A Fully Automated Continuous Flow Synthesis of 4,5-Disbustituted Oxaxoles

A Fully Automated Continuous Flow Synthesis of 4,5-Disbustituted Oxaxoles 
M. Baumann, I.R. Baxendale, S.V. Ley, C.D. Smith and G.K. Tranmer, Org. Lett. 2006, 8, 5231-5234.
 http://pubs.acs.org/doi/abs/10.1021/ol061975c

 A multipurpose mesofluidic flow reactor capable of producing gram quantities of material has been developed as an automated synthesis platform for the rapid on-demand synthesis of key building blocks and small exploratory libraries. The reactor is configured to provide the maximum flexibility for screening of reaction parameters that incorporate on-chip mixing and columns of solid supported reagents to expedite the chemical syntheses.

Versatile, High Quality and Scalable Continuous Flow Production of Metal-Organic Frameworks

The precursor solutions are pumped continuously, mixed via a static-mixer (T-piece) and 

enter the coiled reactor tubes at temperature (T). A backpressure regulator (BPR) situated

after the reactor coil is used to maintain a constant liquid pressure. 

The residence time can be varied by changing the length of the reactor or pumping rates.

Figure 1: Schematic representation showing the general flow reactor

 setup for the production of MOFs.

http://www.nature.com/srep/2014/140625/srep05443/full/srep05443.html#f1

Further deployment of Metal-Organic Frameworks in applied settings 
requires their ready preparation at scale. Expansion of typical batch
 processes can lead to unsuccessful or low quality synthesis for some 
systems. Here we report how continuous flow chemistry can be
 adapted as a versatile route to a range of MOFs, by emulating 
conditions of lab-scale batch synthesis. This delivers ready 
synthesis of three different MOFs, with surface areas that 
closely match theoretical maxima, with production rates 
of 60 g/h at extremely high space-time yields.

Synthesis of Acetal Protected Building Blocks using Flow Chemistry and Flow I.R. Methods: Preparation of Butane 2, 3- Diacetal Tartrates

Synthesis of Acetal Protected Building Blocks using Flow Chemistry and Flow I.R. Methods: Preparation of Butane 2, 3- Diacetal Tartrates 

C.F. Carter, I.R. Baxendale, M. O’Brien, J.B.J. Pavey, S.V. Ley, Org. Biomol. Chem. 2009, 7, 4594.

http://pubs.rsc.org/en/Content/ArticleLanding/2009/OB/b917289k#!divAbstract
http://www.rsc.org/suppdata/ob/b9/b917289k/b917289k.pdf

Catherine F. Carter,^a   Ian R. Baxendale,^a   Matthew O'Brien,^a  John B. J. Pavey^b and   Steven V. Ley*^a  

*

Corresponding authors

^a

Department of Chemistry, Innovative Technology Centre, University of Cambridge, Lensfield Road, Cambridge, UK
E-mail: svl1000@cam.ac.uk

^b

AstraZeneca, Bakewell Road, Loughborough, Leics, UK

The syntheses of butane-2,3-diacetal protected tartrate derivatives are described using continuous flow processing techniques with in-line purification and I.R. analytical protocol
.................

Acceptorless dehydrogenative coupling of primary alcohols to esters by heterogeneous Pt catalysts

Catal. Sci. Technol., 2014, 4,3631-3635
DOI: 10.1039/C4CY00979G, Communication

Sondomoyee Konika Moromi, S. M. A. Hakim Siddiki, Md. Ayub Ali, Kenichi Kon, Ken-ichi Shimizu
Pt/SnO₂ is presented as the first example of a reusable heterogeneous catalyst for acceptorless dehydrogenative coupling of primary alcohols to esters under additive-free and solvent-free conditions.



 Supported platinum catalysts have been studied for the acceptor-free dehydrogenative 
coupling of primary alcohols to esters in the liquid phase under solvent-free conditions in N₂ at 180 °C. 
The activity depends on the support material, and Pt-loaded SnO₂ (Pt/SnO₂) gives the highest activity. Pt/SnO₂ shows higher activity than various transition metals
 (Ir, Re, Ru, Rh, Pd, Ag, Co, Ni, Cu) loaded on SnO₂. The Pt/SnO₂  
catalyst (1 mol%) selectively converted various primary alcohols to their corresponding esters in moderate to 
high isolated yield (53–91%). This is the first example of reusable heterogeneous catalysts for the acceptor-free dehydrogenative coupling of primary alcohols to esters 
under additive-free and solvent-free conditions. Mechanistic and infrared
 (IR) studies are also shown to discuss the reaction pathway and a possible role of the SnO₂ support as Lewis acid sites that activate carbonyl groups of adsorbed aldehyde intermediates.

Acceptorless dehydrogenative coupling of primary alcohols to esters by heterogeneous Pt catalysts

Sondomoyee Konika Moromi,^a   S. M. A. Hakim Siddiki,^b  Md. Ayub Ali,^a   Kenichi Kon^a and   Ken-ichi Shimizu*^ab  

*

Corresponding authors

^a

Catalysis Research Center, Hokkaido University, N-21, W-10, Sapporo 001-0021, Japan 
E-mail: kshimizu@cat.hokudai.ac.jp;
Fax: +81 11 706 9163

^b

Elements Strategy Initiative for Catalysts and Batteries, Kyoto University, Katsura, Kyoto 615-8520, Japan

Catal. Sci. Technol., 2014,4, 3631-3635

DOI: 10.1039/C4CY00979G

read

 http://pubs.rsc.org/en/Content/ArticleLanding/2014/CY/C4CY00979G?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+rss%2Fcy+%28RSC+-+Catalysis+Science+%26+Technology+latest+articles%29#!divAbstract



 MAKE IN INDIA
http://makeinindia.com/
http://makeinindia.com/sector/pharmaceuticals/

A Catalyst That Multitasks To Make Complex Molecules Organic Synthesis: Method leads to complex, biologically relevant molecules on gram scale

A copper catalyst guides this multicomponent reaction. 

A new synthetic strategy that relies on a multitasking copper catalyst allows chemists to construct useful molecules faster and with higher yield. Experts say it promises to fast-track complicated syntheses.

Fewer steps in a chemical synthesis often translate to a better yield of the final product. Chemists therefore prize so-called multicomponent reactions that orchestrate the assembly of multiple building blocks into a complex structure in a single stroke.

Boston College chemists Amir H. Hoveyda, Fanke Meng, and Kevin P. McGrath demonstrate their virtuosity in this regard by using an inexpensive copper catalyst that puts together complex molecules from an allene, a diboron reagent, and an allylic phosphate. The resulting products contain a stereogenic carbon center, a monosubstituted alkene, and a tough-to-synthesize Z-trisubstituted alkenylboron (Nature 2014, DOI: 10.1038/nature13735).

 READ AT

http://cen.acs.org/articles/92/i38/Catalyst-Multitasks-Make-Complex-Molecules.html

Metal-free coupling of saturated heterocyclic sulfonylhydrazones with boronic acids

Metal-free coupling of saturated heterocyclic sulfonylhydrazones with boronic acids 

Daniel M. Allwood *†, David C. Blakemore ‡, Alan D. Brown ‡, and Steven V. Ley †

† Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, U.K.

‡ Neusentis Chemistry, Pfizer Worldwide Research and Development, The Portway Building, Granta Park, Cambridge, CB21 6GS, U.K.

J. Org. Chem., 2014, 79 (1), pp 328–338

DOI: 10.1021/jo402526z

http://pubs.acs.org/doi/abs/10.1021/jo402526z

The coupling of aromatic moieties with saturated heterocyclic partners is currently an area of significant interest for the pharmaceutical industry. Herein, we present a procedure for the metal-free coupling of 4-, 5-, and 6-membered saturated heterocyclic p-methoxyphenyl (PMP) sulfonylhydrazones with aryl and heteroaromatic boronic acids. This procedure enables a simple, two-step synthesis of a range of functionalized sp2–sp3 linked bicyclic building blocks, including oxetanes, piperidines, and azetidines, from their parent ketones.

Flow chemistry syntheses of natural products

 Flow chemistry syntheses of natural products ..click here

J.C. Pastre, D.L. Browne, S.V. Ley, Chem. Soc. Rev. 2013, 42, 8801-9198.

The development and application of continuous flow chemistry methods for synthesis is a rapidly growing area of research. In particular, natural products provide demanding challenges to this developing technology. This review highlights successes in the area with an emphasis on new opportunities and technological advances.

read

http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/c3cs60246j#!divAbstract