Shubham Deolka

Post-Doctorate, Soccer is my pain killer !!!!
Synthetic Chemist/DATA SCIENCE - Multimetallic, Pincer chemistry, Photochemistry, Fluorine Fun !!

[Yulab @YulabJin]

Sp3 Methylene CH coupling with heteroaryls has been limited (really annoying for medichemists). With bifunctional pyridone ligands and new mechanism via Pd(II)/Pd(0), we made a big stride: https://t.co/krVnNkj1Y2

[Clément Ghiazza @ClementGhiazza]

❗New ChemRxiv❗A Nitrogen atom insertion strategy into benzimidazoles that lifts a longstanding bottleneck in the synthesis of 1,2,4-triazines. This work highlights the potential of Skeletal Editing as a powerful synthetic tool for accessing rare heterocyclic scaffolds.

[Nature Catalysis @NatureCatalysis]

Unlocking the Cu-catalysed asymmetric radical azidation of N-heterobenzylic sites through rational ligand design https://t.co/DRKWQcbJWN

[Wang Lab@SIOC @pengwanglab]

Nickel‐Catalyzed 1,2‐Arylalkenylation of Unactivated Alkenes Enabled by a Native Hydroxy Group - Wang - Angewandte Chemie International Edition - Wiley Online Library https://t.co/4TqEwKjpA3

[Boron-Chem-Research @Boron_Chemistry]

Activation-Reactivity Inversion in Au(I)-Complex-Photocatalyzed Borylation of Aryl Chlorides ( @ACSCatalysis ): https://t.co/FYymo4RYrN

[Jacsol Joc @jacsoljoc]

https://t.co/nSbl6wkeEz

[J. Am. Chem. Soc. @J_A_C_S]

N-Aryl-BIP Ligand-Enabled Iron-Catalyzed Asymmetric Synthesis of β-Amino Free Alcohols from Alkenes | Journal of the American Chemical Society https://t.co/q6FfUW2o33

[Jacsol Joc @jacsoljoc]

https://t.co/j0MunDr32w

[Xinglong Zhang @XZhangChem]

Happy to share two recent productive collaborative works with Professor Jun (Joelle) Wang at HKBU published in @J_A_C_S and @angew_chem! In the first one, we found that using different acid additives can modulate regioswitching by having different acid binding modes to Ni

[Ramesh Rasappan Lab @rr_lab]

A proud milestone for @rr_lab - our first JACS publication! Heartiest congratulations to Chandru, Bincy, Sanjai, Sheryl & Venkadesh for this remarkable achievement and well-deserved success. 👏✨https://t.co/7VrDqGcCUD
@rr_prof @Chemie_iisertvm @tvmiiser

[SUSTech 南方科技大学 @SUSTechSZ]

🧪Breaking breakthrough in asymmetric photocatalysis!
#SUSTech researchers developed a novel Relay Energy Transfer photocatalysis paradigm, with findings published in @ScienceMagazine.✨
Read more: https://t.co/KhbzWcqaN7

[Ohmiya Lab @OhmiyaLab]

Our work on deep-red/NIR light-driven Ni-catalyzed C(sp²)–C(sp³) cross-coupling has been published in ACS Catalysis (@ACSPublications). Congrats Kanji and Yusuke! https://t.co/pShlhMynY1

[J. Am. Chem. Soc. @J_A_C_S]

Enantioselective Nickel-Catalyzed Cross-Dehydrogenative Coupling of Aldehydes and Alkenes toward Skipped Enones | Journal of the American Chemical Society https://t.co/IMzwrGOUsA

[Wang Lab@SIOC @pengwanglab]

With a bulky 1,3-diketone ligand, a nickel-catalyzed remote substitution of unprotected alkenyl alcohols with arylboronic acids has been realized, enabling distal C–C bond formation directly from native alcohols. Just out @J_A_C_S | https://t.co/o5c54hNJ98

[Luo Yun @tomluoyun]

Excited to share our new publication in @J_A_C_S, wherein formal carbonyl insertion was achieved at the para or ortho position of pyridines, enabling access to 1,4- or 1,2-azepinones, which could be smoothly downstreamed into bicyclic pyrrolidinones. https://t.co/6tJtWm8R3K

[Jacsol Joc @jacsoljoc]

https://t.co/pRFxrrLfRX

[⏣🈶機の🈴成屋さん⌬ @yuukinogouseiya]

今週の⌬🈶機🈴成系⌬の論文

from 𝐧𝐚𝐭𝐮𝐫𝐞
https://t.co/Zw3JheQoVT (アルケンをアルキンに直接変換)

from 𝐒𝐜𝐢𝐞𝐧𝐜𝐞
https://t.co/G04ryF2LIy (太陽熱エネルギー貯蔵分子)
https://t.co/5pvbCuew4G (フェロセンカーボンフリーアナログ)
https://t.co/6FyKEQnHc2 (不斉C–Hアミノ化)

[GrykoGroup @GroupGryko]

🚀Can CO2 radical anion be a reductant for ConPET process?
Here is our recent @ChemRxiv on "Adaptive Photocatalytic Regimes Enabled by CO2•− and ConPET Synergy"
Excellent work done by @SMChem_ & @Shantanu_JUchem 🥂
🔗Read here:👇
https://t.co/6JXt4im2IK

[Murakami Lab @LabMurakami]

Congrats, Shumpei, Takumi, and Yota! We report "The Synthesis of Tertiary Alkylamines from Alkyl-Substituted Alkenes Using Amine Umpolung Strategy" in J. Am. Chem. Soc. @J_A_C_S https://t.co/fSLVuJpGaI

[nagib lab @nagiblab]

If you like harnessing carbenes from di-chlorides, you’ll LOVE skeletal editing with tri-chlorides!

Congrats to Bethany, Hojin, Victoria, and our collaborators from Chicago (Ethan & Mark Levin) and California (Anna, Zhang & Dave Olson)!

Open access: https://t.co/XKCX5ba0ry