
TY  - JOUR
A1  - Brown, RD 
A1  - Drummond, LJ 
A1  - Lahey, FN 
A1  - Thomas, WC 
T1  - Alkaloids of the Australian Rutaceae: <I>Acronychia baueri</I>. II. Some Reactions of the Alkaloid Acronycine
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1949
VL  - 2
IS  - 4
SP  - 622
EP  - 629
KW  - 
UR  - https://doi.org/10.1071/CH9490622 
N2  - Acronycine, C20H19O3N, is readily converted to noracroaycine, C19H17O3N, a weak base which contains no methoxyl. Acronycine contains a reactive double bond, shown to be present in a dimethylpyran ring by oxidation to an acid which, on heating, yields &#945;-hydroxyisobutyric acid together with a phenol, Cl4H11O3N, and its methyl ether, Cl5H1303N. The action of alcoholic potash on acronycine results in the formation of two phenols, both of which are readily reconverted to acronycine. The bromination of acronycine has also been studied. 
ER  -

