Nicolò Tampellini (@ntampellini_) 's Twitter Profile
Nicolò Tampellini

@ntampellini_

PhD student @MillerGroupYale 🇺🇸
B. Sc. @LabSynthesis 🇮🇹
Asymmetric catalysis with flasks and computers ⚗️💻

ID: 1443918675510239264

linkhttps://ntampellini.github.io/ calendar_today01-10-2021 12:40:33

128 Tweet

133 Followers

107 Following

Nicolò Tampellini (@ntampellini_) 's Twitter Profile Photo

Take a look at our latest in case you don't want to resolve your modafinil analogs😉Led by @se_huth and together with Maria. Computational modeling revealed why the apparently floppy (but broadly successful!) class of Asp-derived catalysts achieve high levels of selectivity.

Take a look at our latest in case you don't want to resolve your modafinil analogs😉Led by @se_huth and together with Maria. Computational modeling revealed why the apparently floppy (but broadly successful!) class of Asp-derived catalysts achieve high levels of selectivity.
Nicolò Tampellini (@ntampellini_) 's Twitter Profile Photo

Ken Wiberg is an absolute physical organic pioneer that left us many concepts and achievements - from a physical organic description of KIEs, to molecular tortures leading to [1.1.1]propellane, to applying computational tools to molecular modeling. Needless to say, so honored!🙏

Nicolò Tampellini (@ntampellini_) 's Twitter Profile Photo

One, two, or three? When trying to get a computational estimate of equilibrium data, which approach do you take? Why? I have the feeling there is not as much consensus on this as I thought in the past, and we have a learning opportunity :)

One, two, or three? When trying to get a computational estimate of equilibrium data, which approach do you take? Why? I have the feeling there is not as much consensus on this as I thought in the past, and we have a learning opportunity :)
Yale Chemistry (@yalechem) 's Twitter Profile Photo

Congrats to Brandon Mercado B. Q. Mercado , our X-ray crystallographer! He received the Lorimer Award for helping to bring MicroED to Yale, positioning the university as a leader in this transformative new method for chemical structural analysis. bit.ly/3CtueHP

Congrats to Brandon Mercado <a href="/Fullerene/">B. Q. Mercado</a> , our X-ray crystallographer! He received the Lorimer Award for helping to bring MicroED to Yale, positioning the university as a leader in this transformative new method for chemical structural analysis. bit.ly/3CtueHP
kazuhiro morisaki (@kmorisakic) 's Twitter Profile Photo

Conceptually new asymmetric transformation—Reflexive Chirality Transfer (RCT)— appeared in ChemRxiv (go.shr.lc/3Z3f03N). 1,3-Dipolar cycloaddition of amino acid Schiff bases proceeds with "preserving chirality" despite the once loss of the chirality at the α-carbon.

Conceptually new asymmetric transformation—Reflexive Chirality Transfer (RCT)— appeared in <a href="/ChemRxiv/">ChemRxiv</a> (go.shr.lc/3Z3f03N).
1,3-Dipolar cycloaddition of amino acid Schiff bases proceeds with "preserving chirality" despite the once loss of the chirality at the α-carbon.
Angewandte Chemie (@angew_chem) 's Twitter Profile Photo

Cationic, Iodine(III)-Mediated and Directed Diastereoselective Oxidation of Inert C-H Bonds in Cyclic Hydrocarbons (Nuno Maulide and co-workers) MaulideGroup #openaccess 🔓 onlinelibrary.wiley.com/doi/10.1002/an…

Baran Lab (@baranlabreads) 's Twitter Profile Photo

🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in ChemRxiv (chemrxiv.org/engage/chemrxi…) the first method for stereoretentive radical cross-coupling is disclosed. No fancy ligands or redox needed—just a Ni-diazene twist. 120 years after Gomberg, a new chapter

🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in <a href="/ChemRxiv/">ChemRxiv</a> (chemrxiv.org/engage/chemrxi…) the first method for stereoretentive radical cross-coupling is disclosed. No fancy ligands or redox needed—just a Ni-diazene twist. 120 years after Gomberg, a new chapter
kazuhiro morisaki (@kmorisakic) 's Twitter Profile Photo

Simple yet Efficient New Method for Direct Site-selective Deoxygenation of Benzylalcohol Derivatives is now out in ChemRxiv (go.shr.lc/4iLL6JI)

Simple yet Efficient New Method for Direct Site-selective Deoxygenation of Benzylalcohol Derivatives is now out in <a href="/ChemRxiv/">ChemRxiv</a> (go.shr.lc/4iLL6JI)