29/01/2019
Social cake party...........
Small compounds and following application of the developed reaction methodology for preparation of focused compound libraries. Obtained compounds are studi
The group’s research covers several complementary areas of organic synthesis for the development of novel efficient reaction methodology, such as:
• Enantioselective catalysis for the synthesis of complex chiral products with multiple stereocenters
• C-H bond activation using transition metal catalysis for direct coupling of non-functionalized compounds
• C-H bond functionalization based on utilization of direct oxidative metal-free methods for synthesis of compounds of interest
29/01/2019
Social cake party...........
Bering L., D’Ottavio L., Sirvinskaite G., Antonchick A. P. Nitrosonium ion catalysis: aerobic, metal-free cross-dehydrogenative carbon–heteroatom bond formation Chem. Commun., 2018, Early View, DOI: 10.1039/C8CC08328B
Nice chemistry.......
29/08/2018
Sweet chemistry developed by Lab, publish in Catalytic Transfer Using as Hydrogen Source
https://onlinelibrary.wiley.com/doi/10.1002/cssc.201801770
Luis and Andrey contributed a book chapter to PATAI'S Chemistry of Functional Groups!
Oxidative Heteroatom–Heteroatom Bond Formation - Bering - - Major Reference Works - Wiley Online Library Oxidative Heteroatom–Heteroatom Bond Formation Hypervalent Halogen Compounds (2018) Luis Bering E-mail address:[email protected] Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany Department of Chemistry and Chemical Biology, Technical Uni...
26/06/2018
Benzylation of arenes was reported in Organic Letters as well!
Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes Metal-Free C–O Bond Functionalization: Catalytic Intramolecular and Intermolecular Benzylation of Arenes
26/06/2018
More work on NO+ catalysis from our group!
Selective, Catalytic, and Metal-Free Coupling of Electron-Rich Phenols and Anilides Using Molecular Oxygen as Terminal Oxidant Selective, Catalytic, and Metal-Free Coupling of Electron-Rich Phenols and Anilides Using Molecular Oxygen as Terminal Oxidant
20/03/2018
Aerobic, Metal-Free, and Catalytic Dehydrogenative Coupling of Heterocycles: En Route to Hedgehog Signaling Pathway Inhibitors published now in Organic letters, Congratulation Luis & Felix!
22/01/2018
Dihydroxylation of simple alkanes was highlighted in Org. Chem. Highlights 2017!
C-H Functionalization: The Inoue Synthesis of Zaragozic Acid C Jennifer M. Schomaker of the University of Wisconsin found (Chem. Commun. 2017, 53, 4346. ) that silver catalysts selectively directed the cyclization of 1 to H1, to give 2. Other catalysts (Rh, Mn, Ru) directed the cyclization to H2. Tian-Sheng Mei of the Shanghai Institute of Organic Chemistry use...
06/12/2017
Luca Laraia, former Postdoc and Project Leader in Prof. Waldmann's lab, is now Assistant Professor at the Danmarks Tekniske Universitet - DTU in Copenhagen. Congrats!🎊
Luca is actually offering a PhD position in synthetic organic chemistry. And this sounds quite convincing...👉"I was lucky to find him as a mentor. Luca understands how to guide and motivate people both on a daily basis as well as in the long term, enabling his co-workers to achieve their full potential." Lucas Robke, former PhD Student in the Waldmann lab.
http://www.kemi.dtu.dk/english/Research/Organic-Inorganic-Chemistry/Kemisk_Biologi/LucaLaraia/Profile
29/11/2017
After 7 years Dr. Marco Potowski leaves the MPI. All the best for the next stage of your career!
23/11/2017
Interested in doing your PhD abroad?
Assistant Professor Dr. Luca Laraia (DTU, Copenhagen, Denmark) is offering a PhD position in synthetic organic chemistry!
http://www.dtu.dk/english/career/job?id=aabecb7f-71cb-44b8-ad31-c275bc98f8cb
For any questions feel free to contact [email protected]
PhD Scholarship in Synthesis of natural product-derived compound collections for phenotypic screening DTU will promote promising fields of research within the technical and the natural sciences, especially based on usefulness to society, relevance to business and sustainability.