
TY  - JOUR
A1  - Davis, M 
A1  - Homfeld, E 
A1  - McVicars, J 
A1  - Pogany, S 
T1  - The chemistry of 2,1-benzisothiazoles. IX. The reaction of 3-chloro-substituted 2,1-benzisothiazoles with nucleophiles and the preparation of(2,1-Benzisothiazol-3-yl)acetic acid
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1975
VL  - 28
IS  - 9
SP  - 2051
EP  - 2055
KW  - 
UR  - https://doi.org/10.1071/CH9752051 
N2  - 3-Chloro-2,1-benzisothiazole (2; R = H, R? = Cl) and 3,5-dichloro-2,1- benzisothiazole (2;R,R? = Cl) react readily with nucleophiles, and yield 3-substituted products. Acid hydrolysis of one such product, ethyl (2,1-benzisothiazol-3-yl)cyanoacetate (2; R = H, R? = CH(CN)CO2Et),affords (2,1-benzisothiazol-3-yl)acetic acid (2; R = H, R? = CH2CO2H), an auxin analogue. 
ER  -

