Facile inversion of configuration of N-Boc-β-aminoalcohols via SN2 cyclization to oxazolidinones
摘要:
Oxazolidinones are obtained by the cyclization of mesylates derived from N-Boc-beta -aminoalcohols. Hydrolysis of the N-Boc-oxazolidinones regenerates the protected aminoalcohols with inverted configuration at the hydroxy group. (C) 2000 Elsevier Science Ltd. All rights reserved.
Facile inversion of configuration of N-Boc-β-aminoalcohols via SN2 cyclization to oxazolidinones
作者:Fabio Benedetti、Stefano Norbedo
DOI:10.1016/s0040-4039(00)01753-6
日期:2000.12
Oxazolidinones are obtained by the cyclization of mesylates derived from N-Boc-beta -aminoalcohols. Hydrolysis of the N-Boc-oxazolidinones regenerates the protected aminoalcohols with inverted configuration at the hydroxy group. (C) 2000 Elsevier Science Ltd. All rights reserved.