The addition of tri-sec-butylborohydrides to the 2-acetyl-1,3-oxazolidine 1 can be directed with high selectivity to either the Si or the Re pi-carbonyl face under chelating or non-coordinating conditions, respectively.

DIASTEREOSELECTIVE ADDITION OF METAL-COORDINATED AND NAKED TRI-SEC-BUTYLBOROHYDRIDES TO A NOREPHEDRINE-DERIVED 2-ACETYLOXAZOLIDINE

MANZONI L;
1992

Abstract

The addition of tri-sec-butylborohydrides to the 2-acetyl-1,3-oxazolidine 1 can be directed with high selectivity to either the Si or the Re pi-carbonyl face under chelating or non-coordinating conditions, respectively.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/236688
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