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Unclogging the problems of flow chemistry

US scientists have found a way to stop solid byproducts clogging channels in continuous flow reactors, a problem that has hampered their progress for use in manufacturing pharmaceuticals.

Klavs Jensen, Stephen Buchwald and their team at the Massachusetts Institute of Technology believe that flow methods will become increasingly important in the future of pharmaceuticals and chemical manufacturing. ‘One of the biggest hurdles is handling solids,’ says group member Timothy Noël. ‘Precipitates can form during the reactions, which usually lead to irreversible clogging of microchannels in the reactors.’ Previous methods suggested to overcome this problem include introducing another solvent to dissolve the solids, but this can reduce the overall efficiency of the reactions. Now, the team have used an ultrasound bath to break up the byproducts to prevent clogging.

Traditionally, pharmaceutical manufacture is done in a batch-based system, but the process suffers from interruptions and the need to transport material between batch reactors. Performing these reactions in a continuous flow system would speed up the process and reduce chemical waste.

Unclogging the problems of flow chemistry

The team tested the method on palladium-catalysed C-N cross-coupling reactions, making amines that are common in biologically active molecules. The reactions couple aryl halides to nitrogen nucleophiles and form byproducts – inorganic salts – that are insoluble in the solvents used.

As a result, says Noël, they were able to obtain diarylamine products with reaction times ranging from 20 seconds to 10 minutes. At very short residence times (time in the reactor under reaction conditions) they observed a significantly higher rate for the reaction in flow compared to the equivalent batch experiments. With high conversions in short reaction times, they were able to reduce the catalyst loading in flow to just 0.1 mol per cent. ‘Extremely low catalyst loadings such as these are of particular interest to the pharmaceutical industry,’ says Noël.

Noël believes that in the future microfluidics will be used to construct increasingly complex molecules. Different devices will automate and integrate many synthetic steps that are currently performed using the more traditional and time-consuming batch-based practices.

Oliver Kappe, from the Christian Doppler Laboratory for Microwave Chemistry, Institute of Chemistry, Karl-Franzens-University Graz says: ‘Jensen and Buchwald clearly demonstrate that immersing a flow device into an ultrasound bath can prevent clogging problems that unfortunately are all too familiar to the flow/microreactor community.’

Sarah Corcoran

Find out more by downloading the Chemical Science Edge article.

Stephen Buchwald is Associate Editor for Chemical Science. Submit your exceptional organic research to him today to be seen with the best.

Also of interest: 
Continuous flow multi-step organic synthesis 
Damien Webb and Timothy F. Jamison 
Chem. Sci., 2010, 1, 675-680, DOI: 10.1039/C0SC00381F, Minireview

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ISACS 4 and 5- oral abstract deadline approaching

Time is running out to submit your oral abstracts for two ISACS meetings taking place in 2011.

Submit by 21st January 2011 for the opportunity to give an oral presentation at:

ISACS4 – Challenges in Renewable Energy (MIT, Boston, USA) and ISACS5 – Challenges in Chemical Biology (University of Manchester, UK).

For more information, visit the ISACS website.

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Total synthesis of diazonamide A

US chemists have developed a new highly stereoselective route to a natural product with potent anticancer properties.

David MacMillan and colleagues at Princeton University made the structurally challenging diazonamide A by exploiting three different types of catalysis – Lewis acid, transition metal and organocatalysis – in the key steps.

The principal challenge was stereoselectively installing the C(10) quaternary carbon stereocentre, explains MacMillan, as this aspect of the structure had not been successfully addressed in any of the three completed total syntheses. Using asymmetric iminium catalysis, the team efficiently synthesised the furanindoline core and C(10) centre with high stereoselectivity, which they believe is the most complex and challenging setting in which organocatalysis has been employed to date.

Graphical abstract: Total synthesis of diazonamide A 

Find out more by downloading MacMillan’s Chemical Science Edge article.

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New Associate Editor for Chemical Science

Wonwoo NamI am pleased to announce the appointment of a new Chemical Science Associate Editor: Professor Wonwoo Nam from the Department of Bioinspired Science at Ewha Womans University in Seoul, Korea. His research focuses on bioinorganic chemistry, including understanding the roles of metal ions in biological systems and biomimetic oxidation reactions.

Professor Nam’s editorial office is now open for submissions in the area of bioinorganic chemistry. We look forward to working with him and welcome him to his new role.

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Chameleon capsules bind anions selectively

UK chemists have created a new class of container molecules that can incorporate different functional groups on their exterior surface, much like a cell displays different biomolecules on its surface.

Jonathan Nitschke and colleagues at the University of Cambridge used subcomponent self-assembly to make tetrahedral metal-organic capsules with twelve exchangeable aniline residues at the vertices of the cage. The modular construction allows their exteriors to be tailored to suit a given environment and reconfigured in response to external stimuli, explains Nitschke. The capsules bind guest species with great selectivity, he adds.

Nitschke talks about this study and his ideas for future work in the latest Chemical Science audio file, which accompanies his Edge article.

For more information about container molecules, read Nitschke’s Chemical Science Mini review and his ChemComm communication, part of the ChemComm Emerging Investigators issue.

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Chemical Science Pacifichem Party

The Chemical Science party at Pacifichem on Saturday went down a storm, as the pictures below suggest. Managing Editor Robert Eagling, Editor-in-Chief David MacMillan and a number of Associate Editors celebrated the journal’s success with leading international researchers.
   

Were you there? Did you get a hot-off-the-press copy of Chemical Science Issue 1, 2011, or a much coveted Chemical Science baseball cap? Let us know your feedback below.

To play a part of the journal’s success in 2011, submit to Chemical Science today.

Photos reproduced with the permission of ACES XP

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Hot article roundup – November

flameHere in the UK we’ve been enduring the coldest start to winter since 1976. Thankfully, we published a great selection of hot Edge articles last month. As per all Chemical Science articles, they are free to access until the end of 2011.

Enjoy!

A ‘hole’ lot of mobility: Chi-Ming Che and colleagues report single crystal organoplatinum complexes with high charge mobility

Fingerprinting red wine: Eric Anslyn and colleagues have developed a sensor that can discriminate between different tannins and fingerprint a wide variety of red wines

Dinitrogen complexation with main group radicals: Spectroscopic evidence for weak but distinct interactions between several main group element radicals and physically dissolved dinitrogen in solution

New class of organic acceptors: A family of push–pull chromophores with a [4]dendralene backbone and a remarkably high propensity for reversible electron uptake

Carbene catalysts for group transfer: Gregory Hillhouse discusses the synthesis and carbene transfer reactivity of dimeric nickel bridging-carbene complexes

Building complex oxides layer-by-layer: Matthew Rosseinsky and colleagues exploit the capabilities of modern thin film deposition to grow an artificial metastable oxide

Carbenoids’ role in silver catalysis: Silver(I)-catalysed reactions of vinyldiazoacetates involve the intermediacy of silver-carbenoid species

Submit your own hot research to Chemical Science today.

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Metal-organic frameworks as nanostructure templates

Nanoporous metal-organic frameworks (MOFs) loaded with silver can serve as templates for ordered nanostructures, say US scientists.

Mark Allendorf, at Sandia National Laboratories, Livermore, and colleagues impregnated a MOF with silver then exposed the MOF to an electron beam. The beam broke down the template, leading to silver coalescence and the formation of ordered silver nanostructures.

The method forms either silver nanoparticles or nanowires depending on the MOF’s structure and the extent of silver loading, explains Allendorf.

Graphical abstract: Ordered metal nanostructure self-assembly using metal–organic frameworks as templates

Although the synthesis of silver nanowires and nanoparticles have been previously reported, this new route can generate structures with diameters less than 10 nanometres, which has previously been very challenging.

Allendorf’s Chemical Science Edge article is available to download for free.

Be seen with the best and submit to Chemical Science today.

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Stereoselective additions with a twist

A helical framework around an electrophilic centre is an effective control element for the stereoselective addition of nucleophiles, according to European scientists.

Stereoselective additions of nucleophiles to trivant carbon atoms are common organic reactions. Chemists often rely on stereogenic elements close to the reactive centres to influence the stereochemical outcome. For example, nucleophiles can preferentially add to one of the two diastereotopic faces of a carbenium ion when there is an α-stereocentre.

Now Jérome Lacour, at the University of Geneva, Switzerland, and colleagues have shown that nucleophiles can also distinguish between the diastereotopic faces of chiral cationic helicenes. Using hydride and organolithium reagents, the group achieved diastereomeric ratios higher than 49:1.

Graphical abstract: Highly selective additions of hydride and organolithium nucleophiles to helical carbenium ions

More information can be found in Professor Lacour’s Edge article.

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Metal free catalysts for aliphatic C-H bond oxidation

Metal-free polymers have the potential to replace toxic metal catalysts in hydrocarbon oxidation reactions, according to an international team of chemists.

Yong Wang, at the Max-Planck Institute of Colloids and Interfaces, Potsdam, Germany, and colleagues replaced some of the carbon atoms in graphitic carbon nitride with boron. The resulting polymeric material was better than previous biomimetic homogeneous oxidation catalysts at oxidising substituted aromatics.

Graphical abstract: Synthesis of boron doped polymeric carbon nitride solids and their use as metal-free catalysts for aliphatic C–H bond oxidation

Oxidations of sp3 hybridised C-H bonds are challenging because the oxidised products are more reactive than the starting materials and so they tend to over-oxidise. This was not a problem for Wang’s catalyst, which was highly selective at forming ketones or aldehydes.

For more information, download Wang’s Edge article for free.

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