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Cyclopentyl iodide

Cydopentanol, 255 Cyclopentanone, 336, 340, 489, 493 Cyclopentyl bromide, 277 Cydopentyl chloride, 276 Cyclopentyl iodide, 285... [Pg.1172]

Cyclopentane Cyclopentyl chloride Cyclopentene Cyclopentyl iodide... [Pg.142]

Naito has also described analogous tandem radical addition-cyclization processes under iodine atom-transfer reaction conditions [16,32], Treatment of 186 with z-PrI (30 eq.) and triethylborane (3x3 eq.) in toluene at 100 °C gave, after cleavage from the resin, the desired lactam product 190 in 69% yield (Scheme 46). Similar reactions involving cyclohexyl iodide, cyclopentyl iodide, and butyl iodide were also reported as well as the reaction with ethyl radical from triethylborane [16,32], The relative stereochemistry of the products was not discussed. [Pg.120]

See other pages where Cyclopentyl iodide is mentioned: [Pg.276]    [Pg.342]    [Pg.276]    [Pg.342]    [Pg.286]    [Pg.283]    [Pg.349]    [Pg.286]    [Pg.85]    [Pg.187]    [Pg.187]    [Pg.37]    [Pg.1264]    [Pg.508]    [Pg.286]    [Pg.254]    [Pg.317]    [Pg.41]    [Pg.532]    [Pg.254]    [Pg.317]    [Pg.1391]    [Pg.1436]    [Pg.1436]    [Pg.426]    [Pg.418]    [Pg.286]    [Pg.142]    [Pg.187]    [Pg.187]    [Pg.271]    [Pg.337]    [Pg.60]    [Pg.304]    [Pg.254]    [Pg.319]    [Pg.7]    [Pg.405]    [Pg.465]    [Pg.702]    [Pg.458]    [Pg.453]    [Pg.464]   
See also in sourсe #XX -- [ Pg.285 ]

See also in sourсe #XX -- [ Pg.285 ]



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4-Cyclopentyl

Cyclopentyl iodide, reaction

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