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1. Full Text 6‑Phosphorylated Phenanthridines from 2‑Isocyanobiphenyls via Radical C–P and C–C Bond Formation
by Zhang, Bo and Daniliuc, Constantin Gabriel and Studer, Armido
Organic letters, ISSN 1523-7060, 01/2014, Volume 16, Issue 1, pp. 250 - 253
Phosphorylation | Phenanthridines - chemical synthesis | Phenanthridines - chemistry | Free Radicals - chemistry | Nitriles - chemistry | Models, Molecular | Crystallography, X-Ray | Molecular Structure | Biphenyl Compounds - chemistry | Index Medicus
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2. Full Text Lewis Acid Catalyzed Stereoselective Dearomative Coupling of Indolylboron Ate Complexes with Donor–Acceptor Cyclopropanes and Alkyl Halides
by Das, Saikat and Daniliuc, Constantin G and Studer, Armido
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2018, Volume 57, Issue 15, pp. 4053 - 4057
multicomponent reactions | ring-opening reactions | donor–acceptor cyclopropanes | boron | stereospecificity | Halides | Esters | Lewis acid | Heterocyclic compounds | Stereospecificity | Coupling | Coordination compounds | Organic compounds
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3. Full Text Functional‐Group Tolerance in Frustrated Lewis Pairs: Hydrogenation of Nitroolefins and Acrylates
by Greb, Lutz and Daniliuc, Constantin‐Gabriel and Bergander, Klaus and Paradies, Jan
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2013, Volume 52, Issue 22, pp. 5876 - 5879
boranes | nitroolefins | hydrogenation | hydrogen activation | frustrated Lewis pairs | Acrylates | Hydrogen | Hydrogenation | Lewis acid | Hydrides | Tolerances | Aggregates
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4. Full Text Stereospecific 1,3‐Aminobromination of Donor–Acceptor Cyclopropanes
by Das, Saikat and Daniliuc, Constantin G and Studer, Armido
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2017, Volume 56, Issue 38, pp. 11554 - 11558
1,3-aminobromination | donor–acceptor cyclopropanes | γ-lactams | stereospecificity | azetidines | Bromination | Diesters | Stereospecificity | Amides | N-Bromosuccinimide | Substrates | Organic compounds
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5. Full Text Conjugate Umpolung of β,β‐Disubstituted Enals by Dual Catalysis with an N‐Heterocyclic Carbene and a Brønsted Acid: Facile Construction of Contiguous Quaternary Stereocenters
by Li, Jun‐Long and Sahoo, Basudev and Daniliuc, Constantin‐G and Glorius, Frank
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2014, Volume 53, Issue 39, pp. 10515 - 10519
carbenes | dual catalysis | quaternary centers | spiro compounds | umpolung | Dual catalysis | Umpolung | Carbenes | Spiro compounds | Quaternary centers | Heterocyclic Compounds - chemistry | Acids - chemistry | Methane - analogs & derivatives | Stereoisomerism | Methane - chemistry | Catalysis | Cycloaddition Reaction | Indoles - chemistry | Spiro Compounds - chemistry | Aldehydes - chemistry | Index Medicus
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6. Full Text 6‑Aroylated Phenanthridines via Base Promoted Homolytic Aromatic Substitution (BHAS)
by Leifert, Dirk and Daniliuc, Constantin Gabriel and Studer, Armido
Organic letters, ISSN 1523-7060, 12/2013, Volume 15, Issue 24, pp. 6286 - 6289
Models, Molecular | Crystallography, X-Ray | Molecular Structure | Phenanthridines - chemical synthesis | Phenanthridines - chemistry | Aldehydes - chemistry | Index Medicus
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7. Full Text N‐Heterocyclic Carbene Catalyzed Formal [3+2] Annulation Reaction of Enals: An Efficient Enantioselective Access to Spiro‐Heterocycles
by Guo, Chang and Schedler, Michael and Daniliuc, Constantin G and Glorius, Frank
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2014, Volume 53, Issue 38, pp. 10232 - 10236
organocatalysis | asymmetric synthesis | N‐heterocyclic carbenes | spiro‐heterocycles | enals | N-heterocyclic carbenes | spiro-heterocycles | Synthesis | Catalysis | Enantiomers | Aldehydes | Heterocyclic compounds | Organic compounds | Beta | Organic chemistry | Purity | Chemical reactions | Derivatives | Carbenes | Bearing
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8. Full Text Unnatural Amino Acid Synthesis Enabled by the Regioselective Cobalt(III)‐Catalyzed Intermolecular Carboamination of Alkenes
by Lerchen, Andreas and Knecht, Tobias and Daniliuc, Constantin G and Glorius, Frank
Angewandte Chemie (International ed.), ISSN 1433-7851, 11/2016, Volume 55, Issue 48, pp. 15166 - 15170
alkene difunctionalization | CpCo(III) catalysis | carboamination | unnatural amino acids | redox-neutral conditions | Amino acids | Synthesis | Catalysis | Cobalt | Olefins | Index Medicus
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9. Full Text Oxidative N‐Heterocyclic Carbene Catalyzed Dearomatization of Indoles to Spirocyclic Indolenines with a Quaternary Carbon Stereocenter
by Bera, Srikrishna and Daniliuc, Constantin G and Studer, Armido
Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2017, Volume 56, Issue 26, pp. 7402 - 7406
organocatalysis | quaternary stereocenter | asymmetric synthesis | spiroannulation | dearomatization | Synthesis | Catalysis | Heterocyclic compounds | Organic compounds | Acylation | Optical activity | Indoles | Enantiomers | Indole
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10. Full Text Cover Picture: Oxidative N‐Heterocyclic Carbene Catalyzed Dearomatization of Indoles to Spirocyclic Indolenines with a Quaternary Carbon Stereocenter (Angew. Chem. Int. Ed. 26/2017)
by Bera, Srikrishna and Daniliuc, Constantin G and Studer, Armido
Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2017, Volume 56, Issue 26, pp. 7321 - 7321
organocatalysis | quaternary stereocenter | asymmetric synthesis | spiroannulation | dearomatization | Ketones | Optical activity | Catalysis | Indoles | Nucleophiles | Enantiomers | Carbon | Intermediates | Acylation
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11. Full Text Efficient Synthesis of Arylated Furans by a Sequential Rh‐Catalyzed Arylation and Cycloisomerization of Cyclopropenes
by Wang, Xiaoming and Lerchen, Andreas and Daniliuc, Constantin G and Glorius, Frank
Angewandte Chemie (International ed.), ISSN 1433-7851, 02/2018, Volume 57, Issue 6, pp. 1712 - 1716
rhodium(III) catalysis | C−H activation | cycloisomerization | furans | cyclopropene | Esters | Furans | Chemical synthesis | Isomerization | Pesticides | Organic compounds
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12. Full Text Highly Enantioselective Intramolecular 1,3‐Dipolar Cycloaddition: A Route to Piperidino‐Pyrrolizidines
by Vidadala, Srinivasa Rao and Golz, Christopher and Strohmann, Carsten and Daniliuc, Constantin‐G and Waldmann, Herbert
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2015, Volume 54, Issue 2, pp. 651 - 655
biology‐oriented synthesis | cycloaddition | asymmetric catalysis | pyrrolizidines | pyrrolidino‐piperidines | Pyrrolidino-piperidines | Cycloaddition | Asymmetric catalysis | Biology-oriented synthesis | Pyrrolizidines | Pyrroles - chemistry | Piperidines - chemistry | Magnetic Resonance Spectroscopy | Stereoisomerism | Cycloaddition Reaction | Enantiomers | Schiff bases | Catalysis | Index Medicus | Stereoselectivity | Synthesis | Catalysts | Scaffolds
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