Dilgam Ahmadli
@DilgamAhmadli
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PhD Candidate at Max-Planck-Institut für Kohlenforschung, Ritter Lab || MSc Bilkent University, Türkmen Group || BSc Bilkent university
Mülheim an der Ruhr
Joined January 2018
Here we go! I am super excited to share my first publication as a first author in @J_A_C_S . Huge congratulations to all involved
'How do I thianthrenate X?' – In our new article in @J_A_C_S, @DilgamAhmadli presents simple guidelines for selecting reaction conditions and with our collaborators from @syngenta developed a robust diversification platform for further functionalizations! https://t.co/nBUsHGB6uU
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It was a pleasure to present my work at Novartis Graduate Colloquium and to meet a great group of scientists! Many thnks for the kind invitation and the opportunity to share my research. I truly enjoyed the insightful discussions and the inspiring scientific environment.
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Come join us in the most livable city in the world! 🌍 We have a fully funded PhD position open 🚨 More info in the thread below and on our website! 👇 https://t.co/xvq473iw4U
mateoslab.com
🚨 PhD Opportunity Alert! RT appreciated! A fully funded PhD position is available in the Mateos Group at the University of Vienna! 🔹 Up to 4y of funding 🔹 Application deadline: April 21, 2025 👉 More info: https://t.co/k4rUCdoRrs
#PhDPosition #Chemistry #Catalysis (1/4)
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Our work on dearomative alkylation of heteroarenium salts via blue light enabled radical reservoir strategy is now online at @JOC_OL
https://t.co/zp6bKj7cJ6
pubs.acs.org
Alkyl substituted nitrogen heterocycles are important building blocks in drug molecules, agrochemicals, and materials. Herein we report a simple and efficient way to prepare such compounds by...
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Congrats to all involved. Thanks to @yunus_turkmen to make it possible.
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Do not miss the recent work from Karimov Lab. Congrats to the former labmate and friend @agshin_garayev and all involved.
Excited to share this preprint from our group where we studied dihydroheteroarene dimers and their coupling with alkyl halides.
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Congrats to the Ritter labs soccer team for a great third place in this years KoFo Cup!! ⚽️
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🚨📢 FULLY-FUNDED PhD POSITION! 📢🚨 Join my research team at the Institute of Organic Chemistry, 𝐔𝐧𝐢𝐯𝐞𝐫𝐬𝐢𝐭𝐲 𝐨𝐟 𝐕𝐢𝐞𝐧𝐧𝐚! Dive into cutting-edge synthetic organic chemistry and unravel complex reaction mechanisms. 🚀🔬
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Congrats @TimSchu34938298. Great work!!!
Looking for an alternative ligand to Cp? Have you tried a phenol? Check out our newest publication in @J_A_C_S about ruthenium phenoxo complexes in pi-arene activation! Congrats to @TimSchu34938298 and all involved! Open access 🔓 https://t.co/q6U13DbED7
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Thianthrene meets nickel catalysis! We are happy to present our newest publication in @NatureCatalysis about C–heteroatom coupling of TT-salts with electron-rich aryls using nickel and light. Great collaboration with @CornellaLab
https://t.co/6kIgTcy0N5
nature.com
Nature Catalysis - Photoredox-catalysed coupling of electron-rich aryl electrophiles based on simple nickel salts usually suffers from a slow oxidative addition. Now, it is shown that...
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We are happy to present our newest publication in @ScienceMagazine about safer aryldiazonium chemistry! Nitrate is reduced to generate aryldiazoniums as fleeting intermediates for the direct conversion of anilines and aminoheterocycles to arylhalides. https://t.co/ZFEoIdmpGe
science.org
Aryldiazonium salts remain a staple in organic synthesis and are still prepared largely in accord with the protocol developed in the 19th century. Because of the favorable reactivity that often...
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This week in Group Meeting, we discussed the career of Viresh Rawal (University of Chicago). Here are some papers selected by the lab: https://t.co/cUm7A5mBkh
https://t.co/zI1YSDlRmk
https://t.co/O1vKttAqFh
https://t.co/7gjtaCmC5v
https://t.co/msJZK1mNx9
https://t.co/s8J3BOtM2Z
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Check out our most recent publication in @J_A_C_S about selective C–H fluorination of quinolines! Out today and open access! https://t.co/5YPHBGG0et Congrats to all involved!
pubs.acs.org
Direct C–H fluorination is an efficient strategy to construct aromatic C–F bonds, but the cleavage of specific C–H bonds in the presence of other functional groups and the high barrier of C–F bond...
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