Once the radicals are generated, they can undergo addition to the olefinic bond in the starting material. This radical addition step creates a new carbon-carbon bond, forming a cyclohexyl radical intermediate.
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erythro-4-benzyloxy-5-methyl-3-(tetrahydro-2-pyranyloxy)-5-hexen-1-yne
(E)-1-
N-(phenylmethoxy)-N-2-propen-1-yl-2-propenamide
(E)-4-[Benzenesulfonyl-(3-oxo-propyl)-amino]-but-2-enoic acid ethyl ester
4'-phenoxy[1,1'-biphenyl]-2-amine
5-(tert-butoxycarbonyl)pentyl benzoate
methyl (R)-N-(benzyloxycarbonyl)-2-amino-5-(methylthio)pentanoate
(Z)-8-(tert-Butyl-diphenyl-silanyloxy)-3-hydroxy-6-methyl-2-methylene-oct-6-enoic acid methyl ester
(5R)-5-methyl-1-(2-propen-1-yl)-2-(2-propen-2-yl)cyclohexene
(+)-PULEGONE
Phentydrone
(4S,5R)-4-(2-hydroxypropan-2-yl)-5-((-)-menthyloxy)-dihydrofuran-2(3H)-one
diethyl (2-oxo-4-(p-methoxyphenyl)-2H-chromen-3-yl)phosphonate
(1S,6R)-N-[N-(S)-(p-toluenesulfonyl)-p-toluenesulfonimidoyl]-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-enamine
3,8-Dimethyl-3,8-diphenyl-2,7-dioxaspiro<4.4>nonane-1,6-dione
Silane, trimethyl[2-(triphenylgermyl)ethenyl]-, (E)-
(E)-(1-iodo-3-methylbut-1-en-1-yl)benzene
cholestane
2-HEXANONE OXIME
