148. L. Li, E. Babaoglu, K. Harms, G. Hilt, Eur. J. Org. Chem. 2017, 4543-4547.
Expanding Blaise-Type Reactions towards Indium-Mediated Transformations of α-Bromo-β-keto Esters with Nitriles.

147. M. Chen, J. Shang, Y. Wang, K. Wu, J. Kuttner, G. Hilt, W. Hieringer, J. M. Gottfried ACS Nano 2017, 11, 134-143.
On-Suface Synthesis and Characterization of Honeycombene Oligophenylene Macrocycles.

146. P. Röse, G. Hilt Adv. Synth. Catal. 2017, 359, 1359- 1372.
Efficient Oxidative Coupling of Arenes via Electrochemical Regeneration of 2,3-Dichloro-5,6-dicyano-1,4-benoquinone (DDQ) under Mild Reaction Conditions.

145. S. M. Weber, G. Hilt Org. Lett. 2017, 19, 564-567.
Control of the Regioselectivity in Cobalt- versus Ruthenium-Catalyzed Alder-ene Reactions of Unsymmetrical 1,3-Diynes.

144. Q. Fan, T. Wang, J. Dai, J. Kuttner, G. Hilt, J. M. Gottfried, J. Zhu, 2017, submitted.

143. F. Weber, P. S. Steinlandt, M. Ballmann, G. Hilt Synthesis 2017, 49, 440-450.
Structure dependent Nickel-catalysed Transposition of N-Allylamides to E- or Z-Enamides.


142. A. Nödling, R. Möckel, R. Tonner, G. Hilt Chem. Eur. J. 2016, 22, 13171-13180.
Lewis acids as activators in CBS-catalysed Diels-Alder reactions - distortion induced Lewis acidity enhancement of SnCl4.

141. E. Babaoglu, K. Harms, G. Hilt Synlett 2016, 27, 1820-1823.
Indium-Mediated Blaise-Type Reaction of Bromomalonates with Nitriles and Isocyanates.

140. Q. Fan, J. Dai, T. Wang, J. Kuttner, G. Hilt, J. M. Gottfried, J. Zhu ACS Nano 2016, 10, 3747-3754. DOI:10.1021/acsnano.6b00366
Confined Synthesis of Organometallic Chains and Macrocycles by Cu-O Surface Templating.

139. J. Dai, Q. Fan, T. Wang, J. Kuttner, G. Hilt, J. M. Gottfried, J. Zhu Physical Chemistry Chemical Physics 2016, 18, 20627-20634.
The role of the substrate structure in the on-surface synthesis of organometallic and covalent oligophenylene chains.

138. F. Weber, M. Ballmann, C. Kohlmeyer, G. Hilt Org. Lett. 2016, 18, 548-551. DOI:10.1021/acs.orglett.5b03585

Nickel-Catalyzed Double Bond Transposition of Alkenyl-Boronates for in situ syn-Selective Allylboration Reactions. 137. P. Röse, G. Hilt Synthesis 2016, 48, 463-492. DOI:10.1055/s-0035-1560378 Cobalt-catalyzed Bond Formation Reactions; Part 2


136. P. Röse, C. C. M. Garcia, F. Pünner, K. Harms, G. Hilt J. Org. Chem. 2015, 80, 7311-7316. DOI:10.1021/acs.joc.5b01198
Cobalt-catalyzed Cross-Benzannulation of Conjugated Enynes and Diynes.

135. F. Weber, A. Schmidt, P. Röse, M. Fischer, O. Burghaus, G. Hilt Org. Lett. 2015, 17, 2952-2955. DOI:10.1021/acs.orglett.5b01230
Double Bond Isomerization - Highly Reactive Nickel Catalyst Applied in the Synthesis of the Pheromone (9Z,12Z)-Tetradeca-9,12-dienyl Acetate.

134. C. Wang, Y. Zheng, H. Huo, P. Röse, L. Zhang, K. Harms, G. Hilt, E. Meggers Chem. Eur. J. 2015, 21, 7355-7359. DOI:10.1002/chem.201500998
Merger of Visible Light Induced Oxidation and Enantioselective Alkylation with a Chiral Iridium Catalyst.

133. G. Hilt ChemCatChem 2015, 7, 1639-1641. DOI:10.1002/cctc.201500177
Asymmetric Nickel-Catalysed Cross-Hydrovinylation of Two Terminal Alkenes.

132. R. Möckel, G. Hilt Org. Lett. 2015, 17, 1644-1647. DOI:10.1021/acs.orglett.5b00306
Synthesis of Polysubstituted Iodobenzene Derivatives from Alkynylsilanes and 1,3-Dienes via Diels-Alder / Oxidation / Iodination Reaction Sequence.

131. J. Kuttner, G. Hilt Synthesis 2015, 47, 1170-1180. DOI:10.1055/s-0034-1380148
Synthesis of Acyclic Polycarbonyl Compounds via Ozonolysis of 1,4-Cyclohexadienes.

130. P. Röse, S. Emge, J.-i. Yoshida, G. Hilt Beilstein J. Org. Chem. 2015, 11, 174-183. DOI:10.3762/bjoc.11.18
Electrochemical Selenium- and Iodonium-Initiated Cyclisation of Hydroxy-functionalised 1,4-Dienes.

129. J. Shang, Y. Wang, M. Chen, J. Dai, X. Zhou, J. Kuttner, G. Hilt, J. M. Gottfried, K. Wu Nature Chem. 2015, 7, 389-393. DOI:10.1038/nchem.2211
Assembling Molecular Sierpinski Triangles Fractals.

128. A. Schmidt, A. Nödling, G. Hilt Angew. Chem. 2015, 127, 814-818 DOI:10.1002/ange.201409902; Angew. Chem. Int. Ed. 2015, 54, 801-804. DOI:10.1002/anie.201409902
An Alternative Mechanism for the Cobalt-Catalyzed Isomerization of Terminal Alkenes to (Z)-2-Alkenes.


127. L. Kersten, G. Hilt J. Org. Chem. 2014, 79, 11661-11673. DOI:10.1021/jo502308d null
Synthesis of Tri-, Tetra- and Pentacarbonyl Derivatives via Ozonolysis of 1,4-Dienes and Cyclisation to Polyaromatic Systems.

126. H. Huo, X. Shen, C. Wang, L. Zhang, P. Röse, L.-A.. Chen, K. Harms, M. Marsch, G. Hilt, E. Meggers, Nature 2014, 515, 100-103.  DOI:10.1038/nature13892 null
Asymmetric photoredox transition-metal catalysis activated by visible light.

125. A. Nödling, G. Jakab, P. R. Schreiner, G. Hilt Eur. J. Org. Chem. 2014, 6394-6398. DOI:10.1002/ejoc.201402871 null 31P NMR Spectroscopically Quantified Hydrogen-Bonding Strength of Thioureas and Their Activity in Diels-Alder Reactions.

124. J. Kuttner, G. Hilt Macromolecules 2014, 47, 5532-5541. DOI:10.1021/ma5012446 null
Regiodivergent Cobalt-Catalysed Diels-Alder Reactions for the Synthesis of Bifunctional Building Blocks and their Suzuki-Cross-Coupling Polymerisations.

123. G. Hilt ChemCatChem 2014, 6, 2484-2485.  DOI:10.1002/cctc.201402341 null
Double Bond Isomerisation and Migration - New Playgrounds for Transition Metal-Catalysis.

122. A. Schmidt, E. Maiterth, G. Hilt Synthesis 2014, 46, 2040-2044.  DOI:10.1055/s-0034-1378375 null
Cobalt-Catalysed Transformations of 1,3,5-Hexatrienes on a Large Scale.

121. P. Susnik, G. Hilt Organometallics 2014, 33, 5907-5910. DOI:10.1021/om500292t null
Homoallylpinacolboronic Ester as Alkene Component in Cobalt-Catalyzed Alder-ene Reactions.

120. F. Pünner, G. Hilt Chem. Commun. 2014, 50, 7310-7313. DOI:10.1039/C4CC03348E null
Zinc-mediated CH-activation of tetrahydrofuran under mild conditions for the regioselective addition to aryl-propiolates.

119. Q. Fan, C. Wang, L. Liu, J. Zhao, J. Kuttner, G. Hilt, J. M. Gottfried J. Phys. Chem. 2014, 118, 13018-13025. DOI:10.1021/jp5037475 null
Covalent, Organometallic and Halogen Bonded Nanomeshes from Tetrabromo-Terphenyl by Surface-Assisted Synthesis on Cu(111).

118. A. Schmidt, G. Hilt Chem. - Asian J. 2014, 9, 2407-2410. DOI:10.1002/asia.201402323 null
Unprecedented Cobalt-Catalysed Isomerisation Reaction to Single Skipped 2,4,7-Trienes Applied in the Synthesis of Urushiol.

117. G. Hilt Chem. Rec. 2014, 14, 386-396. DOI:10.1002/tcr.201400001 null
1,4-Cyclohexadienes - Easy Access to a Versatile Building Block via Transition Metal-Catalysed Diels-Alder Reactions.

116. A. R. Nödling, K. Müther, V. H. G. Rohde, G. Hilt, M. Oestreich Organometallics 2014, 33, 302-308. DOI:10.1021/om401040y null
Ferrocene-Stabilized Silicon Cations as Catalysts for Diels-Alder Reactions: Attempted Experimental Quantification of Lewis Acidity and ReactIR Kinetic Analysis.

115. G. Hilt, J. Janikowski, M. Schwarzer, O. Burghaus, D. Sakow, M. Bröring, M. Drüschler, B. Huber, B. Roling, G. Frenking J. Organomet. Chem. 2014, 749, 219-223. DOI:10.1016/j.bbr.2011.03.031 null
Studies of Electronic Effects of Modified Pyridine-Imine Ligand Utilised in Cobalt-catalysed meta-selective Diels-Alder Reactions.

114. Q. Fan, C. Wang, Y. Han, J. Zhu, J. Kuttner, G. Hilt, J. M. Gottfried ACS Nano 2014, 8, 709-718. DOI:10.1021/nn405370s null
Surface-assisted Formation, Assembly and Dynamics of Planar Organometalic Macrocycles and Zigzag Shaped Polymer Chains with C-Cu-C Bonds.

113. P. Raster, A. Schmidt, M. Rambow, N. Kuzmanovic, B. König, G. Hilt Chem. Commun. 2014, 50, 1864-1866. DOI:10.1039/C3CC48487D null
Immobilisation of Photoswitchable Diarylhexenes Synthesised via Cobalt-Mediated Diels-Alder Reaction.

112. A. Miersch, K. Harms, G. Hilt Chem. Commun. 2014, 50, 542-544. DOI:10.1039/C3CC46788K null
Zinc-Mediated Addition of Diethyl Bromomalonate to Alkynes for the Initiation of Multi-Component Reactions toward Polysubstituted Pyranones and Tetracarbonyl Derivatives.


111. F. Pünner, J. Schieven, G. Hilt Org. Lett. 2013, 15, 4888-4891. DOI:10.1021/ol4023276 null
Synthesis of Fluorenone and Anthraquinone Derivatives from Aryl- and Aroyl-substituted Propiolates.

110. A. Miersch, C. Kohlmeyer, G. Hilt Synthesis 2013, 3228-3232. DOI:10.1055/s-0033-1339616 null
Zinc-Mediated Regiodiverse Synthesis of Vinyl Bromide Derivatives and their in situ Palladium-catalysed Cross-Coupling Reactions.

109. F. Pünner, G. Hilt Eur. J. Org. Chem. 2013, 5580-5584. DOI:10.1002/ejoc.201300726 null
Zinc/Iron-mediated Ring-Opening of Dibromocyclopropanes for in situ Diels-Alder Reactions with Electron-deficient Aldehydes and Imines.

108. L. Fiebig, J. Kuttner, G. Hilt, M. Schwarzer, G. Frenking, H.-G. Schmalz, M. Schäfer J. Org. Chem. 2013, 78, 10485-10493. DOI:10.1021/jo402001g null
Cobalt Catalysis in the Gas Phase: Experimental Characterisation of Cobalt(I) Complexes as Intermediates in Regioselective Diels-Alder Reactions.

107. A. Schmidt, G. Hilt Org. Lett. 2013, 15, 2708-2711. DOI:10.1021/ol401015e null
Scope and Limitations of 1,3,5-Hexatriene Derivatives in Regioselective Cobalt-Catalyzed Reactions.

106. P. Röse, F. Pünner, G. Hilt, K. Harms Synlett 2013, 1101-1104. DOI:10.1055/s-0033-1338384 null
Efficient Synthesis of 2-Pyridylenynes and Application in Cobalt-Catalysed Benzannulation Reactions.

105. Q. Fan, J. Zhu, J. Kuttner, G. Hilt, J. M. Gottfried Angew. Chem. 2013, 125, 4766-4770. DOI:10.1002/anie.201300610 null
Surface-Assisted Organic Synthesis of Hyperbenzene Nanotroughs.

104. G. Hilt, EROS-Reagent 4,4,5,5-Tetramethyl-2-(2-methylene-3-buten-1-yl)-1,3,2-dioxaborolane. DOI:10.1002/047084289X.rn01618 null

96a. Addition to 96.: M. Arndt, G Hilt, A. F. Khlebnikov, S. I. Kozhushkov, A. de Meijere Eur. J. Org. Chem. 2013, 1171-1172. DOI:10.1002/ejoc.201200105 null
Diels-Alder Reactions for the Construction of Cyclopropylarenes.


103. M. Arndt, M. Dindaroğlu, H.-G. Schmalz, G. Hilt Synthesis 2012, 44, 3534-3542. DOI:10.1055/s-0030-1258408 null
Ligand Control of the Cobalt-Catalysed 1,4-Hydrovinylation Reaction.

102. F. Erver, J. R. Kuttner, G. Hilt J. Org. Chem. 2012, 77, 8375-8385. DOI:10.1021/jo301028b null
Multidirectional Cobalt-Catalyzed Diels-Alder / Hydrovinylation Sequences.

101. A. Miersch, G. Hilt Chem. Eur. J. 2012, 18, 9798-9801. DOI:10.1002/chem.201201385 null
Stereodivergent Zinc-Mediated Three-Component Synthesis of Tri- and Tetrasubstituted Alkenes.

100. F. Erver, G. Hilt J. Org. Chem. 2012, 77, 5216-5219. DOI:10.1021/jo3007896 null
Cobalt- versus Ruthenium-catalyzed Alder-ene Reaction for the Synthesis of Credneramides A and B.

99. F. Erver, G. Hilt Org. Lett. 2012, 14, 1884-1887. DOI:10.1021/ol300504f null
Double- and Triple-Cobalt-Catalysis in Multi-Component Reactions.

98. G. Hilt Eur. J. Org. Chem. 2012, 4441-4451. DOI: 10.1002/ejoc.201200212 null
The Hydrovinylation Reactions - Atom-Economic Transformations with Steadily Increasing Synthetic Potential.

97. G. Hilt, F. Pünner, Diels-Alder Reactions, in Transition-Metal-Mediated Aromatic Ring Construction, K. Tanaka, (Ed.), Wiley, 2012. ISBN:978-1-118-14892-1 null

96. M. Arndt, G. Hilt, A. F. Khlebnikov, S. I. Kozhushkov, A. de Meijere Eur. J. Org. Chem. 2012, 3112-3121. DOI:10.1002/ejoc.201200105 null
Diels-Alder Reactions for the Construction of Cyclopropylarenes.

95. F. Pünner, G Hilt Chem. Commun. 2012, 3617-3619. DOI: 10.1039/C2CC30777D null
Regioselective Solvent-dependent Benzannulation of Conjugated Enynes.

94. J. R. Kuttner, S. Warratz, G Hilt Synthesis 2012, 44, 1293-1303. DOI:10.1055/s-0031-1289752 null
Straightforward Synthesis of Non-Conjugated Cyclohex-3-enones and Conjugated 4-Methylene-cyclohex-2-enone Derivatives.

93. L. Kersten, G. Hilt Adv. Synth. Catal. 2012, 354, 863-869. DOI: 10.1002/adsc.201100800 null
Regioselective Cobalt-Catalysed Hydrovinylation for the Synthesis of non-conjugated Enones and 1,4-Diketones.

92. F. Pünner, A. Schmidt, G. Hilt Angew. Chem. 2012, 124, 1296-1299, DOI:10.1002/ange.201107512 null; Angew. Chem. Int. Ed. 2012, 51, 1270-1273. DOI:10.1002/anie.201107512 null
Up the Hill: Selective Double Bond Isomerisation of Terminal 1,3-Dienes towards Z-1,3-Dienes or 2Z,4E-2,4-Dienes.

91. M. Danz, R. Tonner, G. Hilt Chem. Commun. 2012, 377-379. DOI:10.1039/C1CC15980A null
Understanding the Regioselectivity in Scholl Reactions for the Synthesis of Oligoarenes.

90. G. Kiefer, J. Ruiz, E. Solari, G. Hilt, K. Severin Eur. J. Org. Chem. 2012, 93-98. DOI:10.1002/ejoc.201101263 null
Ruthenium-catalyzed Sequential Enyne Cross-Metathesis/ATRA Reactions

Komplette Publikationsliste (PDF-Datei 1993-2013)