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Can I read Lewis acid-mediated reaction with silyl ketene acetals and allylstannane of the aluminum acetals generated by DIBALH reduction of α-amino acid esters on EtoBox?
Lewis acid-mediated reaction with silyl ketene acetals and allylstannane of the aluminum acetals generated by DIBALH reduction of α-amino acid esters by Syun-ichi Kiyooka; Ken Suzuki; Masashi Shirouchi; Yuichi Kaneko; Shinji Tanimori is a Chemistry article available to read on EtoBox.
What is Lewis acid-mediated reaction with silyl ketene acetals and allylstannane of the aluminum acetals generated by DIBALH reduction of α-amino acid esters about?
The intermediates generated by DIBALH reduction of a-amino acid esters undergo condensation without racemization with silyl ketene acetals and allylstannane in the presence of Lewis acid to afford the corresponding p-hydroxy esters and homoallylic alcohols in good yields while achieving high syn selectivity via an aluminum-assisted chelation control.
Who reads Lewis acid-mediated reaction with silyl ketene acetals and allylstannane of the aluminum acetals generated by DIBALH reduction of α-amino acid esters?
It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- Syun-ichi Kiyooka; Ken Suzuki; Masashi Shirouchi; Yuichi Kaneko; Shinji Tanimori
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4039)
- Published
- 1993
- Language
- EN
- Field
- Chemistry (Physical Sciences)
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