Year |
Citation |
Score |
2021 |
Strehl J, Fastie C, Hilt G. The Electrochemical cis-Chlorination of Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 27: 17341-17345. PMID 34648232 DOI: 10.1002/chem.202103316 |
0.39 |
|
2021 |
Li L, Kail S, Weber SM, Hilt G. Indium-Catalysed Transfer-Hydrogenation for the Reductive Cyclisation of 2-Alkynyl Enones towards Trisubstituted Furans. Angewandte Chemie (International Ed. in English). PMID 34476880 DOI: 10.1002/anie.202109266 |
0.376 |
|
2021 |
Hilt G, Fährmann J. Alternating Current Electrolysis as Efficient Tool for the Direct Electrochemical Oxidation of Hydroxamic Acids for Acyl Nitroso Diels-Alder Reactions. Angewandte Chemie (International Ed. in English). PMID 34232547 DOI: 10.1002/anie.202107148 |
0.393 |
|
2021 |
Hilt G, Fährmann J. Alternating Current Electrolysis as Efficient Tool for the Direct Electrochemical Oxidation of Hydroxamic Acids for Acyl Nitroso Diels-Alder Reactions. Angewandte Chemie (International Ed. in English). PMID 34232547 DOI: 10.1002/anie.202107148 |
0.393 |
|
2021 |
Weber SM, Hilt G. Late 3d Metal-Catalyzed (Cross-) Dimerization of Terminal and Internal Alkynes. Frontiers in Chemistry. 9: 635826. PMID 33777899 DOI: 10.3389/fchem.2021.635826 |
0.337 |
|
2020 |
Strehl J, Hilt G. Electrochemical, Iodine-Mediated α-CH Amination of Ketones by Umpolung of Silyl Enol Ethers. Organic Letters. PMID 32700915 DOI: 10.1021/Acs.Orglett.0C02068 |
0.496 |
|
2020 |
Sattler LE, Hilt G. Allylic Oxidation of Ester-substituted 1,4-Dienes. The Journal of Organic Chemistry. PMID 32348141 DOI: 10.1021/Acs.Joc.0C00776 |
0.509 |
|
2020 |
Hilt G, Weber SM, Queder J. Ligand-Controlled Diastereoselective Cobalt-Catalysed Hydroalkynylation of Terminal Alkynes to E- or Z-1,3-Enynes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32271963 DOI: 10.1002/Chem.202001697 |
0.489 |
|
2020 |
Hilt G, Babaoglu E. Electrochemical Iodine-Mediated Oxidation of Enamino-Esters to 2H-Azirine-2-Carboxylates supported by Design of Experiments. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32220135 DOI: 10.1002/Chem.202001465 |
0.397 |
|
2020 |
Li L, Hilt G. Regiodivergent DH or HD Addition to Alkenes: Deuterohydrogenation versus Hydrodeuterogenation. Organic Letters. PMID 32043886 DOI: 10.1021/Acs.Orglett.0C00213 |
0.441 |
|
2020 |
Kohlmeyer C, Schäfer A, Huy PH, Hilt G. Formamide Catalyzed Nucleophilic Substitutions: Mechanistic Insight and Rationalization of Catalytic Activity Acs Catalysis. DOI: 10.1021/Acscatal.0C03348 |
0.431 |
|
2019 |
Christoffers J, Strehl J, Kahrs C, Hilt G, Müller T. Electrochemical Induced Ring Transformation of Cyclic α-(ortho-Iodophenyl)-β-oxoesters. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31850604 DOI: 10.1002/Chem.201905570 |
0.454 |
|
2019 |
Pünner F, Schmidt A, Hilt G. Corrigendum: Up the Hill: Selective Double-Bond Isomerization of Terminal 1,3-Dienes towards Z-1,3-Dienes or 2Z,4E-Dienes. Angewandte Chemie (International Ed. in English). 58: 17103. PMID 31736259 DOI: 10.1002/Anie.201902504 |
0.305 |
|
2019 |
Fan Q, Martin-Jimenez D, Ebeling D, Krug CK, Brechmann L, Kohlmeyer C, Hilt G, Hieringer W, Schirmeisen A, Gottfried JM. Nanoribbons with Non-Alternant Topology from Fusion of Polyazulene: Carbon Allotropes Beyond Graphene. Journal of the American Chemical Society. PMID 31617709 DOI: 10.1021/Jacs.9B08060 |
0.302 |
|
2019 |
Strehl J, Hilt G. Electrochemical, Manganese-Assisted Carbon-Carbon Bond Formation between β-Keto Esters and Silyl Enol Ethers. Organic Letters. PMID 31247778 DOI: 10.1021/Acs.Orglett.9B01866 |
0.359 |
|
2019 |
Weber SM, Hilt G. Chemoselective Cobalt(I)-Catalyzed Cyclotrimerization of (Un)Symmetrical 1,3-Butadiynes for the Synthesis of 1,2,4-Regioisomers. Organic Letters. PMID 31117706 DOI: 10.1021/Acs.Orglett.9B01281 |
0.514 |
|
2018 |
Möckel R, Babaoglu E, Hilt G. Iodine(III)-mediated Electrochemical Trifluoroethoxylactonisation - Rational Reaction Optimisation and Prediction of Mediator Activity. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30133017 DOI: 10.1002/Chem.201804152 |
0.494 |
|
2018 |
Fan Q, Werner S, Tschakert J, Ebeling D, Schirmeisen A, Hilt G, Hieringer W, Gottfried JM. Precise Mono-Selective Aromatic C-H Bond Activation by Chemisorption of Meta-Aryne on a Metal Surface. Journal of the American Chemical Society. PMID 29750508 DOI: 10.1021/Jacs.8B01658 |
0.323 |
|
2018 |
Kohlmeyer C, Klüppel M, Hilt G. Synthesis of Nitrosobenzene Derivatives via Nitrosodesilylation Reaction. The Journal of Organic Chemistry. PMID 29484887 DOI: 10.1021/Acs.Joc.8B00262 |
0.522 |
|
2017 |
Möckel R, Hille J, Winterling E, Weidemüller S, Faber TM, Hilt G. Electrochemical Synthesis of Aryl Iodides by Anodic Iododesilylation. Angewandte Chemie (International Ed. in English). PMID 29215798 DOI: 10.1002/Anie.201711293 |
0.4 |
|
2017 |
Fan Q, Wang T, Dai J, Kuttner J, Hilt G, Gottfried JM, Zhu J. On-Surface Pseudo-High Dilution Synthesis of Macrocycles: Principle and Mechanism. Acs Nano. PMID 28419801 DOI: 10.1021/Acsnano.7B01870 |
0.352 |
|
2017 |
Weber SM, Hilt G. Control of the Regioselectivity in Cobalt- versus Ruthenium-Catalyzed Alder-ene Reaction of Unsymmetrical 1,3-Diynes. Organic Letters. PMID 28103048 DOI: 10.1021/Acs.Orglett.6B03729 |
0.506 |
|
2017 |
Hilt G, Ballmann M, Weber F, Sattler L. Synthesis of Non-Conjugated Trienes via In Situ Hydrovinylation/Wittig Olefination of Unsaturated Phosphonium Salts Synthesis. 50: 1711-1720. DOI: 10.1055/S-0036-1591878 |
0.467 |
|
2017 |
Li L, Babaoglu E, Harms K, Hilt G. Expanding Blaise-Type Reactions towards Indium-Mediated Transformations of α-Bromo-β-keto Esters with Nitriles European Journal of Organic Chemistry. 2017: 4543-4547. DOI: 10.1002/Ejoc.201700868 |
0.412 |
|
2017 |
Möckel R, Hille J, Winterling E, Weidemüller S, Faber TM, Hilt G. Elektrochemische Synthese von Aryliodiden durch anodische Iododesilylierung Angewandte Chemie. 130: 450-454. DOI: 10.1002/Ange.201711293 |
0.33 |
|
2017 |
Röse P, Emge S, König CA, Hilt G. Efficient Oxidative Coupling of ArenesviaElectrochemical Regeneration of 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) under Mild Reaction Conditions Advanced Synthesis & Catalysis. 359: 1359-1372. DOI: 10.1002/Adsc.201601331 |
0.476 |
|
2016 |
Nödling AR, Möckel R, Tonner R, Hilt G. Lewis Acids as Activators in CBS-Catalysed Diels-Alder Reactions: Distortion Induced Lewis Acidity Enhancement of SnCl4. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27492791 DOI: 10.1002/Chem.201602394 |
0.767 |
|
2016 |
Weber F, Ballmann M, Kohlmeyer C, Hilt G. Nickel-Catalyzed Double Bond Transposition of Alkenyl Boronates for in Situ syn-Selective Allylboration Reactions. Organic Letters. PMID 26771707 DOI: 10.1021/Acs.Orglett.5B03585 |
0.498 |
|
2016 |
Hilt G, Weber F, Steinlandt P, Ballmann M. Structure-Dependent Nickel-Catalysed Transposition of N-Allylamides to E- or Z-Enamides Synthesis. 49: 440-450. DOI: 10.1055/S-0036-1588340 |
0.328 |
|
2016 |
Hilt G, Babaoglu E, Harms K. Indium-Mediated Blaise-Type Reaction of Bromomalonates with Nitriles and Isocyanates Synlett. 27: 1820-1823. DOI: 10.1055/S-0035-1561973 |
0.526 |
|
2016 |
Röse P, Hilt G. Cobalt-Catalysed Bond Formation Reactions; Part 2 Synthesis (Germany). 48: 463-492. DOI: 10.1055/S-0035-1560378 |
0.503 |
|
2016 |
Babaoglu E, Harms K, Hilt G. ChemInform Abstract: Indium-Mediated Blaise-Type Reaction of Bromomalonates with Nitriles and Isocyanates. Cheminform. 47. DOI: 10.1002/chin.201649084 |
0.347 |
|
2015 |
Röse P, Garcia CC, Pünner F, Harms K, Hilt G. Cobalt-Catalyzed Cross-Benzannulation of Conjugated Enynes and Diynes. The Journal of Organic Chemistry. 80: 7311-6. PMID 26084604 DOI: 10.1021/Acs.Joc.5B01198 |
0.544 |
|
2015 |
Weber F, Schmidt A, Röse P, Fischer M, Burghaus O, Hilt G. Double-Bond Isomerization: Highly Reactive Nickel Catalyst Applied in the Synthesis of the Pheromone (9Z,12Z)-Tetradeca-9,12-dienyl Acetate. Organic Letters. 17: 2952-5. PMID 26023712 DOI: 10.1021/Acs.Orglett.5B01230 |
0.508 |
|
2015 |
Wang C, Zheng Y, Huo H, Röse P, Zhang L, Harms K, Hilt G, Meggers E. Merger of visible light induced oxidation and enantioselective alkylation with a chiral iridium catalyst. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 7355-9. PMID 25832794 DOI: 10.1002/Chem.201500998 |
0.427 |
|
2015 |
Röse P, Emge S, Yoshida J, Hilt G. Electrochemical selenium- and iodonium-initiated cyclisation of hydroxy-functionalised 1,4-dienes. Beilstein Journal of Organic Chemistry. 11: 174-83. PMID 25815067 DOI: 10.3762/Bjoc.11.18 |
0.532 |
|
2015 |
Möckel R, Hilt G. Synthesis of polysubstituted iodobenzene derivatives from alkynylsilanes and 1,3-dienes via diels-alder/oxidation/iodination reaction sequence. Organic Letters. 17: 1644-7. PMID 25794242 DOI: 10.1021/Acs.Orglett.5B00306 |
0.492 |
|
2015 |
Schmidt A, Nödling AR, Hilt G. An alternative mechanism for the cobalt-catalyzed isomerization of terminal alkenes to (Z)-2-alkenes. Angewandte Chemie (International Ed. in English). 54: 801-4. PMID 25430003 DOI: 10.1002/Anie.201409902 |
0.774 |
|
2015 |
Kuttner JR, Hilt G. Synthesis of acyclic polycarbonyl compounds via ozonolysis of cyclohexa-1,4-dienes Synthesis (Germany). 47: 1170-1180. DOI: 10.1055/S-0034-1380148 |
0.554 |
|
2015 |
Hilt G. Asymmetric nickel-catalysed cross-hydrovinylation of two terminal alkenes Chemcatchem. 7: 1639-1641. DOI: 10.1002/Cctc.201500177 |
0.309 |
|
2014 |
Huo H, Shen X, Wang C, Zhang L, Röse P, Chen LA, Harms K, Marsch M, Hilt G, Meggers E. Asymmetric photoredox transition-metal catalysis activated by visible light. Nature. 515: 100-3. PMID 25373679 DOI: 10.1038/Nature13892 |
0.449 |
|
2014 |
Kersten L, Harms K, Hilt G. Synthesis of tri-, tetra-, and pentacarbonyl derivatives via ozonolysis of 1,4-dienes and cyclization to polyaromatic systems. The Journal of Organic Chemistry. 79: 11661-73. PMID 25371047 DOI: 10.1021/Jo502308D |
0.46 |
|
2014 |
Schmidt A, Hilt G. Unprecedented cobalt-catalyzed isomerization reactions to single skipped 2,4,7-trienes applied in the synthesis of urushiol. Chemistry, An Asian Journal. 9: 2407-10. PMID 24920254 DOI: 10.1002/Asia.201402323 |
0.461 |
|
2014 |
Hilt G. 1,4-Cyclohexadienes--easy access to a versatile building block via transition-metal-catalysed Diels-Alder reactions. Chemical Record (New York, N.Y.). 14: 386-96. PMID 24890660 DOI: 10.1002/Tcr.201400001 |
0.482 |
|
2014 |
Pünner F, Hilt G. Zinc-mediated CH-activation of tetrahydrofuran under mild conditions for the regioselective addition to aryl-propiolates. Chemical Communications (Cambridge, England). 50: 7310-3. PMID 24869771 DOI: 10.1039/C4Cc03348E |
0.335 |
|
2014 |
Raster P, Schmidt A, Rambow M, Kuzmanovic N, König B, Hilt G. Immobilisation of photoswitchable diarylcyclohexenes synthesised via cobalt-mediated Diels-Alder reaction. Chemical Communications (Cambridge, England). 50: 1864-6. PMID 24402313 DOI: 10.1039/C3Cc48487D |
0.526 |
|
2014 |
Miersch A, Harms K, Hilt G. Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives. Chemical Communications (Cambridge, England). 50: 542-4. PMID 24266022 DOI: 10.1039/C3Cc46788K |
0.555 |
|
2014 |
Schmidt A, Maiterth E, Hilt G. Cobalt-catalysed transformations of 1,3,5-hexatrienes on a large scale Synthesis (Germany). 46: 2040-2044. DOI: 10.1055/S-0034-1378375 |
0.521 |
|
2014 |
Sušnik P, Hilt G. Homoallylpinacolboronic ester as alkene component in cobalt-catalyzed alder ene reactions Organometallics. 33: 5907-5910. DOI: 10.1021/Om500292T |
0.541 |
|
2014 |
Nödling AR, Müther K, Rohde VHG, Hilt G, Oestreich M. Ferrocene-stabilized silicon cations as catalysts for diels-alder reactions: Attempted experimental quantification of lewis acidity and reactIR kinetic analysis Organometallics. 33: 302-308. DOI: 10.1021/Om401040Y |
0.386 |
|
2014 |
Kuttner JR, Hilt G. Regiodivergent cobalt-catalyzed diels-alder reactions for the synthesis of bifunctional building blocks and their suzuki-cross-coupling polymerizations Macromolecules. 47: 5532-5541. DOI: 10.1021/Ma5012446 |
0.533 |
|
2014 |
Fan Q, Wang C, Liu L, Han Y, Zhao J, Zhu J, Kuttner J, Hilt G, Gottfried JM. Covalent, organometallic, and halogen-bonded nanomeshes from tetrabromo-terphenyl by surface-assisted synthesis on Cu(111) Journal of Physical Chemistry C. 118: 13018-13025. DOI: 10.1021/Jp5037475 |
0.302 |
|
2014 |
Hilt G, Janikowski J, Schwarzer M, Burghaus O, Sakow D, Bröring M, Drüschler M, Huber B, Roling B, Harms K, Frenking G. Studies of electronic effects of modified pyridine-imine ligands utilized in cobalt-catalyzed meta-selective Diels-Alder reactions Journal of Organometallic Chemistry. 749: 219-223. DOI: 10.1016/J.Jorganchem.2013.09.020 |
0.462 |
|
2014 |
Nödling AR, Jakab G, Schreiner PR, Hilt G. 31P NMR spectroscopically quantified hydrogen-bonding strength of thioureas and their catalytic activity in diels-alder reactions European Journal of Organic Chemistry. 2014: 6394-6398. DOI: 10.1002/Ejoc.201402871 |
0.439 |
|
2013 |
Fiebig L, Kuttner J, Hilt G, Schwarzer MC, Frenking G, Schmalz HG, Schäfer M. Cobalt catalysis in the gas phase: experimental characterization of cobalt(I) complexes as intermediates in regioselective Diels-Alder reactions. The Journal of Organic Chemistry. 78: 10485-93. PMID 24044877 DOI: 10.1021/Jo402001G |
0.615 |
|
2013 |
Pünner F, Schieven J, Hilt G. Synthesis of fluorenone and anthraquinone derivatives from aryl- and aroyl-substituted propiolates. Organic Letters. 15: 4888-91. PMID 24011126 DOI: 10.1021/Ol4023276 |
0.544 |
|
2013 |
Schmidt A, Hilt G. Scope and limitations of 1,3,5-hexatriene derivatives in regioselective cobalt-catalyzed reactions. Organic Letters. 15: 2708-11. PMID 23662814 DOI: 10.1021/Ol401015E |
0.535 |
|
2013 |
Miersch A, Kohlmeyer C, Hilt G. Zinc-mediated regiodiverse synthesis of vinyl bromide derivatives and their in situ palladium-catalysed cross-coupling reactions Synthesis (Germany). 45: 3228-3232. DOI: 10.1055/S-0033-1339616 |
0.549 |
|
2013 |
Röse P, Pünner F, Hilt G, Harms K. Efficient synthesis of 2-pyridylenynes and application in cobalt-catalysed benzannulation reactions Synlett. 24: 1101-1104. DOI: 10.1055/S-0033-1338384 |
0.537 |
|
2013 |
Pünner F, Hilt G. Zinc/iron-mediated ring opening of dibromocyclopropanes for in situ Diels-Alder reactions with electron-deficient aldehydes and imines European Journal of Organic Chemistry. 5580-5584. DOI: 10.1002/Ejoc.201300726 |
0.488 |
|
2013 |
Arndt M, Hilt G, Khlebnikov AF, Kozhushkov SI, Meijere Ad. Diels-Alder Reactions for the Construction of Cyclopropylarenes: Diels-Alder Reactions for the Construction of Cyclopropylarenes European Journal of Organic Chemistry. 2013: 1171-1172. DOI: 10.1002/Ejoc.201201724 |
0.466 |
|
2012 |
Miersch A, Hilt G. Stereodivergent zinc-mediated three-component synthesis of tri- and tetrasubstituted alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9798-801. PMID 22786818 DOI: 10.1002/Chem.201201385 |
0.353 |
|
2012 |
Erver F, Kuttner JR, Hilt G. Multidirectional cobalt-catalyzed Diels-Alder/1,4-hydrovinylation sequences. The Journal of Organic Chemistry. 77: 8375-85. PMID 22694267 DOI: 10.1021/Jo301028B |
0.471 |
|
2012 |
Erver F, Hilt G. Cobalt- versus ruthenium-catalyzed Alder-ene reaction for the synthesis of credneramide A and B. The Journal of Organic Chemistry. 77: 5215-9. PMID 22568728 DOI: 10.1021/Jo3007896 |
0.55 |
|
2012 |
Erver F, Hilt G. Double- and triple-cobalt catalysis in multicomponent reactions. Organic Letters. 14: 1884-7. PMID 22432934 DOI: 10.1021/Ol300504F |
0.543 |
|
2012 |
Pünner F, Hilt G. Regioselective solvent-dependent benzannulation of conjugated enynes. Chemical Communications (Cambridge, England). 48: 3617-9. PMID 22395492 DOI: 10.1039/C2Cc30777D |
0.482 |
|
2012 |
Pünner F, Schmidt A, Hilt G. Up the hill: selective double-bond isomerization of terminal 1,3-dienes towards Z-1,3-dienes or 2Z,4E-dienes. Angewandte Chemie (International Ed. in English). 51: 1270-3. PMID 22173992 DOI: 10.1002/Anie.201107512 |
0.305 |
|
2012 |
Danz M, Tonner R, Hilt G. Understanding the regioselectivity in Scholl reactions for the synthesis of oligoarenes. Chemical Communications (Cambridge, England). 48: 377-9. PMID 22083090 DOI: 10.1039/C1Cc15980A |
0.509 |
|
2012 |
Arndt M, Dindarolu M, Schmalz HG, Hilt G. Ligand control of the cobalt-catalysed 1,4-hydrovinylation reaction Synthesis (Germany). 44: 3534-3542. DOI: 10.1055/S-0032-1316796 |
0.613 |
|
2012 |
Kuttner JR, Warratz S, Hilt G. Straightforward synthesis of nonconjugated cyclohex-3-enone and conjugated 4-methylenecyclohex-2-enone derivatives Synthesis. 44: 1293-1303. DOI: 10.1055/S-0031-1289752 |
0.394 |
|
2012 |
Hilt G. Hydrovinylation reactions - Atom-economic transformations with steadily increasing synthetic potential European Journal of Organic Chemistry. 4441-4451. DOI: 10.1002/Ejoc.201200212 |
0.548 |
|
2012 |
Arndt M, Hilt G, Khlebnikov AF, Kozhushkov SI, De Meijere A. Diels-Alder reactions for the construction of cyclopropylarenes European Journal of Organic Chemistry. 3112-3121. DOI: 10.1002/Ejoc.201200105 |
0.561 |
|
2012 |
Kiefer G, Ruiz J, Solari E, Hilt G, Severin K. Ruthenium-catalyzed sequential enyne cross-metathesis/ATRA reactions European Journal of Organic Chemistry. 93-98. DOI: 10.1002/Ejoc.201101263 |
0.542 |
|
2012 |
Kersten L, Hilt G. Regioselective cobalt-catalysed hydrovinylation for the synthesis of non-conjugated enones and 1,4-diketones Advanced Synthesis and Catalysis. 354: 863-869. DOI: 10.1002/Adsc.201100800 |
0.494 |
|
2011 |
Arndt M, Dindaro?lu M, Schmalz HG, Hilt G. Gaining absolute control of the regiochemistry in the cobalt-catalyzed 1,4-hydrovinylation reaction. Organic Letters. 13: 6236-9. PMID 22040103 DOI: 10.1021/Ol202696N |
0.678 |
|
2011 |
Erver F, Hilt G. Multi-component regio- and diastereoselective cobalt-catalyzed hydrovinylation/allylboration reaction sequence. Organic Letters. 13: 5700-3. PMID 21954907 DOI: 10.1021/Ol202481J |
0.545 |
|
2011 |
Bohn MA, Schmidt A, Hilt G, Dindaro?lu M, Schmalz HG. Cobalt-catalyzed 1,4-hydrobutadienylation of 1-aryl-1,3-dienes with 2,3-dimethyl-1,3-butadiene. Angewandte Chemie (International Ed. in English). 50: 9689-93. PMID 21882314 DOI: 10.1002/Anie.201103613 |
0.677 |
|
2011 |
Hilt G, Erver F, Harms K. Regioselective cobalt-catalyzed alder-ene reaction toward silicon- and boron-functionalized building blocks. Organic Letters. 13: 304-7. PMID 21162547 DOI: 10.1021/Ol102764W |
0.488 |
|
2011 |
Hilt G. Cobalt(I)-catalysed reactions for the synthesis of acyclic 1,4-dienes - Genesis of two synthetic methods Synlett. 1654-1659. DOI: 10.1055/S-0030-1260800 |
0.575 |
|
2011 |
Raster P, Weiss S, Hilt G, König B. Synthesis and photoisomerization of diarylcyclobutenes Synthesis. 905-908. DOI: 10.1055/S-0030-1258435 |
0.493 |
|
2011 |
Erver F, Hilt G, Harms K. Cobalt(I) catalysis in the diastereoselective two-step synthesis of tricyclic systems Synthesis. 972-978. DOI: 10.1055/S-0030-1258433 |
0.532 |
|
2011 |
Hilt G, Roesner S. Substrate-controlled regioselective cobalt(I)-catalysed 1,4-hydrovinylation reactions Synthesis. 662-668. DOI: 10.1055/S-0030-1258408 |
0.788 |
|
2011 |
Hilt G, Nödling A. The correlation of Lewis acidities of silyl triflates with reaction rates of catalyzed diels-alder reactions European Journal of Organic Chemistry. 7071-7075. DOI: 10.1002/Ejoc.201101307 |
0.786 |
|
2011 |
Hilt G, Pünner F, Möbus J, Naseri V, Bohn MA. A lewis acidity scale in relation to rate constants of lewis acid catalyzed organic reactions European Journal of Organic Chemistry. 5962-5966. DOI: 10.1002/Ejoc.201101029 |
0.42 |
|
2011 |
Danz M, Hilt G. Regiodiverse three-component synthesis of arenes Advanced Synthesis and Catalysis. 353: 303-308. DOI: 10.1002/Adsc.201000832 |
0.553 |
|
2010 |
Kersten L, Roesner S, Hilt G. Synthesis and characterization of polycarbonyl compounds via their BF2-adducts. Organic Letters. 12: 4920-3. PMID 20936846 DOI: 10.1021/Ol102083V |
0.778 |
|
2010 |
Arndt M, Reinhold A, Hilt G. Cobalt-catalyzed 1,4-hydrovinylation of allylsilane and allylboronic esters for the synthesis of hydroxy-functionalized 1,4-dienes. The Journal of Organic Chemistry. 75: 5203-10. PMID 20597480 DOI: 10.1021/Jo100951D |
0.57 |
|
2010 |
Auvinet AL, Harrity JP, Hilt G. Ambient-temperature cobalt-catalyzed cycloaddition strategies to aromatic boronic esters. The Journal of Organic Chemistry. 75: 3893-6. PMID 20443638 DOI: 10.1021/Jo1004907 |
0.444 |
|
2010 |
Hilt G, Paul A, Treutwein J. Cobalt catalysis at the crossroads: cobalt-catalyzed Alder-ene reaction versus [2 + 2] cycloaddition. Organic Letters. 12: 1536-9. PMID 20196545 DOI: 10.1021/Ol100266U |
0.532 |
|
2010 |
Hilt G, Arndt M, Weske DF. Cobalt-catalyzed generation of 1,4-dienes as synthons for 1,3-dicarbonyl compounds and their application in natural product syntheses Synthesis. 1321-1324. DOI: 10.1055/S-0029-1219278 |
0.507 |
|
2009 |
Hilt G, Weske DF. Aromatic compounds as synthons for 1,3-dicarbonyl derivatives. Chemical Society Reviews. 38: 3082-91. PMID 19847343 DOI: 10.1039/B902344P |
0.415 |
|
2009 |
Hilt G, Danz M, Treutwein J. Cobalt-catalyzed 1,4-hydrovinylation of styrenes and 1-aryl-1,3-butadienes. Organic Letters. 11: 3322-5. PMID 19583205 DOI: 10.1021/Ol901064P |
0.485 |
|
2009 |
Hilt G. Transition-metal-catalyzed ring opening of hetero-Diels-Alder adducts. Angewandte Chemie (International Ed. in English). 48: 6390-3. PMID 19565592 DOI: 10.1002/Anie.200901939 |
0.339 |
|
2009 |
Hilt G, Treutwein J. Cobalt-catalysed hydrovinylation as the key step in a short synthesis of moenocinol. Chemical Communications (Cambridge, England). 1395-7. PMID 19259599 DOI: 10.1039/B822023A |
0.494 |
|
2009 |
Hilt G, Janikowski J. Regiocontrolled cobalt-catalyzed Diels-Alder reactions of silicon-functionalized, terminal, and internal alkynes. Organic Letters. 11: 773-6. PMID 19125626 DOI: 10.1021/Ol802837M |
0.509 |
|
2009 |
Hilt G, Paul A, Hengst C. Cobalt-Catalyzed [6+2] Cycloadditions with Cycloheptatriene Synfacts. 2009: 1338-1338. DOI: 10.1055/s-0029-1218190 |
0.446 |
|
2009 |
Hilt G, Paul A, Hengst C. Cobalt-catalysed [6+2] cycloaddition of internal alkynes and terminal alkenes with cycloheptatriene Synthesis. 3305-3310. DOI: 10.1055/S-0029-1216900 |
0.533 |
|
2009 |
Hilt G, Hengst C, Arndt M. The Unprecedented cobalt-catalysed oxidative glaser coupling under reductive conditions Synthesis. 395-398. DOI: 10.1055/S-0028-1083316 |
0.373 |
|
2009 |
Nayek HP, Hilt G, Dehnen S. Synthesis, structure and electrochemical properties of a ferrocene-bridged bis[tris(arylselenolato)stannyl] compound European Journal of Inorganic Chemistry. 4205-4208. DOI: 10.1002/Ejic.200900664 |
0.337 |
|
2009 |
Hilt G. Übergangsmetall-katalysierte Ringöffnungen von Hetero-Diels-Alder-Addukten Angewandte Chemie. 121: 6508-6511. DOI: 10.1002/Ange.200901939 |
0.445 |
|
2008 |
Treutwein J, Hilt G. Cobalt-catalyzed [2+2] cycloaddition. Angewandte Chemie (International Ed. in English). 47: 6811-3. PMID 18720333 DOI: 10.1002/Anie.200801778 |
0.534 |
|
2008 |
Mörschel P, Janikowski J, Hilt G, Frenking G. Ligand-tuned regioselectivity of a cobalt-catalyzed Diels-Alder reaction. A theoretical study. Journal of the American Chemical Society. 130: 8952-66. PMID 18558688 DOI: 10.1021/Ja078242N |
0.475 |
|
2008 |
Hilt G, Paul A, Harms K. Cobalt-catalyzed intermolecular [2 + 2 + 2] cycloaddition for the synthesis of 1,3-cyclohexadienes. The Journal of Organic Chemistry. 73: 5187-90. PMID 18543967 DOI: 10.1021/Jo800735X |
0.561 |
|
2008 |
Hilt G, Janikowski J. Cobalt-catalyzed [4+2+2] cycloaddition for the synthesis of 1,3,6-cyclooctatrienes. Angewandte Chemie (International Ed. in English). 47: 5243-5. PMID 18528918 DOI: 10.1002/Anie.200800127 |
0.471 |
|
2008 |
Hilt G, Danz M. Regioselective cobalt-catalyzed Diels-Alder reaction towards 1,3-disubstituted and 1,2,3-trisubstituted benzene derivatives Synthesis. 2257-2263. DOI: 10.1055/S-2008-1078450 |
0.557 |
|
2008 |
Hilt G, Hess W, Harms K. Cobalt-catalyzed [2+2+2] cycloaddition of phenylacetylene with 1,3-dienes for the synthesis of vinyl-substituted 1,4-diphenylcyclohexa-1,3-dienes Synthesis. 75-78. DOI: 10.1055/S-2007-990930 |
0.503 |
|
2008 |
Hess W, Treutwein J, Hilt G. Cobalt-catalysed Carbon-carbon bond-formation reactions Synthesis. 3537-3562. DOI: 10.1055/S-0028-1083210 |
0.491 |
|
2008 |
Hilt G, Hengst C, Hess W. Solvent-dependent regiochemical cyclotrimerisation of phenylacetylene with cobalt catalysts containing disulfide ligands: A case study European Journal of Organic Chemistry. 2293-2297. DOI: 10.1002/Ejoc.200800106 |
0.418 |
|
2008 |
Treutwein J, Hilt G. ChemInform Abstract: Cobalt-Catalyzed [2 + 2] Cycloaddition. Cheminform. 39. DOI: 10.1002/chin.200850054 |
0.365 |
|
2008 |
Hilt G, Janikowski J. Cobalt‐katalysierte [4+2+2]‐Cycloaddition zur Synthese von 1,3,6‐Cyclooctatrienen Angewandte Chemie. 120: 5321-5323. DOI: 10.1002/Ange.200800127 |
0.33 |
|
2008 |
Hilt G, Janikowski J. Iron-Catalyzed Cycloadditions and Ring Expansion Reactions Iron Catalysis in Organic Chemistry: Reactions and Applications. 245-269. DOI: 10.1002/9783527623273.ch9 |
0.314 |
|
2007 |
Hilt G, Treutwein J. Cobalt-catalyzed Alder-ene reaction. Angewandte Chemie (International Ed. in English). 46: 8500-2. PMID 17899617 DOI: 10.1002/Anie.200703180 |
0.527 |
|
2007 |
Hilt G, Hengst C. A concise synthesis of substituted stilbenes and styrenes from propargylic phosphonium salts by a cobalt-catalyzed Diels-Alder/Wittig olefination reaction sequence. The Journal of Organic Chemistry. 72: 7337-42. PMID 17715980 DOI: 10.1021/Jo701406D |
0.523 |
|
2007 |
Hilt G, Bolze P, Harms K. An improved catalyst system for the iron-catalyzed intermolecular ring-expansion reactions of epoxides. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 4312-25. PMID 17323394 DOI: 10.1002/Chem.200601747 |
0.544 |
|
2007 |
Linker T, Krüger T, Hess W, Hilt G. Photooxygenation of chiral 1,3-cyclohexadienes: Strong influence of substituents on the stereo- and mode selectivities Arkivoc. 2007: 85-96. DOI: 10.3998/Ark.5550190.0008.809 |
0.435 |
|
2007 |
Hilt G, Treutwein J. Cobalt-katalysierte Alder-En-Reaktion† Angewandte Chemie. 119: 8653-8655. DOI: 10.1002/Ange.200703180 |
0.386 |
|
2007 |
Hilt G, Bolze P, Heitbaum M, Hasse K, Harms K, Massa W. Synthesis of hexahydrocyclopenta[c]furans by an intramolecular iron-catalyzed ring expansion reaction Advanced Synthesis and Catalysis. 349: 2018-2026. DOI: 10.1002/Adsc.200700035 |
0.45 |
|
2006 |
Hilt G, Janikowski J, Hess W. meta-Directing cobalt-catalyzed Diels-Alder reactions. Angewandte Chemie (International Ed. in English). 45: 5204-6. PMID 16927330 DOI: 10.1002/Anie.200601974 |
0.513 |
|
2006 |
Hilt G, Hess W, Harms K. Asymmetric cobalt-catalyzed Diels-Alder reactions of a boron-functionalized 1,3-diene with alkynes and allylboration with aldehydes. Organic Letters. 8: 3287-90. PMID 16836387 DOI: 10.1021/Ol061153F |
0.529 |
|
2006 |
Hilt G, Galbiati F. Regioselective carbene insertion on polysubstituted dihydroaromatic compounds. Organic Letters. 8: 2195-8. PMID 16671815 DOI: 10.1021/Ol060739Z |
0.471 |
|
2006 |
Hilt G, Hengst C. Propargylic phosphonium salts in cobalt-catalysed Diels-Alder reactions Synlett. 3247-3250. DOI: 10.1055/S-2006-951544 |
0.522 |
|
2006 |
Hilt G, Galbiati F. Rhodium- or copper-catalysed CH-insertion of carbenoids into dihydro-aromatic compounds and acyclic 1,4-dienes Synthesis. 3589-3596. DOI: 10.1055/S-2006-942512 |
0.471 |
|
2006 |
Hilt G, Galbiati F, Harms K. A modular approach for the synthesis of dibenzoazepine derivatives Synthesis. 3575-3584. DOI: 10.1055/S-2006-942511 |
0.497 |
|
2006 |
Hilt G, Walter C, Bolze P. Iron-salen complexes as efficient catalysts in ring expansion reactions of epoxyalkenes Advanced Synthesis and Catalysis. 348: 1241-1247. DOI: 10.1002/Adsc.200606107 |
0.65 |
|
2005 |
Hilt G, Bolze P, Kieltsch I. An iron-catalysed chemo- and regioselective tetrahydrofuran synthesis. Chemical Communications (Cambridge, England). 1996-8. PMID 15834484 DOI: 10.1039/B501100K |
0.439 |
|
2005 |
Hilt G, Vogler T, Hess W, Galbiati F. A simple cobalt catalyst system for the efficient and regioselective cyclotrimerisation of alkynes. Chemical Communications (Cambridge, England). 1474-5. PMID 15756340 DOI: 10.1039/B417832G |
0.516 |
|
2005 |
Hilt G, Lüers S, Smolko KI. A two-step reaction sequence for the syntheses of tetrahydronaphthalenes. Organic Letters. 7: 251-3. PMID 15646970 DOI: 10.1021/Ol0477879 |
0.534 |
|
2005 |
Hilt G, Bolze P. Boron-substituted building blocks in Diels-Alder and other cycloaddition reactions Synthesis. 2091-2115. DOI: 10.1055/S-2005-872084 |
0.471 |
|
2005 |
Hilt G, Galbiati F. Cobalt(I)-catalysed neutral Diels-Alder reactions of nitrogen- functionalised alkynes Synlett. 829-833. DOI: 10.1055/S-2005-863732 |
0.508 |
|
2005 |
Hilt G, Hess W, Vogler T, Hengst C. Ligand and solvent effects on cobalt(I)-catalysed reactions: Alkyne dimerisation versus [2+2+2]-cyclotrimerisation versus Diels-Alder reaction versus [4+2+2]-cycloaddition Journal of Organometallic Chemistry. 690: 5170-5181. DOI: 10.1016/J.Jorganchem.2005.03.067 |
0.566 |
|
2005 |
Hilt G, Hess W, Schmidt F. Dihydroaromatic boronic esters as building blocks for the synthesis of phenanthrenes and phenanthridines European Journal of Organic Chemistry. 2526-2533. DOI: 10.1002/Ejoc.200500025 |
0.516 |
|
2005 |
Hilt G, Galbiati F. Cobalt(I)-Catalyzed Neutral Diels—Alder Reactions of Nitrogen-Functionalized Alkynes. Cheminform. 36. DOI: 10.1002/chin.200531040 |
0.421 |
|
2004 |
Hilt G, Lüers S, Harms K. The first broad application of alkynyl sulfides as dienophiles in cobalt(I)-catalyzed Diels-Alder reactions. The Journal of Organic Chemistry. 69: 624-30. PMID 14750784 DOI: 10.1021/Jo0302915 |
0.562 |
|
2004 |
Hilt G, Lüers S, Schmidt F. Cobalt(I)-catalyzed Diels-Alder, 1,4-hydrovinylation and 1,4-hydrosilylation reactions of non-activated starting materials on a large scale Synthesis. 634-638. DOI: 10.1055/S-2003-44373 |
0.494 |
|
2003 |
Hilt G, Smolko KI. Alkynylboronic esters as efficient dienophiles in cobalt-catalyzed Diels-Alder reactions. Angewandte Chemie (International Ed. in English). 42: 2795-7. PMID 12820271 DOI: 10.1002/Anie.200351404 |
0.53 |
|
2003 |
Hilt G, Lüers S. Alkynyl sulfides as dienophiles in cobalt-catalyzed Diels-Alder reactions Synthesis. 1784-1786. DOI: 10.1055/S-2003-41034 |
0.52 |
|
2003 |
Hilt G. Catalysts for Fine Chemical Synthesis; Volume 1: Hydrolysis, Oxidation and Reduction Synthesis. 2003: 1304-1304. DOI: 10.1055/S-2003-39386 |
0.35 |
|
2003 |
Hilt G, Korn TJ, Smolko KI. A short three-component synthesis of tricyclic compounds Synlett. 241-243. DOI: 10.1055/S-2003-36795 |
0.509 |
|
2003 |
Hilt G. Konvergente gepaarte Elektrolyse zur Drei-Komponenten-Synthese geschützter Homoallylalkohole Angewandte Chemie. 115: 1760-1762. DOI: 10.1002/Ange.200350892 |
0.338 |
|
2002 |
Ohkuma T, Koizumi M, Muñiz K, Hilt G, Kabuto C, Noyori R. trans-RuH(eta1-BH4)(binap)(1,2-diamine): a catalyst for asymmetric hydrogenation of simple ketones under base-free conditions. Journal of the American Chemical Society. 124: 6508-9. PMID 12047151 DOI: 10.1021/Ja026136+ |
0.716 |
|
2002 |
Hilt G, Smolko KI, Lotsch BV. Cobalt(I)-catalyzed neutral Diels-Alder reactions of oxygen-functionalized acyclic 1,3-dienes with alkynes Synlett. 1081-1084. DOI: 10.1055/S-2002-32592 |
0.557 |
|
2002 |
Hilt G, Lüers S. Cobalt(I)-catalyzed 1,4-hydrovinylation reactions of 1,3-dienes with functionalized terminal alkenes under mild conditions Synthesis. 609-618. DOI: 10.1055/S-2002-23549 |
0.51 |
|
2002 |
Hilt G, Smolko KI. Cobalt(I)-catalyzed neutral Diels-Alder reactions of 1,3-diynes with acyclic 1,3-dienes Synthesis. 686-692. DOI: 10.1055/S-2002-23547 |
0.529 |
|
2002 |
Ohkuma T, Koizumi M, Muñiz K, Hilt G, Kabuto C, Noyori R. trans-RuH(η1-BH4)(binap)(1,2-diamine): A catalyst for asymmetric hydrogenation of simple ketones under base-free conditions Journal of the American Chemical Society. 124: 6508-6509. DOI: 10.1021/ja026136+ |
0.428 |
|
2002 |
Hilt G, Smolko KI, Waloch C. Indium-catalyzed allylation of imines with electrochemically assisted catalyst regeneration Tetrahedron Letters. 43: 1437-1439. DOI: 10.1016/S0040-4039(02)00044-8 |
0.496 |
|
2001 |
Hilt G, du Mesnil FX, Lüers S. An Efficient Cobalt(I) Catalyst System for the Selective 1,4-Hydrovinylation of 1,3-Dienes. Angewandte Chemie (International Ed. in English). 40: 387-389. PMID 29712416 DOI: 10.1002/1521-3773(20010119)40:2<387::Aid-Anie387>3.0.Co;2-7 |
0.459 |
|
2001 |
Piotrowski H, Hilt G, Schulz A, Mayer P, Polborn K, Severin K. Self-assembled organometallic [12]metallacrown-3 complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 3196-208. PMID 11531106 DOI: 10.1002/1521-3765(20010803)7:15<3196::Aid-Chem3196>3.0.Co;2-M |
0.332 |
|
2001 |
Piotrowski H, Polborn K, Hilt G, Severin K. A self-assembled metallomacrocyclic ionophore with high affinity and selectivity for Li+ and Na+. Journal of the American Chemical Society. 123: 2699-700. PMID 11456954 DOI: 10.1021/Ja005804T |
0.323 |
|
2001 |
Hilt G, Lüers S, Polborn K. Synthesis of polycyclic polyfunctionalized carbocycles by a cobalt(I)‐initiated tandem diels–alder reaction sequence Israel Journal of Chemistry. 41: 317-328. DOI: 10.1560/8E4X-0U34-Mqyd-0H20 |
0.509 |
|
2001 |
Hilt G, Korn TJ. An efficient cobalt catalyst for the neutral Diels-Alder reaction of acyclic 1,3-dienes with internal alkynes Tetrahedron Letters. 42: 2783-2785. DOI: 10.1016/S0040-4039(01)00289-1 |
0.55 |
|
2001 |
Hilt G, Lüers S, Polborn K. Synthesis of polycyclic polyfunctionalized carbocycles by a cobalt(I)-initiated tandem Diels - Alder reaction sequence Israel Journal of Chemistry. 41: 317-327. |
0.381 |
|
2000 |
Semmelhack MF, Hilt G. Selective functionalization of an isodurene-Cr(CO)3 complex Synlett. 1127-1128. DOI: 10.1055/S-2000-6751 |
0.599 |
|
2000 |
Hilt G, Du Mesnil FX. An improved cobalt catalyst for homo Diels-Alder reactions of acyclic 1,3-dienes with alkynes Tetrahedron Letters. 41: 6757-6761. DOI: 10.1016/S0040-4039(00)01163-1 |
0.535 |
|
1998 |
Semmelhack MF, Hilt G, Colley JH. S(n)AR reactions with fluoroarene-Cr(CO)2L complexes, where L is a potential linker ligand for solid phase synthesis Tetrahedron Letters. 39: 7683-7686. DOI: 10.1016/S0040-4039(98)01720-1 |
0.631 |
|
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 |
0.579 |
|
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. |
0.59 |
|
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 |
0.594 |
|
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