KnochelLab
@KnochelLab
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The student-run Twitter account for the Knochel research group at the LMU Munich!
Munich, Germany
Joined July 2019
Excited to see our work presented on the frontcover of @ChemCatChem! https://t.co/btth8hpoTH Check out more about the current work, that is going on in our group and take a look at our cover profile! https://t.co/HVLhrsDbFU
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In Situ Quench Reactions of Enantioenriched Secondary Alkyllithium Reagents in Batch and Continuous Flow Using an I/Li-Exchange (Knochel) @Knochellab #OpenAccess thanks to #ProjektDEAL
https://t.co/6U3omVccoH
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Check out this article from @angew_chem titled "Exploiting Coordination Effects for the Regioselective Zincation of Diazines Using TMPZnX⋅LiX (X=Cl, Br)." Read here: https://t.co/G5IAwvttue
#OpenAccess
@KnochelLab, @EvaHeviaGroup
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Another metalation riddle solved thanks to the amazing insights gained through @EvaHeviaGroup! Glad we could end this challenging project together. Congrats to all authors for their commitment and contributions. Feel free to check out our latest #OpenAccess article in @angew_chem
Always a treat to work with the @KnochelLab and their intriguing puzzles on reactivity! This time we exploited coordination effects in #Zn chemistry to promote unique C2 #zincation of #pyrimidines @angew_chem
https://t.co/plk79VUx2n
#openaccess #teamwork
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Preparation of Functionalized Amides Using Dicarbamoylzincs (Knochel) @KnochelLab @DimitrijeDjuka2 #openaccess thanks to #projektDEAL
https://t.co/mIbkrkiAh0
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Regioselective Magnesiation and Zincation Reactions of Aromatics and Heterocycles Triggered by Lewis Acids (P. Knochel et al.) @KnochelLab #OpenAccess thanks to #ProjektDEAL
https://t.co/5Mvt6tEujt
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Wondered how to selectively functionalize your desired heterocycle by using organometallic amide bases? We got you! Check out our latest concept article in @ChemEurJ summarizing some of the work that has been done in our group throughout the last decade 🥳 https://t.co/ZLS576Ybp5
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We are happy to share another #openaccess paper demonstrating the power of #flow chemistry in @ChemEurJ. Dimi and Benni used dimethylamides for continuous flow acylations of functionalized aryllithiums in toluene😯Check it out here 👀
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Interested in some more exciting flow chemistry? Ever wondered how to safely handle sodium?🤔A sodium-packed-bed reactor is all you need. Congrats to Johannes and co-authors! Check out our paper in @angew_chem as #openaccess article.
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Here is another project recently published in @ChemicalScience. We used pyrydine intermediates to regioselectively prepare functionalized 2,3,4-substituted pyridines. They could even perform the reaction in continuous flow👀Congrats Benni and Dimi!
pubs.rsc.org
A new regioselective 3,4-difunctionalization of 3-chloropyridines via 3,4-pyridyne intermediates is reported. Regioselective lithiation of 3-chloro-2-ethoxypyridine and a related 2-thio-derivative...
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Thanks to @ChemicalScience for publishing #OpenAccess and Editor @Melchiorre_P for handling our manuscript!!
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Let's start things off with our latest paper in @ChemicalScience. Ever wondered how you could prepare non-stabilized chiral Grignards? @aliakhsander and @wilkehenrik came up with a quite handy approach for that🤩 Check it out here:
pubs.rsc.org
A general preparation of enantiomerically and diastereomerically enriched secondary alkylmagnesium reagents was reported as well as their use for performing highly stereoselective transition-metal...
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"All good things come to an end". After being quiet here on Twitter in the last couple of months, we are thrilled to bring some of our most recent chemistry to you! Stay tuned for the last bits of Knochel-work ever produced in our labs here in Munich😯 #retirement
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It’s great seeing you publish more great work despite having left our lab 🥰😉🙃
Proud to share the first publication arising from DPR Beerse @JanssenGlobal together with Matthieu Jouffroy. If you want to figure out how to transform carboxylic acids into alkynes, and how this helps you with your SAR exploration, check out our paper: https://t.co/dKAbYn4wLx.
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❇️This Synfact of the Month is about ✨ Negishi Cross-Couplings in Water and Deep Eutectic Solvents✨. This study was carried out at @unibait by @Capriati_V and Filippo Perna 👉 https://t.co/sRXae140AS 🔷Highlighted by Knochel (@KnochelLab) and @aliakhsander🔷
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❇️ The research work of Willis (@RhPdCu) and his team from @UniofOxford on the ✨Preparation of Primary #Sulfonamides by 𝘵-BuONSO and #Organometallics✨ was highlighted by Paul Knochel and @aliakhsander (@KnochelLab)! 👏 👉 https://t.co/AYHkFUGgDy
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Attention Master students: 3 #Bioinorganic Chemistry PhD positions available in the group of my awesome colleague Prof. Ivana Ivanović-Burmazović @LMU_Muenchen Please contact her directly via: https://t.co/8QrCBrdk8P
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🕰️ In this Synfact Classic Paul Knochel and Johannes Harenberg (@KnochelLab) highlighted a publication authored by Bartoli and co-authors (@UniCamerino) in 1989. Read about the ✨Bartoli Indole Synthesis✨ here: 👉 https://t.co/n7lNeKgHqU!
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We are very pleased that the newest work from our post-doc @baosheng_wei in collaboration with Prof. Bein was now published in @angew_chem! Feel free to check it out as it is open access :) Congratulations to all authors!🥳
transition-metal-free synthesis of polyfunctional triarylmethanes and 1,1-diarylalkanes by sequential cross-coupling of benzal diacetates with organozinc reagents @KnochelLab #openaccess thanks to #projektDEAL
https://t.co/dwUCEWy3e9
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❇️ The @KonchelLab highlighted the research work of Hartwig and co-workers (@HartwigGroup) from @UCBerkeley: ✨Enantioselective Catalytic Hydroamination of Internal Alkenes✨!🧐 Read more in this Synfact of the Month 👉 https://t.co/gKbD5FRnB8
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