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KMID : 0043319820050020097
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Archives of Pharmacal Research
1982 Volume.5 No. 2 p.97 ~ p.101
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Novel Aspects of Bromolactonization Reaction Using N-Haloimides in an Aprotic Polar Solvent
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Jew SS
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Abstract
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Depending upon the results obtained by the bromolactonization of olefinic acids (9-11) by means of N-bromosaccharin (4), the influence of the stabilities of the imidic anions resulted from heterolytic cleavage of N-haloimides, such as N-bromosuccinimide (1), N-bromophthalimde (2), and N-bromosaccharin (3) in dry N,N-dimethylformamide on the reactivity is elucidated.
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