
TY  - JOUR
A1  - Feutrill, GI 
A1  - Mirrington, RN 
T1  - An approach to the stereospecific synthesis of nordebromolaurinterol
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1973
VL  - 26
IS  - 2
SP  - 357
EP  - 367
KW  - 
UR  - https://doi.org/10.1071/CH9730357 
N2  - The synthesis of 3-(2?-hydroxyphenyl)-2,3-dimethylcyclopent-ene (8) has been effected in six steps from o-iodoanisole; a key step was the conversion of (7) into (8), each being acid-sensitive, by demethylation with sodium thioethoxide in dimethyl-formamide.     The reactions of (8) and its acetate (22) with several methylenating agents were examined, but no cyclopropane-containing products were obtained. 
ER  -

