Organo- Metallic Compounds. 504 



TELLURIUM COMPOUNDS. 



Gutbier u. Flury. 111466. Hexa- 

 halogenotellureate. 



Lederer. 112741. Queeksilber- 

 chlorid-Doppelsalze aromatiechex Tellu- 

 ride. 



Weinzierl. 

 des Tellurs. 



11 5980. Halogenosalze 



TUKGSTi:.\ COMPOUNDS. 



Turner. 115673. Attempt to prepare 



organometallic derivatives of tungsten. 



ZINC COMPOUNDS. 

 Lunijak. 118035. Action des combi- 

 et Mg-organiqnes sur les 

 des acides aliphatiqnes. 



unisons Zn 

 anhydrides 



(Russ.) 



SULPHOXIDES AND 



SULPHONES. 



[Organic sulphur compounds are also 

 indexed under the oxygen compounds in 

 which an equivalent of oxygen takes the 

 place of the sulphur. Sulphonic acids 

 are indexed under acids 1300-1350.] 



2100 



;exeral. 



Gutmann. 111474. Einwirkung von 



alkalischen Reduktionsmitteln auf l>i- 

 sulfoxyde und Sulphoxyde. 



2110 



PARAFFIN COMPOUNDS 



Boeseken et Ockenburg, van. 109705. 

 La dissociation des chlorures des acides 

 methyl- et ethylsulphoniques 0H 3 S0 2 C1 

 et C 2 H 5 SOjCl par le chlorure d'alu- 

 minium. 



Franchimont <& Backer. 110908. 

 a-supho-propionic acid and its separation 

 in optically active isomerides. 



2130 



BENZENOID COMPOUNDS. 



Fries u. Schtirmann. 111067. Re- 

 duktion der Sulfinsauren mittels Brom- 

 wasserstoffs. 



Olivier. 11 8,s 18. Friedel-Crafts'selie 

 Synthese von Sulphonen. 113850: Vi- 

 tesse de reaction dans la synthese de 

 sulfones. 



Smythe. 

 oxide. 



Truttwin. 115081. Umlagerungs- 

 Reaktionen bei Arylamiden der m-Nitro- 



benzolsulfunsaure. 



115191. Benzyl tetrasulph- 



2000 



Si LPHONBS. 

 SULPHONES C 7 rL0,S 



"-Oxyphenyl methyl sulphone 

 Zincke u. Ebel. B., 47, (930). 



/-Oxyphenyl methyl sulphone 

 Zincke u. Ebel. B., 47, J L06). 



SULPHONE C.sH.uO^ 



"'-Phenylene dimethyl disulphone 

 C 6 H 4 SO ..i k 



DlCHLORO DERIVATIVE. 



PoUak u. Wienenberger. M.. 35, 



(1467). 



SULPHONE C 13 H 12 2 S 



Phenyl tolyl sulphone 



Phenyl o-methyi.amino-?u-toi.yl sulphone 



m-)utro derivative 



N0 2 .C 6 H 4 .S0 2 .C 6 H 3 Me.NHlIe 



and the corresponding m-amino and 



azoveij derivatives. 



Witt u. Truttwin B., 47, (2786). 

 SULPHONE C 19 H 16 2 S 



m-Tolyl biphenyl sulphone 

 C 7 H 7 .S< > 2 .C 6 H 4 1 ! 6 1 i, 



o-Methylamino derivative 

 NHHe.C 7 H 6 .S0 2 .C 6 H 4 Ph 



Witt u. Truttwin. B., 47, 2786). 

 SULPHONE C 2 oH 14 04S 



/3-Naphthol sulphone (Ho.C,„H 6 ) 2 S0 2 

 Hinsberg J. pr., 90, (3 15). 



SULPHONE C 26 H 22 04S S 



Bi-m tolyl diphenylene disulphone 

 C 7 H 7 .S0 2 .C 8 H 4 .C 6 H 4 .S0 2 .C 7 H, 



1 tlMETHYLTETRAAMINO DERIVA1 IVE 



[NHMe.C B H 3 Me.S0 2 .C 6 H 3 (NH 2 ).] 2 

 Witt u. Truttwin. B., 47, (2786). 



SULPHOXWES. 

 SULPHOXIDES C 7 H t 2 S 



o- and /)-0xyphenyl methyl 



sulphoxide HO.C 6 H 4 .SO.CH 3 



Zincke u. Ebel. B., 47, (929, 1 106;. 



