Alkaloids. 



872 



3010 



Ergotinine 035113905X5 

 Barger ct Carr, F. H. J.C., 91, (337). 



Kraft. 48411. Ki-ystallisieites lly- 

 droergotiniiisulfat. 



Tanret. .52483. L'ergotinine. 



Ergotoxine CasH^iOeNj 



Barger. 43984. [Das aniorfe Ergo- 

 toxin C35H41O5N5, der wirksame Be- 

 staiidteil des Alutterkorns.] (Hol- 

 landisch.) 



& Carr, F. H. [Ergotoxine 



and its i^hosphate, hydrochloride and 

 oxalates.] J.C, 91, (337j. 



& Dale. 43988. Ergotoxine 



and some other constituents of ergot. 



Hesperidine. 

 Modrakowskl. 49747. Hesperidin 

 in Conmm macidatum. (Polish.) 



Hordenine- 



Gaebel. 4644(1 Hordenin. 



Leger. 487()G. L'hordenine, alcaloide 

 nouveau retire des germes dits tourail- 

 lons de I'orge. 



Lobine C23H3JN3O4 



and its lajdrochloride and aurichloride. 



Mann & Ince. 493.58. [Isolation of 

 lobine from the " Box " poison plant, 

 Oxylohium ■parviflornm.'] 



Lupanine. 



Soldaini e Di Palma. 52100. Azione 

 del calore sul cloridrato dellad-hiiDanina 

 e sulla d-lnpanina ed i-lupanina. 



N-Methylpyrrole dihydride CjHgN 



occurs in tobacco. An isomeride occurs 

 in pepper (from Piper nigr^im). 



Pictet et Court. Bl., 1, (1001). 

 Morphine CnHigOjN 



Bucberer. Konstitutions desMorpliins 

 und Thebains. J. pr., 76, (428). 



Busch. Synthese von 3.4.8-Tri- 



methoxyphenanthren. Oxydation von 

 /3-Methylmorphiniethiu. Diss. Berlin, 

 1907, 



Dittmer. ilorphenol und seine Deri- 

 vate. Diss. Jena, 1907. 



GuUd. 46898. Solubility and melting- 

 point of morphine. 



Lees, F. H. Morpliine. III. J.C, 91, 



(1408). 



Knorr u. Horlein. Isokodeinon ui)d 

 tiber die Isomerie von Kodein, Iso- 

 kodein und Pseudokodein. X. : 3.4-Di 

 methoxy-9-amiuo.phenanthren aus 3.4- 

 Dimethoxy - phenanthren-9-carbonsaure. 

 XL : Oxy-nietliyl-niorphimethin (Keto- 

 diliydro-methylmorphimethin). B., 40, 

 (2032). 



Pschorr u. Einbeck. Konstitution des 

 O.xymethylmopphimethins. B., 40, (1980j. 



u. Halle. Konstitution des 



Morphothebains. B., 40, (2004). 



Vongerichten u. Densdorff. Einwir- 

 kung \-on Halogen auf Morpliinderivate. 

 B., 40, (4146). 



u. Hiibner, 0. Einwirkung 



von Halogen auf Morpliinderivate. B., 

 40, (2827). Hubner. Diss. Jena, 1907. 



Weil. .53 1 90. Derives de la mor- 

 phine. (Polish.) 



a-METHYLMOKPHIMETHlNE C19H23O3X 



Bronio, hromodUiydro, oxybromodiliydro 



and other derivatives. 



Also derivatives of S-methyi.- 



MOHPHIMETHINE. 



Vongerichten. B., 40, (2827). 



OxYilETHYLMOEPHTMETHINE. 



The semicarhazone also the oxime and 

 its hydrochloride. 



Pschorr u. Einbeck. B., 40, (1980). 



/3-Chloiiomorphide CijHigOjNCl 



The acetyl derivative and methiodide. 



Ach u. Steinbock, H. B., 40, (4281). 



Neo'somorphine C17H19O3N 



and its hydrochloride and metJdodide. 

 Lees, F. H. J.C, 91, (1408). 



Narceine. 



Freund. Xarcein. B., 40, (194). 



Narcotine. 



Reichard. 50968. Xarkotin. 



Nornarceine C23H25O8X 



and the hydrochloride and oxime 



Rabe. Qmwandlung des Xarkotins in 

 Nornarcein. Die Chiuatoxine. B., 40, 



(3280). 



I 



