Greener route to carboxylic acids
6 January 2013 Research
Reaction uses water as the oxygen source and solvent for converting primary alcohols
Oxidation in organic synthesis
V K Ahluwalia
CRC Press
2012 | 323pp | £57.99 (HB)
ISBN 9781466506015
Reviewed by John Hayward

The first (and major) section contains an extensive (though at times, oddly selective) list of oxidising methods. For example, sodium hypochlorite, hypobromite and hypoiodite are discussed, yet perhaps the most common alcohol oxidation method – activated DMSO – contains only the Swern protocol, without any reference to the earlier works by Moffatt, Parikh, Doering and others. Likewise, another commonly used reagent (and catalyst), tetrapropylammonium perruthenate, is not mentioned at all. Included as well are several compounds – such as sodium hydroxide – that, while commonly are involved in various redox processes, are not conventionally referred to as oxidising agents.
The second section shows a good selection of reagent combinations to effect desired changes, with the caveat that some of the key reactions mentioned above are absent from those suggested. The third and fourth sections are brief in comparison to the earlier sections, but show a variety of key methods in the respective fields.
Unfortunately, minor typographical and pictorial issues plague this book. Spelling mistakes are to be found throughout and benzene rings consistently have non-120° angles. While perhaps minor issues, they do unfortunately detract from the book as a whole, which to its credit contains an extensive list of reagents and is of some interest as a reference resource, particularly with respect to some of the more exotic reagents.
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