
TY  - JOUR
A1  - Watanabe, S 
A1  - Fujita, T 
A1  - Suga, K 
A1  - Haibara, M 
T1  - A convenient preparative method of jasmone and its related compounds
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1982
VL  - 35
IS  - 8
SP  - 1739
EP  - 1741
KW  - 
UR  - https://doi.org/10.1071/CH9821739 
N2  - The reaction of (2')-hept-4-enoic acid (1) with vinylmagnesium bromide gave (Z)-undeca-1,8-dien- 5-one (2). The oxidation of the terminal vinylic group of (2) affords (Z)-undec-8-ene-2,5-dione (3). Jasmone (4) was obtained by the usual alkali cyclization of (3). A variety of alkylcyclopentenones were prepared by the same method. 
ER  -

