Ketones. 



519 



1540 



1 : 3-Dimethyl l-cyclopentanone 

 CHMe.CE 

 ' CO- ('MM,. 

 HaUer et Cornubert. C.R, 158, 1 1G16). 



Methylcyclohexanone 

 2: l-l 'ioziuiKO-1-UE uni 3 



HEXANONE 



BO.N:C<gg;^gg>CHMe 



\U 2 !-|)l.W!I\n-l-Mi:TllYL-3-CYCLO- 



III. \ r 



Kotz. I. pi., 90. 357). 



KETONES CH„0 



L : 2 : i-Trimethyl-3-cyclopentanone 



CH CHMe.CHMe 



2 CHMe.CO 



also 1:2:4: i -Tetramethyl-3-cyclo- 



pentanone and 1:2:2:4: 1 penta- 



methyl-'5-cyclopentanone. 

 HaUer .t Cornubert. C.lv.,158, 1616;. 



l : l-Methylacetylcyclopentane 



9 H 2 CH 2>CMe.CO.I 

 CH 2 .CB 

 Meerwein A., 405, 172). 



KETONE C H 16 



1:1:3: 3-Tetramethyl---cyclopenta- 



nr . -CMe 

 none CO< 



CMe 2 .CH 2 



Haller et Cornubert. CI.'., 158, (298). 

 KETONE C, H I8 O 



Menthone. 

 Kenyon & Pickard. L12i'77. Rota- 

 tory powers of the menthones. 



KETONE C13H34O 



1:1:3: 3-Tetrapropyl--cyclo- 



hexanoneco<;:;: ; ;;-;';!->cH 2 



Cornubert. C.R., 159. , 5 . 

 KETONES C..H...-.0 



KETONE C H 



Methylcyclopentenone. 

 Oodchot. L11238: Svnthese d'une 

 inethylcyclopentenone. 



KETONE C H, 



2-Methyl-''-ethyl- a -cyclopente- 



1 nn^CMe : CE1 

 none l 1 'K 



CH 



Blaise. CI!., 158, 



KETONES C.H4O 



l Allyl-'-'-cyclohexanone 

 C II -CH<g^-g^>CB 

 Cornubert. C.R., 158, (1900). 



Camplienilone. 

 Sy hi 1 

 Komppa u. Hintikka 1!., 47, (1550 

 Hintikka. 111851. (Finnisch ) 



Fenchocamphorone. 

 Syntl 1 

 Komppa. I'.., 47, (933). 



Santenone. 

 Rimini. 114494. 



KETONES C, H.O 



Methylallylcyclohexanone 



various isomerides 



Also methylcliallylcyclohexanones 

 and methyltriallylcyclohexanones. 

 Cornubert. C.R., 158, (1900). 



Camphor. 



Bohrisch. L09716. Identitatspriil'ung 

 des offizinellen Kampfers. 



Carnot et Cairis. 110049. To.xieite 

 comparative du camphre suivanl 

 dift'erents solvanta. 



Cusmano e Poccianti. 110316. Bi- 

 bromotetraidrocarvone e sua trasfor- 

 mazione in bucci 



Forster <5c Kunz. U<i'j37. Isomeric 

 iiviliazoximes of cauiphorquinone. 



Kausch. 112235. Herstellung von 

 Kampfer auf synthetischem Wege. 



Lowry & Steele. L13000. New 

 chloro-camphor. 



Malosse. 113112. Pouvoir rotatoire 

 specifique du camphre dissous dans 

 l'alcool a 90°. 113113: Pouvoir 

 rotatoire du camphre dissous dans 

 l'huile d'oli 



