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Angewandte Chemie International Edition, ISSN 1433-7851, 08/2015, Volume 54, Issue 33, pp. 9523 - 9527
A CC bond‐forming conjugate reaction was successfully applied to the enantioselective dearomatization of β‐naphthols. A C(sp2)C(sp3) bond is formed by using... 
naphthols | magnesium | arenes | DFT calculations | aromaticity | OXIDATIVE DEAROMATIZATION | COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | MICHAEL ADDITION | KETONES | PHENOLS | CONSTRUCTION | ESTERS | ALLYLIC DEAROMATIZATION | ALKYNONES | GENERATED MAGNESIUM CATALYST | Models, Molecular | Naphthols - chemistry | Magnesium - chemistry | Stereoisomerism | Ketones - chemistry | Conjugates | Ketones | Asymmetry | Catalysts | Transformations | Magnesium | Ethers | Bonding
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2015, Volume 54, Issue 48, pp. 14232 - 14242
Transition‐metal‐catalyzed radical reactions are becoming increasingly important in modern organic chemistry. They offer fascinating and unconventional ways... 
radical reactions | homogeneous catalysis | Michael acceptors | conjugate addition | umpolung | 4-EXO CYCLIZATIONS | O-STANNYL KETYLS | HYDROGEN-ATOM TRANSFER | ALPHA-AMINO RADICALS | CYCLIZATION REACTIONS | COUPLING REACTIONS | ARYL HALIDES | LIGHT PHOTOREDOX CATALYSIS | ELECTRON-DEFICIENT ALKENES | CHEMISTRY, MULTIDISCIPLINARY | CONJUGATE ADDITION
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 2006, Volume 47, Issue 29, pp. 5131 - 5134
Journal Article
Angewandte Chemie. International Edition, ISSN 1433-7851, 2019, Volume 58, Issue 26, pp. 8922 - 8926
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2016, Volume 55, Issue 30, pp. 8571 - 8574
The tripeptide H‐dPro‐Pro‐Asn‐NH2 is presented as a catalyst for asymmetric conjugate addition reactions of aldehydes to maleimide. The peptidic catalyst... 
organocatalysis | peptides | maleimide | asymmetric catalysis | addition reactions | DIELS-ALDER REACTIONS | ENANTIOSELECTIVE SYNTHESIS | 1,3-DICARBONYL COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | MICHAEL ADDITION | ALPHA,ALPHA-DISUBSTITUTED ALDEHYDES | CYCLOADDITION | NITROOLEFINS | STEREOGENIC CENTERS | 1,4-ADDITION | Catalysis | Peptides | Aldehydes | Lactones
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 12/2015, Volume 56, Issue 48, pp. 6722 - 6725
[Display omitted] Nitration of several di- and trisubstituted alkenes with lithium nitrate/TFAA in nitrile solvents afforded N-(β-nitroalkyl)amides in 28–72%... 
Internal H-bonding | Ritter reaction | Alkene nitration | Nitro compound | Diastereoselective Michael addition | NITROALKANES | CHEMISTRY, ORGANIC | ACETONITRILE | Amides | Nitration | Nitriles | Olefins
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2013, Volume 355, Issue 14‐15, pp. 2745 - 2755
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 10/2010, Volume 39, Issue 11, pp. 48 - 412
Journal Article