Year |
Citation |
Score |
2016 |
Trahanovsky WS, Klumpp DA. The chemistry of thiophene-based bis-(p-quinodimethanes): an approach to macrocycles Tetrahedron Letters. 57: 2386-2389. DOI: 10.1016/J.Tetlet.2016.04.062 |
0.653 |
|
2016 |
Klumpp DA, Gilbert TM, Trahanovsky WS. Intramolecular Reactions of Tethered Furan-Based Bis(p-quinodimethanes) European Journal of Organic Chemistry. 2016: 5559-5568. DOI: 10.1002/Ejoc.201600995 |
0.663 |
|
2010 |
TRAHANOVSKY WS, MILLER DL, WANG Y. ChemInform Abstract: Oligomerization of the Thiophene-Based p-Quinodimethanes 2,5-Dimethylene-2,5-dihydrothiophene and 2-Ethylidene-5-methylene-2,5-dihydrothiophene. Cheminform. 29: no-no. DOI: 10.1002/chin.199816060 |
0.32 |
|
2006 |
Zhong Q, He L, Beesley TE, Trahanovsky WS, Sun P, Wang C, Armstrong DW. Development of dinitrophenylated cyclodextrin derivatives for enhanced enantiomeric separations by high-performance liquid chromatography Journal of Chromatography A. 1115: 19-45. PMID 16620856 DOI: 10.1016/J.Chroma.2006.02.065 |
0.634 |
|
2006 |
Trahanovsky WS, Lorimor SP. Room temperature observation of p-xylylenes by 1H NMR and evidence for diradical intermediates in their oligomerization. The Journal of Organic Chemistry. 71: 1784-94. PMID 16496962 DOI: 10.1021/Jo0516279 |
0.69 |
|
2006 |
Zhong Q, He L, Beesley TE, Trahanovsky WS, Sun P, Wang C, Armstrong DW. Optimization of the Synthesis of 2,6–Dinitro-4-trifluoromethylphenyl Ether Substituted Cyclodextrin Bonded Chiral Stationary Phases Chromatographia. 64: 147-155. DOI: 10.1365/S10337-006-0014-8 |
0.623 |
|
2006 |
Trahanovsky WS, Lorimor SP. Room temperature observation of p-xylylenes by 1H NMR and evidence for diradical intermediates in their oligomerization Journal of Organic Chemistry. 71: 1784-1794. DOI: 10.1021/jo0516279 |
0.683 |
|
2005 |
Zhong Q, Han X, He L, Beesley TE, Trahanovsky WS, Armstrong DW. Chromatographic evaluation of poly (trans-1,2-cyclohexanediyl-bis acrylamide) as a chiral stationary phase for HPLC Journal of Chromatography A. 1066: 55-70. PMID 15794555 DOI: 10.1016/J.Chroma.2004.12.088 |
0.645 |
|
1997 |
Trahanovsky WS, Miller DL, Wang Y. Oligomerization of the Thiophene-Based p-Quinodimethanes 2,5-dihydrothiophene and 2-Ethylidene-5-methylene-2,5-dihydrothiophene Journal of Organic Chemistry. 62: 8980-8986. |
0.311 |
|
1990 |
Summerfelt ST, Selosse EJM, Reilly PJ, Trahanovsky WS. 1H-Nuclear magnetic resonance spectroscopy of reducing-residue anomeric protons of pertrifluoroacetylated carbohydrates Carbohydrate Research. 203: 163-172. PMID 2276122 DOI: 10.1016/0008-6215(90)80014-T |
0.317 |
|
1989 |
Sustmann R, Daute P, Sauer R, Sommer A, Trahanovsky WS. Cycloadditions of substituted 1,2-dimethylenecyclopentanes. — The influence of methyl groups on the rate of diels-alder reactions Chemische Berichte. 122: 1551-1558. DOI: 10.1002/Cber.19891220827 |
0.301 |
|
1977 |
Riemann JM, Trahanovsky WS. Formation of methyl-substituted 2-indanones and 1,2-dihydrobenzo-cyclobutenes by the pyrolysis of o-, and m and p-tolyl propargyl ethers Tetrahedron Letters. 18: 1863-1866. DOI: 10.1016/S0040-4039(01)83626-1 |
0.347 |
|
1975 |
Howell BA, Trahanovsky WS. Arene-metal complexes. IX. Carbon-13 NMR spectra of benzonorbornadiene, syn-(η6-benzonorbornadiene)tricarbonylchromium, and (η8-benzonorbornadiene)dicarbonylchromim Journal of Magnetic Resonance (1969). 20: 141-145. DOI: 10.1016/0022-2364(75)90161-4 |
0.323 |
|
1971 |
Trahanovsky WS, Mullen PW. Organic oxalates. Cyclizations of the ortho-methyl- and ortho-trifluoromethyl-cinnamyl radicals to the corresponding indenes Journal of the Chemical Society D: Chemical Communications. 102-103. DOI: 10.1039/C29710000102 |
0.333 |
|
1970 |
TRAHANOVSKY WS, DOYLE MP, MULLEN PW. ChemInform Abstract: HERSTELLUNG VON CYCLOHEPTANON UEBER EINE DURCH LEWISSAEUREN KATALYSIERTE CYCLISIERUNG VON 6-HEPTENOYLCHLORID ZUM BETA-CHLOR-CYCLOHEPTANON Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197010122 |
0.366 |
|
1969 |
Trahanovsky WS, Doyle MP, Mullen PW, Ong CC. Cycloheptanone via a Lewis acid-catalyzed cyclization of 6-heptenoyl chloride to .beta.-chlorocycloheptanone The Journal of Organic Chemistry. 34: 3679-3681. DOI: 10.1021/Jo01263A120 |
0.398 |
|
1968 |
Trahanovsky WS, Doyle MP. Medium effects. II. Cyclization of 6-heptenyl p-nitrobenzenesulfonate during solvolysis in 2,2,2-trifluoroethanol Tetrahedron Letters. 9: 2155-2158. DOI: 10.1016/S0040-4039(00)89709-9 |
0.361 |
|
1968 |
Trahanovsky WS, Smyser G, Doyle MP. Acetolysis of 4-bromobutyl-1,1-d2 p-nitrobenzenesulfonate. Evidence for 1,4-bromine participation and the existence of a 5-membered cyclic bromonium ion during acetolysis. Tetrahedron Letters. 9: 3127-3130. DOI: 10.1016/S0040-4039(00)89569-6 |
0.36 |
|
1968 |
Trahanovsky WS, Smyser GL, Doyle MP. Acetolysis of 4-bromobutyl-1,1-d2 p-nitrobenzenesulfonate. Evidence for 1,4-bromine participation and the existence of a 5-membered cyclic bromonium ion during acetolysis. Tetrahedron Letters. 9: 3127-3130. DOI: 10.1016/S0040-4039(00)89569-6 |
0.304 |
|
1967 |
Trahanovsky WS, Doyle MP. Failure of the principle of hard and soft acids and bases to explain the amount of cyclization of various hex-5-enyl derivatives during acetolysis Chemical Communications (London). 1021-1022. DOI: 10.1039/C19670001021 |
0.397 |
|
1967 |
Trahanovsky WS, Doyle MP, Bartlett PD. Nucleophilic reactivity of the carbon-carbon double bond. VI. The use of urea as a base in acetolysis reactions The Journal of Organic Chemistry. 32: 150-153. DOI: 10.1021/jo01277a037 |
0.357 |
|
1967 |
Trahanovsky WS, Doyle MP, Bartlett PD. Nucleophilic reactivity of the carbon-carbon double bond. VI. The use of urea as a base in acetolysis reactions Journal of Organic Chemistry. 32: 150-153. DOI: 10.1021/Jo01277A037 |
0.605 |
|
1967 |
Trahanovsky WS, Doyle MP. Thermal decomposition of tert-butylperoxy 6-bromohexanoate. Lack of evidence for radical displacement on carbon and 1,5-bridged bromine radicals The Journal of Organic Chemistry. 32: 146-150. DOI: 10.1021/jo01277a036 |
0.345 |
|
1967 |
Trahanovsky WS, Doyle MP. Medium effects. I. Solvolysis of 5-hexenyl p-nitrobenzenesulfonate in acetic acid-nonhydroxylic solvent (20:80) mixtures Journal of the American Chemical Society. 89: 4867-4872. DOI: 10.1021/Ja00995A009 |
0.367 |
|
1967 |
Trahanovsky WS, Doyle MP. Medium effects. I. Solvolysis of 5-hexenyl p-nitrobenzenesulfonate in acetic acid-nonhydroxylic solvent (20:80) mixtures Journal of the American Chemical Society. 89: 4867-4872. DOI: 10.1021/ja00995a009 |
0.417 |
|
1965 |
Bartlett PD, Trahanovsky WS, Bolon DA, Schmid GH. Nucleophilic reactivity of the carbon-carbon double bond. IV. The effect of chain elongation. 3-(△3-Cyclopentenyl- and 3,4-dimethyl-△3-cyclopentenyl)-propyl p-nitrobenzenesulfonates Journal of the American Chemical Society. 87: 1314-1319. DOI: 10.1021/Ja01084A028 |
0.594 |
|
1964 |
Snavely FA, Trahanovsky WS, Suydam FH. Metal derivatives of arylazopyrazolone compounds. VI. Molarity quotients of azo derivatives of 1-phenyl-3-methyl-5-thiopyrazolone Inorganic Chemistry. 3: 123-126. |
0.662 |
|
1962 |
Snavely FA, Trahanovsky WS, Suydam FH. Infrared study of arylazopyrazolone compounds and their copper derivatives Journal of Organic Chemistry. 27: 994-997. |
0.656 |
|
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