After the olefinic C-H activation, the carbon atom from the heptadiene forms a new bond with another carbon atom, resulting in the formation of a cyclic structure. The specific regioselectivity and stereochemistry of this cyclization are controlled by the catalyst and reaction conditions.
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(2-bromoethenylidene)cyclohexane
(2-bromoethenylidene)cyclohexane
3-bromo-1-phenyl-prop-2-yn-1-ol
(R)-2-Oxo-5-phenyl-cyclopentanecarboxylic acid (1S,2R,3R,4S)-4,7,7-trimethyl-3-naphthalen-1-yl-bicyclo[2.2.1]hept-2-yl ester
(E)-(R)-3-(Dimethyl-phenyl-silanyl)-hex-4-en-1-ol
