WebMay 21, 2024 · employed as versatile coupling reagents for the construction of multifunctional chiral bicyclo [3.2.1]octanes with one all-carbon quaternary and two tertiary carbon stereogenic centers in high ... WebMay 21, 2024 · Various bicyclo [3.2.1]octanes bearing one chiral all-carbon quaternary and two tertiary carbon stereogenic centers were obtained in moderate to good yields with …
chirality - How is the cavity of a cyclodextrin chiral? - Chemistry ...
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Synthesis of Enantioenriched α-Chiral Bicyclo[1.1.1]pentanes
WebOct 2, 2014 · An enantio- and diastereoselective organocatalytic domino Michael/Aldol reaction for the direct preparation of synthetically and medicinally relevant bicyclo[3.2.1]octane derivatives with four stereogenic centers, including two quaternary carbons, has been described. The reaction tolerates a large variety of substituents on β,γ … WebFeb 1, 2024 · A similar strategy was reported by Duan and co-workers [13] where a pair of complementary systems afforded both R and S enantiomers of P-stereogenic dibenzophospholes 11 through intramolecular asymmetric C–H bond activation by Pd-complexes.Chiral phosphoric acid 8 together with chiral phosphoramidate ligand 9 led … WebApr 5, 2024 · Bicyclo[1.1.1]pentanes (BCPs), useful surrogates for para-substituted arenes, alkynes, and tert-butyl groups in medicinal chemistry, are challenging to prepare when featuring stereogenic centers adjacent to the BCP. We report the development of an efficient route to α-chiral BCPs, via highly diaster … ray morris hall