Acids. 



604 



1310 



Elektroch., Halle, 12, 1906, (i59-463) ; 

 LichtT, M. Diss. Heidelberg, 1906. 



Parsons, C. L. mid Robinson, Wm. 0. 

 Gleichgewichte im System : Beryllium- 

 oxyd, Oxalsiiure unci Wasser. I. Die 

 Berviliumoxalate. Zs. anorg. Chem., 

 Hambiu-g, 49, 1906, (178-189). 



Sheppard, S. E. and Mees, C. E. K. 

 The niolecidar condition in solution of 

 ferrous oxalate. A correction. London, 

 Proc. Chem. Soc, 22, 1906, (105-106). 



Ethyl ester Et2C204 



Bieber, A. Einwirkung von Oxal- 

 ester auf cyklische Ketone. Diss., 

 Gottingen. 1905. 



Brass, R. Condensationen von Oxal- 

 ester niit Derivaten des Acetessigesters. 

 Diss. Tii])ingen, 1904. 



Muenk, K. Condensationen zwischen 

 Oxalester und ilethvlaethvlketon. Diss. 

 Kiel, 1905. 



OXAMIDE NH2.CO.CO.NH2 



p-Chlovo-oxa nilaniide 



C6H4CI.NH.CO.CO.NH2 



s-Di-p-cMorophenyloxodicMoronmide 



CeH^CI.XCLCO.CO.NCl.CeH.Cl 



p-Chloro-oxanilamide 



C6H4CI.NH.CO.CO.NH2 



s-Di-p-cMoro-oxan'dide 



C6H4CI.NH.CO.CO.NH.C6H4CI 



2 : i-Dichloro-oxanilamide 



C6H3Cl2.XH.CO.CO.NH2 



s-Di m ethyl oxodieJdoroa mide 



CH3.XCI.CO.CO.NCI.CH3 



s-Diethyloxodichloroamide 



C2H5.NCI.CO.CO.NCI.C2H5 



s-Dhnethyloxodihromoamide 



CH3.NBr.CO.CO.NBr.CH3 



8-Diethyloxodihromoainide 



C.Hs.NIJr.CO.CO.NBr.CjHs 



Chattaway, F. D. and Lewis, W. H. 

 Halogen derivatives of substituted oxa- 

 mides. London, J. Chem. Soc, 89, 

 1906, (155-161); [abstract] Loudon, 

 Proc. Chem. Soc, 22, 1906, (18-19). 



p-Xitrop]ienyloxnmide 

 XO2.C6H4.XH.CO.CO.NII,, 



Scbultz, 1!., Rohde, CJ. und Herzog, 



(;. J. iir:ikt. Chem., Leipzig, (N.F.), 

 74, 1900, (71-91;. 



OXAMIC ACID XH2.CO.CO2H 



EiJnjl p-chloi'0-oxanilate 



C6H4Cl.XH.CO.C02Et 



Ethyl 2 : 4-dicJdoro-oxanilate 



CeHaClj.XH.CO.COjEt 



Chattaway, F. D. and Lewis, W. H. 



Halogen derivatives of substituted oxa- 



mides. London, J. Chem. Soc, 89, 



1906, (155-101); [abstract] London, 



Proc. Chem. Soc, 22, 1906, (18-19). 



Plieuyloxamia acid 

 yUrUe CoHs.NH.CO.CX 



Scliultz, G., Robde, G. und Herzog, G. 



J. prakt. Chem., Leipzig, (N.F.), 74, 

 1900, (74-91j. 



Oxanilhydroxamic acid C8H8O3N2 i.e. 

 PhXH.CO.C(:X.OH).OH and the 



anilide. 



Dimroth, 0. und Taub. L. Berlin? 

 Ber. D. chem. Ges., 39, 1900, (3912- 



3920). 



p-DiphenyJoxamic acid C^4Hii03N 

 i.e. C6H5.C6H4.XH.CO.CO2H 

 p^-Chloro-, bromo- and iodo-couipounds. 

 Gelmo, P. t.c. (4175-4183). 



DiPIlENYLAMIDlNEOXAUC ACID. 



Aviide C14H13ON3 i.e. 



PhNH.C( : NPh).C0.NH2 

 and the di-p-nitro derivative. 



Schultz, G.,Rolide, G. und Herzog. G. 



J. prakt. Chem., Leipzig, (N.F.), 74, 

 1900, (74-911 



ACIDS C3H4O4 



Malonic acid CO2H.CH2.CO2H 

 Haller, A. et Blanc, G. Condensation 



de I'ether 3/3-dimetliylglycidique avec 



I'ether malouique sode ; synthese des 



acides terebique et pvroterebique. 



Paris, C.-R. Acad, sci., "^142, 1900, 



(1471-1474). 

 Leucbs, H. Die Zersetzung des 



Malonesterchlorids. Berlin, Ber. D. 



chem. Ges., 39, 1900, (2641-2043). 



Perkin, \V. H. jun. and Simonsen, J. 

 Ij. Tlie action of tribromoin-(j2jane on 

 tbe sodium derivative of ethvl malonate. 

 London, Proc. Chem. Soc.', 22, 19i)6, 

 (133-134). 



Piloty, (). und Neresbeimer, J. 

 Amido- und Diazo-Malonsiiureester. Ber- 

 lin, Ber. D. chem. Ges., 39, 1906, (514- 

 517). 



