Happy to share our latest work, now published in Nature!
Ligand-enabled remote C–H activation converts abundant saturated fatty acids into desaturated lactones.
https://t.co/cCpMO9idcM
https://t.co/Yl6ERXsAPG
Thanks to @NandanNilekani Foundation, @ANRFIndia@iitbombay@dm_lab
Solvent-Free/Scalable Mechanochemical-Assisted Addition of Phosphine Oxides to Aldehydes: Sustainable Protocol for One-Pot Tandem P-C Bond Formation - now published in Green Chemistry https://t.co/oD9hGp2C8p
In @Nature, we show that redox-active esters can be transformed into alkyl zinc species useful for transmetalation, providing a solution to rate matching in XEC reactions! First application: alkylation of alkenes via polar decarboxylative cross-coupling!
https://t.co/mOBf4ChHk0
🚨 New Publication Alert 🚨
Strategic installation of the –CH₂CF₃ motif via transition-metal-catalyzed C–H functionalization is out @ChemCommun@RoySocChem@dcsiiserkol
🔗https://t.co/PJjtepSRma
📌Fluorine chemistry | C–H activation | Catalysis
Photocatalytic remote C(sp3)–H alkylation of long-chain alkenes: A tandem multicomponent approach via radical translocation - now published in @ChemicalScience from Catalysis Lab @dcsiiserkol@iiserkol
https://t.co/kRrfu0jpEv
🚀Ring-expansion of ketones with [1.1.1]propellane to access functionalized MCB-ketones and spirocyclic scaffolds is out @J_A_C_S. A great collaboration with @MykhailiukChem. Thank you, @ANRFIndia and @iiscbangalore, for the financial support. https://t.co/kSouq7umuH
🔖Our latest work on 𝐙𝐢𝐧𝐜𝐤𝐞-𝐈𝐦𝐢𝐧𝐞-𝐁𝐚𝐬𝐞𝐝 𝐏𝐞𝐫𝐢𝐩𝐡𝐞𝐫𝐚𝐥 𝐄𝐝𝐢𝐭𝐢𝐧𝐠 𝐨𝐟 𝟐‑𝐀𝐫𝐲𝐥𝐩𝐲𝐫𝐢𝐝𝐢𝐧𝐞𝐬 𝐭𝐨 𝐀𝐜𝐜𝐞𝐬𝐬 𝟑‑𝐀𝐜𝐲𝐥𝐩𝐲𝐫𝐢𝐝𝐢𝐧𝐞𝐬 just now out in @JOC_OL
Great work by Piotr, Antoni, @kittiszabo07 🥂
🔗Link: https://t.co/ajqpphXdtA
♨️Hot of the Press!
Our freshly brewed @J_A_C_S on Redirecting Formate Delivery toward Alkenes is now live!
Huge congratulations to @Shantanu_JUchem & @SMChem_ 🥂
Indeed a great collaboration with @funes_ardoiz for DFT studies! @GrykoDorota
🔗Read here: https://t.co/Zm90jZ6Bd1
Hodan and Sarah's work in collaboration with @jamesabull and Phil Miller on transforming trifluoromethane (HFC-23) into fluoroalkenes is now out in @angew_chem here is the link: https://t.co/HkU29jdX4L
🚨Just out in @angew_chem: cross couplings fuel synthesis, but C–S bonds over #SACs were uncharted territory, until now. Here, the first SAC for C–S coupling: selective, recyclable & thiol-poisoning resistant.👏 @GazisTheo, @PalitShilpa & coauthors!
Link: https://t.co/52z4tngsGJ
Attractive route for the synthesis of chiral allylic amines ⚗️ Palladium-Catalyzed Enantioselective α-Alkenylation of Alkylamines with Vinyl Bromides and Triflates | ACS Catalysis https://t.co/WbMg9Ebk7M
New Fe(0) precatalyst enables mild, Grignard-free C–H alkenylation—room temp, broad scope, and gives one clean diastereomer!|Well-Defined Iron(0) Precatalysts for Grignard-Free C–H Alkenylation at Room Temperature
https://t.co/zekkcfMRMA
Did you know that monofluoromethyl radical can act as XAT reagent? Check out our @j_veliks@anette_patte@RamKumar9687 latest research! @osi_lv @J_A_C_S
https://t.co/REPYm5KHzi
The chameleonic nature of a new photocatalyst!
Consecutive Multiphoton-Mediated Defluorinative Amination of Fluoroarenes | Journal of the American Chemical Society https://t.co/mz1Gwoc1Z9
Enantioselective CH activation is still on gas pedal. for broad applications, we must develop new catalysts for reacting CH with nucleophiles: https://t.co/Tyusk6wcHt. What is your wish list? NaF? NaCl? H2O? NH3?
"C–H acylation as an enabling tool to tag phenolic drugs" featuring mechanistic insights now published in @OrgChemFront Excellent experimental work performed by @gironcarlota@ehu_kimika. Zorionak Carlota! https://t.co/Wby7jWHRVe
We are hiring for a 1.5 yrs postdoc in our lab. Backgrnd in any of the following would be great: organic + supra-molecular chem, hydrogels, phase separation. Xperience in microscopy, rheology, UV-PL highly valued. More info by email or group website 👇1/2 Please share🙏