Year |
Citation |
Score |
2020 |
Kaczmarek R, Korczyński D, Green JR, Dembinski R. Extension of the 5-alkynyluridine side chain via C-C-bond formation in modified organometallic nucleosides using the Nicholas reaction. Beilstein Journal of Organic Chemistry. 16: 1-8. PMID 31976010 DOI: 10.3762/Bjoc.16.1 |
0.42 |
|
2019 |
Mishra M, Twardy D, Ellstrom C, Wheeler KA, Dembinski R, Török B. Catalyst-free ambient temperature synthesis of isoquinoline-fused benzimidazoles from 2-alkynylbenzaldehydes via alkyne hydroamination Green Chemistry. 21: 99-108. DOI: 10.1039/C8Gc02520G |
0.452 |
|
2018 |
Kaczmarek R, Korczyński D, Królewska-Golińska K, Wheeler KA, Chavez FA, Mikus A, Dembinski R. Organometallic Nucleosides: Synthesis and Biological Evaluation of Substituted Dicobalt Hexacarbonyl 2'-Deoxy-5-oxopropynyluridines. Chemistryopen. 7: 237-247. PMID 29531887 DOI: 10.1002/Open.201700168 |
0.375 |
|
2016 |
Young J, Schäfer C, Solan A, Baldrica A, Belcher M, Nişanci B, Wheeler KA, R. Trivedi E, Török B, Dembinski R. Regioselective “hydroamination” of alk-3-ynones with non-symmetrical o-phenylenediamines. Synthesis of diversely substituted 3H-1,5-benzodiazepines via (Z)-3-amino-2-alkenones Rsc Advances. 6: 107081-107093. DOI: 10.1039/C6Ra24291J |
0.419 |
|
2015 |
Goel OP, Dembinski R. Synthesis of dimebon and of its tetrathiomolybdate Organic Preparations and Procedures International. 47: 220-226. DOI: 10.1080/00304948.2015.1025017 |
0.426 |
|
2014 |
Solan A, Nişanci B, Belcher M, Young J, Schäfer C, Wheeler KA, Török B, Dembinski R. Catalyst-free chemo-/regio-/stereo-selective amination of alk-3-ynones. Synthesis of 1,5-benzodiazepines and 3-amino-2-alkenones Green Chemistry. 16: 1120-1124. DOI: 10.1039/C3Gc41898G |
0.474 |
|
2012 |
Borkin DA, Puscau M, Carlson A, Solan A, Wheeler KA, Török B, Dembinski R. Synthesis of diversely 1,3,5-trisubstituted pyrazoles via 5-exo-dig cyclization. Organic & Biomolecular Chemistry. 10: 4505-8. PMID 22575899 DOI: 10.1039/C2Ob25580D |
0.449 |
|
2012 |
Li Y, Wheeler KA, Dembinski R. Room temperature syntheses of entirely diverse substituted β-fluorofurans Organic and Biomolecular Chemistry. 10: 2395-2408. PMID 22261647 DOI: 10.1039/C1Ob06693E |
0.522 |
|
2011 |
Li Y, Wheeler KA, Dembinski R. Electrophilic cyclizations of 2-fluoroalk-3-yn-1-ones: Room-temperature synthesis of diversely 2,5-disubstituted 3,4-fluorohalofurans European Journal of Organic Chemistry. 2767-2771. DOI: 10.1002/Ejoc.201100344 |
0.521 |
|
2010 |
Li Y, Wheeler KA, Dembinski R. Gold(I)-catalyzed cycloisomerization of 2-fluoroalk-3-yn-1-ones: Synthesis of 2,5-substituted 3-fluorofurans Advanced Synthesis and Catalysis. 352: 2761-2766. DOI: 10.1002/Adsc.201000411 |
0.457 |
|
2009 |
Sniady A, Sevilla MD, Meneni S, Lis T, Szafert S, Khanduri D, Finke JM, Dembinski R. Synthesis and EPR studies of 2'-deoxyuridines with alkynyl, rodlike linkages. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 7569-77. PMID 19609983 DOI: 10.1002/Chem.200900481 |
0.746 |
|
2009 |
Wyrebek P, Sniady A, Bewick N, Li Y, Mikus A, Wheeler KA, Dembinski R. Microwave-assisted zinc chloride-catalyzed synthesis of substituted pyrroles from homopropargyl azides Tetrahedron. 65: 1268-1275. DOI: 10.1016/J.Tet.2008.11.094 |
0.49 |
|
2009 |
Sniady A, Sevilla M, Meneni S, Lis T, Szafert S, Khanduri D, Finke J, Dembinski R. Cover Picture: Synthesis and EPR Studies of 2′-Deoxyuridines with Alkynyl, Rodlike Linkages (Chem. Eur. J. 31/2009) Chemistry - a European Journal. 15: 7507-7507. DOI: 10.1002/Chem.200990116 |
0.758 |
|
2008 |
Sniady A, Durham A, Morreale MS, Marcinek A, Szafert S, Lis T, Brzezinska KR, Iwasaki T, Ohshima T, Mashima K, Dembinski R. Zinc-catalyzed cycloisomerizations. Synthesis of substituted furans and furopyrimidine nucleosides. The Journal of Organic Chemistry. 73: 5881-9. PMID 18597532 DOI: 10.1021/Jo8007995 |
0.775 |
|
2008 |
Sergeant CD, Ott I, Sniady A, Meneni S, Gust R, Rheingold AL, Dembinski R. Metallo-nucleosides: synthesis and biological evaluation of hexacarbonyl dicobalt 5-alkynyl-2'-deoxyuridines. Organic & Biomolecular Chemistry. 6: 73-80. PMID 18075651 DOI: 10.1039/B713371E |
0.758 |
|
2008 |
Sniady A, Morreale MS, Wheeler KA, Dembinski R. Room-Temperature Electrophilic 5-endo-digChlorocyclization of Alk-3-yn-1-ones with the Use of Pool Sanitizer: Synthesis of 3-Chlorofurans and 5-Chlorofuropyrimidine Nucleosides (Eur. J. Org. Chem. 20/2008) European Journal of Organic Chemistry. 2008: 3415-3415. DOI: 10.1002/Ejoc.200890051 |
0.756 |
|
2008 |
Sniady A, Morreale MS, Wheeler KA, Dembinski R. Room-temperature electrophilic 5-endo-dig chlorocyclization of alk-3-yn-1-ones with the use of pool sanitizer: Synthesis of 3-chlorofurans and 5-chlorofuropyrimidine nucleosides European Journal of Organic Chemistry. 3449-3452. DOI: 10.1002/Ejoc.200800397 |
0.786 |
|
2008 |
Dembinski R, Espinet P, Lentijo S, Markowicz MW, Martín-Alvarez JM, Rheingold AL, Schmidt DJ, Sniady A. Fluorophobic effect in metallomesogens - The synthesis and mesomorphism of Ag, Au, Cu, Fe, Pd, and Pt fluorous isocyanide complexes European Journal of Inorganic Chemistry. 1565-1572. DOI: 10.1002/Ejic.200701341 |
0.741 |
|
2007 |
Meneni S, Ott I, Sergeant CD, Sniady A, Gust R, Dembinski R. 5-Alkynyl-2'-deoxyuridines: chromatography-free synthesis and cytotoxicity evaluation against human breast cancer cells. Bioorganic & Medicinal Chemistry. 15: 3082-8. PMID 17336074 DOI: 10.1016/J.Bmc.2007.01.048 |
0.755 |
|
2007 |
Sniady A, Durham A, Morreale MS, Wheeler KA, Dembinski R. Room temperature zinc chloride-catalyzed cycloisomerization of Alk-3-yn-1-ones: synthesis of substituted furans. Organic Letters. 9: 1175-8. PMID 17328552 DOI: 10.1021/Ol062539T |
0.775 |
|
2007 |
Sniady A, Durham A, Morreale MS, Wheeler KA, Dembinski R. Room temperature zinc chloride-catalyzed cycloisomerization of alk-3-yn-1-ones: Synthesis of substituted furans Organic Letters. 9: 1175-1178. DOI: 10.1021/ol062539t |
0.418 |
|
2007 |
Sniady A, Morreale MS, Dembinski R. Electrophilic cyclization with N-iodosuccinimide: Preparation of 5-(4-Bromophenyl)-3-iodo-2-(4-methylphenyl)furan Organic Syntheses. 84: 199-208. DOI: 10.1002/0471264229.Os084.20 |
0.757 |
|
2006 |
Kaleta Z, Makowski BT, Soós T, Dembinski R. Thionation using fluorous Lawesson's reagent. Organic Letters. 8: 1625-8. PMID 16597126 DOI: 10.1021/Ol060208A |
0.364 |
|
2005 |
Sniady A, Wheeler KA, Dembinski R. 5-Endo-dig electrophilic cyclization of 1,4-disubstituted but-3-yn-1-ones: regiocontrolled synthesis of 2,5-disubstituted 3-bromo- and 3-iodofurans. Organic Letters. 7: 1769-72. PMID 15844902 DOI: 10.1021/Ol050372I |
0.779 |
|
2005 |
Sniady A, Wheeler KA, Dembinski R. 5-Endo-dig electrophilic cyclization of 1,4-disubstituted but-3-yn-1-ones: Regiocontrolled synthesis of 2,5-disubstituted 3-bromo- and 3-iodofurans Organic Letters. 7: 1769-1772. DOI: 10.1002/CHIN.200537105 |
0.396 |
|
2004 |
Markowicz MW, Dembinski R. Fluorous Coupling Reagents: Application of 2-Chloro-4,6- bis[(heptadecafluorononyl)oxy]-1,3,5-triazine in Peptide Synthesis Synthesis. 80-86. DOI: 10.1055/S-2004-812541 |
0.434 |
|
2004 |
Dembinski R. Recent advances in the Mitsunobu reaction: Modified reagents and the quest for chromatography-free separation European Journal of Organic Chemistry. 2763-2772. DOI: 10.1002/Ejoc.200400003 |
0.336 |
|
2003 |
Rao MS, Esho N, Sergeant C, Dembinski R. 5-Endo-dig electrophilic cyclization of alpha-alkynyl carbonyl compounds: synthesis of novel bicyclic 5-iodo- and 5-bromofuranopyrimidine nucleosides. The Journal of Organic Chemistry. 68: 6788-90. PMID 12919049 DOI: 10.1021/Jo0345648 |
0.434 |
|
2002 |
Markowicz MW, Dembinski R. Fluorous, chromatography-free Mitsunobu reaction. Organic Letters. 4: 3785-7. PMID 12599458 DOI: 10.1021/Ol0264511 |
0.406 |
|
2002 |
Esho N, Davies B, Lee J, Dembinski R. Synthesis of dicobalt hexacarbonyl 5-p-tolylethynyl-2'-deoxyuridine. Chemical Communications (Cambridge, England). 332-3. PMID 12120060 DOI: 10.1039/B109501C |
0.33 |
|
1995 |
Wieczorek MW, Błaszczyk J, Potrzebowski MJ, Skowrońska A, Dembiński R. Crystal And Molecular Structure And Solid State Nmr Studies Of Bis(5,5-Dimethyl-2-Oxo-1,3,2-Dioxaphosphorinan-2-Yl) Selenide Phosphorus Sulfur and Silicon and the Related Elements. 102: 15-24. DOI: 10.1080/10426509508042537 |
0.322 |
|
1994 |
Dembiński R, Skowrońska A, Michalski J. An expedient synthesis of symmetrical tetra-alkyl monothiopyrophosphates Tetrahedron Letters. 35: 6331-6334. DOI: 10.1016/S0040-4039(00)73425-3 |
0.407 |
|
1990 |
Dembinski R, skowronska A. The Simple Synthesis of Tetra-Alkyl Sym-Monothiopyrophosphates Phosphorus Sulfur and Silicon and the Related Elements. 51: 204-204. DOI: 10.1080/10426509008544256 |
0.466 |
|
1988 |
Dembinski R, Krawczyk E, Skowronska A. Reaction Of Diphosphoryl Diselenides With Dialkyltrimethylsilyl Phosphites. A New Route To Symmetrical Monoselenopyrophosphates Phosphorus Sulfur and Silicon and the Related Elements. 35: 345-348. DOI: 10.1080/03086648808074339 |
0.436 |
|
1988 |
Skowrońska A, Dembiński R, Gwara J, Michalski J. CHLORINATION REACTIONS OF PHOSPHORUS THIONOESTERS > P(S)OSiMe3; GENERAL SYNTHESIS OF COMPOUNDS CONTAINING > P(O)SCI FUNCTIONAL GROUP Phosphorus Sulfur and Silicon and the Related Elements. 39: 119-122. DOI: 10.1080/03086648808072862 |
0.418 |
|
1988 |
Skowrońska A, Dembiński R, Kamiński R, Michalski J. Reaction of oxophosphorane-sulphenyl and -selenenyl chlorides with dialkyl trimethylsilyl phosphites. Novel synthesis of compounds containing a sulphur or selenium bridge between two phosphoryl centres Journal of the Chemical Society-Perkin Transactions 1. 2197-2201. DOI: 10.1039/P19880002197 |
0.396 |
|
1987 |
Burski J, Dembinski R, Kaminski R, Krawczyk E, Skowronska A. Novel Mild Synthesis of Phosphorus Acid Anhydrides Phosphorus Sulfur and Silicon and the Related Elements. 30: 728-728. DOI: 10.1080/03086648708079222 |
0.439 |
|
1987 |
Skowrońska A, Dembiński R, Kamiński R, Michalski J. Novel synthesis of symmetrical tetra-alkyl monothiopyrophosphates Tetrahedron Letters. 28: 4209-4210. DOI: 10.1016/S0040-4039(00)95581-3 |
0.398 |
|
1986 |
Dembiński R, Kamiński R, Michalski J, Skowrońska A. Synthesis of symmetrical tetra-alkyl monoselenopyrophosphates: compounds containing a selenium bridge between two phosphoryl centres Journal of the Chemical Society, Chemical Communications. 1770-1771. DOI: 10.1039/C39860001770 |
0.372 |
|
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