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2001 esterification, transesterification esterification, transesterification O 0315 32 - 064 Lewis Acid Promoted Transesterification of N-Acyl Oxazolidinones under Mild Conditions. In the presence of mild Lewis acid catalysts TLA, MgBr 2 , or Sc(O-Tf) 3 N-acyl oxazolidinones are smoothly converted to the corresponding methyl esters. The mild conditions suppress racemization of chiral substrates and methanolysis of acid-sensitive groups. — (ORITA, AKIHIRO; NAGANO, YOSHIFUMI; HIRANO, JUNICHI; OTERA, JUNZO; Synlett (2001) 5, 637-639; Dep. Appl. Chem., Okayama Univ. Sci., Ridai, Okayama 700, Japan; EN) 1

ChemInform Abstract: Lewis Acid Promoted Transesterification of N-Acyl Oxazolidinones under Mild Conditions

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Page 1: ChemInform Abstract: Lewis Acid Promoted Transesterification of N-Acyl Oxazolidinones under Mild Conditions

2001 esterification, transesterification

esterification, transesterificationO 0315

32 - 064Lewis Acid Promoted Transesterification of N-Acyl Oxazolidinonesunder Mild Conditions. — In the presence of mild Lewis acid catalystsTLA, MgBr2, or Sc(O-Tf)3 N-acyl oxazolidinones are smoothly converted tothe corresponding methyl esters. The mild conditions suppress racemizationof chiral substrates and methanolysis of acid-sensitive groups. — (ORITA,AKIHIRO; NAGANO, YOSHIFUMI; HIRANO, JUNICHI; OTERA, JUNZO;Synlett (2001) 5, 637-639; Dep. Appl. Chem., Okayama Univ. Sci., Ridai,Okayama 700, Japan; EN)

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Page 2: ChemInform Abstract: Lewis Acid Promoted Transesterification of N-Acyl Oxazolidinones under Mild Conditions

2001 esterification, transesterification

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