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1942 Publications


2016 | Journal Article | LibreCat-ID: 37984
M.-L. Schirmer, A. Spannenberg, and T. Werner, “Highly functionalized alkenes produced from base-free organocatalytic Wittig reactions: (E)-3-benzylidenepyrrolidine-2,5-dione, (E)-3-benzylidene-1-methylpyrrolidine-2,5-dione and (E)-3-benzylidene-1-tert-butylpyrrolidine-2,5-dione,” Acta Crystallographica Section C Structural Chemistry, vol. 72, no. 6, pp. 504–508, 2016, doi: 10.1107/s2053229616008159.
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2016 | Journal Article | LibreCat-ID: 37987
W. Desens, C. Kohrt, A. Spannenberg, and T. Werner, “A novel zinc based binary catalytic system for CO2utilization under mild conditions,” Organic Chemistry Frontiers, vol. 3, no. 2, pp. 156–164, 2016, doi: 10.1039/c5qo00356c.
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2016 | Journal Article | LibreCat-ID: 37986
M.-L. Schirmer, S. Adomeit, A. Spannenberg, and T. Werner, “Novel Base-Free Catalytic Wittig Reaction for the Synthesis of Highly Functionalized Alkenes,” Chemistry - A European Journal, vol. 22, no. 7, pp. 2458–2465, 2016, doi: 10.1002/chem.201503744.
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2016 | Journal Article | LibreCat-ID: 37985
J. Diebler, A. Spannenberg, and T. Werner, “Regio- and Stereoselective Synthesis of Dithiocarbonates under Ambient and Solvent-Free Conditions,” ChemCatChem, vol. 8, no. 12, pp. 2027–2030, 2016, doi: 10.1002/cctc.201600242.
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2016 | Journal Article | LibreCat-ID: 37988
W. Desens and T. Werner, “Convergent Activation Concept for CO2Fixation in Carbonates,” Advanced Synthesis and Catalysis, vol. 358, no. 4, pp. 622–630, 2016, doi: 10.1002/adsc.201500941.
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2016 | Journal Article | LibreCat-ID: 37981
J. Diebler, A. Spannenberg, and T. Werner, “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, vol. 14, no. 31, pp. 7480–7489, 2016, doi: 10.1039/c6ob01081d.
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2016 | Journal Article | LibreCat-ID: 37983
N. Tenhumberg, H. Büttner, B. Schäffner, D. Kruse, M. Blumenstein, and T. Werner, “Cooperative catalyst system for the synthesis of oleochemical cyclic carbonates from CO2and renewables,” Green Chemistry, vol. 18, no. 13, pp. 3775–3788, 2016, doi: 10.1039/c6gc00671j.
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2016 | Journal Article | LibreCat-ID: 37982
J. Diebler, H. Komber, L. Häußler, A. Lederer, and T. Werner, “Alkoxide-Initiated Regioselective Coupling of Carbon Disulfide and Terminal Epoxides for the Synthesis of Strongly Alternating Copolymers,” Macromolecules, vol. 49, no. 13, pp. 4723–4731, 2016, doi: 10.1021/acs.macromol.6b00728.
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2016 | Journal Article | LibreCat-ID: 37980
H. Büttner, C. Grimmer, J. Steinbauer, and T. Werner, “Iron-Based Binary Catalytic System for the Valorization of CO2 into Biobased Cyclic Carbonates,” ACS Sustainable Chemistry & Engineering, vol. 4, no. 9, pp. 4805–4814, 2016, doi: 10.1021/acssuschemeng.6b01092.
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2016 | Journal Article | LibreCat-ID: 37978
H. Büttner, J. Steinbauer, C. Wulf, M. Dindaroglu, H.-G. Schmalz, and T. Werner, “Organocatalyzed Synthesis of Oleochemical Carbonates from CO2and Renewables,” ChemSusChem, vol. 10, no. 6, pp. 1076–1079, 2016, doi: 10.1002/cssc.201601163.
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2016 | Book (Editor) | LibreCat-ID: 38085
J. Steigerwald, R. Behrens, and Hallesche Beiträge zur Europäischen Aufklärung, Eds., Aufklärung und Imagination in Frankreich (1675-1810) - Anthologie und Analyse. , vol. 54. Berlin: De Gruyter, 2016.
LibreCat
 

2016 | Journal Article | LibreCat-ID: 35708
P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “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, vol. 358, no. 23, pp. 3656–3656, 2016, doi: 10.1002/adsc.201601149.
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2016 | Journal Article | LibreCat-ID: 22253
S. Tamke, Z.-W. Qu, N. A. Sitte, U. Flörke, S. Grimme, and J. Paradies, “Cycloisomerisierung von 1,5-Eninen über eine 5-endo-dig- Cyclisierungs-Protodeborylierungs-Sequenz mit einem frustrierten Lewis-Paar als Katalysator,” Angewandte Chemie, pp. 4408–4411, 2016, doi: 10.1002/ange.201511921.
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22254
P. Oechsle, P. Hou, U. Flörke, and J. Paradies, “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, pp. 3656–3656, 2016, doi: 10.1002/adsc.201601149.
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22256
A. F. G. Maier et al., “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles,” Angewandte Chemie International Edition, pp. 12219–12223, 2016, doi: 10.1002/anie.201606426.
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22255
A. F. G. Maier et al., “Dehydrierende Oxidation von Indolinen und anderen Heterocyclen durch frustrierte Lewis-Paare,” Angewandte Chemie, pp. 12407–12411, 2016, doi: 10.1002/ange.201606426.
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22252
S. Tamke, Z.-W. Qu, N. A. Sitte, U. Flörke, S. Grimme, and J. Paradies, “Frustrated Lewis Pair-Catalyzed Cycloisomerization of 1,5-Enynes via a 5-endo-dig Cyclization/Protodeborylation Sequence,” Angewandte Chemie International Edition, pp. 4336–4339, 2016, doi: 10.1002/anie.201511921.
LibreCat | DOI
 

2016 | Journal Article | LibreCat-ID: 22250
A. F. G. Maier et al., “Frustrated Lewis Pair Catalyzed Dehydrogenative Oxidation of Indolines and Other Heterocycles,” Angewandte Chemie International Edition, pp. 12219–12223, 2016, doi: 10.1002/anie.201606426.
LibreCat | DOI
 

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

2016 | Journal Article | LibreCat-ID: 22251
S. Tussing, K. Kaupmees, and J. Paradies, “Structure-Reactivity Relationship in the Frustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Imines,” Chemistry - A European Journal, pp. 7422–7426, 2016, doi: 10.1002/chem.201600716.
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