Acids. 



621 



1330 



O-BROMOniEXYLPROriOXIC ACID 



c6H5.CH2.CBBr.c02H 



d- and Z- and the racemic forms. 



Fisclier, E. nnd Carl, H. Berlin, Ber. 

 D. chem. Ges., 39, 190G, (3996-4003). 



DiCIILOROPUENYLPROriOXIC ACID 



CgUs.CHCI.CHCl.COgH 



Sudborough, J. J. and James, T. C. 

 [Action of aliialis on a3-dicliloro-/3- 

 jDhenylpropionic acid and its method and 

 ethyl esters.] London, J. Chem. Soc, 

 89.'1906, (105-115). 



a-AMINOPHENVI.PROriON'IC ACID 



C6H5.CH2.CH(XH2).C02H 



Flienylalan'ine. 



Miiller, E. Kondensationen von 

 Hippurazid niit Pheuvlalanin. Diss. 

 Heidelberg, 1904. 



Schoeller, W. Spaltung des Phemd- 

 alanin in seiue optiscliaktiven Kompo- 

 nenten mittels der Fornndverbindung. 

 Die d-Bromhydrozimtsaure und zwei 

 aktive Dipeptide, Derivate des 1-Pheiiyl- 

 alanin. Diss. Berlin, 1906. 



;8-HTDROXYLAMI.\"0-;3-PnEN'YLPROPIONIC ACID 



PhCH(XH.OH).CH2.C02H 



and its diacetate aud dibenzoate. 



Posner, Th. Berlin, Ber. D. chem. 

 Ges., 39, 1906, (3515-3529). 



a-Phenylpropionic acid 



CH3.CIlPh.CO2H 



O-AMtSO-a-rUEXYL-PROriONIC ACID 



C9Hii02N 

 Amide and nitrile NHj.CPhile.CN 

 Jawelow, J. i.e. (1195-1200). 



O-PHENYLAillNO-a-PUENTLPROPIONIC ACID 



Nitrile C15H14N2 i.e. 



CX.CPhMe.XHPh 



Bucherer, H. und Grol^e, A. t.c. 

 (986-1013). 



Dimethybenzoic acid 



CeH3Me2.C02H [5:2: 1] 

 XiTRiLE CgHjMej.CN 



Ciesielski, K. Derivate des p-Xylyl- 

 cyanids. Krakow, Bull. Intern. Acad., 

 1906, (270-276); (Polish) Krakow, 

 Rozpr. Akad., 46 A, 1906, (1 11-146). 

 (i>-6534) 



ACIDS CyEnOi 



a-Phenylbutyric acid 



CH3.CH2.CHPh.CO2H 



O-AmINO-O-PHENYLBUTYRIC ACID 



XiTRiLE Ph.CEt(NH2).CN 



Jawelow, J. Berlin, Ber. D. chem. 

 Ges., 39, itlOO, 1 1105-1200). 



^-Phenylbutyric acid 



Pl1MeCH.CH2.CO2H 



Fischer, E. und Schmitz, W. t.c. 



(2208-2215). 



7-Phenylbutyric acid 



PhCH2.CHo.CH2.CO2H 



a-AMISO-y-PIIENYLBLTYRIC ACID 



CioH,302X i.e. 

 C6H5.CH2.CH2.CH(XH2).C02H 



Fischer, E. und Schmitz, W. t.c. 

 (351-356, 2208-2215) : Knoop, Fr. und 

 HoessU, H. t.c. (1477-1480). 



a p-Tolylpropionic acid 



CHj.CHMe.COjH 



a-AMIXO-a-TOLYL-PROPIONIC ACID 



CH3.C6H,.CMe(NH2).C0.2H 

 aud the nitrile. 

 Jawelow, .J. t.c. (1195-1200). 



;8/>ToIylpropionic acid 

 CjH^.CHz.CHz.COjH 



yS-AMINOTOLY'LPROPIONIC ACID 



and /S-Ure'ido-tolylprojDionic acid. 



Posner, Th. und Oppermann, H. t.a. 

 (3705-3713). 



^-HyDROXTLAMIXO-TOLYLPROPIGNIC ACID 



C,H,.CH(XH.OH).CH2.C02H 



and its diacetyl, /3-methoxyl aud 



j3-ethoxyl derivatives. 



Posner, Th. und Oppermann, H. I.e. 



ACIDS CnH2„-,o02 



ACIDS C9H8O2 



Cinnamic acid PhCH : CH.CO2H 



Asser, E. Die Claisensche Zimmt- 

 sauresynthese. Diss. Rostock, 1906. 



Erlenmeyer juu., E. und Barkow, C. 



Stereoisoniere Zimmtsiiuren. Berlin, 

 Ber. D. chem. Ges., 39, 1906, (285-292, 

 1570-1585) ; Erklarung dazu von 

 Marckwald, W.und Meth, R. t.c. (1966). 



Herz, W. und Mylius, B. Die Ge- 

 schwindigkeit der Addition von Brom 

 an Zimmtsaure. t.c. (3816-3820). 



2 s 



