Year |
Citation |
Score |
2021 |
Kim SK, Ngo HX, Dennis EK, Thamban Chandrika N, DeShong P, Garneau-Tsodikova S, Lee VT. Inhibition of Alginate Synthesis by Ebselen Oxide and Its Analogues. Acs Infectious Diseases. PMID 33871968 DOI: 10.1021/acsinfecdis.1c00045 |
0.489 |
|
2020 |
Stein DC, H Stocker L, Powell AE, Kebede S, Watts D, Williams E, Soto N, Dhabaria A, Fenselau C, Ganapati S, DeShong P. Extraction of Membrane Components from Using Catanionic Surfactant Vesicles: A New Approach for the Study of Bacterial Surface Molecules. Pharmaceutics. 12. PMID 32825235 DOI: 10.3390/Pharmaceutics12090787 |
0.648 |
|
2019 |
Nguyen HT, Ganapati S, Watts D, Nanayakkara IA, DeShong P, White IM. New Trimodal Phenotypic Reporter of Extended-Spectrum β-Lactamase Activity. Acs Infectious Diseases. PMID 31478368 DOI: 10.1021/Acsinfecdis.9B00138 |
0.641 |
|
2014 |
Richard K, Mann BJ, Stocker L, Barry EM, Qin A, Cole LE, Hurley MT, Ernst RK, Michalek SM, Stein DC, Deshong P, Vogel SN. Novel catanionic surfactant vesicle vaccines protect against Francisella tularensis LVS and confer significant partial protection against F. tularensis Schu S4 strain. Clinical and Vaccine Immunology : Cvi. 21: 212-26. PMID 24351755 DOI: 10.1128/Cvi.00738-13 |
0.727 |
|
2014 |
DeShong P, E. Nytko F, H. Shukla K. Advances in Siloxane-Based Coupling Reactions: Novel 16-Electron Palladium(0) Tri-alkene Catalysts for Allyl-Aryl Coupling in Precursors to Amaryllidaceae Alkaloids Heterocycles. 88: 1465. DOI: 10.3987/Com-13-S(S)113 |
0.514 |
|
2013 |
Stein D, Zimmerman L, Park J, Stocker L, DeShong P. O19.6 Use of Surfactant Vesicles as a Potential Gonococcal Vaccine Delivery System to Generate Antibody Against Neisserial Lipooligosaccharide Sexually Transmitted Infections. 89. DOI: 10.1136/Sextrans-2013-051184.0196 |
0.726 |
|
2012 |
LeVan A, Zimmerman LI, Mahle AC, Swanson KV, DeShong P, Park J, Edwards VL, Song W, Stein DC. Construction and characterization of a derivative of Neisseria gonorrhoeae strain MS11 devoid of all opa genes. Journal of Bacteriology. 194: 6468-78. PMID 23002223 DOI: 10.1128/Jb.00969-12 |
0.397 |
|
2012 |
Shukla KH, DeShong P. Advances in siloxane-based coupling reactions: Application of palladium-mediated allyl-aryl coupling to the synthesis of pancratistatin derivatives. The formal total synthesis of (±)-7-deoxypancratistatin Heterocycles. 86: 1055-1069. DOI: 10.3987/Com-12-S(N)35 |
0.853 |
|
2010 |
Dowling MB, Li L, Park J, Kumi G, Nan A, Ghandehari H, Fourkas JT, DeShong P. Multiphoton-absorption-induced-luminescence (MAIL) imaging of tumor-targeted gold nanoparticles. Bioconjugate Chemistry. 21: 1968-77. PMID 20964333 DOI: 10.1021/Bc100115M |
0.429 |
|
2009 |
Thomas GB, Rader LH, Park J, Abezgauz L, Danino D, DeShong P, English DS. Carbohydrate modified catanionic vesicles: probing multivalent binding at the bilayer interface. Journal of the American Chemical Society. 131: 5471-7. PMID 19323555 DOI: 10.1021/Ja8076439 |
0.442 |
|
2008 |
Shukla KH, DeShong P. Studies on the mechanism of allylic coupling reactions: a hammett analysis of the coupling of aryl silicate derivatives. The Journal of Organic Chemistry. 73: 6283-91. PMID 18616321 DOI: 10.1021/Jo8010254 |
0.827 |
|
2008 |
Stanford CJ, Dagenais M, Park JH, DeShong P. Real-time monitoring of siloxane monolayer film formation on silica using a fiber Bragg grating Current Analytical Chemistry. 4: 356-361. DOI: 10.2174/157341108785914916 |
0.412 |
|
2008 |
Park J, Rader LH, Thomas GB, Danoff EJ, English DS, DeShong P. Carbohydrate-functionalized catanionic surfactant vesicles: preparation and lectin-binding studies Soft Matter. 4: 1916. DOI: 10.1039/B806059B |
0.445 |
|
2007 |
Sandelier MJ, DeShong P. Reductive cyclization of o-nitrophenyl propargyl alcohols: facile synthesis of substituted quinolines. Organic Letters. 9: 3209-12. PMID 17645347 DOI: 10.1021/Ol0710921 |
0.759 |
|
2007 |
Kadalbajoo M, Park J, Opdahl A, Suda H, Kitchens CA, Garno JC, Batteas JD, Tarlov MJ, DeShong P. Synthesis and structural characterization of glucopyranosylamide films on gold. Langmuir : the Acs Journal of Surfaces and Colloids. 23: 700-7. PMID 17209623 DOI: 10.1021/La062678J |
0.395 |
|
2007 |
Saini SS, Stanford C, Lee SM, Park J, DeShong P, Bentley WE, Dagenais M. Monolayer detection of biochemical agents using etched-core fiber Bragg grating sensors Ieee Photonics Technology Letters. 19: 1341-1343. DOI: 10.1109/Lpt.2007.902345 |
0.415 |
|
2006 |
Shukla KH, Boehmler DJ, Bogacyzk S, Duvall BR, Peterson WA, McElroy WT, Deshong P. Application of palladium-catalyzed allylic arylation to the synthesis of a (+/-)-7-deoxypancratistatin analogue. Organic Letters. 8: 4183-6. PMID 16956182 DOI: 10.1021/Ol061070Z |
0.843 |
|
2006 |
Seganish WM, DeShong P. Application of aryl siloxane cross-coupling to the synthesis of allocolchicinoids. Organic Letters. 8: 3951-4. PMID 16928046 DOI: 10.1021/ol061413t |
0.794 |
|
2006 |
McElroy WT, DeShong P. Synthesis of the CD-ring of the anticancer agent streptonigrin : studies of aryl-aryl coupling methodologies Tetrahedron. 62: 6945-6954. DOI: 10.1016/J.Tet.2006.04.074 |
0.471 |
|
2005 |
Seganish WM, Handy CJ, DeShong P. Efforts directed toward the synthesis of colchicine: application of palladium-catalyzed siloxane cross-coupling methodology. The Journal of Organic Chemistry. 70: 8948-55. PMID 16238332 DOI: 10.1021/Jo051636H |
0.84 |
|
2005 |
Handy CJ, Manoso AS, McElroy WT, Seganish WM, DeShong P. Recent advances in siloxane-based aryl-aryl coupling reactions: Focus on heteroaromatic systems Tetrahedron. 61: 12201-12225. DOI: 10.1016/J.Tet.2005.08.057 |
0.784 |
|
2005 |
Seganish WM, Mowery ME, Riggleman S, DeShong P. Palladium-catalyzed homocoupling of aryl halides in the presence of fluoride Tetrahedron. 61: 2117-2121. DOI: 10.1016/J.Tet.2004.12.040 |
0.815 |
|
2004 |
Manoso AS, Ahn C, Soheili A, Handy CJ, Correia R, Seganish WM, Deshong P. Improved synthesis of aryltrialkoxysilanes via treatment of aryl Grignard or lithium reagents with tetraalkyl orthosilicates. The Journal of Organic Chemistry. 69: 8305-14. PMID 15549801 DOI: 10.1021/Jo048667H |
0.779 |
|
2004 |
Seganish WM, DeShong P. Palladium-catalyzed cross-coupling of aryl triethylammonium bis(catechol) silicates with aryl bromides using microwave irradiation. Organic Letters. 6: 4379-81. PMID 15524488 DOI: 10.1021/Ol048044Q |
0.817 |
|
2004 |
Seganish WM, DeShong P. Application of directed orthometalation toward the synthesis of aryl siloxanes. The Journal of Organic Chemistry. 69: 6790-5. PMID 15387604 DOI: 10.1021/Jo0492057 |
0.82 |
|
2004 |
Seganish WM, DeShong P. Preparation and palladium-catalyzed cross-coupling of aryl triethylammonium bis(catechol) silicates with aryl triflates. The Journal of Organic Chemistry. 69: 1137-43. PMID 14961662 DOI: 10.1021/Jo035309Q |
0.826 |
|
2003 |
Ahn C, Correia R, DeShong P. Mechanistic Study of the Mitsunobu Reaction. The Journal of Organic Chemistry. 68: 1176. PMID 27518842 DOI: 10.1021/jo027970k |
0.593 |
|
2003 |
McElroy WT, DeShong P. Siloxane-Based Cross-Coupling of Bromopyridine Derivatives: Studies for the Synthesis of Streptonigrin and Lavendamycin Organic Letters. 5: 4779-4782. PMID 14653672 DOI: 10.1021/Ol0357503 |
0.538 |
|
2003 |
Riggleman S, DeShong P. Application of silicon-based cross-coupling technology to triflates. Journal of Organic Chemistry. 68: 8106-8109. PMID 14535790 DOI: 10.1021/Jo034809G |
0.538 |
|
2003 |
Damkaci F, DeShong P. Stereoselective synthesis of alpha- and beta-glycosylamide derivatives from glycopyranosyl azides via isoxazoline intermediates. Journal of the American Chemical Society. 125: 4408-9. PMID 12683796 DOI: 10.1021/Ja028694U |
0.768 |
|
2002 |
Ahn C, DeShong P. An approach to the stereoselective synthesis of syn- and anti-1,3-diol derivatives. Retention of configuration in the Mitsunobu reaction. Journal of Organic Chemistry. 67: 1754-1759. PMID 11895389 DOI: 10.1021/Jo001525C |
0.463 |
|
2002 |
Ahn C, Correia R, DeShong P. Mechanistic study of the Mitsunobu reaction. The Journal of Organic Chemistry. 67: 1751-3. PMID 11895388 DOI: 10.1021/Jo001590M |
0.593 |
|
2002 |
Hoke ME, Brescia MR, Bogaczyk S, DeShong P, King BW, Crimmins MT. Regioselectivity in the palladium-catalyzed addition of carbon nucleophiles to carbocyclic derivatives. The Journal of Organic Chemistry. 67: 327-35. PMID 11798302 DOI: 10.1021/Jo010672N |
0.795 |
|
2001 |
Manoso AS, DeShong P. Improved synthesis of aryltriethoxysilanes via palladium(0)-catalyzed silylation of aryl iodides and bromides with triethoxysilane. The Journal of Organic Chemistry. 66: 7449-55. PMID 11681960 DOI: 10.1021/Jo010621Q |
0.814 |
|
2001 |
Correia R, DeShong P. Palladium-catalyzed arylation of allylic benzoates using hypervalent siloxane derivatives. The Journal of Organic Chemistry. 66: 7159-65. PMID 11597246 DOI: 10.1021/Jo010627F |
0.747 |
|
2001 |
Bogaczyk S, Brescia MR, Shimshock YC, DeShong P. A highly stereoselective approach to the synthesis of functionalized pyran derivatives by Lewis acid assisted ketal reduction and allylation. The Journal of Organic Chemistry. 66: 4352-5. PMID 11397176 DOI: 10.1021/Jo010252Y |
0.799 |
|
2000 |
Handy CJ, Lam YF, DeShong P. On the synthesis and NMR analysis of tetrabutylammonium triphenyldifluorosilicate. The Journal of Organic Chemistry. 65: 3542-3. PMID 10843644 DOI: 10.1021/Jo991771S |
0.782 |
|
2000 |
DeShong P, Handy CJ, Mowery ME. Hypervalent siloxane derivatives. An alternative to Stille and Suzuki couplings Pure and Applied Chemistry. 72: 1655-1658. DOI: 10.1351/Pac200072091655 |
0.795 |
|
2000 |
DeShong P, Soli ED, Slough GA, Sidler DR, Elango V, Rybczynski PJ, Vosejpka LJS, Lessen TA, Le TX, Anderson GB, Philipsborn Wv, Vöhler M, Rentsch D, Zerbe O. Glycosylmanganese pentacarbonyl complexes: an organomanganese-based approach to the synthesis of C-glycosyl derivatives Journal of Organometallic Chemistry. 593: 49-62. DOI: 10.1016/S0022-328X(99)00431-3 |
0.38 |
|
1999 |
Mowery ME, DeShong P. Synthesis of Unsymmetrical Biaryls by Palladium-Catalyzed Cross Coupling Reactions of Arenes with Tetrabutylammonium Triphenyldifluorosilicate, a Hypervalent Silicon Reagent. The Journal of Organic Chemistry. 64: 3266-3270. PMID 11674429 DOI: 10.1021/Jo990072C |
0.843 |
|
1999 |
Soli ED, Manoso AS, Patterson MC, DeShong P, Favor DA, Hirschmann R, Smith AB. Azide and Cyanide Displacements via Hypervalent Silicate Intermediates. The Journal of Organic Chemistry. 64: 3171-3177. PMID 11674417 DOI: 10.1021/Jo982302D |
0.808 |
|
1999 |
Mowery ME, DeShong P. Cross-Coupling Reactions of Hypervalent Siloxane Derivatives: An Alternative to Stille and Suzuki Couplings. The Journal of Organic Chemistry. 64: 1684-1688. PMID 11674236 DOI: 10.1021/Jo982463H |
0.837 |
|
1999 |
Mowery ME, DeShong P. Improvements in cross coupling reactions of hypervalent siloxane derivatives. Organic Letters. 1: 2137-40. PMID 10836067 DOI: 10.1021/Ol991186D |
0.819 |
|
1999 |
Soli ED, DeShong P. Advances in Glycosyl Azide Preparation via Hypervalent Silicates Journal of Organic Chemistry. 64: 9724-9726. DOI: 10.1021/Jo991161S |
0.309 |
|
1998 |
Brescia M, DeShong P. Stereoselective Phenylation Of Allylic Alcohol Derivatives By Palladium-Catalyzed Cross-Coupling With Hypervalent Silicon Complexes Journal of Organic Chemistry. 63: 3156-3157. DOI: 10.1021/Jo980069D |
0.445 |
|
1998 |
Rentsch D, Nill L, Philipsborn Wv, Sidler DR, Rybczynski PJ, DeShong P. 13C, 17O and 55Mn NMR studies on substituted manganese carbonyl complexes. A contribution to the mechanism of demetalation reactions†† Magnetic Resonance in Chemistry. 36. DOI: 10.1002/(Sici)1097-458X(199806)36:133.0.Co;2-L |
0.328 |
|
1997 |
Brescia M, Shimshock YC, DeShong P. Regioselectivity in the Palladium-Catalyzed Addition of Carbon Nucleophiles to Dihydropyran Derivatives Journal of Organic Chemistry. 62: 1257-1263. DOI: 10.1021/Jo961973D |
0.428 |
|
1996 |
Pilcher AS, DeShong P. Utilization of Tetrabutylammonium Triphenyldifluorosilicate as a Fluoride Source for Silicon-Carbon Bond Cleavage. Journal of Organic Chemistry. 61: 6901-6905. PMID 11667585 DOI: 10.1021/Jo960922D |
0.435 |
|
1995 |
Class YJ, DeShong P. A formal total synthesis of (±)-pseudomonic acid A Tetrahedron Letters. 36: 7631-7634. DOI: 10.1016/0040-4039(95)01590-E |
0.373 |
|
1994 |
Ahn C, Kennington JW, DeShong P. A new approach to the synthesis of monocyclic β-lactam derivatives Journal of Organic Chemistry. 59: 6282-6286. DOI: 10.1021/Jo00100A033 |
0.314 |
|
1994 |
Shimshock SJ, DeShong P. Synthesis of the Tetramic Acid Antibiotics Studies in Natural Products Chemistry. 14: 97-141. DOI: 10.1016/B978-0-444-81780-8.50009-0 |
0.312 |
|
1993 |
Kennington JW, Li W, Deshong P. Synthesis of Δ4-isoxazolines at high pressures. A new approach to the preparation of β-lactam derivatives? High Pressure Research. 11: 163-166. DOI: 10.1080/08957959208201702 |
0.32 |
|
1993 |
Pilcher AS, DeShong P. Improved protocols for the selective deprotection of trialkylsilyl ethers using fluorosilicic acid Journal of Organic Chemistry. 58: 5130-5134. DOI: 10.1021/Jo00071A023 |
0.337 |
|
1993 |
Dowler ME, Le TX, DeShong P, von Philipsborn W, Vöhler M, Rentsch D. Probing the chemistry of organomanganese complexes. a kinetic study of the role of coordinate bonds in a demetalation reaction Tetrahedron. 49: 5673-5682. DOI: 10.1016/S0040-4020(01)87276-8 |
0.305 |
|
1991 |
DeShong P, Rybczynski PJ. A Novel Method For The Synthesis Of Spiroketal Systems. Synthesis Of The Pheromones Of The Common Wasp And The Olive Fruit Fly Journal of Organic Chemistry. 56: 3207-3210. DOI: 10.1021/Jo00010A005 |
0.38 |
|
1991 |
DeShong P, Li W, Kennington JW, Ammon HL, Leginvs JM. A nitrone-based cycloaddition approach to the synthesis of the glycosyl system of nogalomycin, menogaril, and their congeners Journal of Organic Chemistry. 56: 1364-1373. DOI: 10.1021/Jo00004A008 |
0.385 |
|
1989 |
DeShong P, Simpson DM, Lin M. Acid-catalyzed rearrangement of pyran derivatives. An approach to the stereoselective synthesis of 1,3-diol derivatives Tetrahedron Letters. 30: 2885-2888. DOI: 10.1016/S0040-4039(00)99149-4 |
0.43 |
|
1988 |
DeShong P, Sidler DR. Regioselective opening of epoxides and ethers by (trialkylsilyl)manganese pentacarbonyl complexes: a general strategy for the synthesis of spiroketal lactone and cyclopentenone derivatives Journal of Organic Chemistry. 53: 4892-4894. DOI: 10.1021/Jo00255A051 |
0.413 |
|
1988 |
DeShong P, Cipollina JA, Lowmaster NK. A general method for the synthesis of tetramic acid derivatives Journal of Organic Chemistry. 53: 1356-1364. DOI: 10.1021/Jo00242A003 |
0.343 |
|
1988 |
DeShong P, Waltermire RE, Ammon HL. A general approach to the stereoselective synthesis of spiroketals. A total synthesis of the pheromones of the olive fruit fly and related compounds Journal of the American Chemical Society. 110: 1901-1910. DOI: 10.1021/Ja00214A039 |
0.312 |
|
1987 |
DeShong P, Sidler DR, Slough GA. Synthesis of enones and butenolides using organomanganese pentacarbonyl complexes. Tetrahedron Letters. 28: 2233-2236. DOI: 10.1016/S0040-4039(00)96088-X |
0.329 |
|
1987 |
DeShong P, Slough GA, Rheingold AL. Synthesis of carbonyl compounds using organomanganese pentacarbonyl complexes. Tetrahedron Letters. 28: 2229-2232. DOI: 10.1016/S0040-4039(00)96087-8 |
0.329 |
|
1986 |
DeShong P, Leginus JM, Lander SW. A stereoselective approach to the synthesis of allylic and homoallylic amines Journal of Organic Chemistry. 51: 574-576. DOI: 10.1021/Jo00354A040 |
0.389 |
|
1986 |
DeShong P, Lin MT, Perez JJ. Total synthesis of the (+)-pheromone of the male swift moth hepialus hecta L Tetrahedron Letters. 27: 2091-2094. DOI: 10.1016/S0040-4039(00)84456-1 |
0.311 |
|
1986 |
DeShong P, Lin M, Perez JJ. Total synthesis of the (+)-pheromone of the male swift moth hepialus hecta L. Tetrahedron Letters. 27: 2091-2094. DOI: 10.1002/Chin.198643322 |
0.315 |
|
1985 |
DeShong P, Kell DA, Sidler DR. Intermolecular And Intramolecular Azomethine Ylide (3 + 2) Dipolar Cycloadditions For The Synthesis Of Highly Functionalized Pyrroles And Pyrrolidines Journal of Organic Chemistry. 16: 2309-2315. DOI: 10.1021/Jo00213A022 |
0.436 |
|
1985 |
Deshong P, Ramesh S, Elango V, Perez JJ. Total Synthesis Of (.+-.)-Tirandamycin A Cheminform. 16. DOI: 10.1002/Chin.198551332 |
0.38 |
|
1985 |
Deshong P, Dicken CM, Leginus JM, Whittle RR. Stereoselection In Acyclic Systems. The Synthesis Of Amino Sugars Via Nitrone Cycloadditions Cheminform. 16. DOI: 10.1002/Chin.198502341 |
0.38 |
|
1984 |
DeShong P, Leginus JM. Nitrone cycloadditions. An efficient method for the homologation of aldehydes to .alpha.,.beta.-unsaturated aldehydes Journal of Organic Chemistry. 49: 3421-3423. DOI: 10.1021/Jo00192A047 |
0.305 |
|
1984 |
Deshong P, Dicken CM, Leginus JM, Whittle RR. Stereoselection in acyclic systems. The synthesis of amino sugars via nitrone cycloadditions Journal of the American Chemical Society. 106: 5598-5602. DOI: 10.1021/Ja00331A033 |
0.38 |
|
1984 |
DeShong P, Leginus JM. Nitrone cycloadditions with vinyl silanes: the total synthesis of deoxysugars. Tetrahedron Letters. 25: 5355-5358. DOI: 10.1016/S0040-4039(01)91282-1 |
0.385 |
|
1983 |
Deshong P, Lowmaster NE. High Pressure Diels-Alder Reaction of Furan and Methyl Acrylate Synthetic Communications. 13: 537-543. DOI: 10.1080/00397918308059526 |
0.382 |
|
1983 |
DeShong P, Ramesh S, Perez JJ. Total synthesis of tirandamycin. A short, efficient synthesis of the Ireland alcohol Journal of Organic Chemistry. 14: 2117-2118. DOI: 10.1021/Jo00160A044 |
0.348 |
|
1983 |
DeShong P, Lowmaster NE, Baralt O. Methodology for the synthesis of 3-acyltetramic acids Journal of Organic Chemistry. 14: 1149-1150. DOI: 10.1021/Jo00155A060 |
0.337 |
|
1983 |
DeShong P, Leginus JM. Stereospecific synthesis of racemic daunosamine. Diastereofacial selectivity in a nitrone cycloaddition Journal of the American Chemical Society. 105: 1686-1688. DOI: 10.1021/Ja00344A063 |
0.37 |
|
1982 |
Deshong P, Dicken CM, Perez JJ, Shoff RM. A Simple, Inexpensive System For Performing High Pressure Reactions Organic Preparations and Procedures International. 14: 369-372. DOI: 10.1080/00304948209354935 |
0.326 |
|
1982 |
Dicken CM, DeShong P. Reactions at high pressures. [3+2] Dipolar cycloaddition of nitrones with vinyl ethers Journal of Organic Chemistry. 13: 2047-2051. DOI: 10.1021/Jo00132A014 |
0.373 |
|
1982 |
DeShong P, Ramesh S, Perez JJ, Bodish C. Preparation of 2,9-dioxabicyclo[3.3.1]nonanes. A model for tirandamycin Tetrahedron Letters. 23: 2243-2246. DOI: 10.1016/S0040-4039(00)87311-6 |
0.365 |
|
1979 |
Büchi G, Deshong PR, Katsumura S, Sugimura Y. Total synthesis of tryptoquivaline G [18] Journal of the American Chemical Society. 101: 5084-5086. |
0.521 |
|
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