
TY  - JOUR
A1  - D'Arcy, BR 
A1  - Lewis, KG 
A1  - Mulquiney, CE 
T1  - Reactions of Stenhouse Salts. III. Transformation Products Under Acidic and Basic Conditions
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1985
VL  - 38
IS  - 6
SP  - 953
EP  - 965
KW  - 
UR  - https://doi.org/10.1071/CH9850953 
N2  - Mild acid treatment of alcoholic solutions of Stenhouse salts has been shown to yield a mixture of the corresponding N-arylpyrrole-2-carbaldehyde and the N-aryl-3-hydroxypyridinium salt. Treatment of alcoholic solutions of the Stenhouse salts with a variety of bases leads to 4-substituted 2-arylaminocyclopent-2-enones. 
ER  -

