前往化源商城

The Journal of Organic Chemistry

Structure and Reactivity. I. The Oximation Rates of Some Straight-Chain and Monomethyl-Substituted Alkanones

PG Kletzke

文献索引:Kletzke,P.G. Journal of Organic Chemistry, 1964 , vol. 29, p. 1363 - 1366

全文:HTML全文

被引用次数: 10

摘要

'The oxinration rates have been determined for 65 straight-chain and monomethyl- substituted alkanones. The methyl ketones are the most reactive of the straight-chain ketones studied, followed by the ethyl ketones, The propyl and higher ketones have the same rate. A methyl group on the first carbon adjacent to the carbonyl group lo\ rers the rate the most as compared to the corresponding straight-rhain cwrnpounds. This decreased ...

 相关合成线路

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%

~%