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Stereoselectivity in the Formation and Radical Reduction of Cyclic Bromoacetals, Key Intermediates for the Synthesis of δ-Hydroxy- and ε-Hydroxy-α-methylcarboxylic Acid Esters by Hajime Nagano; Ayako Mikami; Tomoko Yajima is a Chemistry article available to read on EtoBox.
What is Stereoselectivity in the Formation and Radical Reduction of Cyclic Bromoacetals, Key Intermediates for the Synthesis of δ-Hydroxy- and ε-Hydroxy-α-methylcarboxylic Acid Esters about?
We report the stereoselectivity in the formation and radical reduction of six-and seven-membered cyclic bromoacetals. The oxidative ring cleavage of the resulting acetals gave the corresponding acyclic d-hydroxyand o-hydroxy-a-methylcarboxylic acid esters.
Who reads Stereoselectivity in the Formation and Radical Reduction of Cyclic Bromoacetals, Key Intermediates for the Synthesis of δ-Hydroxy- and ε-Hydroxy-α-methylcarboxylic Acid Esters?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- Hajime Nagano; Ayako Mikami; Tomoko Yajima
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
- Published
- 2003
- Language
- EN
- Field
- Chemistry (Physical Sciences)
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