1310 



ACIDS CsHinO. 



n-Valeric Acid 



CII3 . CH2 . CH, . CH2 . COjH 



Valeryl chloride. 

 Compound CH3 [CH,]3C0 . CI, SI) Clj 



Rosenheim, Arthur und Loewenstamm, 



Willy. Berlin, Ber. D. chem. Ges., 35, 

 rj02, (1115-1130). 



0/875-TETRABROMOVALERIC ACID 



C5He02Br4 I.e. 



( "HjBr . CHBr . CHBr . CHBr . CO,H 



Doebner, 0[skar]. Ueber die der 

 Soiljinsiiure homologen ungesiittigten 

 Siiiiren mit zwei Doppelbiiidungen. 

 Berlin, Ber. D. chem. Ges., 35, ]'d02, 

 (1136-1147). 



a-AMINO-n- VALERIC ACID CsHjiOzN 



Preparation, Etkyl ester, benzoi/l and 

 plienylisocyanate compounds. 



Slimmer, Max D. Ueber Amino- 

 valeriaiisauren. Berlin, Ber. D. chem. 

 Ges., 35, 1902, (400-410). 



o5-l)lA.MIN0VALERIC ACID C5Hi,02N2 



{Ornithin). 



Herzoff, R. 0. Ueher den Xachvveis 

 v(in Lysin und Ornithin. Hoppe-Seylers 

 Zs. physiol. Chem., Strassbarg, 34, 1002, 



(525-527). 



Isovaleric Acid 



CH3 . CHMe . CH2 . CO2H 



Kinzel, W. Kupferisovaleriauat, 

 Cn(C5H902)2. Pharm. Centralhalle, 

 Dresden, 43, l!»02, (37-38). 



a-AMINO-iso-VALERlC ACID C5H11O2N I.e. 



Me2CH . CH(XH2) . COOH 



I'leparation. Also its ethyl ester, 

 benzoyl and plienylisocyanate com- 

 pounds. 



490 1310 



)3-AmIN0-IS0VALERIC ACID C5H11O2N 



Preparation, ethyl ester, benzoyl ami 

 phenylisocyanate compounds. 



Slimmer, Max D. Berlin, Ber. D. 

 chem. (^es., 35, 1902, (400-410). 



Methylethylacetic acid 



CH3 . CH2 . CHMe . CO.H 



a-AMlNO-METHYLETHYLACETIC ACID 



C5Hn02N i.e. 



CH3 . CH2 . CMe(NH2) . COzH 



Preimration, ethyl ester, hejizoyl anJ 

 plienylisocyanate compounds. 



Slimmer, Max I). Ueber Amino- 

 valeriansiuiren. Berlin, Ber. D. chem. 

 Ges., 35, 1902, (400-410). 



ACIDS CeHisG: 



«-Hexoic acid 



CH3 . CHj . CH2 . CH2 . CH2 . CO2H 



a-AMINO-)l-HEXOIC .\CID 



{Leucine^. 



Etard. Sur les prodnits basiqnes de 

 I'hvdrolyse profonde du muscle. Paris, 

 Bui. soc' chim., (ser. 3), 27, 1902, (093- 

 696). 



Vila, A. et Valine, E. Mecauisme de 

 synthese de la leucine. Paris, C.-R. 

 .lead, sci., 134, J902, (1.394-1597). 



Leucyllcueine C12HJ4O3X, i.e. 

 NH . CH(C4Hg) . CO2H 

 CO.CH(C\H9i.XH2 



Fischer, Emil. Ueber einige Derivate 



des Glykocolls, Alanins und Leucins. 



Berlin, Ber. I), chem. Ges., 35, 1902, 

 (1095-1106). 



(J arhoxynminoacctyJ am'i noacct yl - amino- 



liexoie acid. Diethyl ester 



C15H27O6N3 



"' l^t 

 5t 



(Carho.Kctliyl-i/lycyl-glycyl-leucine-ester). 



o PTT A'^^ ■ NH . CHfC^Hg) . CO2 

 .e. ^«2^>,Tpj_cQ _ QYi. . XH. CO, 



Slimmer, Max D. Berlin, Ber. 

 «;hem. Ges., 35, 1902, (400-410). 



J). 



Fischer, Emil. Berlin, Ber. D. chem. 

 (Jcs., 35, 1902, (1095-1106). 



