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作 者:Guang Yu XU Yi ZHOU Man Cai XU
机构地区:[1]College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081
出 处:《Chinese Chemical Letters》2006年第3期302-304,共3页中国化学快报(英文版)
摘 要:A convenient synthesis of oxazolidinone antibacterial linezolid from readily available L-ascorbic acid is described. The key steps include reductive amination of arylamine and (S)-glyceraldehyde acetonide in the presence of NaBH4 and 4A sieve, followed by hydrolysis and regioselective cyclization.A convenient synthesis of oxazolidinone antibacterial linezolid from readily available L-ascorbic acid is described. The key steps include reductive amination of arylamine and (S)-glyceraldehyde acetonide in the presence of NaBH4 and 4A sieve, followed by hydrolysis and regioselective cyclization.
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