Acyclic Stereocontrol of Free Radical Reactions Involving Alkyl 2-(1-Hydroxyalkyl)propenoates
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The addition of cyclohexyl and t-butyl free radicals to silylated derivatives of alkyl 2-(1-hydroxyalkyl) propenoates was found to be stereoselective . In the case of the cyclohexyl radical the stereoselectivity was dependent upon the conditions used to generate the free radical and to quench the intermediate. Stereoselectivity in additions of the t-butyl radical was found to be temperature-dependent. In all cases stereoselectivity increased as the steric bulk of the group attached to the carbinol oxygen increased. A simple model which accounts for the stereoselectivity is proposed.
1978 ◽
Vol 43
(2)
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pp. 224-228
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2016 ◽
Vol 50
(12)
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pp. 1361-1373
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1961 ◽
Vol 83
(8)
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pp. 2017-2018
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1964 ◽
Vol 3
(9)
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pp. 602-608
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1973 ◽
Vol 95
(8)
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pp. 2643-2646
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1964 ◽
Vol 85
(5)
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pp. 307-312,A25
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1959 ◽
Vol 81
(5)
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pp. 1120-1126
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