https://www.selleckchem.com/products/GDC-0941.html Molecular balances based on the dibenzobicyclo[3.2.2]nonane template enable probing of the competition between halogen-π and CH-π interactions. Structural, NMR spectroscopic, and computational analyses revealed that the π system can favorably interact both with C-X or C-H functionalities, depending on the size of the functional group.Synthesis of bacterial cell surface l-glycero-d-manno-heptose (l,d-Hep)- and d-glycero-d-manno-heptose (d,d-Hep)-containing higher carbon sugars is a challenging task. Here, we report a convenient and efficient approach for the synthesis of the l,d-Hep and d,d-Hep building blocks. Using l-lyxose and d-ribose as starting materials, this approach features diastereoselective Mukaiyama-type aldol reactions as the key steps. On the basis of the synthetic l,d-Hep and d,d-Hep building blocks, we achieved the first stereoselective synthesis of the unique α-l,d-Hep-(1→3)-α-d,d-Hep-(1→5)-α-Kdo core trisaccharide of the lipopolysaccharide of Vibrio parahemolyticus O2.Hybrid organic-inorganic perovskites (HOIPs) with chiral organic ligands exhibit highly spin-dependent transport and strong natural optical activity (NOA). Here we show that these remarkable features can be traced to a chirality-induced spin-orbit coupling (SOC), Hso = ατk z σ z , which connects the carrier's spin (σ z ), its wave vector (k z ), and the material's helicity (τ) along the screw direction with strength α controlled by the geometry of the organic ligands. This SOC leads to a macroscopic spin polarization in the presence of an electrical current and is responsible for the observed spin-selective transport. NOA originates from a coupling between the exciton's center-of-mass wave vector K z and its circular polarization j z ex, Hso' = α'τK z j z ex, contributed jointly from the electron's and the hole's SOCs in an exciton. Our model provides a roadmap to achieve a strong and tunable chirality in HOIPs for novel applications