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11711 Publications


2016 | Journal Article | LibreCat-ID: 37988
Desens, W., & Werner, T. (2016). Convergent Activation Concept for CO2Fixation in Carbonates. Advanced Synthesis and Catalysis, 358(4), 622–630. https://doi.org/10.1002/adsc.201500941
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2016 | Journal Article | LibreCat-ID: 37981
Diebler, J., Spannenberg, A., & Werner, T. (2016). Atom economical synthesis of di- and trithiocarbonates by the lithium tert-butoxide catalyzed addition of carbon disulfide to epoxides and thiiranes. Organic and Biomolecular Chemistry, 14(31), 7480–7489. https://doi.org/10.1039/c6ob01081d
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2016 | Journal Article | LibreCat-ID: 37983
Tenhumberg, N., Büttner, H., Schäffner, B., Kruse, D., Blumenstein, M., & Werner, T. (2016). Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO2and renewables. Green Chemistry, 18(13), 3775–3788. https://doi.org/10.1039/c6gc00671j
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2016 | Journal Article | LibreCat-ID: 37982
Diebler, J., Komber, H., Häußler, L., Lederer, A., & Werner, T. (2016). Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers. Macromolecules, 49(13), 4723–4731. https://doi.org/10.1021/acs.macromol.6b00728
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2016 | Journal Article | LibreCat-ID: 37980
Büttner, H., Grimmer, C., Steinbauer, J., & Werner, T. (2016). Iron-Based Binary Catalytic System for the Valorization of CO2 into Biobased Cyclic Carbonates. ACS Sustainable Chemistry & Engineering, 4(9), 4805–4814. https://doi.org/10.1021/acssuschemeng.6b01092
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2016 | Journal Article | LibreCat-ID: 37978
Büttner, H., Steinbauer, J., Wulf, C., Dindaroglu, M., Schmalz, H.-G., & Werner, T. (2016). Organocatalyzed Synthesis of Oleochemical Carbonates from CO2and Renewables. ChemSusChem, 10(6), 1076–1079. https://doi.org/10.1002/cssc.201601163
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2016 | Book (Editor) | LibreCat-ID: 38085
Steigerwald, J., Behrens, R., & Hallesche Beiträge zur Europäischen Aufklärung (Eds.). (2016). Aufklärung und Imagination in Frankreich (1675-1810) - Anthologie und Analyse. (Vol. 54). De Gruyter.
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2016 | Journal Article | LibreCat-ID: 35708
Oechsle, P., Hou, P., Flörke, U., & Paradies, J. (2016). Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). Advanced Synthesis & Catalysis, 358(23), 3656–3656. https://doi.org/10.1002/adsc.201601149
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2016 | Journal Article | LibreCat-ID: 22253
Tamke, S., Qu, Z.-W., Sitte, N. A., Flörke, U., Grimme, S., & Paradies, J. (2016). Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator. Angewandte Chemie, 4408–4411. https://doi.org/10.1002/ange.201511921
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2016 | Journal Article | LibreCat-ID: 22254
Oechsle, P., Hou, P., Flörke, U., & Paradies, J. (2016). Cover Picture: Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence (Adv. Synth. Catal. 23/2016). Advanced Synthesis & Catalysis, 3656–3656. https://doi.org/10.1002/adsc.201601149
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22256
Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., & Paradies, J. (2016). Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. Angewandte Chemie International Edition, 12219–12223. https://doi.org/10.1002/anie.201606426
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2016 | Journal Article | LibreCat-ID: 22255
Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., & Paradies, J. (2016). Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare. Angewandte Chemie, 12407–12411. https://doi.org/10.1002/ange.201606426
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2016 | Journal Article | LibreCat-ID: 22252
Tamke, S., Qu, Z.-W., Sitte, N. A., Flörke, U., Grimme, S., & Paradies, J. (2016). Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence. Angewandte Chemie International Edition, 4336–4339. https://doi.org/10.1002/anie.201511921
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2016 | Journal Article | LibreCat-ID: 22250
Maier, A. F. G., Tussing, S., Schneider, T., Flörke, U., Qu, Z.-W., Grimme, S., & Paradies, J. (2016). Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles. Angewandte Chemie International Edition, 12219–12223. https://doi.org/10.1002/anie.201606426
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22249
Oechsle, P., Hou, P., Flörke, U., & Paradies, J. (2016). Concise Synthesis of Dithiophene Derivatives by a Palladium- Catalyzed Multiple C-S Cross Coupling/Cyclization Sequence. Advanced Synthesis & Catalysis, 3770–3776. https://doi.org/10.1002/adsc.201600802
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22251
Tussing, S., Kaupmees, K., & Paradies, J. (2016). Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines. Chemistry - A European Journal, 7422–7426. https://doi.org/10.1002/chem.201600716
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2016 | Journal Article | LibreCat-ID: 22248
Oechsle, P., Flörke, U., Egold, H., & Paradies, J. (2016). Heteroacene Synthesis through C−S Cross-Coupling/5-endo-digCyclization. Chemistry - A European Journal, 18559–18563. https://doi.org/10.1002/chem.201603737
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 35710
Tussing, S., Kaupmees, K., & Paradies, J. (2016). Inside Cover: Structure–Reactivity Relationship in the Frustrated Lewis Pair (FLP)‐Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). Chemistry – A European Journal, 22(22), 7302–7302. https://doi.org/10.1002/chem.201601558
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22257
Tussing, S., Kaupmees, K., & Paradies, J. (2016). Inside Cover: Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines (Chem. Eur. J. 22/2016). Chemistry - A European Journal, 7302–7302. https://doi.org/10.1002/chem.201601558
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 24653
Mahnken, R., Cheng, C., Düsing, M., Ehlenbröker, U., & Leismann, T. (2016). The concept of generalized stresses for computational manufacturing and beyond. GAMM-Mitteilungen, 229–265. https://doi.org/10.1002/gamm.201610014
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