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L-Iodo-5-decyne

Bromo- and l-iodo-5-decyne were studied because they do not possess electroactive carbon-carbon triple bonds and therefore the electrolytic cleavage of the carbon-halogen bonds can be investigated over a relatively wide range of potentials. The reduction product distribution proved to be dependent upon the potentials employed during the... [Pg.584]

The reaction of l-iodo-5-decyne, nickel carbonyl, and potassium tert-butoxide leads to a mixture of three ester products (CLXXXIII)-(CLXXXV) (Crandall and Michaely, 1973). [Pg.140]


See other pages where L-Iodo-5-decyne is mentioned: [Pg.350]    [Pg.586]   
See also in sourсe #XX -- [ Pg.140 ]




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