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ChemInform Abstract: Highly Regioselective Opening of Optically Active N-Boc-2,3-aziridino Alcohol Derivatives with Metal Halides. by G. RIGHI; T. FRANCHINI; C. BONINI is a Chemistry article available to read on EtoBox.
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Highly Regioselective Opening of Optically Active N-Boc-2,3aziridino Alcohol Derivatives with Metal Halides. -Treatment of silyl-protected N-Boc-aziridino alcohols (chiral and racemic) with MgBr 2 as activated metal halide results in regio-and stereoselective ring opening to give brominated derivatives of amino alcohols. -(RIGHI, G.; FRANCHINI, T.;
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It is typically read by researchers, students, and practitioners in Chemistry.
- Author
- G. RIGHI; T. FRANCHINI; C. BONINI
- Publisher
- John Wiley and Sons; Wiley (John Wiley & Sons); Wiley (ISSN 0931-7597)
- Published
- 1998
- Language
- EN
- Field
- Chemistry (Physical Sciences)