
TY  - JOUR
A1  - Crank, G 
A1  - Khan, HR 
T1  - Formation of Thioamide Derivatives from Reactions of Isothiocyanates with Oxazol-2-amines
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1985
VL  - 38
IS  - 3
SP  - 447
EP  - 458
KW  - 
UR  - https://doi.org/10.1071/CH9850447 
N2  - 4-Substituted oxazol-2-amines react with isothiocyanates to give products having a thioamide function at C5. The reaction is considered to be an electrophilic process in competition with the usual reaction of the amino group with the isothiocyanate . The nature of the isothiocyanate and the type of substituent at C4 affect the amount of the thioamide product formed. Some chemical properties of the thioamides are also investigated. 
ER  -

