1240 



474 



1240 



Perkin, W. H., sen. [IMagnetic rota- 

 tion and refractive value of borneol.] 

 London, J. Chem. Soc, 81, 1902, (309- 

 317). 



ISOBOENYL FORMATE, ACETATE, BDTYRATE, 



and isovALERATE and their physical 

 constants. 



Kondakow, I[van]. Synthesen unter 

 Eiuwirkuiig von Zinkchlorid in der 

 hydroaromatischen Reihe. J. prakt. 

 Chem., Leipzig, (N.F.), 65, 1902, (201- 

 238). 



DiBOItNEOL.VillNE C20H35O2N i.e. 



C8Hi4<9^^ I : NH 



' ' CH(OH)J. 



Einhom, Alfred und Jalin, Stephan. 

 Zur Kenutuiss des Aminocamphers. 

 Berlin, Ber. D. chem. Ges., 35, 1902, 

 (3057-3608). 



Isofenchyl alcohol. 



ISOFESCHYL FuRMATK, ACETATE and VALER- 

 ATE and their physical constants. 



Kondakow, l[van]. Syntliesen uuter 

 Einwirkung von Zinkchlorid in der 

 hydroaromatischen Reihe. J. prakt. 

 Chem., Leipzig, (N.F.), 65, 1902, (201- 

 238). 



Cineol. 



Compound of cineol uith reaorchi and 

 ■with pyroganoJ. 



Baeyer, Adolf imd Villiger, Victor. 

 Ueber die 1)asischen Eigenschaften des 

 Sauerstoffs. (3. Mitt.) Berlin, Ber. D. 

 chem. Ges., 35, 1902, (1201-1212). 



a-Oxycamphor 



CjoHieOj i.e. CsU,,<^^^^ ' 



Its methijl and ethyl ethers and plienyl- 

 urethanc. 



Manasse, 0. Ueher Oxycampher. 

 (2. Mitt.) Berlin, Ber. D. chem. Ges., 

 35, 1902, (3811-3828). 



CH.OH 

 )3-0xy camphor C8Hi4<^q 



Its oxune, phcnylhydrazone, semi- 

 carbazone and benzenesulphojiate. 



Manasse, 0. Berlin, Ber. D. chem. 

 Ges., 35. 1902, (.3811-3828). 



OLS CnH2„-40 



OLS CioHuO 



Hydroxycamphene. 



Forster, Martin Onslow. . . . 

 Conversion of hydroxycamphene into 

 )3-halogen derivatives of camphor. 

 [Methyl and ethyl ethers of hydroxy- 

 camphene.] London, J. Chem. Soc, 81, 

 1902, (204-274); [abstract] London, 

 Proc. Chem. Soc, 18, 1902, (25-26). 



DI-OLS. 



DI-OLS CnH2n-202 



DI-OLS CioH.sOz 



Caraphor-glycol. 



Phcnylurcthnne C24H2(i04N2 



pf, .CH.O.CO.NH.Ph 

 i.e. ^'8au<(^^ Q (;,Q^jj j,j, 



Manasse, 0. Ueber Oxycampher. 

 (2. Mitt.) Berlin, Ber. D. chem. Ges., 

 35, 1902, (3811-3828). 



DI-OLS C14H26O2 



Disuberyl glycol 



LCH2 . CH2 . (Mi J 2 



Markovnikov, V. St. Peterl)urg, 

 Znrn. russ. iiz.chim. Obsc., 34, .1902, 

 (904-916). 



DI-OLS CnH2n-302 

 DI-OLS C,4H2o02 



Oxybenzyl-methylcyclohexanol. 



Compound. Ci4H2o02 proloably 

 CHMe< gg^ ; gg^°^^>C2H2(01I)Ph 



T^try, L. Derives de la /3-methyl- 

 cyclohexanone. Paris, Bui. soc. chim., 

 (ser, 3), 27, 1902, (302-307). 



