A one-pot synthesis of dihydrobenzosiloles from styrenes has been developed. The reaction involves the nickel-catalyzed hydrosilylation of styrene with diphenylsilane, followed by the irridium-catalyzed dehydrogenative cyclization. This method is efficient for both electron rich and electron deficient styrenes, and exhibits good functional group tolerance, as well as excellent regioselectivity. The forming dihydrobenzosiloles can be efficiently converted into valuable benzosiloles or 2-hydroxyphenethyl alcohols.
We demonstrate an efficient conversion of highly-multimode (M2∼34) pump beam from fiber-combined 938-nm laser diodes into a 976-nm Stokes beam of high quality (M2=1.7-2 at output powers 10-52 W) that results in record brightness enhancement (BE=73) for Raman lasers based on graded-index fiber (GIF) and other fibers. The measured shapes of the output beams in GIF show that the near-parabolic pump beam becomes depleted above the Raman threshold so that the hole in the pump beam profile is much broader than the generated Stokes beam of near-Gaussian shape. The effect is analyzed in frames of a radially-dependent balance model with an account for the mode-selective feedback by FBG, which qualitatively describes the high-quality Stokes beam generation and the hole formation, but the hole width (and its power broadening) as well as the BE values are not consistent with experiment. Possible reasons for the difference are discussed.
Brönsted acid-catalyzed one-pot synthesis of indoles from o-aminobenzyl alcohols and furans has been developed. This method operates via the in situ formation of aminobenzylfuran, followed by its recyclization into the indole core. The method proved to be efficient for substrates possessing different functional groups, including -OMe, -CO2Cy, and -Br. The resulting indoles can easily be transformed into diverse scaffolds, including 2,3- and 1,2-fused indoles, and indole possessing an α,β-unsaturated ketone moiety at the C-2 position.