Inner-Bond-Cleavage Approach to Figure-Eight Macrocycles from Planar Aromatic Hydrocarbons.

Figure-eight-shaped nonplanar π-systems adopt distinctive chiral -symmetric structures, which are ideal for realizing efficient circularly polarized luminescence (CPL). However, the short-step and enantioselective synthesis of figure-eight π-systems represents a considerable challenge for the conventional bottom-up synthetic strategy. Herein, we report that the oxidative cleavage of the internal double bond of a commercially available polycyclic aromatic hydrocarbon, i.

Expanded [2,1][]Carbohelicenes with 15- and 17-Benzene Rings.

Expanded carbohelicenes with structures fused to 15- and 17-benzene were successfully synthesized. Establishing a new synthetic strategy is crucial to realize the development of longer expanded [2,1][]helicenes with a kekulene-like projection drawing structure. This article describes the sequential integration of the π-elongating Wittig reaction of functionalized phenanthrene units and ring-fusing Yamamoto coupling for the synthesis of [2,1][15]helicenes and [2,1][17]helicenes.

Clinical characteristics of hidradenitis suppurativa patients in Okinawa, Japan: Differences between East Asia and Western countries.

Hidradenitis suppurativa (HS) is a long-term inflammatory follicular disease. In Western countries, the prevalence of HS has been estimated to be 0.1-4% in the general population.