
Sachin Giri🇮🇳🇺🇲
@gsachin187
PhD Candidate, The University of Texas at Dallas | #PhotoChemistry #Methodologies #RadioChemistry | @GevorgyanLab | @SunLab
ID: 2180365826
07-11-2013 15:58:20
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294 Followers
827 Following


One-Pot Formal Carboradiofluorination of Alkenes: A Toolkit for Positron Emission Tomography Imaging Probe Development J. Am. Chem. Soc. Top Science #Chemistry #chemed #scicomm #news #Technology #Tech #NewsBreak #research #science #AcademicTwitter pubs.acs.org/doi/10.1021/ja…


Kudos to you and the team, Filo!! We can now have this paper presented in your fantastic course – Total Synthesis and Natural Products! Waiting to read more of these in the near future. Filippo Romiti J. Am. Chem. Soc.




Check out our new work, now out in Angewandte Chemie, featuring chemoselective hydropalladation of conjugated dienes/enynes over acrylic acids & amides to furnish lactones. This cascade annulation was conducted by Ziyan, who has joined Frances Arnold's lab as a postdoc. Congrats,Ziyan!



Check out our invited review on "Recent Advances in Visible Light Induced Palladium Catalysis"– Published in Angewandte Chemie today! Congratulations, Sumon and Kelvin! onlinelibrary.wiley.com/doi/10.1002/an…


+ Yusuf, Sashi Debnath. Thank you Chemistry at Thieme and the contributors!


***We are hiring!*** My group is looking for a postdoc with comp chem experience to join us at UT Dallas Chemistry from August '24. You can find out more about the position and submit your application here: jobs.utdallas.edu/postings/26587 Please share! #compchem


We're excited to share our work on C−H Oxygenation that is out in J. Am. Chem. Soc. today. This protocol utilizes Pd(0/I/II) manifold that allows a regio- and diastereoselective oxygenation of internal alkenes. Congrats Kyohei and Kelvin! Link: pubs.acs.org/doi/10.1021/ja…


We're excited to share our work on direct allylic C−H sulfonylation, now out in Angewandte Chemie. Building on to our Pd(0/I/II) manifold, a diverse set of cyclic and acyclic internal alkenes are covered with post-functionalization featuring formal alkene transposition!



Join us in congratulating Nikita and Valeriia for discovering a new reactivity of diazo compounds, undergoing branch-selective hydroalkylation with alkenes. Initial findings suggest a carbene-type mechanism which is unusual for nickel catalysis. Published today in J. Am. Chem. Soc.


