New publication in JACS! https://t.co/as8q677d2D Congratulations to the Dydio group for the excellent piece of work! ValleyPhos rocks! Great Collaboration!
Recent advances in transition metal-catalyzed organic transformations using hemilabile P,P=O ligands - now published in Organic Chemistry Frontiers https://t.co/nMz7SzdkHD The future is bright for hemilabile P,P=O ligands in asymmetric catalysis and thank Professor Zhenming Zhang's tremendous job!
Asymmetric Reductive Cross-Coupling of Aldimines | Organic Letters https://t.co/AD6wOkqHAu Congratulations to Yuhao for developing cross-coupling of aldimines templated by chiral diboron!
Enantioselective Ruthenium-Catalyzed Hydrogenation of Substituted 3-Acylamino Pyridinium Salts | ACS Catalysis https://t.co/a00COmIJ6t Interesting findings on Ru-catalyzed AH of pyridinium salts with good practicality and surprising mechanism! Thanks Wang Nan's great efforts!
Chiral 2,3‐Dihydrobenzo[d][1,3]oxaphosphole Ligands - Zhu - Major Reference Works - Wiley Online Library https://t.co/X5N1vLm7Op Our ligands are in collection of EROS.
The AntPhos #ligands allow for efficient metal-catalyzed cross-coupling and asymmetric cyclization reactions. #chemistry#ligand https://t.co/9TvljDLxcS
Just out in #OrgLett from @WenjunTangLab & @janssen
colleagues, an unprecedented deuterated monophosphorus ligand CD3-AntPhos is shown to be effective for enantioselective C-H arylation under mild conditions at low palladium loadings. Please have a look: https://t.co/BLpfwDF1Bb
Efficient Synthesis of (-)-Corynoline by Enantioselective Palladium-Catalyzed alpha-Arylation with Sterically Hindered Substrates (Tang) https://t.co/mK2KEnKEkq
kang Du
@kangdu12
Our recent work in Chem. Sci. ( Tang group @WenjunTangLab at SIOC /HIAS, Chen at ECUST, and us ) on Acyl-oxyallenes as α, β-Unsaturated Ketone Surrogates for Giese Radical Addition.https://t.co/rYsTdV7umR
Copper-catalyzed cyclizative aminoboration for chiral substituted piperidines! Congratulations to Dazhuang and thank Professor Qinghai Zhou for the excellent collaboration! https://t.co/F9igJD5hxd
"Hours spent on chemical reactions can’t be recycled. Let’s make sure we conserve the ultimate nonrenewable resource" -- couldn’t agree more.
https://t.co/J5qgXhGOrR
Check our recent work in Org. Lett. ( Tang group at SIOC /HIAS, Smith group at Oxford, and us ) on construction of cage-like frameworks by sequential [2+2] cycloaddition.https://t.co/O00vfT4omG