Environmental exposures impact gamete function and fertility, but the mechanisms are poorly understood. Here we show that pheromones sensed by ciliated neurons in the C. elegans nose alter the lipid microenvironment within the oviduct, thereby affecting sperm motility. In favorable environments, pheromone-responsive sensory neurons secrete a TGF-β ligand called DAF-7, which acts as a neuroendocrine factor that stimulates prostaglandin-endoperoxide synthase (Cox)-independent prostaglandin synthesis in the ovary. Oocytes secrete F class prostaglandins that guide sperm toward them. These prostaglandins are also synthesized in Cox knockout mice, raising the possibility that similar mechanisms exist in other animals. Our data indicate environmental cues perceived by the female nervous system affect sperm function.

Mild conditions are reported for the hydroxylation of aliphatic C-H bonds through radical translocation, oxidation to carbocation, and nucleophilic trapping with H2O. This remote functionalization employs fac-[Ir(ppy)3] together with Tz(o) sulfonate esters and sulfonamides to facilitate the site-selective replacement of relatively inert C-H bonds with the more synthetically useful C-OH group. The hydroxylation of a range of substrates and the methoxylation of two substrates through 1,6- and 1,7-hydrogen-atom transfer are demonstrated. In addition, a synthesis of the antidepressant fluoxetine using remote hydroxylation as a key step is presented.

The nematode Caenorhabditis elegans secretes ascarosides, structurally diverse derivatives of the 3,6-dideoxysugar ascarylose, and uses them in chemical communication. At high population densities, specific ascarosides, which are together known as the dauer pheromone, trigger entry into the stress-resistant dauer larval stage. In order to study the structure-activity relationships for the ascarosides, we synthesized a panel of ascarosides and tested them for dauer-inducing activity. This panel includes a number of natural ascarosides that were detected in crude pheromone extract, but as yet have no assigned function, as well as many unnatural ascaroside derivatives. Most of these ascarosides, some of which have significant structural similarity to the natural dauer pheromone components, have very little dauer-inducing activity. Our results provide a primer to ascaroside structure-activity relationships and suggest that slight modifications to ascaroside structure dramatically influence binding to the relevant G protein-coupled receptors that control dauer formation.

Mild conditions are reported for the hydroxylation of aliphatic CH bonds through radical translocation, oxidation to carbocation, and nucleophilic trapping with H2O. This remote functionalization employs fac‐[Ir(ppy)3] together with Tzo sulfonate esters and sulfonamides to facilitate the site‐selective replacement of relatively inert CH bonds with the more synthetically useful COH group. The hydroxylation of a range of substrates and the methoxylation of two substrates through 1,6‐ and 1,7‐hydrogen‐atom transfer are demonstrated. In addition, a synthesis of the antidepressant fluoxetine using remote hydroxylation as a key step is presented.

Remote Hydroxylation Through Radical Translocation and Polar Crossover. -The site-selective replacement of relatively inert aliphatic C-H bonds with the hydroxy group is facilitated by employing the photocatalyst together with sulfonate esters and sulfonamides and involves a radical translocation, oxidation to carbocation, and nucleophilic trapping with H 2O under mild reaction conditions. The methoxylation of two substrates is also demonstrated. -(HOLLISTER, K. A.; CONNER, E. S.; SPELL, M. L.; DEVEAUX, K.; MANEVAL, L.; BEAL, M. W.; RAGAINS*, J. R.; Angew. Chem., Int. Ed. 54 (2015) 27, 7837-7841, http://dx.doi.org/10.1002/anie.201500880 ; Dep. Chem., La. State Univ., Baton Rouge, LA 70803, USA; Eng.) -Toeppel 43-044

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