Alcohol. 



553 



1210 



DI-OLS. 

 ALCOHOLS CnH2..+.02 



Lydtin, F. Reindarstellung liocli- 

 niolekiilarer Derlvate des (ilycols im 

 Vacuum des Ivathodeuliclits. Diss. 

 Heidelberg, 1903. 



Stoermer, R. Synthese von Alde- 

 hyden uiid Ketonen aus asyinm. 

 disubstituirten Aetliylenglykolen iind 

 dereii Aethern. Berlin, Her. D. chem. 

 Cies., 39, 1906, (2i'8S-2.30r)). 



ALCOHOLS C2H6O2 



Ethylene Glycol 



Favorskij, A. L'ether diethyleniqne, 

 etlier simple complet de Tetliylene- 

 glycole. Transformation de Tethylene- 

 glycole en aldehyde acetique. (Russ.) 

 St. Peterburg, Zurn. russ. fis.-chim. 

 Obsc., 38, 1906, (741-755j. 



Henry, L. Preparation du glycol 

 ethvlenique et de queiques autres alcools. 

 Bruxelles, Bui. Acad, rov., 1906, (732- 

 740). 



ALCOHOL C4H,o02 



Butylene Glycol 



CH3.CH(OHj.CH(OH}.CH3 

 Mono- and di- plienylnretlianes. 



Harden, A. and Walpole, G. S. 

 Chemical action of BaciUits hicfis aero- 

 genes (Escherich) on glucose and 

 mannitol ; production of 2 : 3-butylene- 

 glycol and acetylmethvlcarljinol. Lon- 

 don, Proc. R. Soc, (Ser. B), 77, 1900, 

 (399-405). 



Butylene Glycol 



CH3.CH(OH).CH2.CH2.0H 



Acetyl derivative 

 CH3.CH(6h).CH2.CH20Ac 

 Voronkov, M. P. Action de I'amal- 

 game de magnesium sur I'aldehyde 

 acetique. (Russ.) St. Peterlmrg, Zurn. 

 russ. fis.-chim. ObSc., 38, VJ06, (547- 

 550). 



ALCOHOLS C5H,202 



Pentanediol. 



TrICIILORO-DERIYATIVE of the iloNOMETHYL 



ETHER MeO.CH2.CH2.CH2.CH(OH).CCl3 

 Hamonet, J. L. Metho.Kytrichloropeu- 

 tanol 1.5.4 et a trichloromethyltetrahv- 

 drofurfurane. Paris, C.-R. Acad, sci 

 142, 1906, (210-211). 



ALCOHOLS C6H14O2 



Hexane-af diol. 



Derivatives. 



Dionneau, R. Derives asymetriques 

 de rhexanediol-l.(). Paris, C.-R. Acad, 

 sci., 142, 1906, v91-92). 



Hexane-diol 



HO.CHMe.CHMe.CHMe.OH 



Salkind, J. St. Peterburg, Zurn. mss. 

 fis.-chim. ObSc., 37, 1905, ("484-492). 



Hexane-diol 



PIO.[CH2]3.CMe2.0H 



(Dimethylsiicei nic glycol). 



Henry, L. Paris, C.-R. Acad, sci., 

 143, 1906, (1221-1225). 



Hexane-diol 



OH.CMe2.Ci\le2.0H 



(Pinacone). 



Holleman, A. F. [Un meilleur mode 

 de] .... preparation de la 

 pinacone. Rec. Trav. chim., Leiden, 

 25, 1906, (206-207). 



ALCOHOLS C7H16O2 



Heptane-diol OIl.CH2.LcH2l5.CH2.OH 



Diethyl ether EtO.LCHjJj.OEt 



Dionneau, R. Paris, C.-R. Acad. 

 sci., 142, 1906, (91-92). 



Dimethyl ether o£ cni.ouo-DERivATiVE 

 MeO.CCH2J3.CHCl.LCH2J3.OMe 



Hamonet, J. L. Sj-ntlieses dans la 

 serie de I'heptanetriol symetrique-1.4.7. 

 op. cil. 141, 1905, (1244-1245). 



ALCOHOLS C0H1SO2 



Octane-diol 



OH.CMe2.CH2.CH2.CMe2.OH 



{Be-Dimethylhexane-^i-diol). 

 Henry, L. Sur la pinacone suc- 

 cinique. op. cit. 143, 1906, (496-500). 



ALCOHOLS C<,H2o02 



Ennane-diol 



HO.C.Mej.CMej.CMej.OH 



(Uexamethijltrimethylene glycol). 



Kalisev, A. P. St. Peterlmrg, Zurn. 

 russ. fis.-chim. Obsc., 38, 1906, (proc- 

 verb. 464-465). 



Slavianov, A. N. i.e. (proc.-verh. 



465-466). 



