Anilides natural waters

In a study covering a wide range of polar and acidic pesticides deethylatrazine and atrazine besides anilide, phenoxy acid, phenylurea, carbamates and other types of specific pesticides in river water were determined by ESI-LC-MS and MS/MS. Recoveries, depending on preconcentration steps, obtained with different SPE materials (PLRS-S, Hyshere-1, LiChrolut EN and Isolute ENV -i-) and at different pH values were reported [502]. Sixteen of the most widely used pesticides in Southern Italy were monitored in surface water samples taken in the Calabria region. Triazines were determined quantitatively by LC-UV and ESI-LC-MS(-i-) and were confirmed by MS [537]. In another study the simultaneous determination of 26 non-acidic (base and neutral e.g. triazine, carbamate, anilide, N-substituted amine, urea and organophosphorus type) and 13 acidic (sulfuron and phenoxy acid type) pesticides in natural waters was performed using ESI-LC-MS. Recoveries... 

The Dess-Martin periodinane 8 is also able to oxidize aromatic compounds to the corresponding quinones. The presence of water is important and, starting from anilides 42 substituted in the 2-position, the rare class of ortho-imido-quinones 43 is accessible, Scheme 21. It has been shown that compounds of type 43 are interesting building blocks and can lead to polycyclic molecules of diverse molecular architecture [95,96]. They can undergo subsequent Diels-Alder reactions and intramolecular versions have been used for a rapid access to natural products and for synthesis of scaffolds for further manipulation.para-Quinones 45 are also easily accessible, however, only in modest yields by reacting 4-sub-stituted anilines 44 under the same reaction conditions, Scheme 21 [97]. 

Iodine(V) reagents such as Dess-Martin periodinane (DMP) and o-iodoxyben-zoic acid (IBX) are known as general reagents for oxidation of alcohols and have been utilized widely for natural product syntheses. Besides their general use for alcoholic oxidation, recently, the active studies on novel utilization of iodine( V) reagents such as DMP and IBX have been pursued mainly by Nicolaou and coworkers [26]. In particular, the versatile reactivities of anilides (62) with IBX or DMP are interesting and involve unprecedented features as follows. o-Imido-quinones (63) are prepared from 62 by the action of DMP and water. This reaction has been investigated extensively and was found to lead to p-quinones (64)... 

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