| Year |
Citation |
Score |
| 2010 |
WIEST O, STECKHAN E. ChemInform Abstract: Electron Transfer Catalyzed Diels-Alder Reactions with 2-Vinylindoles. Cheminform. 24: no-no. DOI: 10.1002/chin.199340094 |
0.569 |
|
| 2004 |
Lütz S, Steckhan E, Liese A. First asymmetric electroenzymatic oxidation catalyzed by a peroxidase Electrochemistry Communications. 6: 583-587. DOI: 10.1016/J.Elecom.2004.04.009 |
0.629 |
|
| 2003 |
Schröder I, Steckhan E, Liese A. In situ NAD+ regeneration using 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonate) as an electron transfer mediator Journal of Electroanalytical Chemistry. 541: 109-115. DOI: 10.1016/S0022-0728(02)01420-1 |
0.383 |
|
| 2002 |
Zelgert M, Nieger M, Lennartz M, Steckhan E. Two directional electroorganic synthesis - Electrochemical oxidation and application of a C2-symmetric building block Tetrahedron. 58: 2641-2646. DOI: 10.1016/S0040-4020(02)00147-3 |
0.383 |
|
| 2001 |
Hollmann F, Schmid A, Steckhan E. The First Synthetic Application of a Monooxygenase Employing Indirect Electrochemical NADH Regeneration. Angewandte Chemie (International Ed. in English). 40: 169-171. PMID 29711966 DOI: 10.1002/1521-3773(20010105)40:1<169::Aid-Anie169>3.0.Co;2-T |
0.59 |
|
| 2001 |
Steckhan E, Arns T, Heineman WRHilt G, Hoormann D, Jörissen J, Kröner L, Lewall B, Pütter H. Environmental protection and economization of resources by electroorganic and electroenzymatic syntheses. Chemosphere. 43: 63-73. PMID 11233827 DOI: 10.1016/S0045-6535(00)00325-8 |
0.329 |
|
| 2001 |
Hollmann F, Schmid A, Steckhan E. The First Synthetic Application of a Monooxygenase Employing Indirect Electrochemical NADH Regeneration This work was supported by BASF AG. We thank DEGUSSA AG for the gift of chemicals. Angewandte Chemie (International Ed. in English). 40: 169-171. PMID 11169702 DOI: 10.1002/1521-3773(20010105)40:1<169::AID-ANIE169>3.0.CO;2-T |
0.531 |
|
| 2001 |
Hollmann F, Schmid A, Steckhan E. Erste synthetische Anwendung einer Monooxygenase unter indirekter elektrochemischer NADH-Regenerierung Angewandte Chemie. 113: 190-193. DOI: 10.1002/1521-3757(20010105)113:1<190::Aid-Ange190>3.0.Co;2-Z |
0.583 |
|
| 2000 |
Gutenberger G, Blechert S, Steckhan E. α-Cyano-γ-lactones by photoinduced electron transfer-catalyzed oxidation of α-hydroxyalkylsilanes in the presence of α-cyano acrylates Tetrahedron Letters. 41: 461-464. DOI: 10.1016/S0040-4039(99)02093-6 |
0.366 |
|
| 1999 |
Peglow T, Blechert S, Steckhan E. Radical cation Diels-Alder reaction between indoles and exocyclic 1,3-dienes with incorporated intentional cleaving points Chemical Communications. 433-434. DOI: 10.1039/A900078J |
0.302 |
|
| 1999 |
Haberl U, Wiest O, Steckhan E. Ab initio studies of the radical cation Diels-Alder reaction Journal of the American Chemical Society. 121: 6730-6736. DOI: 10.1021/Ja983993Y |
0.489 |
|
| 1999 |
Hofbauer M, Heineman WR, Kreishman GP, Steckhan E. Hydrophobic interaction of analytes with permselective poly(N-vinyl amide) films on electrodes Analytical Chemistry. 71: 399-406. DOI: 10.1021/Ac980315L |
0.433 |
|
| 1999 |
Rößler U, Blechert S, Steckhan E. Single electron transfer induced total synthesis of canthin-6-one Tetrahedron Letters. 40: 7075-7078. DOI: 10.1016/S0040-4039(99)01472-0 |
0.363 |
|
| 1999 |
Haberl U, Steckhan E, Blechert S, Wiest O. Electron-transfer-induced Diels - Alder reactions of indole and exocyclic dienes: Synthesis and quantum-chemical studies Chemistry - a European Journal. 5: 2859-2865. DOI: 10.1002/(Sici)1521-3765(19991001)5:10<2859::Aid-Chem2859>3.0.Co;2-R |
0.591 |
|
| 1999 |
Tomuschat P, Kröner L, Steckhan E, Nieger M, Dötz KH. Benzannulation of axial chiral biscarbene complexes of chromium: An approach to novel C2-symmetrical redox-active Bi(phenanthrenequinones) Chemistry - a European Journal. 5: 700-707. DOI: 10.1002/(Sici)1521-3765(19990201)5:2<700::Aid-Chem700>3.0.Co;2-D |
0.368 |
|
| 1998 |
Kardassis G, Brungs P, Steckhan E. Electrogenerated chiral cationic glycine equivalents - Part 1: The 6-methoxy derivative of cyclo(L-Pro-Gly) Tetrahedron. 54: 3471-3478. DOI: 10.1016/S0040-4020(98)00081-7 |
0.33 |
|
| 1998 |
Schierle K, Vahle R, Steckhan E. Efficient pathways to precursors of pyrrolidine azasugar structures European Journal of Organic Chemistry. 509-514. DOI: 10.1002/(Sici)1099-0690(199803)1998:3<509::Aid-Ejoc509>3.0.Co;2-V |
0.329 |
|
| 1997 |
Wend R, Steckhan E. Polymersupported triarylamines as redox catalysts in electroorganic synthesis - On the way to a redox active polyelectrolyte system Electrochimica Acta. 42: 2027-2039. DOI: 10.1016/S0013-4686(97)85478-3 |
0.333 |
|
| 1997 |
Hilt G, Lewall B, Montero G, Utley JHP, Steckhan E. Efficient In‐Situ Redox Catalytic NAD(P)+ Regeneration in Enzymatic Synthesis Using Transition‐Metal Complexes of 1,10‐Phenanthroline‐5,6‐dione and Its N‐Monomethylated Derivative as Catalysts Liebigs Annalen. 1997: 2289-2296. DOI: 10.1002/Jlac.199719971117 |
0.349 |
|
| 1997 |
Gürtler CF, Blechert S, Steckhan E. Radical cation initiated cycloaddition reactions between 2-vinylindoles and β-substituted enaminonitriles Chemistry - a European Journal. 3: 447-452. DOI: 10.1002/Chem.19970030317 |
0.413 |
|
| 1997 |
Hilt G, Jarbawi T, Heineman WR, Steckhan E. An analytical study of the redox behavior of 1,10-phenanthroline-5,6-dione, its transition-metal complexes, and its N-monomethylated derivative with regard to their efficiency as mediators of NAD(P)+ regeneration Chemistry - a European Journal. 3: 79-88. DOI: 10.1002/Chem.19970030114 |
0.633 |
|
| 1997 |
Hilt G, Lewall B, Montero G, Utley JHP, Steckhan E. Efficient in-situ redox catalytic NAD(P)+ regeneration in enzymatic synthesis using transition-metal complexes of 1,10-phenanthroline-5,6-dione and its N-monomethylated derivative as catalysts Liebigs Annales. 2289-2296. |
0.508 |
|
| 1996 |
Danielmeier K, Schierle K, Steckhan E. Electrochemical oxidation of chiral 5-substituted 2-oxazolidinones: A key building block for dichiral β-amino alcohols Tetrahedron. 52: 9743-9754. DOI: 10.1016/0040-4020(96)00506-6 |
0.346 |
|
| 1996 |
Höfer E, Steckhan E, Ramos B, Heineman WR. Polymer-modified electrodes with pendant [RhIII(C5Me5)(L)Cl]+-complexes formed by γ-irradiation cross-linking Journal of Electroanalytical Chemistry. 402: 115-122. DOI: 10.1016/0022-0728(95)04243-1 |
0.481 |
|
| 1996 |
Windeck AK, Hess U, Steckhan E, Reck G. Electrochemically initiated hydrocyanomethylation of N-heteroaryl-substituted azomethines Liebigs Annales. 1471-1476. DOI: 10.1002/Jlac.199619960920 |
0.384 |
|
| 1995 |
Meggers E, Steckhan E, Blechert S. Radical C-C bond formation by photoinduced electron transfer addition of α-silyl carbamates to acceptor-substituted alkenes Angewandte Chemie (International Edition in English). 34: 2137-2139. DOI: 10.1002/Anie.199521371 |
0.343 |
|
| 1995 |
Gürtler CF, Blechert S, Steckhan E. Radical cation [4 + 2] cycloadditions with 2-vinylindoles Angewandte Chemie (International Edition in English). 34: 1900-1901. DOI: 10.1002/Anie.199519001 |
0.312 |
|
| 1994 |
Gürtler CF, Blechert S, Steckhan E. Formation of Pyrido[1,2a]indoles by Electron Transfer Catalyzed Diels-Alder Reaction between 2-Vinylindoles and β-Enamidoesters Synlett. 1994: 141-142. DOI: 10.1055/S-1994-22770 |
0.365 |
|
| 1994 |
Kandzia C, Steckhan E. Electrochemical epoxidation of electron-poor olefins using silver bipyridine based redox mediators Tetrahedron Letters. 35: 3695-3698. DOI: 10.1016/S0040-4039(00)73074-7 |
0.365 |
|
| 1994 |
Stahl A, Steckhan E, Nieger M. Diastereoselective [3+2] cycloaddition of allyltrialkylsilanes to intermediate N-acyliminoesters obtained from methyl-4-methoxy-2-imidazolidinone- and 2-oxazolidinone-4-carboxylates Tetrahedron Letters. 35: 7371-7374. DOI: 10.1016/0040-4039(94)85317-7 |
0.328 |
|
| 1993 |
Hilt G, Steckhan E. Transition metal complexes of 1,10-phenanthroline-5,6-dione as efficient mediators for the regeneration of NAD+ in enzymatic synthesis Journal of the Chemical Society, Chemical Communications. 1706-1707. DOI: 10.1039/C39930001706 |
0.546 |
|
| 1993 |
Kandzia C, Steckhan E, Knoch F. Efficient and short synthesis of new camphor sultam based chiral bipyridines and phenanthrolines Tetrahedron: Asymmetry. 4: 39-42. DOI: 10.1016/S0957-4166(00)86012-7 |
0.318 |
|
| 1993 |
Wiest O, Steckhan E. Radical cation Diels-Alder reaction of indoles and exocyclic dienes Tetrahedron Letters. 34: 6391-6394. DOI: 10.1016/0040-4039(93)85053-Y |
0.611 |
|
| 1993 |
Martiny M, Steckhan E, Esch T. Cycloaddition Reactions Initiated by Photochemically Excited Pyrylium Salts Chemische Berichte. 126: 1671-1682. DOI: 10.1002/Cber.19931260726 |
0.41 |
|
| 1993 |
Wiest O, Steckhan E. Electron Transfer‐Catalyzed Diels–Alder Reactions with 2‐Vinylindoles Angewandte Chemie. 32: 901-903. DOI: 10.1002/Anie.199309011 |
0.585 |
|
| 1993 |
Wiest O, Steckhan E. Electron transfer-catalyzed Diels-Alder reactions with 2-vinylindoles Angewandte Chemie (International Edition in English). 32: 901-903. |
0.564 |
|
| 1992 |
Steckhan E, Kandzia C. Ruthenium-Catalysed, Electrochemical Cleavage of Aryl Olefins for the Synthesis of Benzaldehydes Synlett. 1992: 139-140. DOI: 10.1055/S-1992-21294 |
0.385 |
|
| 1992 |
Wiest O, Steckhan E, Grein F. Selectivity in radical-cation Diels-Alder reactions of indole and electron-rich dienes: A semiempirical approach Journal of Organic Chemistry. 57: 4034-4037. DOI: 10.1021/Jo00040A060 |
0.597 |
|
| 1991 |
Gieseler A, Steckhan E, Wiest O, Knoch F. Photochemically induced radical cation Diels-Alder reaction of indole and electron-rich dienes Journal of Organic Chemistry. 56: 1405-1411. DOI: 10.1021/Jo00004A013 |
0.601 |
|
| 1991 |
Frede M, Steckhan E. Continuous electrochemical activation of flavoenzymes using polyethyleneglycol-bound ferrocenes as mediators: a model for the application of oxidoreductases as oxidation catalysts in organic synthesis Tetrahedron Letters. 32: 5063-5066. DOI: 10.1016/S0040-4039(00)93428-2 |
0.321 |
|
| 1991 |
Papadopoulos A, Lewall B, Steckhan E, Ginzel KD, Knoch F, Nieger M. Anodic oxidation of N-acyl and N-alkoxycarbonyl dipeptide esters as a key step for the formation of chiral heterocyclic synthetic building blocks Tetrahedron. 47: 563-572. DOI: 10.1016/S0040-4020(01)87046-0 |
0.354 |
|
| 1991 |
Dapperheld S, Steckhan E, Brinkhaus KG, Esch T. Organic Electron Transfer Systems, II Substituted Triarylamine Cation‐Radical Redox Systems – Synthesis, Electrochemical and Spectroscopic Properties, Hammet Behavior, and Suitability as Redox Catalysts Chemische Berichte. 124: 2557-2567. DOI: 10.1002/Cber.19911241127 |
0.353 |
|
| 1991 |
Vögtle F, Alfter F, Steckhan E, Mavili S, Nieger M. Makrocyclisch modifizierte Verbindungen vom TTF- und TCNQ-Typ Chemische Berichte. 124: 897-902. DOI: 10.1002/Cber.19911240433 |
0.346 |
|
| 1990 |
Gieseler A, Steckhan E, Wiest O. Photoinduced, Electron-Transfer-Catalyzed Diels-Alder Reaction Between Indole and 1,3-Cyclohexadienes1 Synlett. 1990: 275-277. DOI: 10.1055/S-1990-21063 |
0.604 |
|
| 1990 |
GIESELER A, STECKHAN E, WIEST O. ChemInform Abstract: Photoinduced, Electron-Transfer-Catalyzed Diels-Alder Reaction Between Indole and 1,3-Cyclohexadienes. Cheminform. 21. DOI: 10.1002/chin.199039168 |
0.571 |
|
| 1990 |
Steckhan E, Herrmann S, Ruppert R, Thömmes J, Wandrey C. Continuous generation of NADH from NAD⊕ and formate using a homogeneous catalyst with enhanced molecular weight in a membrane reactor Angewandte Chemie (International Edition in English). 29: 388-390. |
0.444 |
|
| 1989 |
Ginzel KD, Brungs P, Steckhan E. Indirect electrochemical α-methoxylation of N-acyl and N-carboalkoxy α-amino acid esters and application as cationic glycine equivalents Tetrahedron. 45: 1691-1701. DOI: 10.1016/S0040-4020(01)80034-X |
0.335 |
|
| 1989 |
Papadopoulos A, Heyer J, Ginzel K, Steckhan E. Regioselective anodic oxidation ofN-acyl,N-alkoxycarbonyl, andN-(2-Nitrophenylsulfenyl) dipeptide esters Chemische Berichte. 122: 2159-2164. DOI: 10.1002/Cber.19891221117 |
0.305 |
|
| 1988 |
Ruppert R, Herrmann S, Steckhan E. Very efficient reduction of NAD(P)+ with formate catalysed by cationic rhodium complexes Journal of the Chemical Society, Chemical Communications. 1150-1151. DOI: 10.1039/C39880001150 |
0.313 |
|
| 1988 |
Töteberg-Kaulen S, Steckhan E. Intramoleculer arylsulphoetherificatiom and lactonization of unsaturated alcohols and carboxylic acids initiated by anodic oxidation of disulphides Tetrahedron. 44: 4389-4397. DOI: 10.1016/S0040-4020(01)86141-X |
0.411 |
|
| 1988 |
Komoschinski J, Steckhan E. Efficient indirect electrochemical in situ regeneration of NAD+ and NADP+ for enzymatic oxidations using iron bipyridine and phenanthroline complexes as redox catalysts Tetrahedron Letters. 29: 3299-3300. DOI: 10.1016/0040-4039(88)85145-1 |
0.322 |
|
| 1988 |
Heyer J, Dapperheld S, Steckhan E. Convenient Syntheses of 2-Nitrophenylsulfen-(NPS-)imines by Oxidation of NPS-Protected Amines and Amino Acid Derivatives Chemische Berichte. 121: 1617-1623. DOI: 10.1002/Cber.19881210913 |
0.343 |
|
| 1987 |
Ruppert R, Herrmann S, Steckhan E. Efficient indirect electrochemical in-situ regeneration of nadh:electrochemically driven enzymatic reduction of pyruvate catalyzed by d-ldh Tetrahedron Letters. 28: 6583-6586. DOI: 10.1016/S0040-4039(00)96919-3 |
0.325 |
|
| 1987 |
Mlcoch J, Steckhan E. Electrochemically induced [4+2]-cycloadditions - a mechanistic interpretation of the cation radical Diels-Alder reaction based on preparative results Tetrahedron Letters. 28: 1081-1084. DOI: 10.1016/S0040-4039(00)95916-1 |
0.411 |
|
| 1987 |
Ginzel KD, Steckhan E, Degner D. Indirect electrochemical α-methoxylation of aliphatic ethers and acetals - reactivity and regioselectivity of the anodic oxidation using tris(2,4-dibromophenyl)amine as redox catalyst Tetrahedron. 43: 5797-5805. DOI: 10.1016/S0040-4020(01)87786-3 |
0.37 |
|
| 1987 |
Grammenudi S, Franke M, Vögtle F, Steckhan E. The rhodium complex of a tris(bipyridine) ligand-Its electrochemical behaviour and function as mediator for the regeneration of NADH from NAD+ Journal of Inclusion Phenomena. 5: 695-707. DOI: 10.1007/Bf00656589 |
0.331 |
|
| 1986 |
Brinkhaus KHG, Steckhan E, Degner D. Indirect electrochemical side-chain oxidation of alkyl aromatic compounds - selective synthesis of methyl benzoates or ortho-benzoic acid trimethylesters Tetrahedron. 42: 553-560. DOI: 10.1016/S0040-4020(01)87454-8 |
0.363 |
|
| 1984 |
Platen M, Steckhan E. Oxidative Deblocking of the 4-Methoxybenzyl Thioether Protecting Group: Application to the Directed Synthesis of Poly-cystinyl Peptides European Journal of Organic Chemistry. 1984: 1563-1576. DOI: 10.1002/Jlac.198419840905 |
0.322 |
|
| 1984 |
Platen M, Steckhan E. Mild and Effective Removal of Dithioketal Protecting Groups by Triarylamine Cation Radicals as Homogeneous Electron Transfer Agents Chemische Berichte. 117: 1679-1694. DOI: 10.1002/Cber.19841170505 |
0.375 |
|
| 1978 |
Baltes H, Steckhan E, Schäfer HJ. Anodische Oxidation von konjugierten Dienen Chemische Berichte. 111: 1294-1314. DOI: 10.1002/Cber.19781110409 |
0.504 |
|
| 1977 |
Steckhan E. Spectroelectrochemical study of olefins-I. The mechanism of the anodic oxidation of tetraphenylethylene Electrochimica Acta. 22: 395-399. DOI: 10.1016/0013-4686(77)85093-7 |
0.31 |
|
| 1977 |
Mackey L, Steckhan E, Kuwana T. Korrektur der spektrochemisch bestimmten Geschwindigkeitskonstanten für die Reaktion von Bipyridylium-Radikalkationen mit Cytochrome C Colloid and Polymer Science. 255: 1022-1022. DOI: 10.1007/BF01776263 |
0.381 |
|
| 1975 |
MacKey L, Steckhan E, Kuwana T. Correction to spectroelectrochemically determined rates for bipyridylium radical cation reactions with cytochrome C [1] Berichte Der Bunsengesellschaft FüR Physikalische Chemie. 79: 587-588. DOI: 10.1002/bbpc.19750790706 |
0.488 |
|
| 1974 |
Steckhan E, Schäfer H. Hydroxylating Dimerization of Styrene at the Anode Angewandte Chemie International Edition in English. 13: 472-473. DOI: 10.1002/Anie.197404721 |
0.459 |
|
| 1970 |
Schäfer H, Steckhan E. Anodic mixed coupling of olefins Tetrahedron Letters. 11: 3835-3838. DOI: 10.1016/S0040-4039(01)98602-2 |
0.406 |
|
| 1969 |
Schäfer H, Steckhan E. Oxidative Dimerisierung von Olefinen Angewandte Chemie. 81: 532-532. DOI: 10.1002/Ange.19690811408 |
0.433 |
|
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