Asymmetric Synthesis of N‐tert‐Butoxycarbonyl α‐Amino Acids. Synthesis of (5S,6R)‐4‐tert‐Butoxycarbonyl‐5,6‐Diphenylmorpholin‐2‐one
Asymmetric Synthesis of N‐tert‐Butoxycarbonyl α‐Amino Acids. Synthesis of (5S,6R)‐4‐tert‐Butoxycarbonyl‐5,6‐Diphenylmorpholin‐2‐one
复制标题
N-叔丁氧基羰基 α-氨基酸的不对称合成 (5S,6R)-4-叔丁氧基羰基-5,6-二苯基吗啉-2-酮的合成。
DOI：
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发表时间：
2003
期刊：
影响因子：
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通讯作者：
D. Zhai
中科院分区：
文献类型：
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作者：
Robert M. Williams;P. Sinclair;D. Demong;Daimo. Chen;D. Zhai
Ethylbromoacetate
Di-tert-butyl carbonate
p-Toluenesulfonic acid
Benzeneethanol, beta amino-alpha phenyl-
Ethyl-N-(1′2-diphenyl-2-hydroxyethyl)glycinate
Ethyl N-tert-butyloxycarbonyl-N-(1′2′-diphenyl-2-hydroxyethyl)glycinate
(5S,6R)-4-tert-Butyloxycarbonyl-5,6-diphenymorpholin-2-one
4-Morpholinecarboxylic acid, 6-oxo-2,3-diphenyl, 1,1, dimethylethyl-2-one
Keywords:
asymmetric synthesis;
alpha-amino acids;
waste disposal;
lactones;
morpholine;
bromination;
stereoselective coupling;
organometallic reagents
