Azanator

Azabon 115 Azacosterol 2, 161 Azaclorzine T, 241 Azacyclonol 1, 47 Azanator T57 Azaperone 300 Azarole 2 129 Azastene 2 ... 

T23. Tsujino, S Servidei, S Tonin, P., Shanske, S., Azan, G., and DiMauro, S., Identification of three novel mutations in non-Ashkenazi Italian patients with muscle phosphofructokinase deficiency. Am. J. Hum. Genet. 54,812-819 (1994). 

Azanator (59) represents a more classical anti-histaminic structure, since the more basic nitrogen in this case occurs in the side chain. Preparation... 

Azanator Azatadine Clemastine Closiramine Antihypertensives Dorastine Mianserin Rotoxamine Terfenadine... 

Skeletal Stabilization as the Basis for Synthesis of Novel Phosph(lH)azane Oligomers and Polymers... 

Reactions that in principle could yield linear phosph(III)azanes generally do not (7, 8) instead they produce low molecular weight oligomers. Among these, the four-membered ring... 

The reactions of azofurazans have been used to obtain the hydrazine and the amino derivatives. For example, reactions of azofurazans, including macrocyclic azofurazan 196, with BunLi and the lithium derivatives of methylfur-azans were studied. Several competitive processes were found to occur (1) the addition of a Li reagent at the N=N bond (2) the redox reaction giving rise to hydrazofurazans and (3) the reaction of the side chain of azofurazan (Scheme 44) <2004RCB615>. 

In a similar manner these hypervalent iodine derivatives promote the addition of the non-nucleophilic 4-nitrofur-azan-3-olate functions to cycloalkenes to give product 210 (Scheme 49) <2001RCB2479>. 

Methoxybenzodifurazan 227 can be nitrated by nitric acid at room temperature to give methoxynitrobenzodifur-azan 228, which reacts with arylamines to yield a series of substituted compounds 229 (Scheme 56) <2003PCJ578>. 

Dimethylbenzofurazan 255 was transformed by 02 produced by irradiation of C60 into 4,7-dimethylbenzofur-azan 4,7-endoperoxide 256 in CDCI3 or CD2CI2 at 0°C in excellent yields. The endoperoxide 256 decomposed back to compound 255 at room temperature. When tetramethylethylene (TME) was added to the decomposing endoperoxide 256 at 37 °C, the hydroperoxide from reaction of TME with 02 was detected (Scheme 67) <2001TL987>. 

Asymmetric /) .vamidocyclodiphosph(V,III)azane monochalcogenides (40), containing a phosphorus (V) and a phosphorus (III) centre, are accessible from stoichiometric oxidation of the parent feamidocyclodiphosphazane with... 

Attempts to synthesize the compound Me2N-N=PNR1R2 resulted in the formation of a cyclodiphospha(m)azane (19). Scheme 2 shows the products of reaction of... 

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