Bromine perchlorate, bis

Bromine(III) compounds, 317 [Br(OS02F)]2-, 320 Bromine fluorosulfate, 320 Bromine hexafluoroantimonate, difluoro-, 313 Bromine perchlorate, bis(quinoline)-, 319 Bromine tetrafiuoroborate, bis(quinuclidine)-, 319 Bromine trifluoride, 313, 314 Butane, rflc-p,p -diaminodiphcnyl-alkali metal complexes, 14... 

Ammonium perchlorate, Impurities, 4004 Azidoacetic acid, 0774 f Aziridine, Acids, 0863 Benzoyl azide, 2698 Benzyl chloroformate, 2931 1,2-Bis(dilluoroamino)-A-nitroethylamine, 0803 Bromine trioxide, 0259 2-Butanone oxime, 1654 2-Butyne-l,4-diol, 1526... 

Acrylic acid, Initiator, Water, 1148 Aluminium chloride, Water, 0062 Barium peroxide, Propane, 0216 1,3-Benzodithiolium perchlorate, 2677 1,1 -Bis(fluorooxy)tetrafluoroethane, 0641 Borane-tetrahydrofuran, 0138 Boron tribromide, Water, 0122 Bromine, Aluminium, Dichloromethane, 0261 Bromine, Tungsten, Tungsten trioxide, 0261 f 1,3-Butadiene, 1480 Calcium oxide, Water, 3937 Chlorine trifluoride, Refractory materials, 3981 Chromium trioxide, Acetic acid, 4242 Copper(II) oxide, Boron, 4281 Diazoacetonitrile, 0675 Dihydroxymaleic acid, 1447 Ethyl azide, 0872... 

These preparations of bis(2,4,6-trimethylpyridine)iodine(l) and bromine(l) hexa-fluorophosphate are adaptations of methods previously reported for obtaining the corresponding perchlorates.2... 

Treatment of bis(dimethylaminomethylene)pyrrolizinium perchlorate (29) with cyclopentadiene-NaH in DMF gave the diatropic cyclopenta-[fc]cycl[4,2,2]azine (77), which was also obtained from the fulvene derivative (78) and 3//-pyrrolizine (25). Electrophilic substitutions (deuteration, nitration, nitrosation, acylation, bromination, Mannich reaction) occur in the 6- and 8-positions.32... 

Cyclization of allylic alcohols to form epoxides has been particularly problematical, and the reactions have been more of mechanistic than of synthetic interest. For reactions conducted under basic conditions, it is possible that epoxide formation involves initial halogen addition followed by nucleophilic displacement to form the epoxide. Early examples of direct formation of epoxides from allylic alcohols with sodium hypobromite," bromine and 1.5 M NaOH,12 and r-butyl hypochlorite13 have been reviewed previously.fr Recently it has been shown that allylic alcohols can be cyclized effectively with bis(jym-collidine)iodine(I) perchlorate (equation 3).14 An unusual example of epoxide formation competing with other cyclization types is shown in equation (4).15 In this case, an allylic benzyl ether competes effectively with a -/-hydroxyl group as the nucleophile. 

Intramolecular bromoalkylamine addition to alkenes has been perfmned using bis(sym-col-lidine)bromine(l) perchlorate (62 equation 31). The method plays an important role in the key stq i of ( )-sporamine synthesis (63) (65 The reaction of I(py)2BF4 and alkenes in the presence of nucleo-... 

TIN or TIN POWDER (7440-31-5) Sn Finely divided material is combustible and forms explosive mixture with air [autoignition temp (dust cloud) 1166°F/630°C]. Contact with moisture in 911 forms tin dioxide. A reducing agent the powder is very reactive. Violent reaction with strong acids, strong oxidizers, ammonium perchlorate, ammonium nitrate, bis-o-azido benzoyl peroxide, bromates, bromine, bromine pentafluoride, bromine trifluoride, bromine azide, cadmium, carbon tetrachloride + water, chlorine, chlorine monofluoride, chlorine nitrate, chlorine pentafluoride, chlorites, copper(II) nitrate, dimethylarsinic acid, fluorine, hydriodic acid, iodine heptafluoride, nitrosyl fluoride, oxygen difluoride, perchlorates, perchloroethylene, potassium dioxide, phosphorus pentoxide, sulfur, sulfur dichloride, turpentine (fire or explosion). 

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