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TrustedReviews 01/23/2020 03:31
With Microsoft’s Surface Duo dual-screen Android smartphone due later this year, the company has opened up the device’s SDK (software development kit) to developers eager to see what’ll make it tick when it launches. “Today, developers can download the preview SDK for Surface Duo, access documentation and samples for best practices, see UX design patterns, […]. .
PR Newswire 01/23/2020 03:30
PUNE, India, Jan. 23, 2020 /PRNewswire/ -- The global semiconductor manufacturing equipment market size is projected to reach USD 119.00 billion by 2026, thereby exhibiting a CAGR of 8.0% during the forecast period. It is expected to gain impetus from the launch of advanced process...
insideHPC 01/23/2020 03:24
RJM International, a provider of emissions reduction and combustion improvement solutions, has deployed its first HPC cluster. The move supports the growth of the company’s business in the EU and the UK, particularly in the biomass and Energy from Waste segments of the market. The new HPC environment is designed, integrated and supported by HPC, storage and data analytics integrator, OCF. .
ForexLive 01/23/2020 03:24
Wuhan has been effectively quarantined in fears that the new coronavirus outbreak will become more widespread. ForexLive. Adds to the other stories surrounding the situation from earlier today. The suspension doesn't just apply to buses and ships, it is apparently for all passenger transportation routes involving roads and waterways, according to the Chinese ministry of transport.
An efficient chlorination of indoles and electron‐rich arenes with chlorine anion as nucleophile is described. With the use of ethyl phenyl sulfoxide as the promoter, the reaction went smoothly under metal‐free and mild conditions. Various indoles and electron‐rich arenes are converted into the corresponding chlorinated compounds in moderate to excellent yields. A plausible interrupted Pummerer reaction mechanism was proposed without the oxidation of chloride anion. In addition, the byproduct thioether could be easily converted to the starting material sulfoxide just by a simple oxidation reaction.
Abstract. The challenging bioamination of hydrophobic substrates has been attained through the employment of a disperse system consisting of a combination of a low polarity solvent (e.g. isooctane or methyl‐tert‐butylether), a non‐ionic surfactant and a minimal amount of water. In these conditions, amine transaminases (ATA) were shown to efficiently carry out the reductive amination of variously substituted cyclohexanones, providing good conversions often coupled with a superior stereoselectivity if compared with the corresponding chemical reductive amination. An array of synthetically useful 4‐substituted aminocyclohexanes was consequentially synthesized for the first time through biocatalysis, analyzed and stereochemically characterized.

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