Theoretical and Physical. 



086 



7035 



McKenzie & Mtiller. Kaceinisation 

 by alkali as applieil to the resolution of 

 7'-manilelic acid into its optically active 

 isonierides. J.C, 91, (1814). 



& Wren. Asymmetric 



synthesis of the optically active tartaric 

 acids. J.C, 91, (1215). 



Mamlock. Stereochemie. Leipzig, 

 1907. 



Michael, A. Die van't Iloff- 



Wi.slicenussche Konfigurationslehre. J. 

 pr., 75, (105). 



Patterson & Kaye. Ojnical super- 

 position. [Rotations of Z-menthyl di- 

 acetyl-j-tartrate in the homogeneous 

 condition and in solution in ethj"l 

 alcohol, benzene and nitrobenzene, and 

 comparison of these data with those of 

 Z-menthyl diacetyl-cZ- and -/-tartrates.] 

 J.C, 91. (705). 



& McMillan. Influence of 



solvents on the rotation of optically 

 active compounds. A new general 

 method for studying intramolecnlar 

 change. [Influence of benzan/mldoxinie, 

 beuz-s(/tialdosime, anisfnifialdo.xime, 



aniss//Haldosime, and ethyl formyl- 

 phenylacetate on the rotation of ethyl 

 tartrate.] J.C, 91, (504). 



Pfeiffer. 50524. Stereochemie des 

 Chroms. Systematik der stereoisonieren 

 Chromsalze. — Die isomeren Dibromo- 

 salze. 



Pickard & Kenyon. Resolution of 

 sec.-octvl alcohol (methyhexvlcarbiuol, 

 octane-2-ol). J.C, 91, (2058)". 



&■ Littlebury. Alcohols of 



the hydroaroinatic and terpene series. 

 Resolution of the alcohols into their 

 optically active components and the 

 preparation of the borneols. J.C, 91, 

 (1973). 



Pope. 50G85. Stereochemistry. 



Ranken & Taylor. 50894. Physical 

 properties of mixed solutions of in- 

 dependent optically active substances. 

 [Tartrates with sucrose or maltose.] 



Rosanofif. Prinzip der optischen 

 Superposition. Z. p. C, 57, (739). 



Scholtz. 51755. Die optisch-aktiven 

 Verbindungen des Schwefels, Selens, 

 Zinns, Siliziums und Stickstoffs. 



Smiles. 52048. Nitrates of dimethyl- 

 and methylethyl-thetine menthyl esters. 

 [Attempts to resolve methylethylthetine 

 into its optical isonierides.] 



Isomerism of Nitruuex Cci.mi'0unds. 



Buckney, F. 44890. [Resolution of 

 oi)tically active allylkairolinium iodide.] 



& Jones. Optical activity 



of cyclic annnonium compounds. J.C, 



91,(1821). 



Frohlicli. Asymmetrischer Stickstoff 

 in den Ammoniumsalzen. Diss. Tu- 

 bingen, 1907. 



Homer. 47G23. Resolution of salts 

 of asymmetric nitrogen compounds and 

 weak organic acids. 



Jones. 47893. Resolution of optically 

 active annnonium salts bj^ means of tar- 

 taric acid. 



Pope & Beck. Resolution of tetra- 

 hydro-p-toluquinaldine into its optically 

 active components [by means of d-a y8- 

 bromocainphoi-sulphonic acid]. J.C, 

 91, (4.58). 



Scholtz u. Wassermann. Stereoiso- 

 merie bei Verbindungen mit fiinfwerti- 

 gem as3'nimetrischem Stickstoffatom und 

 asymmetrischem Kohlenstoffatom. B., 

 40, (685). 



Wassermann. Sterische Hinderung 

 und opli&che Isomerie von Stickstoff- 

 verbindungen. Diss. Greifswald, 1907. 



WedeMnd, E. Stereochemie des fiinf- 

 wertigen Stickstoffes. Leij^zig, 1907. 



Isomerieverhiiltnisse des 



asymmetrischen Stickstoffs. Diss. 

 Tiibingen, 1907. 



7040 PHYSICAL PROPERTIES 



IN RELATION TO STRUC- 

 TURE. 



Badenhausen. Farbe, Fluoreszenz, 

 Phototropie und einige Synthesen der 

 Fulgide. Diss. Leipzig, 1906. 



Baeyer, A. Abkoramlinge des Tri- 

 phenylcarbinols. A., 354, (152). 



Dibenzahiceton und Tri- 



phenylmethan. B., 40, (3083). 



Baly & Stewart. 43941. Origin of 

 color. 



Benrath. 44207. Farbenwechsel 

 von Kobalt- uud Kupferchlorid in 



Losung. 



Byk. Absorption komplexer Kupfer- 

 verbindungea im Violett und Ultra- 

 violett ; farbvertiefende Wirkungen von 

 Schwermetallen. Z. p. C, 61, (1). 



