The reactivity of cyclic ketones is influenced by the ring strain. Smaller ring sizes (e.g., cyclopropyl ketones) often have higher ring strain, making them more reactive. Larger rings may be less strained and therefore less reactive.
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1-Cycloundecene-1-carboxylic acid, methyl ester, (E)-
1-p-methoxybenzyloxy-3-methylbut-3-en-2-ol
7-Azabicyclo[2.2.1]heptane, 7-benzoyl-
4,4-Dimethyl-5-oxo-2-phenethyl-tetrahydro-furan-3-carboxylic acid ethyl ester
2-tosyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid methyl ester
2-[2-(4-Bromo-phenyl)hydrazono]cyclohexanone
methyl 6-O-benzyl-2,3-dideoxy-2,3-C-ethylene-2,4-di-C-methyl-α-D-allopyranoside
[2-(Isopropylamino-methyl)-phenyl]-methyl-amine
1-Propanone, 1-(2-naphthalenyl)-2-phenyl-
3-Azabicyclo[3.2.0]heptane-2,4-dione, 3-butyl-
2-Methyl-6-(toluene-4-sulfonyloxy)-3-vinyl-hexanoic acid ethyl ester
(1S,2R,3S)-2,3-Dimethyl-2-vinyl-cyclohexanol
2,6-di-tert-butyl-4-methylphenyl (cyclohexen-3-yl)acetate
2-benzyl-5-(2-bromo-phenylethynyl)-isoxazolidine
(3S,4R,5R,6S)-3,4,5,6-Tetrakis-benzyloxy-cyclohexane-1,2-diol
4-(1α,5α,6β-3,6-Dimethyl-3-azabicyclo[3.1.0]hex-6-yl)morpholine
5-[ISOCYANO-(TOLUENE-4-SULFONYL)-METHYL]-BENZO[1,3]DIOXOLE
Spiro[2.4]hepta-4,6-diene-1-carboxaldehyde, 2,2-dimethyl-, (R)- (9CI)
N-benzyl-N-<1-hydroxypent-2(Z)-en-5-yl>crotonamide
