
TY  - JOUR
A1  - Birch, AJ 
A1  - Keogh, KS 
A1  - Mamdapur, VR 
T1  - Conversion of 2,5-disubstituted furam into (Z)-jasmone
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1973
VL  - 26
IS  - 12
SP  - 2671
EP  - 2674
KW  - 
UR  - https://doi.org/10.1071/CH9732671 
N2  - Two new syntheses of (Z)-jasmone (3; R = (Z)-CH2CH=CHCH2Me) are reported. One is based on an initial oxidative opening of a 2,5- disubstituted furan (1; R = (Z)-CH2CH2CH=CHCH2Me) to an enedione (2; R = (Z)-CH2CH2- CH=CHCH2Me), the other on an efficient procedure for obtaining the keto acid (3; R = CH2CO2H) and the extension of the acetic acid side chain stereospecifically. 
ER  -

