Total Synthesis of Lignan Lactone (-)-Hinokinin.

This research paper is aimed at studying the total synthesis of pharmacologically active lignan (-)-hinokinin. The synthesis features a three-step cascade reaction involving highly stereoselective Michael addition, anion-oxidative hydroxylation, and oxygen anion cyclization to construct the pivotal butyrolactonimidate intermediate.

Linear dislocation tunes chirality: STM study of chiral transition and amplification in a molecular assembly on an HOPG surface.

Molecular arrangement and transition in the domain boundary of a chiral two-dimensional assembly is clearly revealed by high-resolution STM images on an HOPG surface and a linear dislocation formed by molecular trimers and located at opposite chiral domains is found to directly reverse the chirality on DTCD self-assembly.