Abstract:The direct γ-C(sp3)-H activation of saturated α-keto esters has long been an elusive transformation. We found that photo-redox catalysis IrIII in combination with DABCO as dual hydrogen-bonding donor and organic...
“…The absolute configuration of 8a was assigned to be R based on a previous report. 11 Based on the same plausible mechanism analysis, the stereochemistry of the other products 8 was assigned by analogy.…”
Section: Resultsmentioning
confidence: 99%
“…10 However, due to the high reactivity of indoles 6 and β,γ-unsaturated α-ketoesters 7 , low reaction temperatures were generally applied to ensure high stereoselectivity of the reactions. 11 It is desirable to develop new and effective asymmetric synthetic protocols, which can be easily handled and operated under mild conditions.…”
This work diversified the Py-2NO ligand library recently developed by our group and further expanded the application of chiral Py-2NO ligands in asymmetric catalysis.
“…The absolute configuration of 8a was assigned to be R based on a previous report. 11 Based on the same plausible mechanism analysis, the stereochemistry of the other products 8 was assigned by analogy.…”
Section: Resultsmentioning
confidence: 99%
“…10 However, due to the high reactivity of indoles 6 and β,γ-unsaturated α-ketoesters 7 , low reaction temperatures were generally applied to ensure high stereoselectivity of the reactions. 11 It is desirable to develop new and effective asymmetric synthetic protocols, which can be easily handled and operated under mild conditions.…”
This work diversified the Py-2NO ligand library recently developed by our group and further expanded the application of chiral Py-2NO ligands in asymmetric catalysis.
As phenanthroline (phen) possesses great coordination ability with various ions, the development of new chiral phen ligands is in great demand in asymmetric catalysis. Herein, we rationally designed and developed...
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