| Year |
Citation |
Score |
| 2020 |
Fessner WD, Mertsch A, He N, Yi D, Kickstein M. An α2,3-sialyltransferase from Photobacterium phosphoreum with broad substrate scope: Controlling hydrolytic activity by directed evolution. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32596832 DOI: 10.1002/Chem.202002277 |
0.331 |
|
| 2020 |
Hecquet L, Casajus H, Lagarde A, Leremboure M, Miguel TDD, Nauton L, Thery V, Fessner W, Duguet N, Charmantray F. Enzymatic Synthesis of Aliphatic Acyloins Catalyzed by Thermostable Transketolase Chemcatchem. DOI: 10.1002/Cctc.202001160 |
0.354 |
|
| 2020 |
Lorillière M, Guérard‐Hélaine C, Gefflaut T, Fessner W, Clapés P, Charmantray F, Hecquet L. Convergent in situ Generation of Both Transketolase Substrates via Transaminase and Aldolase Reactions for Sequential One‐Pot, Three‐Step Cascade Synthesis of Ketoses Chemcatchem. 12: 812-817. DOI: 10.1002/Cctc.201901756 |
0.332 |
|
| 2019 |
Roldán R, Hernández K, Joglar J, Bujons J, Parella T, Fessner WD, Clapés P. Aldolase-Catalyzed Asymmetric Synthesis of N-Heterocycles by Addition of Simple Aliphatic Nucleophiles to Aminoaldehydes. Advanced Synthesis & Catalysis. 361: 2673-2687. PMID 31680790 DOI: 10.1002/Adsc.201801530 |
0.345 |
|
| 2019 |
L'enfant M, Bruna F, Lorillière M, Ocal N, Fessner W, Pollegioni L, Charmantray F, Hecquet L. One‐Pot Cascade Synthesis of (3S)‐Hydroxyketones Catalyzed by Transketolase via Hydroxypyruvate Generated in Situ from d‐Serine by d‐Amino Acid Oxidase Advanced Synthesis & Catalysis. 361: 2550-2558. DOI: 10.1002/Adsc.201900109 |
0.372 |
|
| 2018 |
Roldán R, Hernandez K, Joglar J, Bujons J, Parella T, Sánchez-Moreno I, Hélaine V, Lemaire M, Guérard-Hélaine C, Fessner WD, Clapés P. Biocatalytic Aldol Addition of Simple Aliphatic Nucleophiles to Hydroxyaldehydes. Acs Catalysis. 8: 8804-8809. PMID 30221031 DOI: 10.1021/Acscatal.8B02486 |
0.356 |
|
| 2018 |
Fessner WD, Junker S, Roldan R, Joosten HJ, Clapés P. Complete switch of reaction specificity of an aldolase by directed evolution in vitro: Synthesis of generic aliphatic aldol products. Angewandte Chemie (International Ed. in English). PMID 29882622 DOI: 10.1002/Anie.201804831 |
0.327 |
|
| 2017 |
Saravanan T, Junker S, Kickstein M, Hein S, Link MK, Ranglack J, Witt S, Lorillière M, Hecquet L, Fessner WD. Donor Promiscuity of a Thermostable Transketolase by Directed Evolution: Efficient Complementation of 1-Deoxy-d-xylulose-5-phosphate Synthase Activity. Angewandte Chemie (International Ed. in English). PMID 28378514 DOI: 10.1002/Anie.201701169 |
0.312 |
|
| 2017 |
Roldán R, Sanchez-Moreno I, Scheidt T, Hélaine V, Lemaire M, Parella T, Clapés P, Fessner WD, Guérard-Hélaine C. Breaking the dogma of aldolase specificity: Simple aliphatic ketones and aldehyde are nucleophiles for fructose-6-phosphate aldolase. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28266745 DOI: 10.1002/Chem.201701020 |
0.349 |
|
| 2017 |
Saravanan T, Reif M, Yi D, Lorillière M, Charmantray F, Hecquet L, Fessner W. Engineering a thermostable transketolase for arylated substrates Green Chemistry. 19: 481-489. DOI: 10.1039/C6Gc02017H |
0.346 |
|
| 2016 |
Güclü D, Szekrenyi A, Garrabou X, Kickstein M, Junker S, Clapés P, Fessner WD. Minimalist Protein Engineering of an Aldolase Provokes Unprecedented Substrate Promiscuity Acs Catalysis. 6: 1848-1852. DOI: 10.1021/Acscatal.5B02805 |
0.338 |
|
| 2015 |
Güclü D, Rale M, Fessner WD. Modular synthesis of dihydroxyacetone monoalkyl ethers and isosteric 1-hydroxy-2-alkanones European Journal of Organic Chemistry. 2015: 2960-2964. DOI: 10.1002/Ejoc.201403695 |
0.341 |
|
| 2014 |
Heyl D, Fessner WD. Facile direct synthesis of acetylenedicarboxamides Synthesis (Germany). 46: 1463-1468. DOI: 10.1055/S-0033-1341101 |
0.301 |
|
| 2012 |
Fessner WD, Heyl D, Rale M. Multi-enzymatic cascade synthesis of d-fructose 6-phosphate and deoxy analogs as substrates for high-throughput aldolase screening Catalysis Science and Technology. 2: 1596-1601. DOI: 10.1039/C2Cy20092A |
0.336 |
|
| 2011 |
Samland AK, Rale M, Sprenger GA, Fessner WD. The transaldolase family: new synthetic opportunities from an ancient enzyme scaffold. Chembiochem : a European Journal of Chemical Biology. 12: 1454-74. PMID 21574238 DOI: 10.1002/Cbic.201100072 |
0.319 |
|
| 2011 |
Rale M, Schneider S, Sprenger GA, Samland AK, Fessner WD. Broadening deoxysugar glycodiversity: natural and engineered transaldolases unlock a complementary substrate space. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 2623-32. PMID 21290439 DOI: 10.1002/Chem.201002942 |
0.336 |
|
| 2011 |
He N, Yi D, Fessner WD. Flexibility of substrate binding of cytosine-5′-monophosphate-N- acetylneuraminate synthetase (CMP-sialate synthetase) from Neisseria meningitidis: An enabling catalyst for the synthesis of neo-sialoconjugates Advanced Synthesis and Catalysis. 353: 2384-2398. DOI: 10.1002/Adsc.201100412 |
0.303 |
|
| 2010 |
Clapés P, Fessner WD, Sprenger GA, Samland AK. Recent progress in stereoselective synthesis with aldolases. Current Opinion in Chemical Biology. 14: 154-67. PMID 20071212 DOI: 10.1016/J.Cbpa.2009.11.029 |
0.327 |
|
| 2010 |
FESSNER W, GRUND C, PRINZBACH H. ChemInform Abstract: π-Facial Stereoselectivity in the Diels-Alder Reaction. Part 3. An Unsymmetrically Birdcage-Annulated Cyclohexadiene. Cheminform. 23: no-no. DOI: 10.1002/chin.199227084 |
0.405 |
|
| 2010 |
FESSNER WD, PRINZBACH H. ChemInform Abstract: The Pagodane Route to Dodecahedrane Cheminform. 22: no-no. DOI: 10.1002/chin.199119311 |
0.368 |
|
| 2008 |
Grundmann P, Fessner WD. One-pot, regioselective synthesis of substituted arylglycines for kinetic resolution by penicillin G acylase Advanced Synthesis and Catalysis. 350: 1729-1735. DOI: 10.1002/Adsc.200800203 |
0.303 |
|
| 2003 |
Phung AN, Zannetti MT, Whited G, Fessner WD. Stereospecific biocatalytic synthesis of pancratistatin analogues. Angewandte Chemie (International Ed. in English). 42: 4821-4. PMID 14562359 DOI: 10.1002/Anie.200352023 |
0.316 |
|
| 2003 |
González-García E, Helaine V, Klein G, Schuermann M, Sprenger GA, Fessner WD, Reymond JL. Fluorogenic stereochemical probes for transaldolases. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 893-9. PMID 12584704 DOI: 10.1002/Chem.200390110 |
0.315 |
|
| 2002 |
Riemann I, Papadopoulos MA, Knorst M, Fessner WD. C-glycosides by aqueous condensation of β-dicarbonyl compounds with unprotected sugars Australian Journal of Chemistry. 55: 147-154. DOI: 10.1071/Ch02012 |
0.306 |
|
| 2002 |
Warwel M, Fessner WD. Indium-mediated stereoselective synthesis of truncated, 6- and 7-carbon sialic acids Synlett. 2104-2106. DOI: 10.1055/S-2002-35564 |
0.32 |
|
| 2001 |
Fessner WD, Helaine V. Biocatalytic synthesis of hydroxylated natural products using aldolases and related enzymes. Current Opinion in Biotechnology. 12: 574-86. PMID 11849940 DOI: 10.1016/S0958-1669(01)00265-8 |
0.321 |
|
| 2001 |
Knorst M, Fessner WD. CMP-Sialate Synthetase from Neisseria meningitidis - Overexpression and Application to the Synthesis of Oligosaccharides Containing Modified Sialic Acids Advanced Synthesis and Catalysis. 343: 698-710. DOI: 10.1002/1615-4169(200108)343:6/7<698::Aid-Adsc698>3.0.Co;2-J |
0.321 |
|
| 2000 |
Fessner W, Goße C, Jaeschke G, Eyrisch O. Short Enzymatic Synthesis ofL-Fucose Analogs European Journal of Organic Chemistry. 2000: 125-132. DOI: 10.1002/(Sici)1099-0690(200001)2000:1<125::Aid-Ejoc125>3.0.Co;2-F |
0.327 |
|
| 1999 |
Zimmermann FT, Schneider A, Schörken U, Sprenger GA, Fessner WD. Efficient multi-enzymatic synthesis of D-xylulose 5-phosphate Tetrahedron Asymmetry. 10: 1643-1646. DOI: 10.1016/S0957-4166(99)00166-4 |
0.315 |
|
| 1999 |
Junker HD, Phung N, Fessner WD. Diastereoselective free-radical synthesis of α-substituted C-glycosyl phosphonates, and their use as building blocks in the HWE reaction Tetrahedron Letters. 40: 7063-7066. DOI: 10.1016/S0040-4039(99)01459-8 |
0.329 |
|
| 1999 |
Zannetti MT, Walter C, Knorst M, Fessner W. Fructose 1,6-Bisphosphate Aldolase fromStaphylococcus carnosus: Overexpression, Structure Prediction, Stereoselectivity, and Application in the Synthesis of Bicyclic Sugars Chemistry - a European Journal. 5: 1882-1890. DOI: 10.1002/(Sici)1521-3765(19990604)5:6<1882::Aid-Chem1882>3.0.Co;2-C |
0.326 |
|
| 1997 |
Arth HL, Fessner WD. Practical synthesis of 4-hydroxy-3-oxobutylphosphonic acid and its evaluation as a bio-isosteric substrate of DHAP aldolase. Carbohydrate Research. 305: 313-21. PMID 9648254 DOI: 10.1016/S0008-6215(97)10026-X |
0.352 |
|
| 1997 |
Petersen M, Zannetti MT, Fessner W. Tandem asymmetric C-C bond formations by enzyme catalysis Topics in Current Chemistry. 186: 87-117. DOI: 10.1007/Bfb0119221 |
0.347 |
|
| 1996 |
Fessner W, Walter C. Enzymatic C-C bond formation in asymmetric synthesis Topics in Current Chemistry. 184: 97-194. DOI: 10.1007/3-540-61388-9_63 |
0.341 |
|
| 1996 |
Fessner WD, Schneider A, Held H, Sinerius G, Walter C, Hixon M, Schloss JV. The mechanism of class II, metal-dependent aldolases Angewandte Chemie - International Edition in English. 35: 2219-2221. DOI: 10.1002/Anie.199622191 |
0.319 |
|
| 1995 |
Arth H, Sinerius G, Fessner W. Enzymes in organic synthesis. Expedient enantioselective synthesis of (S)-(−)-3,4-dihydroxybutylphosphonate, an isosteric substrate mimic for glycerol phosphate oxidase Liebigs Annalen. 1995: 2037-2042. DOI: 10.1002/Jlac.1995199511285 |
0.335 |
|
| 1995 |
Eyrisch O, Fessner WD. Disaccharide mimetics by enzymatic tandem aldol additions Angewandte Chemie (International Edition in English). 34: 1639-1641. DOI: 10.1002/Anie.199516391 |
0.309 |
|
| 1994 |
Fessner WD, Sinerius G. Phosphoenolpyruvate as a dual purpose reagent for integrated nucleotide/nicotinamide cofactor recycling. Bioorganic & Medicinal Chemistry. 2: 639-45. PMID 7858970 DOI: 10.1016/0968-0896(94)85012-7 |
0.317 |
|
| 1993 |
Fessner WD, Schneider A, Eyrisch O, Sinerius G, Badía J. 6-deoxy-L-lyxo- and 6-deoxy-L-arabino-hexulose 1-phosphates. Enzymatic syntheses by antagonistic metabolic pathways1 1 Enzymes in Organic Synthesis, part 6. For part 5. Tetrahedron: Asymmetry. 4: 1183-1192. DOI: 10.1016/S0957-4166(00)80227-X |
0.33 |
|
| 1993 |
Eyrisch O, Sinerius G, Fessner WD. Facile enzymic de novo synthesis and NMR spectroscopic characterization of d-tagatose 1,6-bisphosphate Carbohydrate Research. 238: 287-306. DOI: 10.1016/0008-6215(93)87020-S |
0.307 |
|
| 1993 |
Gleiter R, Sigwart C, Fessner W, Müller-Bötticher H, Prinzbach H. Electronic Interactions in Saturated and Unsaturated [1.1.1]-, [2.1.1]-, [2.2.1]-, and [2.2.2]Triblattanes — PE-Spectroscopic Investigations Chemische Berichte. 126: 2299-2307. DOI: 10.1002/Cber.19931261019 |
0.44 |
|
| 1993 |
Müller-Bötticher H, Fessner W, Melder J, Prinzbach H, Gries S, Irngartinger H. Functionalized Enantiomerically Pure [1.1.1]-, [2.1.1]-, [2.2.1]-, and [2.2.2]Triblattanes Chemische Berichte. 126: 2275-2297. DOI: 10.1002/Cber.19931261018 |
0.462 |
|
| 1992 |
Fessner WD, Badía J, Eyrisch O, Schneider A, Sinerius G. Enzymatic syntheses of rare ketose 1-phosphates Tetrahedron Letters. 33: 5231-5234. DOI: 10.1016/S0040-4039(00)79140-4 |
0.302 |
|
| 1992 |
Lutz G, Pinkos R, Murty BARC, Spurr PR, Fessner W, Wörth J, Fritz H, Knothe L, Prinzbach H. The Pagodane Route to Dodecahedranes Scope and Limitation of the Dehydrocyclization Stratagem Chemische Berichte. 125: 1741-1751. DOI: 10.1002/Cber.19921250729 |
0.498 |
|
| 1992 |
Murty BARC, Pinkos R, Spurr PR, Fessner W, Lutz G, Fritz H, Hunkler D, Prinzbach H. The Pagodane Route to Dodecahedranes Unsaturated (Hyperstable) and Saturated Bissecododecahedranes Chemische Berichte. 125: 1719-1739. DOI: 10.1002/Cber.19921250728 |
0.479 |
|
| 1992 |
Fessner W, Murty BARC, Spurr PR, Pinkos R, Melder J, Fritz H, Prinzbach H. The Pagodane Route to Dodecahedranes Directed Conversions – The Pagodane → Bissecododecahedradiene Stage Chemische Berichte. 125: 1697-1717. DOI: 10.1002/Cber.19921250727 |
0.507 |
|
| 1991 |
Fessner WD, Scheumann K, Prinzbach H. π-Facial stereoselectivity in the diels-alder reaction-IV.1 the directing influence of proximate unsaturation Tetrahedron Letters. 32: 5939-5942. DOI: 10.1016/S0040-4039(00)79431-7 |
0.473 |
|
| 1991 |
Fessner WD, Grund C, Prinzbach H. π-Facial stereoselectivity in the diels-alder reaction-III.1 an unsymmetrically birdcage-annulated cyclohexadiene Tetrahedron Letters. 32: 5935-5938. DOI: 10.1016/S0040-4039(00)79430-5 |
0.473 |
|
| 1991 |
Herges R, Schleyer PVR, Schindler M, Fessner WD. Tetramethylene dications (CH2)4 2+: Are the norbornadiene dication, the pagodane dication, and related systems aromatic? Journal of the American Chemical Society. 113: 3649-3656. |
0.376 |
|
| 1989 |
Prakash GKS, Fessner WD, Olah GA, Lutz G, Prinzbach H. Stable carbocations. Part 274. 2-Seco[1.1.1.1]pagodyl cation. Strong stabilization of a trivalent carbocation by carbon-carbon .sigma.-bond hyperconjugation Journal of the American Chemical Society. 111: 746-748. DOI: 10.1021/Ja00184A061 |
0.435 |
|
| 1989 |
Klärner FG, Artschwager-Perl U, Fessner WD, Grund C, Pinkos R, Melder JP, Prinzbach H. Domino and pincer cycloadditions with syn-o,o′-dibenzenes pressure dependence and mechanistic implications Tetrahedron Letters. 30: 3137-3140. DOI: 10.1016/S0040-4039(00)99184-6 |
0.42 |
|
| 1989 |
Fessner WD, Grund C, Prinzbach H. Domino and pincer cycloadditions with syn-o,o′-dibenzenes scope and π-facial stereoselectivity Tetrahedron Letters. 30: 3133-3136. DOI: 10.1016/S0040-4039(00)99183-4 |
0.419 |
|
| 1989 |
Bednarski MD, Simon ES, Bischofberger N, Fessner WD, Kim MJ, Lees W, Saito T, Waldmann H, Whitesides GM. Rabbit muscle aldolase as a catalyst in organic synthesis Journal of the American Chemical Society. 111: 627-635. |
0.673 |
|
| 1989 |
Prakash GKS, Fessner WD, Olah GA, Lutz G, Prinzbach H. 2-Seco[1.1.1.1]pagodyl cation. Strong stabilization of a trivalent carbocation by C-C σ-bond hyperconjugation Journal of the American Chemical Society. 111: 746-748. |
0.343 |
|
| 1988 |
Prakash GKS, Krishnamurthy VV, Herges R, Bau R, Yuan H, Olah GA, Fessner WD, Prinzbach H. Stable carbocations. 273. [1.1.1.1]- and [2.2.1.1]Pagodane dications: frozen two-electron Woodward-Hoffmann transition-state models Journal of the American Chemical Society. 110: 7764-7772. DOI: 10.1021/Ja00231A029 |
0.557 |
|
| 1988 |
DREWELLO T, FESSNER W, KOS AJ, LEBRILLA CB, PRINZBACH H, VON RAGUE SCHLEYER P, SCHWARZ H. ChemInform Abstract: Gas-Phase Oxidation (“Charge Stripping”) of Pagodane Radical Cations and Related Cage Hydrocarbons. - A Theoretical-Experimental Search into Tetramethylene Dications. Cheminform. 19. DOI: 10.1002/chin.198816093 |
0.326 |
|
| 1988 |
VON E. DOERING W, ROTH WR, BREUCKMANN R, FIGGE L, LENNARTZ H, FESSNER W, PRINZBACH H. ChemInform Abstract: Forbidden Reactions. (2 + 2) Cycloreversion of Rigid Cyclobutanes. Cheminform. 19. DOI: 10.1002/chin.198816088 |
0.388 |
|
| 1988 |
FESSNER W, SEDELMEIER G, KNOTHE L, PRINZBACH H, RIHS G, YANG Z, KOVAC B, HEILBRONNER E. ChemInform Abstract: ′Face-to-Face′Benzo-Anellated Homologous Hypostrophenes. Syntheses, X-Ray Structure Analyses and PE Spectra. Cheminform. 19. DOI: 10.1002/chin.198805154 |
0.341 |
|
| 1988 |
Drewello T, Fessner W, Kos AJ, Lebrilla CB, Prinzbach H, von Ragué Schleyer P, Schwarz H. Gasphasenoxidation („Charge-Stripping”) von ionisierten Pagodanen und verwandten Käfigkohlenwasserstoffen. — Eine theoretisch-experimentelle Studie zu Tetramethylen-Dikationen Chemische Berichte. 121: 187-189. DOI: 10.1002/Cber.19881210126 |
0.358 |
|
| 1988 |
Doering WvE, Roth WR, Breuckmann R, Figge L, Lennartz H, Fessner W, Prinzbach H. Verbotene Reaktionen. — [2 + 2]-Cycloreversion starrer Cyclobutane Chemische Berichte. 121: 1-9. DOI: 10.1002/Cber.19881210102 |
0.454 |
|
| 1988 |
Müller H, Melder J, Fessner W, Hunkler D, Fritz H, Prinzbach H. Functionalized, Enantiomerically Pure [2.1.1]-, [2.2.1]-, and [2.2.2]-Triblattanes Angewandte Chemie International Edition in English. 27: 1103-1106. DOI: 10.1002/Anie.198811031 |
0.403 |
|
| 1988 |
Müller H, Melder J, Fessner W, Hunkler D, Fritz H, Prinzbach H. Funktionalisierte, enantiomerenreine [2.1.1]-, [2.2.1]- und [2.2.2]-Triblattane Angewandte Chemie. 100: 1140-1143. DOI: 10.1002/Ange.19881000835 |
0.403 |
|
| 1988 |
Surya Prakash GK, Krishnamurthy VV, Herges R, Bau R, Yuan H, Olah GA, Fessner WD, Prinzbach H. [1.1.1.1]- and [2.2.1.1]pagodane dications: Frozen two-electron Woodward-Hoffmann transition-state models Journal of the American Chemical Society. 110: 7764-7772. |
0.319 |
|
| 1987 |
Fessner W, Sedelmeier G, Knothe L, Prinzbach H, Rihs G, Yang Z, Kova? B, Heilbronner E. ?Face-to-Face?-Benzo-anellierte homologe Hypostrophene. Synthesen, R�ntgenstrukturanalysen und PE-Spektren Helvetica Chimica Acta. 70: 1816-1842. DOI: 10.1002/Hlca.19870700718 |
0.448 |
|
| 1987 |
FESSNER W, MURTY BARC, PRINZBACH H. ChemInform Abstract: The Pagodane Route to Dodecahedranes. Thermal, Reductive, and Oxidative Pagodane Rearrangements. Cheminform. 18. DOI: 10.1002/chin.198736140 |
0.35 |
|
| 1987 |
MURTY BARC, SPURR PR, PINKOS R, GRUND C, FESSNER WD, HUNKLER D, FRITZ H, ROTH WH, PRINZBACH H. ChemInform Abstract: Photochemistry of Tetracyclo(7.2.1.04,11.06,10)dodeca-2,7-diene Based Systems Cheminform. 18. DOI: 10.1002/chin.198730348 |
0.328 |
|
| 1987 |
SEDELMEIER G, FESSNER W, PINKOS R, GRUND C, MURTY BARC, HUNKLER D, RIHS G, FRITZ H, KRUEGER C, PRINZBACH H. ChemInform Abstract: Studies Towards Functionalized/Annulated acs-Tetracyclo(7.2.1.04,11.06,10)dodeca-2,7-diene Skeletons - X-Ray Structural Analyses of a “face-to-face” Dibenzo Compound and a Tetraoxadihydropagodane. Cheminform. 18. DOI: 10.1002/chin.198711126 |
0.346 |
|
| 1987 |
Prinzbach H, Murty BARC, Fessner W, Mortensen J, Heinze J, Gescheidt G, Gerson F. One- and Two-Electron Oxidations of Pagodanes and Bissecododecahedradienes: Unusually Persistent Radical Cations Angewandte Chemie International Edition in English. 26: 457-458. DOI: 10.1002/Anie.198704571 |
0.416 |
|
| 1987 |
Spurr PR, Murty BARC, Fessner W, Fritz H, Prinzbach H. Bissecododecahedraenes, Unusual Hyperstable Olefins Angewandte Chemie International Edition in English. 26: 455-456. DOI: 10.1002/Anie.198704551 |
0.478 |
|
| 1987 |
Fessner W, Murty BARC, Wörth J, Hunkler D, Fritz H, Prinzbach H, Roth WD, Schleyer PvR, McEwen AB, Maier WF. Dodecahedranes from[1.1.1.1]Pagodanes Angewandte Chemie International Edition in English. 26: 452-454. DOI: 10.1002/Anie.198704521 |
0.445 |
|
| 1987 |
Fessner W, Murty BARC, Prinzbach H. The Pagodane Route to Dodecahedranes—Thermal, Reductive, and Oxidative Transformations of Pagodanes Angewandte Chemie International Edition in English. 26: 451-452. DOI: 10.1002/Anie.198704511 |
0.414 |
|
| 1987 |
Prinzbach H, Murty BARC, Fessner W, Mortensen J, Heinze J, Gescheidt G, Gerson F. Ein- und Zweielektronenoxidationen von Pagodanen und Bissecododecahedradienen – ungewöhnlich persistente Radikalkationen Angewandte Chemie. 99: 488-490. DOI: 10.1002/Ange.19870990528 |
0.415 |
|
| 1987 |
Spurr PR, Murty BARC, Fessner W, Fritz H, Prinzbach H. Bissecododecahedraene, ungewöhnliche, hyperstabile Olefine Angewandte Chemie. 99: 486-488. DOI: 10.1002/Ange.19870990527 |
0.475 |
|
| 1987 |
Fessner W, Murty BARC, Wörth J, Hunkler D, Fritz H, Prinzbach H, Roth WD, Schleyer PvR, McEwen AB, Maier WF. Dodecahedrane aus [1.1.1.1]Pagodanen Angewandte Chemie. 99: 484-486. DOI: 10.1002/Ange.19870990526 |
0.41 |
|
| 1987 |
Fessner W, Murty BARC, Prinzbach H. Die Pagodan-Route zu Dodecahedranen – thermische, reduktive und oxidative Pagodan-Umwandlungen Angewandte Chemie. 99: 482-484. DOI: 10.1002/Ange.19870990525 |
0.425 |
|
| 1987 |
Fessner WD, Sedelmeier G, Spurr PR, Rihs G, Prinzbach H. "Pagodane": The efficient synthesis of a novel, versatile molecular framework Journal of the American Chemical Society. 109: 4626-4642. |
0.379 |
|
| 1986 |
Elschenbroich C, Schneider J, Prinzbach H, Fessner WD. Metal .pi.-complexes of benzene derivatives. 26. (5,12:6,11-Dimethano-5,5a,6,11,11a,12-hexahydro-.eta.12-tetracene)chromium - a model compound to study 1H NMR coordination shift anisotropy in the periphery of bis(.eta.6-arene)metal complexes Organometallics. 5: 2091-2096. DOI: 10.1021/Om00141A028 |
0.336 |
|
| 1986 |
Prakash GK, Krishnamurthy VV, Herges R, Bau R, Yuan H, Olah GA, Fessner WD, Prinzbach H. Stable carbocations. Part 267. Pagodane dication, a unique 2.pi.-aromatic cyclobutanoid system Journal of the American Chemical Society. 108: 836-838. DOI: 10.1021/Ja00264A046 |
0.595 |
|
| 1986 |
Fessner WD, Prinzbach H. D3-trishomocubanetrione synthesis and optical resolution Tetrahedron. 42: 1797-1803. DOI: 10.1016/S0040-4020(01)87598-0 |
0.349 |
|
| 1986 |
SEDELMEIER G, FESSNER W, GRUND C, SPURR PR, FRITZ H, PRINZBACH H. ChemInform Abstract: Photochemical Transformations. Part 68. [6 + 6]-Benzo/Benzo-Photocycloaddition Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198635093 |
0.378 |
|
| 1986 |
PRAKASH GKS, KRISHNAMURTHY VV, HERGES R, BAU R, YUAN H, OLAH GA, FESSNER W, PRINZBACH H. ChemInform Abstract: Considered Stable Carbocations. Part 267. Pagodane Dication, a Unique Zn-Aromatic Cyclobutanoid System. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198625072 |
0.588 |
|
| 1986 |
Sedelmeier G, Fessner W, Pinkos R, Grund C, Murty BARC, Hunkler D, Rihs G, Fritz H, Krüger C, Prinzbach H. Studien im Umfeld funktionalisierter/anellierteracs-Tetracyclo[7.2.1.04,11.06,10]dodeca-2,7-dien-Gerüste — Röntgenstrukturanalysen einer „face-to-face”-Dibenzoverbindung und eines Tetraoxadihydro-pagodans Chemische Berichte. 119: 3442-3472. DOI: 10.1002/Cber.19861191121 |
0.46 |
|
| 1986 |
Prakash GKS, Krishnamurthy VV, Herges R, Bau R, Yuan H, Olah GA, Fessner WD, Prinzbach H. Pagodane dication, a unique 2π-aromatic cyclobutanoid system Journal of the American Chemical Society. 108: 836-838. |
0.551 |
|
| 1986 |
Eischenbroich C, Schneider J, Prinzbach H, Fessner WD. (5,12:6,11-Dimethano-5,5a,6,11,11a,12-hexahydro-η 12-tetracene)chromium - A model compound to study 1H NMR coordination shift anisotropy in the periphery of bis(η6-arene)metal complexes Organometallics. 5: 2091-2096. |
0.33 |
|
| 1985 |
Gleiter R, Zimmermann H, Fessner W, Prinzbach H. Dominance of through-bond interaction in asyn-tricyclo[6.4.0.02,7]dodecatetraene moiety Chemische Berichte. 118: 3856-3860. DOI: 10.1002/Cber.19851180935 |
0.417 |
|
| 1983 |
Fessner WD, Prinzbach H, Rihs G. Pagodane - An undecacyclic C20H20-polyquinane Tetrahedron Letters. 24: 5857-5860. DOI: 10.1016/S0040-4039(00)94220-5 |
0.343 |
|
| Show low-probability matches. |
