Under the influence of the rhodium catalyst, the ester-tethered 1,6-diynes undergo a cycloisomerization reaction. This involves the formation of new carbon-carbon bonds, typically through the opening of the cyclopropanol ring and subsequent rearrangement of the atoms.
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((1-(2-iodophenyl)vinyl)oxy)trimethylsilane
7-pentadeuteriophenyl-4,4-bis(methoxycarbonyl)-1,6-enyne
PLATINUM(II)
N-(3-(4-bromophenyl)prop-2-yn-1-yl)-4-methylbenzenesulfonamide
(1E,5E)-1-(2,5-bis-trimethylsilyl-hepta-1,5-dien-3-ynyl)-4-methoxybenzene
2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate
2-benzyloxycarbonylamino-2-methylhexa-3,4-dienoic acid methyl ester
1-((4-methoxyphenyl)ethynyl)-2-vinylbenzene
4-methyl-N-[2-(prop-2-yn-1-yl)phenyl]benzenesulfonamide
2-(3-methoxy-prop-1-ynyl)-4,5-dimethyl-6-(5-phenyl-pent-1-ynyl)-pyrimidine
1H-Indole, 2-(pentafluorophenyl)-
C17H26O3Si
1-[5-(1-ethynyl)-2,2-dimethyl-(4S,5R)-1,3-dioxolan-4-yl]-3-triphenylmethyloxy-(1S)-propan-1-ol
cinnamyl 2-butynyl ether
