Cyanide hexafluorophosphate

It has been reported that diphenyliodonium triflate reacts with the lithium enolates of some cyclic ketones in the presence of copper cyanide to yield the corresponding a-phenylated or a-diphenylated ketones.58 There has been a detailed analysis of the products of thermal decomposition of diphenyliodonium tetrafluoroborate and hexafluorophosphate salts.59... 

Hydride abstraction from dienyl tricarbonyl iron complexes furnishes cationic dienyl tricarbonyl iron complexes. For example, reaction of the diene-iron tricarbonyl complex (115) with triphenyhnethyl hexafluorophosphate followed by trimethylsilyl cyanide furnished with excellent regio- and stereoselectivity a new diene iron tricarbonyl complex (116) (Scheme 170). Excellent regio- and stereoselectivity is seen upon reaction of the cationic complex (116) with trimethylsilyl cyanide (TMS-CN) (Scheme 170). Reduction of the nitrile affords a spirocyclic lactam complex. Intramolecular cyclization of in situ formed enols furnishes spirocyclic compounds again with excellent stereoconfrol (Scheme 171). An interesting example of hydride transfer from a cyclohexadiene ring to a pendant aldehyde followed by nucleophilic addition is seen in Scheme 172. 

KETONES Lithium diisopropylamide. Nickel carbonyl. Sodium tetiacarbonyl-ferrale(-II). Thallium(IIl) nilrale. 2,4,4,6-Tetramethyl-5,6-dihydro-l,3-(4/0-oxazine. Triphenylmcthyl hexafluorophosphate. y-KETONlTRILES Sodium cyanide. d-LACTONES Silver nitrate. 7-LACTONES a-Chloro-N-cyclohexylpro-panaldoximc. 

The reaction has been shown to be of very broad scope with a multitude of nucleophiles Nu such as imides.23,24,29,32,33,36,37,42 amines,10,32 cyanide,25,32 hydroxide,10,32 alkox-ide,10,26,32 electron-rich isocyclic or heterocyclic aromatic compounds,28 carboxamides,31 lactams,31 ureas,31 sulfonamides,31 cyanate,31 formate (to give products with Nu = H),34 C-H acidic compounds,35 hydrazines and hydrazides,38 and sulfinates.38 The amino group NR R2 of cyclopropane-1,1-diamines and the nucleophile Nu in bicycles 8, 9 or 12, respectively, can be easily replaced with other nucleophiles Nu, such as water,10,32,33 alkoxide,10,32-34,42 Grignard compounds,27,42 amines,29,30,36,37,42,43 cyanide,29,33,42,44 hydride,34,42,44 and C-H acidic compounds39-41,43,44 (see Section 5.2.1.). Therefore, it is currently the most important method for the preparation of substituted bicyclic cyclopropylamines. The toxic and costly reagent methyl fluorosulfate can be avoided in a modified synthetic route, which instead of the fluorosulfate 5 proceeds via the corresponding tetraphenylborate, hexafluorophosphate, or (most conveniently) via the tosylate.23 The different steps of the method can often be combined in a one-pot procedure. Results are summarized in Table 3. 

The employment of suitable organic solvents, such as acetonitrile and acetic acid, with oxidation-resistant supporting electrolytes permits the anodic formation of reactive radical cations from many organic materials. Most aromatic compounds and olefins, as well as those alkanes which have particularly weak C—H bonds, are oxidised in acetonitrile containing fluoroborate or hexafluorophosphate electro-lytes. °" 2 Some aromatic radical cations can be further oxidised to dications within the available potential range. Radical cations in general either deprotonate or attack nucleophiles present in the medium reactions with pyridine, methanol, water, cyanide ion, acetate ion or acetonitrile itself produce addition or substitution products. The complete reactions involve a second electron transfer and coupled chemical... 

The two ends of the bipyridyl-bis-crown ether ligand LI 154 can be clipped together by K+. Reaction of [Cu(MeCN)4]+ with two equivalents of LI 154 gave the precursor [Cu(Ll 154)2]+, which with an excess of KPFe gave the novel alkali-metallated catenate [Cu(KL1154)2](PF6)3. The potassium binds the benzo-15-crown-5 units sufficiently tightly for demetallation, with potassium or tetramethy-lammonium cyanide, to be feasible, giving the [2]-catenane (KL 1154)2 as its hexafluorophosphate salt [299] (Scheme 4-32),... 

Abbreviations CDMT = 2-chloro-4,6-dimethoxy-l,3,5-triazine EDCI = l-ethyl-3-(3-dimethyla-minopropyl)carbodiimide BOP = benzotriazol-l-yloxy-tris-(dimethylamino)phosphonium hexa-fluorophosphate DIPEA = diisopropylethylamine DEPC = diethylphosphoryl cyanide CBM IT = l,l-carbonylbis(3-methylimidazolium triflate HOBt = 1-hydroxybenzotriazole hydrate HBPyU = 0-(benzotriazole-l-yl)-iV,Af,A,Af-bis(tetramethylene)uronium hexafluorophosphate. 

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