Alcohols. 



17:: 



1240 



Phloroglucinol. 



Sera. L15058. Phloroglucinglukuron- 

 Baure. 



Votocek & Potm6sil. I LIS 15. Le 

 dosage de La phloroglucine. 



Wenzel. Condensation des I'hloro- 

 glucins i.iit Aldehyden. M., 34, (1915). 



Oxyquiiiol C B H ■ oii,.[i : 2 : ij 

 Oxyhydroquinone. 

 Monti. L13553. A.zione del cloruro 

 di alluminio sul triacetato dell'ossiidro- 

 chinone, 



1 : 3-DlOXY- 1-SOLPHYDROBENZENE 



C 6 H 3 (OH) 2 .SH 

 Dimethyl ether 6 rJ 3 (< )Me) 2 .SH. 

 Pollak it. Wienenberger M., 35, 

 (1467/ 



Trisulphydrobenzene i'JLSII ;1 :2:4] 

 Derivativ 

 PoUak. M., 35, (1445). 



PHENOLS CsHioO 



Ethylpyrogallol 

 C 6 H 2 Et(Ofl) 3 [l:2:3:4] 

 Cleinniensen. B., 47, (57). 



Dioxymethylbenzyl alcohol 



(HO) 2 C 6 H 2 Me.CH 2 .OH 



Methylene ether and dimethyl ether 



(MeO) 2 C 6 H 2 Me.CH 2 OH 



Robinson (Mrs). L14533. Reaction 



of homopiperonyl and of bouioveratryl 



alcohols. 



PHENOL C 10 H 14 O3 



Diethylpyrogallol 

 -; OH) 3 [l:5:2:3:4] 

 Clemmensen. B., 47, 58 



PHENOL C,,H„,- 12 0., 

 PHENOL CiuHsOs 



1:4: s-Trioxynaphthalene. 

 a-Hydrojuglone. 

 WiUstatter ii. Wbeeler. L16099. lso- 

 merie der Hydro-juglone. 



TETROLS. 

 PHENOLS CmH 2 „ . o 0< 



PHENOLS C 6 H 6 04 



1:3:4: O-Tetraoxybenzene. 



1 : 3-DIOXY-4 : 6-DIS0LPHYDROBENZENE. 



Dimethyl ether L' 6 II 2 v01Ie) 2 (SH) 2 

 Pollak u. Wienenberger. M., 35, 

 (1467). 



1:3:4:6- u rRA Ul PHI DROBENZEHE 



C 6 H 2 (SH) 4 



Methyl ether and other derivatives. 



PoUak. M., 35, (1445). 



PHENOLS CnH 2 u- 14 4 



PHENOLS C 12 H 10 04 



Diresorcinol C 8 H 3 (OH) 2 ] 2 

 Friedrichs. 1 1 IU.~>~). Oxydation des 

 Tetraoxy-biphenyls zu Tartronsaure. 



3:4:3': 4'-Tetraoxydiphenyl 



(HO) 2 C 6 H 3 .C 6 H 3 (OB ., 



Tetramethyl ether. 



Seer u. Ehrenreich. M., 34, (646). 



1240 REDUCED BENZENOID- 

 OLS. CYCL1C-OLS OTHER 

 THAN BENZENOID-OLS. 



Tarbouriech. L15496. Transpositions 

 pinacoliques dans la seTie du cyclo- 

 hexane. 



OLS C„H 2 ,,0 



ol C S H I6 



2 ■. 2DimethylcyclohexanoM 

 Meerwein. A., 405, (142). 



OL CioH 20 



Menthol. 

 Don. 110506. Ein Thymol-Menthol- 

 Emulsoid in Glyzerin. 



OLS C„H 2 n- 2 



OL CioH 8 



Borneol C 10 H 17 .OH 



Aloy et Brustier. L09063, Catalyse 

 du borneol en presence de metaux et 

 d'oxydes metalliques. 



Kenyon & Pickard. 112277. Rotatory 



powers of the borneols. 



Meerwein. L13328. Reaktions- 

 mechanismus der Umwandlung von 

 Borneol in Camphen. 



Peacock. 114011. Rotatory powers, 

 refractivities, and molecular solution- 

 volumes of borneol in certain solvents. 



Epiborneol (',,11, 

 Bredt u. Perkin. J. pi , 89, 254 



Thujenol. 



Thujyl alcohol. 



6ugaev et Fomin. 110295. Les 

 alcools thuyiliques isomeres. ^Russe.) 



