Nitnle groups

Dimerization involves addition of the cyanamide anion to the nitnle group of an undissociated molecule to give the anion of cyanoguanidine, or dicyandiamide. This reaction takes place most readily at pH 8—10 where the reactants are present in favorable proportion. The product is a weaker acid than cyanamide and is protonated at once with generation of a new cyanamide anion. 

Although isolated fluonne atoms can survive reductions with hthium aluminum hydnde when they are not m a position a to an ester or nitnle group [79] (equauons 63a and 63b), those in an a position arc reducti vely cleaved The milder borohydride reagents convert an a fluorocarboxylate ester to the corresponding alcohol without loss of fluonne [501 (equation 64)... 

Huonnations with DAST proceed with high chemoselectivity In general, under very mild reaction conditions usually required for the replacement of hydroxyl groups, other functional groups, including phenolic hydroxyl groups [112], remain intact This provides a method for selective conversion of hydroxy esters [95 97] (Table 6), hydroxy ketones [120, 121], hydroxy lactones [722, 123], hydroxy lactams [124] and hydroxy nitriles [725] into fluoro esters, fluoro ketones, fluoro lactones, fluoro lactams, and fluoro nitnles, respectively (equations 60-63)... 

Unsaturated compounds containing both a double bond and a charactensbc group such as hydroxyl, carbonyl, or nitnle or an organophosphorus, -selenium sulfur, -iodine, or -boron group are also included in this section even when only the double bond IS oxidized... 

Reactions offluorinated dipoles. In recent years, much effort has been devoted to the preparation of tnfluoromethyl-substituted 1,3-dipoles with the goal of using them to introduce trifluoromethyl groups into five-membered nng heterocycles Fluorinated diazoalkanes were the first such 1,3-dipoles to be prepared and used in synthesis A number of reports of cycloadditions of mono- and bis(tnfluo-romethyl)diazomethane appeared prior to 1972 [9] Other types of fluonne-substi-tuted 1,3-dipoles were virtually unknown until only recently However, largely because of the efforts of Tanaka s group, a broad knowledge of the chemistry of tnfluoromethyl-substituted nitrile oxides, nitnle imines, nitnle ylides, and nitrones has been accumulated recently... 

In 1970, a new reacdon, the displacement of a nitro group from ct-nitro esters, ct-nitro nitnles, ct-nitro ketones, iind ct,ct-dinitro compounds by nitroalkiine salts, was described. These displacements, which are exemplified by the reacdon presented in Eq. 7.1, take place at room temperanire iind give excellent yields of pure products. The reacdon proceeds via a radiciil chain mechanism involving one electron-transfer processes as shovmin Scheme 7.1 the details of the mechanism are described in a review. ... 

Nitnles. Nitriles can be prepared by a number of methods, including (1) the reaction of alkyl haHdes with alkaH metal cyanides, (2) addition of hydrogen cyanide to a carbon—carbon, carbon—oxygen, or carbon—nitrogen multiple bond, (i) reaction of hydrogen cyanide with a carboxyHc acid over a dehydration catalyst, and (4) ammoxidation of hydrocarbons containing an activated methyl group. For reviews on the preparation of nitriles see references 14 and 15. 

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