 37626264 DOI: 10.1038/s41416-023-02399-4 |
0.445 |
|
| 2023 |
Usama SM, Gao Z, Arancillo M, Burgess K. Cytotoxicities Of Tumor Seeking Dyes: Impact On Future Clinical Trials. Chemmedchem. PMID 36630600 DOI: 10.1002/cmdc.202200561 |
0.479 |
|
| 2022 |
Gao Z, Yang Z, Li Z, Burgess K. Fluorescent PARP Inhibitors Applied To Intracranial Glioblastoma: Accumulation and Persistence In Vivo. Acs Medicinal Chemistry Letters. 13: 911-915. PMID 35707158 DOI: 10.1021/acsmedchemlett.1c00712 |
0.487 |
|
| 2020 |
Lin CM, Jiang Z, Gao Z, Arancillo M, Burgess K. Small molecules targeting the NEDD8·NAE protein-protein interaction. Chemical Science. 12: 1535-1543. PMID 34163916 DOI: 10.1039/d0sc00958j |
0.502 |
|
| 2019 |
Thavornpradit S, Usama SM, Park GK, Shrestha JP, Nomura S, Baek Y, Choi HS, Burgess K. QuatCy: A Heptamethine Cyanine Modification With Improved Characteristics. Theranostics. 9: 2856-2867. PMID 31244928 DOI: 10.7150/Thno.33595 |
0.346 |
|
| 2019 |
Usama SM, Thompson T, Burgess K. Productive Manipulation of Cyanine Dye π-Networks. Angewandte Chemie (International Ed. in English). PMID 31124257 DOI: 10.1002/Anie.201902956 |
0.303 |
|
| 2018 |
Lin CM, Usama SM, Burgess K. Site-Specific Labeling of Proteins with Near-IR Heptamethine Cyanine Dyes. Molecules (Basel, Switzerland). 23. PMID 30405016 DOI: 10.3390/Molecules23112900 |
0.323 |
|
| 2018 |
Zhao B, Burgess K. Click-Addressable Cassette for Photoaffinity Labeling. Acs Medicinal Chemistry Letters. 9: 155-158. PMID 29456805 DOI: 10.1021/Acsmedchemlett.7B00516 |
0.301 |
|
| 2018 |
Taechalertpaisarn J, Zhao B, Liang X, Burgess K. Small Molecule Inhibitors Of The PCSK9•LDLR Interaction. Journal of the American Chemical Society. PMID 29378408 DOI: 10.1021/Jacs.7B09360 |
0.313 |
|
| 2017 |
Xin D, Jeffries A, Burgess K. Interplay Of Stereochemistry, Conformational Rigidity, And Ease Of Synthesis For 13-Membered Cyclic Peptidomimetics Containing APC Residues. Acs Combinatorial Science. PMID 28561582 DOI: 10.1021/Acscombsci.7B00041 |
0.341 |
|
| 2016 |
Xin D, Burgess K. Anthranilic acid-containing cyclic tetrapeptides: at the crossroads of conformational rigidity and synthetic accessibility. Organic & Biomolecular Chemistry. PMID 27173439 DOI: 10.1039/C6Ob00693K |
0.316 |
|
| 2015 |
Kamkaew A, Thavornpradit S, Puangsamlee T, Xin D, Wanichacheva N, Burgess K. Oligoethylene glycol-substituted aza-BODIPY dyes as red emitting ER-probes. Organic & Biomolecular Chemistry. 13: 8271-6. PMID 26138325 DOI: 10.1039/C5Ob01104C |
0.342 |
|
| 2015 |
Kamkaew A, Burgess K. Aza-BODIPY dyes with enhanced hydrophilicity. Chemical Communications (Cambridge, England). 51: 10664-7. PMID 26051677 DOI: 10.1039/C5Cc03649F |
0.339 |
|
| 2015 |
Xin D, Raghuraman A, Burgess K. Extended piperidine-piperidinone protein interface mimics. The Journal of Organic Chemistry. 80: 4450-8. PMID 25866317 DOI: 10.1021/Acs.Joc.5B00300 |
0.73 |
|
| 2014 |
Xin D, Burgess K. A chemoselective route to β-enamino esters and thioesters. Organic Letters. 16: 2108-10. PMID 24679218 DOI: 10.1021/Ol5005643 |
0.319 |
|
| 2014 |
Lim SH, Wu L, Kiew LV, Chung LY, Burgess K, Lee HB. Rosamines targeting the cancer oxidative phosphorylation pathway. Plos One. 9: e82934. PMID 24622277 DOI: 10.1371/Journal.Pone.0082934 |
0.48 |
|
| 2014 |
Brahimi F, Ko E, Malakhov A, Burgess K, Saragovi HU. Combinatorial assembly of small molecules into bivalent antagonists of TrkC or TrkA receptors Plos One. 9. PMID 24603864 DOI: 10.1371/Journal.Pone.0089617 |
0.576 |
|
| 2014 |
Khumsubdee S, Burgess K. Metathesis for catalyst design: Metacatalysis Tetrahedron. 70: 1326-1335. DOI: 10.1016/J.Tet.2013.12.040 |
0.318 |
|
| 2013 |
Khumsubdee S, Burgess K. Comparison Of Asymmetric Hydrogenations Of Unsaturated- Carboxylic Acids And -Esters. Acs Catalysis. 3: 237-249. PMID 24729943 DOI: 10.1021/Cs3007389 |
0.305 |
|
| 2013 |
Khumsubdee S, Zhou H, Burgess K. Homo-Roche ester derivatives by asymmetric hydrogenation and organocatalysis Journal of Organic Chemistry. 78: 11948-11955. PMID 24219839 DOI: 10.1021/Jo401996M |
0.328 |
|
| 2013 |
Xin D, Ko E, Perez LM, Ioerger TR, Burgess K. Evaluating minimalist mimics by exploring key orientations on secondary structures (EKOS). Organic & Biomolecular Chemistry. 11: 7789-801. PMID 24121516 DOI: 10.1039/C3Ob41848K |
0.575 |
|
| 2013 |
Raghuraman A, Xin D, Perez LM, Burgess K. Expanding the scope of oligo-pyrrolinone-pyrrolidines as protein-protein interface mimics. The Journal of Organic Chemistry. 78: 4823-33. PMID 23654284 DOI: 10.1021/Jo400323K |
0.712 |
|
| 2013 |
Ko E, Raghuraman A, Perez LM, Ioerger TR, Burgess K. Exploring key orientations at protein-protein interfaces with small molecule probes. Journal of the American Chemical Society. 135: 167-73. PMID 23270593 DOI: 10.1021/Ja3067258 |
0.761 |
|
| 2013 |
Zhu Y, Burgess K. Highly stereoselective syntheses of all 1,2,3-Me,OH,Me triads via asymmetric hydrogenation reactions Advanced Synthesis and Catalysis. 355: 107-115. DOI: 10.1002/Adsc.201200709 |
0.485 |
|
| 2013 |
Cerdán L, Martínez-Martínez V, García-Moreno I, Costela A, Pérez-Ojeda ME, Arbeloa IL, Wu L, Burgess K. Naturally assembled excimers in xanthenes as singular and highly efficient laser dyes in liquid and solid media Advanced Optical Materials. 1: 984-990. DOI: 10.1002/Adom.201300383 |
0.492 |
|
| 2012 |
Ko E, Kamkaew A, Burgess K. Small Molecule Ligands For Active Targeting Of TrkC-expressing Tumor Cells. Acs Medicinal Chemistry Letters. 3: 1008-1012. PMID 23411915 DOI: 10.1021/Ml300227D |
0.555 |
|
| 2012 |
Zhu Y, Burgess K. Filling gaps in asymmetric hydrogenation methods for acyclic stereocontrol: application to chirons for polyketide-derived natural products. Accounts of Chemical Research. 45: 1623-36. PMID 23035731 DOI: 10.1021/Ar200145Q |
0.47 |
|
| 2012 |
Fedoseyenko D, Raghuraman A, Ko E, Burgess K. Omegatides: constrained analogs of peptide primary sequence. Organic & Biomolecular Chemistry. 10: 921-4. PMID 22179815 DOI: 10.1039/C2Ob06692K |
0.742 |
|
| 2012 |
Zhu Y, Burgess K. Iridium catalyzed enantioselective hydrogenation of α-alkoxy and β-alkoxy vinyl ethers Rsc Advances. 2: 4728-4735. DOI: 10.1039/C2Ra01350A |
0.485 |
|
| 2011 |
Zhu Y, Khumsubdee S, Schaefer A, Burgess K. Asymmetric syntheses of α-methyl γ-amino acid derivatives. The Journal of Organic Chemistry. 76: 7449-57. PMID 21851084 DOI: 10.1021/Jo201215C |
0.488 |
|
| 2011 |
Thivierge C, Loudet A, Burgess K. Brilliant BODIPY-fluorene Copolymers With Dispersed Absorption and Emission Maxima. Macromolecules. 44: 4012-4015. PMID 21804648 DOI: 10.1021/Ma200174W |
0.769 |
|
| 2011 |
Raghuraman A, Ko E, Perez LM, Ioerger TR, Burgess K. Pyrrolinone-pyrrolidine oligomers as universal peptidomimetics. Journal of the American Chemical Society. 133: 12350-3. PMID 21780756 DOI: 10.1021/Ja2033734 |
0.764 |
|
| 2011 |
Thivierge C, Han J, Jenkins RM, Burgess K. Fluorescent proton sensors based on energy transfer. The Journal of Organic Chemistry. 76: 5219-28. PMID 21618970 DOI: 10.1021/Jo2005654 |
0.784 |
|
| 2011 |
Ko E, Liu J, Burgess K. Minimalist and universal peptidomimetics. Chemical Society Reviews. 40: 4411-21. PMID 21483946 DOI: 10.1039/C0Cs00218F |
0.584 |
|
| 2011 |
Jose J, Loudet A, Ueno Y, Wu L, Chen HY, Son DH, Barhoumi R, Burghardt R, Burgess K. Energy transfer cassettes in silica nanoparticles target intracellular organelles. Organic & Biomolecular Chemistry. 9: 3871-7. PMID 21455504 DOI: 10.1039/C0Ob00967A |
0.774 |
|
| 2011 |
Loudet A, Ueno Y, Wu L, Jose J, Barhoumi R, Burghardt R, Burgess K. Organelle-selective energy transfer: a fluorescent indicator of intracellular environment. Bioorganic & Medicinal Chemistry Letters. 21: 1849-51. PMID 21316231 DOI: 10.1016/J.Bmcl.2011.01.040 |
0.779 |
|
| 2011 |
Ko E, Burgess K. Pyrrole-based scaffolds for turn mimics. Organic Letters. 13: 980-3. PMID 21268601 DOI: 10.1021/Ol103022M |
0.586 |
|
| 2011 |
Ko E, Liu J, Perez LM, Lu G, Schaefer A, Burgess K. Universal peptidomimetics. Journal of the American Chemical Society. 133: 462-77. PMID 21182254 DOI: 10.1021/ja1071916 |
0.552 |
|
| 2011 |
Ueno Y, Jose J, Loudet A, Pérez-Bolívar C, Anzenbacher P, Burgess K. Encapsulated energy-transfer cassettes with extremely well resolved fluorescent outputs. Journal of the American Chemical Society. 133: 51-5. PMID 21105708 DOI: 10.1021/Ja107193J |
0.791 |
|
| 2011 |
Pérez-Ojeda ME, Thivierge C, Martín V, Costela A, Burgess K, García-Moreno I. Highly efficient and photostable photonic materials from diiodinated BODIPY laser dyes Optical Materials Express. 1: 243-251. DOI: 10.1364/Ome.1.000243 |
0.74 |
|
| 2010 |
Zhu Y, Loudet A, Burgess K. An asymmetric hydrogenation route to (-)-spongidepsin. Organic Letters. 12: 4392-5. PMID 20822172 DOI: 10.1021/Ol1018773 |
0.767 |
|
| 2010 |
Brahimi F, Liu J, Malakhov A, Chowdhury S, Purisima EO, Ivanisevic L, Caron A, Burgess K, Saragovi HU. A monovalent agonist of TrkA tyrosine kinase receptors can be converted into a bivalent antagonist. Biochimica Et Biophysica Acta. 1800: 1018-26. PMID 20600627 DOI: 10.1016/J.Bbagen.2010.06.007 |
0.313 |
|
| 2010 |
Bai Y, Shi Z, Zhuo Y, Liu J, Malakhov A, Ko E, Burgess K, Schaefer H, Esteban PF, Tessarollo L, Saragovi HU. In glaucoma the upregulated truncated TrkC.T1 receptor isoform in glia causes increased TNF-alpha production, leading to retinal ganglion cell death. Investigative Ophthalmology & Visual Science. 51: 6639-51. PMID 20574020 DOI: 10.1167/Iovs.10-5431 |
0.533 |
|
| 2010 |
Liu J, Brahimi F, Saragovi HU, Burgess K. Bivalent diketopiperazine-based tropomysin receptor kinase C (TrkC) antagonists. Journal of Medicinal Chemistry. 53: 5044-8. PMID 20540510 DOI: 10.1021/Jm100148D |
0.341 |
|
| 2010 |
Shi Q, Nguyen AT, Angell Y, Deng D, Na CR, Burgess K, Roberts DD, Brunicardi FC, Templeton NS. A combinatorial approach for targeted delivery using small molecules and reversible masking to bypass nonspecific uptake in vivo. Gene Therapy. 17: 1085-97. PMID 20463761 DOI: 10.1038/gt.2010.55 |
0.761 |
|
| 2010 |
Jose J, Loudet A, Ueno Y, Barhoumi R, Burghardt RC, Burgess K. Intracellular imaging of organelles with new water-soluble benzophenoxazine dyes. Organic & Biomolecular Chemistry. 8: 2052-9. PMID 20401381 DOI: 10.1039/B925845K |
0.779 |
|
| 2010 |
Zhu Y, Fan Y, Burgess K. Carbene-metal hydrides can be much less acidic than phosphine-metal hydrides: significance in hydrogenations. Journal of the American Chemical Society. 132: 6249-53. PMID 20377250 DOI: 10.1021/Ja101233G |
0.479 |
|
| 2010 |
Lim SH, Thivierge C, Nowak-Sliwinska P, Han J, van den Bergh H, Wagnières G, Burgess K, Lee HB. In vitro and in vivo photocytotoxicity of boron dipyrromethene derivatives for photodynamic therapy. Journal of Medicinal Chemistry. 53: 2865-74. PMID 20199028 DOI: 10.1016/J.Pdpdt.2011.03.232 |
0.78 |
|
| 2010 |
Han J, Burgess K. Fluorescent indicators for intracellular pH. Chemical Reviews. 110: 2709-28. PMID 19831417 DOI: 10.1021/Cr900249Z |
0.464 |
|
| 2010 |
Burgess K, Zhu Y, Loudet A. Synthesis of (-)-Spongidepsin Synfacts. 2011: 0008-0008. DOI: 10.1055/s-0030-1259132 |
0.703 |
|
| 2010 |
Powell MT, Porte AM, Reibenspies J, Burgess K. ChemInform Abstract: Optically Active C3-Symmetric Triarylphosphines in Asymmetric Allylations. Cheminform. 32: no-no. DOI: 10.1002/chin.200139030 |
0.605 |
|
| 2010 |
THORESEN LH, KIM H, WELCH MB, BURGHART A, BURGESS K. ChemInform Abstract: Synthesis of 3,5-Diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY®) Dyes. Cheminform. 30: no-no. DOI: 10.1002/chin.199908189 |
0.692 |
|
| 2010 |
POWELL MT, PORTE AM, BURGESS K. ChemInform Abstract: On the Efficacy of Propeller-Shaped, C3-Symmetric Triarylphosphines in Asymmetric Catalysis. Cheminform. 30: no-no. DOI: 10.1002/chin.199902114 |
0.603 |
|
| 2009 |
Jose J, Ueno Y, Castro JC, Li L, Burgess K. Energy transfer dyads based on Nile Red. Tetrahedron Letters. 50: 6442-6445. PMID 20160911 DOI: 10.1016/J.Tetlet.2009.08.130 |
0.678 |
|
| 2009 |
Chen D, Brahimi F, Angell Y, Li YC, Moscowicz J, Saragovi HU, Burgess K. Bivalent peptidomimetic ligands of TrkC are biased agonists and selectively induce neuritogenesis or potentiate neurotrophin-3 trophic signals. Acs Chemical Biology. 4: 769-81. PMID 19735123 DOI: 10.1021/Cb9001415 |
0.781 |
|
| 2009 |
Zhao J, Burgess K. Synthesis of vicinal dimethyl chirons by asymmetric hydrogenation of trisubstituted alkenes. Journal of the American Chemical Society. 131: 13236-7. PMID 19719102 DOI: 10.1021/Ja905458N |
0.304 |
|
| 2009 |
Brahimi F, Malakhov A, Lee HB, Pattarawarapan M, Ivanisevic L, Burgess K, Saragovi HU. A peptidomimetic of NT-3 acts as a TrkC antagonist. Peptides. 30: 1833-9. PMID 19647025 DOI: 10.1016/J.Peptides.2009.07.015 |
0.641 |
|
| 2009 |
Cieślik-Boczula K, Burgess K, Li L, Nguyen B, Pandey L, De Borggraeve WM, Van der Auweraer M, Boens N. Photophysics and stability of cyano-substituted boradiazaindacene dyes. Photochemical & Photobiological Sciences : Official Journal of the European Photochemistry Association and the European Society For Photobiology. 8: 1006-15. PMID 19582277 DOI: 10.1039/B905054J |
0.335 |
|
| 2009 |
Wu L, Loudet A, Barhoumi R, Burghardt RC, Burgess K. Fluorescent cassettes for monitoring three-component interactions in vitro and in living cells. Journal of the American Chemical Society. 131: 9156-7. PMID 19566090 DOI: 10.1021/Ja9029413 |
0.778 |
|
| 2009 |
Lim SH, Wu L, Burgess K, Lee HB. New cytotoxic rosamine derivatives selectively accumulate in the mitochondria of cancer cells. Anti-Cancer Drugs. 20: 461-8. PMID 19387338 DOI: 10.1097/Cad.0B013E32832B7Bee |
0.502 |
|
| 2009 |
Han J, Loudet A, Barhoumi R, Burghardt RC, Burgess K. A ratiometric pH reporter for imaging protein-dye conjugates in living cells. Journal of the American Chemical Society. 131: 1642-3. PMID 19146412 DOI: 10.1021/Ja8073374 |
0.774 |
|
| 2009 |
Han J, Gonzalez O, Aguilar-Aguilar A, Peña-Cabrera E, Burgess K. 3- and 5-Functionalized BODIPYs via the Liebeskind-Srogl reaction. Organic & Biomolecular Chemistry. 7: 34-6. PMID 19081940 DOI: 10.1039/B818390B |
0.494 |
|
| 2009 |
Jose J, Ueno Y, Burgess K. Water-soluble Nile Blue derivatives: syntheses and photophysical properties. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 418-23. PMID 19025740 DOI: 10.1002/Chem.200801104 |
0.698 |
|
| 2009 |
Castro JC, Malakhov A, Burgess K. Synthesis of regioisomerically pure 5-functionalized 2′,7′- dichlorofluoresceins Synthesis. 1224-1226. DOI: 10.1055/S-0028-1088010 |
0.32 |
|
| 2009 |
Loudet A, Bandichhor R, Burgess K, Palma A, McDonnell SO, Hall MJ, O’Shea DF. Design and Synthesis of Near-IR Fluorophores Synfacts. 2009: 150-150. DOI: 10.1055/S-0028-1087497 |
0.722 |
|
| 2008 |
Loudet A, Bandichhor R, Wu L, Burgess K. Functionalized BF(2) Chelated Azadipyrromethene Dyes. Tetrahedron. 64: 3642-3654. PMID 19458781 DOI: 10.1016/J.Tet.2008.01.117 |
0.792 |
|
| 2008 |
Loudet A, Han J, Barhoumi R, Pellois JP, Burghardt RC, Burgess K. Non-covalent delivery of proteins into mammalian cells. Organic & Biomolecular Chemistry. 6: 4516-22. PMID 19039359 DOI: 10.1039/B809006H |
0.758 |
|
| 2008 |
Wu L, Burgess K. A new synthesis of symmetric boraindacene (BODIPY) dyes. Chemical Communications (Cambridge, England). 4933-5. PMID 18931743 DOI: 10.1039/B810503K |
0.533 |
|
| 2008 |
Wu L, Burgess K. Synthesis and spectroscopic properties of rosamines with cyclic amine substituents. The Journal of Organic Chemistry. 73: 8711-8. PMID 18928318 DOI: 10.1021/Jo800902J |
0.569 |
|
| 2008 |
Loudet A, Bandichhor R, Burgess K, Palma A, McDonnell SO, Hall MJ, O'Shea DF. B,O-chelated azadipyrromethenes as near-IR probes. Organic Letters. 10: 4771-4. PMID 18816131 DOI: 10.1021/Ol8018506 |
0.741 |
|
| 2008 |
Zhu Y, Burgess K. Asymmetric hydrogenation approaches to valuable, acyclic 1,3-hydroxymethyl chirons. Journal of the American Chemical Society. 130: 8894-5. PMID 18563899 DOI: 10.1021/Ja802909B |
0.468 |
|
| 2008 |
Wu L, Burgess K. Fluorescent amino- and thiopyronin dyes. Organic Letters. 10: 1779-82. PMID 18396890 DOI: 10.1021/Ol800526S |
0.535 |
|
| 2008 |
Wu L, Burgess K. Syntheses of highly fluorescent GFP-chromophore analogues. Journal of the American Chemical Society. 130: 4089-96. PMID 18321105 DOI: 10.1021/Ja710388H |
0.541 |
|
| 2008 |
Li L, Han J, Nguyen B, Burgess K. Syntheses and spectral properties of functionalized, water-soluble BODIPY derivatives. The Journal of Organic Chemistry. 73: 1963-70. PMID 18271598 DOI: 10.1021/Jo702463F |
0.528 |
|
| 2008 |
Angell Y, Chen D, Brahimi F, Saragovi HU, Burgess K. A combinatorial method for solution-phase synthesis of labeled bivalent beta-turn mimics. Journal of the American Chemical Society. 130: 556-65. PMID 18088119 DOI: 10.1021/Ja074717Z |
0.803 |
|
| 2008 |
Zhu Y, Burgess K. Iridium-catalyzed asymmetric hydrogenation of vinyl ethers Advanced Synthesis and Catalysis. 350: 979-983. DOI: 10.1002/Adsc.200700546 |
0.441 |
|
| 2008 |
Thoresen LH, Burgess K. Total Syntheses of Vancomycin Organic Synthesis Set. 297-306. DOI: 10.1002/9783527620784.Ch27D |
0.727 |
|
| 2007 |
Loudet A, Burgess K. BODIPY dyes and their derivatives: syntheses and spectroscopic properties. Chemical Reviews. 107: 4891-932. PMID 17924696 DOI: 10.1021/Cr078381N |
0.744 |
|
| 2007 |
Angell YL, Burgess K. Peptidomimetics via copper-catalyzed azide-alkyne cycloadditions. Chemical Society Reviews. 36: 1674-89. PMID 17721589 DOI: 10.1039/B701444A |
0.773 |
|
| 2007 |
Zhou J, Ogle JW, Fan Y, Banphavichit V, Zhu Y, Burgess K. Asymmetric hydrogenation routes to deoxypolyketide chirons. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 7162-70. PMID 17582818 DOI: 10.1002/Chem.200700390 |
0.699 |
|
| 2007 |
Thivierge C, Bandichhor R, Burgess K. Spectral dispersion and water solubilization of BODIPY dyes via palladium-catalyzed C-H functionalization. Organic Letters. 9: 2135-8. PMID 17455941 DOI: 10.1021/Ol0706197 |
0.76 |
|
| 2007 |
Angell Y, Burgess K. Base dependence in copper-catalyzed Huisgen reactions: efficient formation of bistriazoles. Angewandte Chemie (International Ed. in English). 46: 3649-51. PMID 17410632 DOI: 10.1002/Anie.200700399 |
0.773 |
|
| 2007 |
Han J, Jose J, Mei E, Burgess K. Chemiluminescent energy-transfer cassettes based on fluorescein and nile red. Angewandte Chemie (International Ed. in English). 46: 1684-7. PMID 17397078 DOI: 10.1002/Anie.200603307 |
0.632 |
|
| 2007 |
Zhou J, Zhu Y, Burgess K. Synthesis of (S,R,R,S,R,S)-4,6,8,10,16,18- hexamethyldocosane from Antitrogus parvulus via diastereoselective hydrogenations. Organic Letters. 9: 1391-3. PMID 17338543 DOI: 10.1021/Ol070298Z |
0.442 |
|
| 2007 |
Dianjun C, Banphavichit V, Reibenspies J, Burgess K. New optically active N-heterocyclic carbene complexes for hydrogenation: A tale with an atropisomeric twist Organometallics. 26: 855-859. DOI: 10.1021/Om061013+ |
0.305 |
|
| 2006 |
Jose J, Burgess K. Syntheses and properties of water-soluble Nile Red derivatives. The Journal of Organic Chemistry. 71: 7835-9. PMID 16995693 DOI: 10.1021/Jo061369V |
0.596 |
|
| 2006 |
Bandichhor R, Petrescu AD, Vespa A, Kier AB, Schroeder F, Burgess K. Synthesis of a new water-soluble rhodamine derivative and application to protein labeling and intracellular imaging. Bioconjugate Chemistry. 17: 1219-25. PMID 16984131 DOI: 10.1021/Bc0601424 |
0.334 |
|
| 2006 |
Bandichhor R, Petrescu AD, Vespa A, Kier AB, Schroeder F, Burgess K. Water-soluble through-bond energy transfer cassettes for intracellular imaging. Journal of the American Chemical Society. 128: 10688-9. PMID 16910657 DOI: 10.1021/Ja063784A |
0.339 |
|
| 2006 |
Jiao GS, Thoresen LH, Kim TG, Haaland WC, Gao F, Topp MR, Hochstrasser RM, Metzker ML, Burgess K. Syntheses, photophysical properties, and application of through-bond energy-transfer cassettes for biotechnology. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 7816-26. PMID 16888738 DOI: 10.1002/Chem.200600197 |
0.745 |
|
| 2006 |
Reyes SJ, Burgess K. Heterovalent selectivity and the combinatorial advantage. Chemical Society Reviews. 35: 416-23. PMID 16636725 DOI: 10.1039/B516721N |
0.301 |
|
| 2006 |
Kim TG, Castro JC, Loudet A, Jiao JG, Hochstrasser RM, Burgess K, Topp MR. Correlations of structure and rates of energy transfer for through-bond energy-transfer cassettes. The Journal of Physical Chemistry. A. 110: 20-7. PMID 16392835 DOI: 10.1021/Jp053388Z |
0.743 |
|
| 2006 |
Bandichhor R, Thivierge C, Bhuvanesh NSP, Burgess K. 4,4-Difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene Acta Crystallographica Section E: Structure Reports Online. 62: o4310-o4311. DOI: 10.1107/S1600536806032235 |
0.75 |
|
| 2006 |
Jose J, Burgess K. Benzophenoxazine-based fluorescent dyes for labeling biomolecules Tetrahedron. 62: 11021-11037. DOI: 10.1016/J.Tet.2006.08.056 |
0.568 |
|
| 2006 |
Kim TG, Castro JC, Loudet A, Jiao GS, Burgess K, Hochstrasser RM, Topp MR. Femtosecond-domain dynamical studies of energy-transfer cassettes Femtochemistry Vii. 128-131. DOI: 10.1016/B978-044452821-6/50022-8 |
0.691 |
|
| 2005 |
Angell Y, Burgess K. Ring closure to beta-turn mimics via copper-catalyzed azide/alkyne cycloadditions. The Journal of Organic Chemistry. 70: 9595-8. PMID 16268639 DOI: 10.1021/Jo0516180 |
0.781 |
|
| 2005 |
Zaccaro MC, Lee HB, Pattarawarapan M, Xia Z, Caron A, L'Heureux PJ, Bengio Y, Burgess K, Saragovi HU. Selective small molecule peptidomimetic ligands of TrkC and TrkA receptors afford discrete or complete neurotrophic activities. Chemistry & Biology. 12: 1015-28. PMID 16183026 DOI: 10.1016/J.Chembiol.2005.06.015 |
0.72 |
|
| 2005 |
Cui X, Fan Y, Hall MB, Burgess K. Mechanistic insights into iridium-catalyzed asymmetric hydrogenation of dienes. Chemistry (Weinheim An Der Bergstrasse, Germany). 11: 6859-68. PMID 16163756 DOI: 10.1002/Chem.200500762 |
0.558 |
|
| 2005 |
Cui X, Burgess K. Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes. Chemical Reviews. 105: 3272-96. PMID 16159153 DOI: 10.1021/Cr0500131 |
0.513 |
|
| 2005 |
Cui X, Ogle JW, Burgess K. Stereoselective hydrogenations of aryl-substituted dienes. Chemical Communications (Cambridge, England). 672-4. PMID 15672173 DOI: 10.1039/B413296C |
0.716 |
|
| 2005 |
Burgess K, Perry MC, Cui X. Chiral Imidazolylidine Ligands for Asymmetric Catalysis Cheminform. 36. DOI: 10.1002/chin.200539248 |
0.463 |
|
| 2004 |
Fan Y, Cui X, Burgess K, Hall MB. Electronic effects steer the mechanism of asymmetric hydrogenations of unfunctionalized aryl-substituted alkenes. Journal of the American Chemical Society. 126: 16688-9. PMID 15612683 DOI: 10.1021/Ja044240G |
0.541 |
|
| 2004 |
Jiao GS, Kim TG, Topp MR, Burgess K. A blue-to-red energy-transfer thymidine analogue that functions in DNA. Organic Letters. 6: 1701-4. PMID 15151393 DOI: 10.1021/Ol049684W |
0.326 |
|
| 2004 |
Lee HB, Zaccaro MC, Pattarawarapan M, Roy S, Saragovi HU, Burgess K. Syntheses and activities of new C10 beta-turn peptidomimetics. The Journal of Organic Chemistry. 69: 701-13. PMID 14750794 DOI: 10.1021/Jo034167X |
0.67 |
|
| 2004 |
Burgess K, Ueno Y, Jiao G. Preparation of 5- and 6-Carboxyfluorescein Synthesis. 2004: 2591-2593. DOI: 10.1055/S-2004-829194 |
0.515 |
|
| 2003 |
Jiao GS, Thoresen LH, Burgess K. Fluorescent, through-bond energy transfer cassettes for labeling multiple biological molecules in one experiment. Journal of the American Chemical Society. 125: 14668-9. PMID 14640617 DOI: 10.1021/Ja037193L |
0.746 |
|
| 2003 |
Pattarawarapan M, Burgess K. Molecular basis of neurotrophin-receptor interactions. Journal of Medicinal Chemistry. 46: 5277-91. PMID 14640536 DOI: 10.1021/Jm030221Q |
0.613 |
|
| 2003 |
Cui X, Burgess K. Iridium-mediated asymmetric hydrogenation of 2,3-diphenylbutadiene: a revealing kinetic study. Journal of the American Chemical Society. 125: 14212-3. PMID 14624534 DOI: 10.1021/Ja037653A |
0.544 |
|
| 2003 |
Thoresen LH, Jiao GS, Haaland WC, Metzker ML, Burgess K. Rigid, conjugated, fluoresceinated thymidine triphosphates: syntheses and polymerase mediated incorporation into DNA analogues. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 4603-10. PMID 14566865 DOI: 10.1002/Chem.200304944 |
0.755 |
|
| 2003 |
Jiao GS, Han JW, Burgess K. Syntheses of regioisomerically pure 5- or 6-halogenated fluoresceins. The Journal of Organic Chemistry. 68: 8264-7. PMID 14535816 DOI: 10.1021/Jo034724F |
0.474 |
|
| 2003 |
Jiao GS, Castro JC, Thoresen LH, Burgess K. Microwave-assisted syntheses of regioisomerically pure bromorhodamine derivatives. Organic Letters. 5: 3675-7. PMID 14507202 DOI: 10.1021/Ol035327U |
0.737 |
|
| 2003 |
Wan CW, Burghart A, Chen J, Bergström F, Johansson LB, Wolford MF, Kim TG, Topp MR, Hochstrasser RM, Burgess K. Anthracene-BODIPY cassettes: syntheses and energy transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 4430-41. PMID 14502630 DOI: 10.1002/Chem.200304754 |
0.376 |
|
| 2003 |
Pattarawarapan M, Reyes S, Xia Z, Zaccaro MC, Saragovi HU, Burgess K. Selective formation of homo- and heterobivalent peptidomimetics. Journal of Medicinal Chemistry. 46: 3565-7. PMID 12904060 DOI: 10.1021/Jm034103E |
0.742 |
|
| 2003 |
Lee HB, Pattarawarapan M, Roy S, Burgess K. Syntheses of second generation, 14-membered ring beta-turn mimics. Chemical Communications (Cambridge, England). 1674-5. PMID 12877497 DOI: 10.1039/B304454H |
0.653 |
|
| 2003 |
Jiao GS, Burgess K. Oligonucleotides with strongly fluorescent groups pi-conjugated to a nucleobase: syntheses, melting temperatures, and conformation. Bioorganic & Medicinal Chemistry Letters. 13: 2785-8. PMID 12873515 DOI: 10.1016/S0960-894X(03)00555-9 |
0.311 |
|
| 2003 |
Lane BS, Burgess K. Metal-catalyzed epoxidations of alkenes with hydrogen peroxide. Chemical Reviews. 103: 2457-73. PMID 12848577 DOI: 10.1021/Cr020471Z |
0.65 |
|
| 2003 |
Perry MC, Cui X, Powell MT, Hou DR, Reibenspies JH, Burgess K. Optically active iridium imidazol-2-ylidene-oxazoline complexes: preparation and use in asymmetric hydrogenation of arylalkenes. Journal of the American Chemical Society. 125: 113-23. PMID 12515512 DOI: 10.1021/Ja028142B |
0.735 |
|
| 2003 |
Jiao GS, Loudet A, Lee HB, Kalinin S, Johansson LBA, Burgess K. Syntheses and spectroscopic properties of energy transfer systems based on squaraines Tetrahedron. 59: 3109-3116. DOI: 10.1016/S0040-4020(03)00383-1 |
0.759 |
|
| 2003 |
Han JW, Castro JC, Burgess K. Microwave-assisted functionalization of bromo-fluorescein and bromorhodamine derivatives Tetrahedron Letters. 44: 9359-9362. DOI: 10.1016/J.Tetlet.2003.10.063 |
0.313 |
|
| 2002 |
Lane BS, Vogt M, DeRose VJ, Burgess K. Manganese-catalyzed epoxidations of alkenes in bicarbonate solutions. Journal of the American Chemical Society. 124: 11946-54. PMID 12358539 DOI: 10.1021/Ja025956J |
0.687 |
|
| 2002 |
Pattarawarapan M, Zaccaro MC, Saragovi UH, Burgess K. New templates for syntheses of ring-fused, C(10) beta-turn peptidomimetics leading to the first reported small-molecule mimic of neurotrophin-3. Journal of Medicinal Chemistry. 45: 4387-90. PMID 12238916 DOI: 10.1021/Jm0255421 |
0.653 |
|
| 2002 |
Hou DR, Reibenspies J, Colacot TJ, Burgess K. Enantioselective hydrogenations of arylalkenes mediated by [Ir(cod) (JM-Phos) ]+ complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 5391-400. PMID 11822439 DOI: 10.1002/1521-3765(20011217)7:24<5391::Aid-Chem5391>3.0.Co;2-1 |
0.315 |
|
| 2002 |
Perry MC, Cui X, Burgess K. A modular approach to trans-chelating, N-heterocyclic carbene ligand complexes Tetrahedron: Asymmetry. 13: 1969-1972. DOI: 10.1016/S0957-4166(02)00535-9 |
0.531 |
|
| 2002 |
Jiang L, Burgess K. Fluorinated and iodinated templates for syntheses of β-turn peptidomimetics Tetrahedron. 58: 8743-8750. DOI: 10.1016/S0040-4020(02)01086-4 |
0.315 |
|
| 2001 |
Powell MT, Hou DR, Perry MC, Cui X, Burgess K. Chiral imidazolylidine ligands for asymmetric hydrogenation of aryl alkenes. Journal of the American Chemical Society. 123: 8878-9. PMID 11535106 DOI: 10.1021/Ja016011P |
0.726 |
|
| 2001 |
Lane BS, Burgess K. A cheap, catalytic, scalable, and environmentally benign method for alkene epoxidations. Journal of the American Chemical Society. 123: 2933-4. PMID 11457001 DOI: 10.1021/Ja004000A |
0.692 |
|
| 2001 |
Hou DR, Reibenspies JH, Burgess K. New, optically active phosphine oxazoline (JM-Phos) ligands: syntheses and applications in allylation reactions. The Journal of Organic Chemistry. 66: 206-15. PMID 11429902 DOI: 10.1021/Jo001333H |
0.35 |
|
| 2001 |
Pattarawarapan M, Chen J, Steffensen M, Burgess K. A rigid linker-scaffold for solid-phase synthesis of dimeric pharmacophores. Journal of Combinatorial Chemistry. 3: 102-16. PMID 11148071 DOI: 10.1021/Cc000081V |
0.687 |
|
| 2001 |
Park C, Burgess K. Facile macrocyclizations to β-turn mimics with diverse structural, physical, and conformational properties Journal of Combinatorial Chemistry. 3: 257-266. DOI: 10.1021/Cc010003N |
0.343 |
|
| 2001 |
Powell MT, Porte AM, Reibenspies J, Burgess K. Optically active C3-symmetric triarylphosphines in asymmetric allylations Tetrahedron. 57: 5027-5038. DOI: 10.1016/S0040-4020(01)00346-5 |
0.665 |
|
| 2000 |
Pattarawarapan M, Burgess K. A Linker Scaffold to Present Dimers of Pharmacophores Prepared by Solid-Phase Syntheses. Angewandte Chemie (International Ed. in English). 39: 4299-4301. PMID 29711923 DOI: 10.1002/1521-3773(20001201)39:23<4299::Aid-Anie4299>3.0.Co;2-N |
0.649 |
|
| 2000 |
Chen J, Pattarawarapan M, Zhang AJ, Burgess K. Solution- and solid-phase syntheses of substituted guanidinocarboxylic acids. Journal of Combinatorial Chemistry. 2: 276-81. PMID 10827936 DOI: 10.1021/Cc990084B |
0.644 |
|
| 2000 |
Chen J, Burghart A, Derecskei-Kovacs A, Burgess K. 4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes modified for extended conjugation and restricted bond rotations. The Journal of Organic Chemistry. 65: 2900-6. PMID 10814176 DOI: 10.1021/Jo991927O |
0.331 |
|
| 2000 |
Burghart A, Thoresen LH, Chen J, Burgess K, Bergström F, Johansson LB-. Energy transfer cassettes based on BODIPY® dyes Chemical Communications. 2203-2204. DOI: 10.1039/B006769P |
0.738 |
|
| 2000 |
Chen J, Burghart A, Wan CW, Thai L, Ortiz C, Reibenspies J, Burgess K. Synthesis and spectroscopic properties of 2-ketopyrrole-BF2 complexes: A new class of fluorescent dye Tetrahedron Letters. 41: 2303-2307. DOI: 10.1016/S0040-4039(00)00166-0 |
0.35 |
|
| 2000 |
Reyes S, Pattarawarapan M, Roy S, Burgess K. Preferred Secondary Structures as a Possible Driving Force for Macrocyclization Tetrahedron. 56: 9809-9818. DOI: 10.1016/S0040-4020(00)00888-7 |
0.675 |
|
| 2000 |
Pattarawarapan M, Burgess K. A linker scaffold to present dimers of pharmacophores prepared by solid-phase syntheses Angewandte Chemie - International Edition. 39: 4299-4301. DOI: 10.1002/1521-3773(20001201)39:23<4299::AID-ANIE4299>3.0.CO;2-N |
0.62 |
|
| 1999 |
Feng Y, Pattarawarapan M, Wang Z, Burgess K. Solid-phase SN2 macrocyclization reactions to form beta-turn mimics. Organic Letters. 1: 121-4. PMID 10822547 DOI: 10.1021/Ol990597R |
0.667 |
|
| 1999 |
Martinez CI, Thoresen LH, Gibbs RA, Burgess K. An allylic/acyclic adenosine nucleoside triphosphate for termination of DNA synthesis by DNA template-dependent polymerases. Nucleic Acids Research. 27: 1271-4. PMID 9973613 DOI: 10.1093/Nar/27.5.1271 |
0.72 |
|
| 1999 |
Feng Y, Burgess K, Pledger D, Cairns N, Linthicum DS. A labeled guanidine ligand for studying sweet taste. Bioorganic & Medicinal Chemistry Letters. 8: 881-4. PMID 9871559 DOI: 10.1016/S0960-894X(98)00130-9 |
0.313 |
|
| 1999 |
Feng Y, Pattarawarapan M, Wang Z, Burgess K. Stereochemical implications on diversity in β-turn peptidomimetic libraries Journal of Organic Chemistry. 64: 9175-9177. DOI: 10.1021/Jo991150Z |
0.646 |
|
| 1999 |
Burghart A, Kim H, Welch MB, Thoresen LH, Reibenspies J, Burgess K, Bergström F, Johansson LBA. 3,5-diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) dyes: Synthesis, spectroscopic, electrochemical, and structural properties Journal of Organic Chemistry. 64: 7813-7819. DOI: 10.1021/Jo990796O |
0.756 |
|
| 1999 |
Feng Y, Burgess K. Solid-Phase SNAr Macrocyclizations To Give Turn-Extended-Turn Peptidomimetics Chemistry - a European Journal. 5: 3261-3272. DOI: 10.1002/(Sici)1521-3765(19991105)5:11<3261::Aid-Chem3261>3.0.Co;2-H |
0.313 |
|
| 1998 |
Powell MT, Porte AM, Burgess K. On the efficacy of propeller-shaped, C3-symmetric triarylphosphines in asymmetric catalysis Chemical Communications. 2161-2162. DOI: 10.1039/A806811I |
0.66 |
|
| 1998 |
Moye-Sherman D, Welch MB, Reibenspies J, Burgess K. Asymmetric synthesis of 3-phenyl-2,3-methanophenylalanine developed by panning catalysts in a library format Chemical Communications. 2377-2378. DOI: 10.1039/A805454A |
0.309 |
|
| 1998 |
Hay CM, Leadbeater NE, Lewis J, Raithby PR, Burgess K. Photochemistry of Os3(CO)12 with AuPPh3Cl: synthesis and structural characterisation of (μ-AuPPh3)(μ-Cl)Os3(CO)10 New Journal of Chemistry. 22: 787-788. DOI: 10.1039/A802946F |
0.587 |
|
| 1998 |
Porte AM, Reibenspies J, Burgess K. Design and Optimization of New Phosphine Oxazoline Ligands via High-Throughput Catalyst Screening Journal of the American Chemical Society. 120: 9180-9187. DOI: 10.1021/Ja981217K |
0.311 |
|
| 1998 |
Moye-Sherman D, Jin S, Ham I, Lim D, Scholtz JM, Burgess K. Conformational preferences of RNase A C-peptide derivatives containing a highly constrained analogue of phenylalanine Journal of the American Chemical Society. 120: 9435-9443. DOI: 10.1021/Ja981153D |
0.305 |
|
| 1997 |
Burgess K, Lim D. Resin type can have important effects on solid phase asymmetricalkylation reactions Chemical Communications. 785-786. DOI: 10.1039/A608524E |
0.3 |
|
| 1997 |
Burgess K, Jacutin SE, Lim D, Shitangkoon A. An Approach to Photolabile, Fluorescent Protecting Groups The Journal of Organic Chemistry. 62: 5165-5168. DOI: 10.1021/Jo9702608 |
0.343 |
|
| 1997 |
Burgess K, Ibarzo J, Linthicum DS, Russell DH, Shin H, Shitangkoon A, Totani R, Zhang AJ. Solid Phase Syntheses of Oligoureas Journal of the American Chemical Society. 119: 1556-1564. DOI: 10.1021/Ja9631256 |
0.305 |
|
| 1996 |
Burgess K, Lim D, Martinez CI. Nucleophilic Aromatic Substitution—A Possible Key Step in Total Syntheses of Vancomycin Angewandte Chemie International Edition in English. 35: 1077-1078. DOI: 10.1002/Anie.199610771 |
0.321 |
|
| 1994 |
Burgess K, Gibbs RA, Metzker ML, Raghavachari R. Synthesis of an oxyamide linked nucleotide dimer and incorporation into antisense oligonucleotide sequences Journal of the Chemical Society, Chemical Communications. 915-916. DOI: 10.1039/C39940000915 |
0.31 |
|
| 1994 |
Burgess K, Lim D, Ho K, Ke C. Asymmetric Syntheses of Protected Derivatives of Carnosadine and Its Stereoisomers as Conformationally Constrained Surrogates for Arginine The Journal of Organic Chemistry. 59: 2179-2185. DOI: 10.1021/Jo00087A039 |
0.322 |
|
| 1993 |
Burgess K, Jaspars M. Ruthenium-catalyzed hydroborations of alkenes Organometallics. 12: 4197-4200. DOI: 10.1021/Om00034A065 |
0.302 |
|
| 1992 |
Burgess K, Ohlmeyer MJ, Whitmire KH. Stereochemically matched (and mismatched) bisphosphine ligands: DIOP-DIPAMP hybrids Organometallics. 11: 3588-3600. DOI: 10.1021/Om00059A023 |
0.497 |
|
| 1992 |
Burgess K, Ho KK. Asymmetric syntheses of all four stereoisomers of 2,3-methanomethionine The Journal of Organic Chemistry. 57: 5931-5936. DOI: 10.1021/Jo00048A028 |
0.335 |
|
| 1992 |
Burgess K, Ho KK. Asymmetric syntheses of protected derivatives of ornithine- and arginine-2,3-methanologs Tetrahedron Letters. 33: 5677-5680. DOI: 10.1016/0040-4039(92)89003-U |
0.313 |
|
| 1991 |
Burgess K, Cassidy J, Henderson I. Optically active building blocks from the SPAC reaction: a completely asymmetric synthesis of (4S-cis)-5-(cyclohexylmethyl)-4-hydroxy-2-pyrrolidinone, a statine analog The Journal of Organic Chemistry. 56: 2050-2058. DOI: 10.1021/Jo00006A017 |
0.306 |
|
| 1990 |
Burgess K, Ohlmeyer MJ, Whitmire KH. Stereochemical assignments via cyclic derivatives: a cautionary note The Journal of Organic Chemistry. 55: 1359-1361. DOI: 10.1021/Jo00291A051 |
0.481 |
|
| 1989 |
Burgess K, Ohlmeyer MJ. Substrate-controlled diastereoselectivity in catalyzed and uncatalyzed hydroborations of allylic amine derivatives Tetrahedron Letters. 30: 5857-5860. DOI: 10.1016/S0040-4039(01)93489-6 |
0.301 |
|
| 1987 |
Burgess K. Regioselective and stereoselective nucleophilic addition to electrophilic vinylcyclopropanes The Journal of Organic Chemistry. 52: 2046-2051. DOI: 10.1021/Jo00386A028 |
0.311 |
|
| 1985 |
Burgess K, Holden HD, Johnson BFG, Lewis J, Hursthouse MB, Walker NPC, Deeming AJ, Manning PJ, Peters R. Metallation of 2-ethenylpyridine at triosmium clusters: X-ray crystal structures of the open trinuclear clusters [Os3H(CO)9L(NC5H4CHCH)](L = CO or PMe2Ph) Journal of the Chemical Society-Dalton Transactions. 85-90. DOI: 10.1039/Dt9850000085 |
0.425 |
|
| 1985 |
Trost BM, Burgess K. Addition-cyclization catalysed by palladium(II) Journal of the Chemical Society, Chemical Communications. 1084-1086. DOI: 10.1039/C39850001084 |
0.411 |
|
| 1985 |
Burgess K. Conjugate nucleophilic ring opening of activated vinylcyclopropanes facilitated by homogenous palladium catalysis Tetrahedron Letters. 26: 3049-3052. DOI: 10.1016/S0040-4039(00)98615-5 |
0.301 |
|
| 1985 |
Burgess K, Guerin C, Johnson B, Lewis J. The synthesis and characterisation of new triosmium and triruthenium main-group metal clusters M3(H)(CO)11(M′R3) and Os3(H)(CO)10(CH3CN)(M′R3) (M = Os, Ru; M′ = Ge, Sn; R, aryl, alkyl) Journal of Organometallic Chemistry. 295: c3-c6. DOI: 10.1016/0022-328X(85)88081-5 |
0.395 |
|
| 1985 |
TROST BM, BURGESS K. ChemInform Abstract: ADDITION-CYCLIZATION CATALYZED BY PALLADIUM(II) Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198550147 |
0.384 |
|
| 1985 |
BURGESS K, HOLDEN HD, JOHNSON BFG, LEWIS J, HURSTHOUSE MB, WALKER NPC, DEEMING AJ, MANNING PJ, PETERS R. ChemInform Abstract: METALATION OF 2-ETHENYLPYRIDINE AT TRIOSMIUM CLUSTERS: X-RAY CRYSTAL STRUCTURES OF THE OPEN TRINUCLEAR CLUSTERS (OS3H(CO)9L(NC5H4CH:CH)) (L = CO OR PME2PH) Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198518286 |
0.36 |
|
| 1983 |
Burgess K, Holden HD, Johnson BFG, Lewis J. Synthesis of triosmium clusters containing amidine ligands: X-ray structural characterization of [Os3(µ-H)(CO)9{NPhC(Ph)NH}] Journal of the Chemical Society-Dalton Transactions. 1199-1202. DOI: 10.1039/Dt9830001199 |
0.428 |
|
| 1983 |
Burgess K, Johnson BFG, Kaner DA, Lewis J, Raithby PR, Azman SN, Syed-Mustaffa B. Reaction of the unsaturated mixed metal cluster [Os3(µ-H)(CO)10(µ-AuPR3)](R = Ph, Et) with carbon monoxide and the chemistry of the products; the X-ray crystal structure of [Os3(CO)10(µ-AuPEt3)2] Journal of the Chemical Society, Chemical Communications. 455-457. DOI: 10.1039/C39830000455 |
0.4 |
|
| 1983 |
Burgess K, Johnson BF, Lewis J. Syntheses of goldtriosmium-isocyanate clusters Journal of Organometallic Chemistry. 247: c42-c44. DOI: 10.1016/S0022-328X(00)98767-9 |
0.563 |
|
| 1983 |
KATRITZKY AR, YEUNG WK, PATEL RC, BURGESS K. ChemInform Abstract: PREPARATION AND REACTIONS OF 1-CYANOMETHYL-2,4,6-TRISUBSTITUTED PYRIDINIUM YLIDES Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198338226 |
0.402 |
|
| 1983 |
BURGESS K, HOLDEN HD, JOHNSON BFG, LEWIS J. ChemInform Abstract: SYNTHESIS OF TRIOSMIUM CLUSTERS CONTAINING AMIDINE LIGANDS: X-RAY STRUCTURAL CHARACTERIZATION OF NONACARBONYL-μ-HYDRIDO-(μ3-N2-PHENYLBENZAMIDIDO-N1,N1,N2)-TRIANGULO-TRIOS# MIUM Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198337309 |
0.389 |
|
| 1983 |
BURGESS K, JOHNSON BFG, LEWIS J, RAITHBY PR. ChemInform Abstract: REACTIONS OF (OS3(μ-H)2(CO)10)) WITH ORGANIC AZIDES: STRUCTURAL CHARACTERIZATION OF (OS3(μ-H)(CO)10(μ-HN3PH)) AND (OS3(μ-H)2(CO)9(μ3-NPH)) Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198302289 |
0.391 |
|
| 1982 |
Burgess K, Johnson BFG, Lewis J, Raithby PR. Reactions of [Os3(µ-H)2(CO)10] with organic azides: structural characterization of [Os3(µ-H)(CO)10(µ-HN3Ph)] and [Os3(µ-H)2(CO)9(µ3-NPh)] Journal of the Chemical Society-Dalton Transactions. 2085-2092. DOI: 10.1039/Dt9820002085 |
0.409 |
|
| 1982 |
Burgess K, Johnson BFG, Lewis J, Raithby PR. Reactions of [Os3(µ-H)2(CO)10] with diazo-compounds: structural characterization of [Os3(µ-H)(CO)10(µ-NHNCPh2)] and [Os3(µ-H)(CO)10(µ-NHNCPhMe)] Journal of the Chemical Society-Dalton Transactions. 263-269. DOI: 10.1039/Dt9820000263 |
0.412 |
|
| 1982 |
Oxton IA, Powell DB, Sheppard N, Burgess K, Johnson BFG, Lewis J. The infrared vibrational assignment for the μ2-bridging methylene ligand in metal cluster complexes and its comparison with frequencies assigned to CH2 species chemisorbed on metal surfaces Journal of the Chemical Society, Chemical Communications. 719-721. DOI: 10.1039/C39820000719 |
0.369 |
|
| 1982 |
Burgess K, Johnson BF, Lewis J, Raithby PR. Reactions of triosmium clusters with organic azides; x-ray crystal structures of [Os3(CO)10(NCMe)(N3COPh)], [Os3(μ-H)(CO)10(HN3Ph)], and [Os3(μ-H)2(CO)9(μ3-NPh)] Journal of Organometallic Chemistry. 224: C40-C44. DOI: 10.1016/S0022-328X(00)93183-8 |
0.559 |
|
| 1982 |
Burgess K, Johnson BF, Lewis J. Synthesis and reactivity of triosmium clusters containing a 2-substituted pyridine moiety Journal of Organometallic Chemistry. 233: C55-C58. DOI: 10.1016/S0022-328X(00)85587-4 |
0.563 |
|
| 1982 |
Katritzky AR, Burgess K, Patel RC. Pyridiniums as potential synthetic substitutes for nitrogen mustards Journal of Heterocyclic Chemistry. 19: 741-745. DOI: 10.1002/Jhet.5570190408 |
0.414 |
|
| 1982 |
BURGESS K, JOHNSON BFG, LEWIS J, RAITHBY PR. ChemInform Abstract: REACTIONS OF (OS3(μ-H)2(CO)10) WITH DIAZO COMPOUNDS: STRUCTURAL CHARACTERIZATION OF (OS3(μ-H)(CO)10(μ-NHNCPH2)) AND (OS3(μ-H)(CO)10(μ-NHNCPHME)) Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198220303 |
0.406 |
|
| 1981 |
KATRITZKY AR, BURGESS K, PATEL RC. ChemInform Abstract: THE SYNTHESIS OF CONDENSED QUINOLIZINIUM SYSTEMS Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198139232 |
0.365 |
|
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