Noel Research Group (@noelgroupuva) 's Twitter Profile
Noel Research Group

@noelgroupuva

Our research focuses on #FlowChemistry, #Engineering, #Synthetic #OrganicChemistry & catalytic methodology development. Headed by @tnoel82. @UvA_Amsterdam

ID: 3432425985

linkhttp://www.NoelResearchGroup.com calendar_today20-08-2015 06:38:45

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6,6K Followers

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Noel Research Group (@noelgroupuva) 's Twitter Profile Photo

Thionyl fluoride is an incredibly useful but challenging reagent to work with. In our JACS Au article, we detail the on-demand generation of gaseous SOF2 from thionyl chloride and its application as a deoxyfluorinating reagent. 🔗: pubs.acs.org/doi/10.1021/ja… #FlowChemistry

Thionyl fluoride is an incredibly useful but challenging reagent to work with. 

In our <a href="/JACS_Au/">JACS Au</a> article, we detail the on-demand generation of gaseous SOF2 from thionyl chloride and its application as a deoxyfluorinating reagent. 

🔗: pubs.acs.org/doi/10.1021/ja…

#FlowChemistry
Noel Research Group (@noelgroupuva) 's Twitter Profile Photo

Discover our new paper on photocatalytic activation of volatile alkanes with SO2 to create valuable sulfinates, key building blocks in many applications. The paper also shows the power of #FlowChemistry to handle gaseous reactants 🦸 Now Nature Communications: nature.com/articles/s4146…

Discover our new paper on photocatalytic activation of volatile alkanes with SO2 to create valuable sulfinates, key building blocks in many applications. 

The paper also shows the power of #FlowChemistry to handle gaseous reactants 🦸

Now <a href="/NatureComms/">Nature Communications</a>: nature.com/articles/s4146…
Noel Research Group (@noelgroupuva) 's Twitter Profile Photo

Check out our new paper on ligated boryl radicals as photocatalytic XAT mediators, enabling C(sp3)‒C(sp2) bond formation to yield valuable vinyl chlorides with excellent E/Z diastereoselectivity. Out now in Chemical Science: pubs.rsc.org/en/content/art… #photocatalysis #LBR #boron

Check out our new paper on ligated boryl radicals as photocatalytic XAT mediators, enabling C(sp3)‒C(sp2) bond formation to yield valuable vinyl chlorides with excellent E/Z diastereoselectivity.

Out now in <a href="/ChemicalScience/">Chemical Science</a>: pubs.rsc.org/en/content/art…

#photocatalysis #LBR #boron
Dell'Amico Group (@dellamico_group) 's Twitter Profile Photo

We're celebrating 🎉🎉 !! Our most recent work related to radical strain release photocatalysis for the synthesis of azetidines is now available Nature Catalysis in open access!!! 🔓🔓 A humongous job by all the team! 🐸nature.com/articles/s4192…🐸

We're celebrating 🎉🎉 !! Our most recent work related to radical strain release photocatalysis for the synthesis of azetidines is now available <a href="/NatureCatalysis/">Nature Catalysis</a> in open access!!! 🔓🔓
A humongous job by all the team! 
🐸nature.com/articles/s4192…🐸
Andrei Yudin (@andrei_yudin) 's Twitter Profile Photo

Visible light-induced halogen-atom transfer by N-heterocyclic carbene-ligated boryl radicals for diastereoselective C(sp3)–C(sp2) bond formation by ⁦Noel Research Group⁩ and co-workers at the U. Amsterdam ⁦Chemical Science⁩ pubs.rsc.org/en/content/art…

Boron-Chem-Research (@boron_chemistry) 's Twitter Profile Photo

Visible light-induced halogen-atom transfer by N-heterocyclic carbene-ligated boryl radicals for diastereoselective C(sp3)–C(sp2) bond formation (Chemical Science): pubs.rsc.org/en/content/art… (Noel Research Group, Timothy Noël).

Visible light-induced halogen-atom transfer by N-heterocyclic carbene-ligated boryl radicals for diastereoselective C(sp3)–C(sp2) bond formation (<a href="/ChemicalScience/">Chemical Science</a>): pubs.rsc.org/en/content/art… (<a href="/NoelGroupUvA/">Noel Research Group</a>, <a href="/tnoel82/">Timothy Noël</a>).
Daniele Mazzarella (@dmz_mazda) 's Twitter Profile Photo

Honored to have been selected to be part of the #IUPAC young observer 2024-2025! Really looking forward to discuss about chemistry in this international community 🤩

Noel Research Group (@noelgroupuva) 's Twitter Profile Photo

Alkylating Ar-Br with light alkanes? Previously thought impossible. Now, it's feasible using a combination of #flowchemistry, #HATphotocatalysis and #nickelcatalysis! 🔗Angewandte Chemie: onlinelibrary.wiley.com/doi/10.1002/an… Great collaborative effort, with DFT insights from Trevor A. Hamlin!

Alkylating Ar-Br with light alkanes? Previously thought impossible.

Now, it's feasible using a combination of #flowchemistry, #HATphotocatalysis and #nickelcatalysis!

🔗<a href="/angew_chem/">Angewandte Chemie</a>: onlinelibrary.wiley.com/doi/10.1002/an…  

Great collaborative effort, with DFT insights from <a href="/TrevorAHamlin/">Trevor A. Hamlin</a>!
Luca Capaldo (@_lucapaldo) 's Twitter Profile Photo

Feeling incredibly honored to receive the SCI Chimica Organica Junior Award "Organic Chemistry in its Methodological Aspects"! 🙏🤩🥳 Huge thanks to everyone who has supported me and believed in me. Grateful beyond words! 🫶 #Award #SCI2024

Feeling incredibly honored to receive the <a href="/SCIorganica/">SCI Chimica Organica</a> Junior Award "Organic Chemistry in its Methodological Aspects"! 🙏🤩🥳

Huge thanks to everyone who has supported me and believed in me. Grateful beyond words! 🫶

#Award #SCI2024
Procter Group (@groupprocter) 's Twitter Profile Photo

#ProcterPOW: Check out two effective flow strategies reported by Noel Research Group - the alkylation of aryl bromides using gaseous alkanes💡 and the environmentally friendly generation of reactive NCF3(PG), SCF3, and OCF3 anions for the introduction of heteroatom-CF3 motifs👀👇

#ProcterPOW: Check out two effective flow strategies reported by <a href="/NoelGroupUvA/">Noel Research Group</a> - the alkylation of aryl bromides using gaseous alkanes💡 and the environmentally friendly generation of reactive NCF3(PG), SCF3, and OCF3 anions for the introduction of heteroatom-CF3 motifs👀👇