Qiang

Wuhan University

[Qiang @Qiang2048]

Thrilled to see our first independent research work published in @NatureSynthesis. We provided an alternative way for pyridine meta-halogenation. This time it's single step under mild conditions. For details: https://t.co/e1aaCORbvb

[Qiang @Qiang2048]

@javiml_94 Congrats Javier! Super fast and excellent research!

[Qiang @Qiang2048]

@junwu54104779 @NatureSynthesis Thanks

[Qiang @Qiang2048]

Thrilled to see our first independent research work published in @NatureSynthesis. We provided an alternative way for pyridine meta-halogenation. This time it's single step under mild conditions. For details: https://t.co/e1aaCORbvb

[Qiang @Qiang2048]

Free link available:
https://t.co/sLEb5RKxOl

[Nature Synthesis @NatureSynthesis]

Now online:

Article by Xiaotian Qi, Qiang Cheng @Qiang2048 & co-workers

Spin-density-controlled radical coupling for meta-selective C–H halogenation of pyridines

https://t.co/uEdr7lSNvC ($)

[Qiang @Qiang2048]

@javiml_94 @NatureSynthesis Thanks Javier

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

Formal meta-C–H-Fluorination of Pyridines and Isoquinolines through Dearomatized Oxazinopyridine Intermediates | Journal of the American Chemical Society @uni_muenster #CH #Fluorination #Pyridines #Isoquinolines #Oxazinopyridine @TotalSyntheses https://t.co/f2L0nXR203

[Qiang @Qiang2048]

@elvahupin Thanks😁😁

[Qiang @Qiang2048]

The first credit from Wiley. We thank Wiley-China for the certificate and encouragement. That's a good start!

[Qiang @Qiang2048]

@Michael16762400 谢谢😁

[Qiang @Qiang2048]

@Zibo_White 😁😁😁

[Universität Münster @uni_muenster]

Chemical synthesis: new strategy for skeletal editing on pyridines. A team led by Armido Studer @chem_pharm_ms realised “chemical surgery” on ring-shaped compounds / Results published in “Nature Chemistry”. https://t.co/dtLrMW6NaG & https://t.co/FX7Djzh92d

[Qiang @Qiang2048]

Last dance in Studer group. We use the redox-neutral activation strategy for pyridine editing.
https://t.co/c5TvE0qZEZ

[Universität Münster @uni_muenster]

Scientists led by Armido Studer from the Organic Chemistry Inst. have published in the @ScienceMagazine a strategy that could give a boost to the development of pyridine-containing drugs and organic functional materials.#chemistry https://t.co/r4C8Yv6bVz & https://t.co/fJEgqkZwNn

[Chemistry News @ChemistryNews]

Researchers solve the problem of functionalizing pyridine in the meta-position https://t.co/BZ4RDCZ22D

[Jake Yeston @JakeYeston]

In @ScienceMagazine this week, two groups report innovative ways of substituting pyridine at the 3-position--@AndyMcNally367 by temporary ring opening and Studer by reversible dearomatization https://t.co/3VYk5V0gnr
https://t.co/Ytij9StftG

[The Nobel Prize @NobelPrize]

BREAKING NEWS:
The Royal Swedish Academy of Sciences has decided to award the 2022 #NobelPrize in Chemistry to Carolyn R. Bertozzi, Morten Meldal and K. Barry Sharpless “for the development of click chemistry and bioorthogonal chemistry.”

[Qiang @Qiang2048]

New Journey to Synthesis of Multiple N-Heterocycles https://t.co/8HNQDmMQRg

[Yunus Turkmen @yunus_turkmen]

Very nice transformation developed by @ritter_lab on the construction of N-heterocycles directly from alkenes👇 @NatureChemistry

https://t.co/5Tpkc1QTjJ

[Chemistry News @ChemistryNews]

Bifunctional sulfilimines enable synthesis of multiple N-heterocycles from alkenes https://t.co/UOQV2Kdd41