Recent advances in chiral sulfide-catalyzed asymmetric halocyclizations are summarized.
This review systematically discusses the last two-decade advances in asymmetric CO2 fixation including chemical, electrochemical and photochemical pathways.
This review explores MOFs, COFs, and POPs as advanced framework materials for the efficient conversion of CO2 into bioactive oxazolidinones.
Chiral tertiary-amine catalysts with a urea group can afford 3-substituted isoindolinones both in higher yields (87% vs. 77%) and enantioselectivities (95% ee vs. 46% ee) than chiral bifunctional phase-transfer catalysts under mild conditions.
This review has summarized the development of organocatalytic asymmetric [3 + 3] cycloadditions and given insights into the remaining challenges to promote the future development of this field.