7000 



1102 



Theoretical and Physical. 



Bolland, A. Les principes de l;i 

 Stereoehimie. (Polish) Lwow, 1901, 

 (65). 23 cm. 2 tor. 



Les principes de la Stereo- 



ehimie. (Polish) Lwow, Sprawozdanie 

 Dyrekcyi 1 Szkofy reahiej, 1901, (1-3G). 



Byk, A. Zur Frage der Si)altbarkeit 

 von RacemverhinduuiTen durch zirkular- 

 polarisiertes Licht, ein Beitrag zur pri- 

 maren Entstehung optischaktiver Suh- 

 stanz. Zs. phvsik. Cliem., Leipzig, 49, 

 1901,(011-687); Berlin, Ber. D. chem. 

 Ges., 37, 1901, (1096-1700). 



Cohen, J. B. and Raper, H. S. The 

 relation of position isomerism to oj)tical 

 activity. 11. The relation of the raen- 

 thyl esters of the isomeric chlorobromo- 

 benzoic acids. III. The rotation of the 

 menthyl esters of the isomeric iodoben- 

 zoic acids London, J. Chem. Soc, 85, 

 1904, (1262-1274); [abstract] Proc. 

 Chem. Soc, 20, 1904, (179). 



Daldn, H. D. The hydrolysis of 

 optically inactive esters by means of 

 enzymes. Part 1. The action of lipase 

 upon esters of mandelic acid. The 

 resolution of inactive raaudelic acid. J. 

 Physiol., Cambridge, 30, 1903, (213- 

 263). 



Elbs, K. Ueber stereochemische Hin- 

 dei-ung bei elektrochemischen Reduk- 

 tionen. Zs. Elektroch., Halle, 10, 1901, 

 (579-582). 



Erlemneyer, Emil, jim. uud Arnold, 

 Alfred. Stereochemische Studien. 1. 

 Ueber eine nene Trennungsmethode 

 racemischer Verbindnngen. — 2. Ueber 

 eine nene Isomeric bei Aethylenderi- 

 vaten. — 3. Ueber einige Derivate der 

 racemischen und der optisch activen 

 Isodiphenyloxathylamiubasen. Liebigs 

 Ann. Chem., Leipzig, 337, 1901, (.307- 

 353). 



Frankland, Percy Faraday and Harger, 

 John. Position-isomerism aiad optical 

 activity. The methyl and ethyl esters 

 of di-o-, -m-, and -2>nitrobpnzoyltartaric 

 acids. London, J. Chem. Soc, 85, 19U1, 

 (1571-1580); [abstract] London, Proc. 

 Chem. Soc, 20, (203-201). 



Hann, A. C. 0. andLapworth, Arthnr. 

 [The resolution of |8-l)euz(iyl-a-phcnyl- 

 propionic acid into its optical isomerides.] 

 London, J. Chem. Sec, 85, 1904, (1355- 

 1370) ; [abstract] London, Proc, Chem. 

 Soc, 20, 1904, (183). 



Henrick, Ferd. luid Wirth, A. tJber 

 Stereoisomeric bei den Oximen des Dyp- 

 nons (Diphenyl-l-Methvlpropenons-3). 

 Wien, SitzBer. "Ale. Wiss., 113, 1901, 

 (Abt. lib, 58-77) ; Wien, MonHfte 

 chem., 25, 1901, (123-112); Berlin, Ber. 

 D. chem. Ges., 37. 1901, (731-731). 



Hiittner, Karl. Stndieu tiber die 

 Leiickartsche Peaktion zur Darstellung 

 von Basen. [Stereoisomerie.] Diss. 

 Gottinoeu (Druck v. ' Dieterich), 1903, 

 (09). '21 cm. 



Kipping, F. S. and Salway, A. H. 

 The arrangement in space, of the groups 

 combined with the tervalent nitrogen 

 atom. London, J. Chem. Soc, 85, 

 1901, (438-155) ; [ai)stract] London, 

 Proc Chem. Soc, 20, 1901, (39-41). 



Krapf, Hermann. Ueber stereoiso- 

 mere llydrazone der Dithiokohlensaure- 

 ester. Diss. Erlangen (Druck v. E. Th. 

 Jacob), 1902, (47). 21 cm. 



Lippmann, E. 0. von. Chemie der 

 Zuckera'-ten [Konstitution]. 3. Aufl. der 

 Sclirift : Die Zuckerarten und ihre Deri- 

 vate. 1. n. 2. Halbbd. Braunschweig, 

 1901, (XXXIX + 2003). 



Lutz, 0. Ueber die optisch-isomeren 

 Benzylmalamidsauren. Berlin, Ber. D. 

 chem. Ges., 37, 1901, (2123-2129). 



McKenzie Alexander. [The resolution 

 of (-compounds.] The esterification of 

 7--maudelic acid by menthol and borneol. 

 London, J. Chem. Soc, 85, 1901, (378- 

 3S0) ; [abstract] London, Proc. Chem. 

 Soc, 20, 1904, (41). 



Studies in asymmetric 



synthesis. 1. Reduction of mentliyl 

 benzoylformate. 11. Action of magne- 

 sium aikyl haloids on menthyl benzoyl- 

 formate. London, J. Cliem. Soc, 85, 

 1904, (1219-1202); [abstract] London, 

 Proc. Chem. Soc, 20, 190L (NS). 



MeyerhofFer, W. Stereochemische 

 Notizen. (Die Pasteur'sche Siraltungs- 

 methode raitttels activer Verbindnngen. 

 — Die Loslichkeit eines Tartrats, ver- 

 glichen mit der des Raceraats.) Berlin, 

 Ber. D. chem. Ges., 37, 1904, (2604- 

 2610). 



Morrell, Robert Selby and Hanson, 

 Edward Kenneth. The resolution of 

 ai3-dihydroxybutyric acid into its opti- 

 cally active constituents. London, J. 

 Chem. Soc, 85, 1901, (197-2(33); 

 [abstract] London, Proc. Chem. Soc, 

 20, 1901, (20-21). 



