The halex reaction is a great way to introduce a fluorine atom in to an aromatic ring, but the reaction often requires high temperatures and or long reaction times if metal fluorides are used. Tetralkylammonium fluorides are a better option due to their higher solubility in the reaction medium, however these salts are often hydrated
Month: July 2017
How many named organic reactions do you think we can find in biological systems? 10-20, 20-30, 30-40, or 40-50? The answer can be found in this review in Angewandte¹. C.-I. Lin, R.M. McCarty, and H.-w. Liu, Angew. Chem. Int. Ed., 2017, 56, 3446-3489.
Cyanation of aromatic/heteroaromatic halides/pseudohalides is still not always a straightforward transformation, especially if the reaction needs to be scaled up. 2 Ar-X + Zn(CN)2 ® 2 ArCN + ZnX2 Workers at BMS have recently published a paper where they describe an improved protocol for this transformation1. They found that Pd2(dba)3 with XantPhos, Zn(CN)2 and i-Pr2NEt
Oxazoles are relatively common heterocyclic rings, but are not always the easiest rings to prepare by de novo synthesis. Two recent papers describe new methods for the preparation of these compounds1,2. In the first paper1, a heterogeneous gold catalyst (MCM-41-Ph3PAuNTf2) is used prepare oxazoles from an acetylene, a nitrile with the oxygen atom coming from
Francis Arnold and her group have published a series of papers using modified Cytochrome P450 enzymes to cyclopropanate olefins with diazo esters1. More recently they have used a related system to create chiral carbon-silicon bonds2. P.S. Coelho, E.M. Brustad, A. Kannan, and F.H. Arnold et al, Science, 2013, 339, 307-310; Z.J. Wang, H. Ranata, N.E.
There have been a number of papers on the subject of how to specify regulatory starting materials, with a bench marking exercise carried out by the IQ Consortium1. Now a sub-group has published a risk assessment tool to evaluate potential regulatory starting materials2, particularly in early development. For any proposed RSM a score is built
Flow chemistry is big news at the moment, but one of the issues from a scale up perspective has been carrying out some of the process hazard analysis, and in particular reaction calorimetry. If reactants are unstable either thermally or chemically is it possible to get meaningful results from a conventional reaction calorimeter? A recent
Photochemistry has to me always seemed to be an area whose potential for industrial manufacture has never been realized. I may be biased (I did my PhD on photochemistry from 1967-1970) but I feel the tremendous synthetic potential of photoreactions has not been exploited enough. One of the reasons is that scale up of batch