作者:G. Yu. Ishmuratov、E. R. Latypova、P. Ya. Kharisov、R. R. Muslukhov、A. A. Bannova、R. F. Talipov、G. A. Tolstikov
DOI:10.1134/s1070428008050035
日期:2008.5
(R)-4-Menthenone compared with common cyclic enones exhibits considerably lower reactivity in 1,4-conjugate addition of organometallic reagents, is inert in Michael reactions and pyrazoline formation evidently due both to the distorted polarization in the enone system and to steric hindrances from the alpha-isopropyl group in the cyclohexene ring.