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ChemInform Abstract: Highly Regioselective Opening of Optically Active N-Boc-2,3-aziridino Alcohol Derivatives with Metal Halides.

✍ Scribed by G. RIGHI; T. FRANCHINI; C. BONINI

Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
29
Category
Article
ISSN
0931-7597

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✦ Synopsis

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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✍ G. RIGHI; R. D'ACHILLE; C. BONINI πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 1 views

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