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Cyclonite boiling vats .

Cyclonona-l,4,7-triyne, 1, and tricyclopropabenzene, 2.

Cyclonucleoside formation from C5 -radicals.

Cycloocta c e biphenylene and related structures studied by Wilcox.

Cyclooctane oxidation catalyzed by Ru colloids in biphasic water-organic media.

Cyclooctane transfer dehydrogenation using tbe as a sacrificial hydrogen acceptor.

Cyclooctanones by oxy-Cope reairangement

Cyclooctanones by oxy-Cope rearrangement

Cyclooctatetraene synthesis throngh Pd-catalyzed homocoupling of horylvinyl iodohenzenes.

Cyclooctatetraene synthesis through Nickel-catalyzed 2-I-2-I-2-I-2 cycloadditions of diynes.

Cyclooctatetraene, an example of a molecule that has alternating single and double bonds but is not aromatic

Cyclooctatetraeneactinide complexes

Cyclooctatriene synthesis through Ga-mediated cycloisomerization of enynes.

Cyclooctene conversion 2- 1,9-tetradecadiene 3- 5,13-octadecadiene 4- 1,9-decadiene 5- 1,9,17-octadecatriene

Cyclooctene conversion 2- l,9E,17-octadecatriene 3- 5E,13E-octadecadiene 4- 5Z,13E-octadecadiene 5- 5Z,13Z-octadecadiene.

Cyclooctene conversion 2- l,9Z-tetradecadiene

Cyclooctene epoxidation.

Cyclooctene synthesis through Re-catalyzed two-carbon ring expansion.

Cyclooctene synthesis through Rh-mediated four-carbon ring expansion.

Cyclooctyne derivatives can be used as alternative click chemistry reactants, as they are capable of reacting with an azide group without the presence of Cu1 to form a cycloaddition product. This reaction proceeds at a slower rate than the Cu1 -catalyzed process, but it avoids the cytotoxic effects that copper addition can have on cells.

Cyclooctyne derivatives for use in copper-free, strain-promoted azide-alkyne cycloadditions designed by Bertozzi 81,83, and Boons j- The second-generation difluorinated derivative 84 is easier to synthesize than 83

Cyclooctynes for strain-promoted cycloadditions with azides in living systems. Fluorination accelerates the cycloaddition because the electron-withdrawing fluoro substituents increase the reactivity of the ring-strained cyclooctyne.

Cyclooligomerization of 1,2-diethynylbenzene and some of its derivatives.

Cyclooligomerization of diazoacetates 1 by cycloaddition reactions.

Cyclooligomerization of ethylene oxide leading to crown ether.



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