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Accounts of chemical research, ISSN 0001-4842, 11/2008, Volume 41, Issue 11, pp. 1523 - 1533
N-Heterocyclic carbenes (NHCs), especially monodentate ones, have become the ligand of choice for many transition-metal-catalyzed transformations. They... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2019, Volume 58, Issue 25, pp. 8572 - 8576
A systematic, user‐friendly assessment tool that delivers a clear overview of the sensitivity of reactions to key parameters is highly desirable. Herein, the... 
photochemistry | radar diagram | reproducibility | robustness screen | sensitivity assessment | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Radar systems | Analysis | Organic chemistry | Sensitivity | Sensitivity analysis | Photochemical reactions | Reproducibility | Photochemicals | Parameter sensitivity | Assessments | Index Medicus
Journal Article
Organic letters, ISSN 1523-7060, 05/2016, Volume 18, Issue 9, pp. 2090 - 2093
Journal Article
Chemical Society reviews, ISSN 1460-4744, 2018, Volume 47, Issue 19, pp. 7190 - 7202
Visible-light-mediated energy transfer has experienced a renaissance in organic synthesis within the last ten years. This tutorial review covers its diverse... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2012, Volume 68, Issue 26, pp. 5185 - 5192
A short and efficient synthesis of ent-corsifuran A by a highly asymmetric hydrogenation of a benzofuran precursor is reported. In addition, the electronic... 
Asymmetric hydrogenation | Ruthenium | N-Heterocyclic carbenes | Benzofuran | 2,3-Dihydrobenzofuran | Hydrogenation | Synthesis | Organic compounds
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2015, Volume 54, Issue 39, pp. 11577 - 11580
A visible‐light‐mediated photoredox‐catalyzed semipinacol‐type rearrangement proceeding via 1,2 alkyl migration was developed. In this transformation,... 
radical reactions | photocatalysis | ring expansion | fluorine | Fluorides | Catalysis | Expansion | Styrenes | Cationic | Migration | Transformations | Derivatives | Bonding | Radicals | Rings (mathematics)
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 03/2011, Volume 133, Issue 8, pp. 2350 - 2353
An efficient Rh(III)-catalyzed oxidative olefination by directed C−H bond activation of N-methoxybenzamides is reported. In this mild, practical, selective,... 
Alkenes - chemistry | Oxidation-Reduction | Stereoisomerism | Molecular Structure | Catalysis | Benzamides - chemical synthesis | Rhodium - chemistry | Benzamides - chemistry | Chemical properties | Rhodium | Carbon compounds | Electric properties | Index Medicus | Chemical Sciences
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 05/2014, Volume 50, Issue 34, pp. 4459 - 4461
An experimentally simple additive-free Rh(III)-catalysed direct alkynylation of alkenes has been developed. This protocol employs commercially available... 
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 09/2014, Volume 356, Issue 13, pp. 2794 - 2800
Intermolecular three‐component oxyarylation reactions of simple alkenes have been developed using a dual gold and photoredox catalytic system. Inexpensive... 
gold | dual catalysis | alkenes | cross‐coupling | photocatalysis | Dual catalysis | Gold | Cross-coupling | Alkenes | Photocatalysis | cross-coupling | Organic dyes | Olefins | Catalysis | Dyes | Catalysts | Accessibility | Joining | Ethers
Journal Article
Accounts of chemical research, ISSN 0001-4842, 03/2015, Volume 48, Issue 3, pp. 619 - 627
Conspectus Synthetic organic chemistry underpins many scientific disciplines. The development of new synthetic methods proceeds with the ultimate intention of... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Research | Ring formation (Chemistry) | Intermolecular forces | Chemical synthesis | Economics | Screening | Stability | Chemical reactions | Tolerances | Catalysis | Screens | Functional groups
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 37, pp. 11287 - 11291
A cobalt‐catalyzed dehydrogenative cross‐coupling of thiols and indoles is reported. Using a cooperative reaction system, a new mode of action for the... 
cross-coupling | cobalt | C−H activation | C−heteroatom coupling | thiolation | Cobalt | Thiols | Catalysis
Journal Article