
TY  - JOUR
A1  - Jones, RA 
A1  - Lindner, JA 
T1  - Pyrrole studies. V. Applications of the Wittig reaction to the synthesis of substituted pyrroles
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1965
VL  - 18
IS  - 6
SP  - 875
EP  - 885
KW  - 
UR  - https://doi.org/10.1071/CH9650875 
N2  -     trans-1-(2-Pyrrolyl)but-1-en-3-one, trans-1-(1-methyl-2-pyrrolyl)but-1-en-3-one, ethyl trans-2-(2-pyrrolyl)acrylate, ethyl trans-2-(1-methyl-2-pyrrolyl)acrylate, 2-vinylpyrrole, 1-methyl-2-vinylpyrrole, and the cis and trans isomers of 2-styrylpyrrole, 1-methyl-2-styrylpyrrole, and 1-phenyl-2-(2-pyrrolyl)prop-1-ene have been prepared using the Wittig reaction. The electronic and infrared spectra of these compounds are recorded. The modified Wittig reaction, using diethyl phosphonates, is only satisfactory with N-substituted carbonylpyrroles. 
ER  -

