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(2S,3R,4S)-4-羟基异亮氨酸的不对称合成
Asymmetric Synthesis of (2S,3R,4S)-4-Hydroxyisoleucine
【摘要】 对甲氧基苯胺和乙醛酸乙酯依次经缩合、(S)-脯氨酸催化不对称Mannich反应和DBU不对称转化制得(2S,3R)-2-(4-甲氧基苯胺基)-3-甲基-4-氧代戊酸乙酯,再经CAN氧化脱保护、硼氢化钠还原和氢氧化锂水解得(2S,3R,4S)-4-羟基异亮氨酸,总收率约30%。
【Abstract】 (2S,3R,4S)-4-Hydroxyisoleucine was synthesized from p-anisidine and ethyl glyoxalate with an overall yield of about 30% by condensation,(S)-proline-catalyzed asymmetric Mannich reaction,DBU-catalyzed asymmetric transformation to afford ethyl(2S,3R)-2-(4-methoxyphenylamino)-3-methyl-4-oxo-pentanoate,which was subjected to deprotection with ceric ammonium nitrate,reduction with NaBH4 and then hydrolysis with lithium hydroxide.
【关键词】 (2S,3R,4S)-4-羟基异亮氨酸;
葫芦巴;
胰岛素分泌促进剂;
不对称合成;
【Key words】 (2S,3R,4S)-4-hydroxyisoleucine; Trigonella foenum-graecum; insulinotropic; asymmetric synthesis;
【Key words】 (2S,3R,4S)-4-hydroxyisoleucine; Trigonella foenum-graecum; insulinotropic; asymmetric synthesis;
- 【文献出处】 中国医药工业杂志 ,Chinese Journal of Pharmaceuticals , 编辑部邮箱 ,2010年07期
- 【分类号】R914
- 【被引频次】4
- 【下载频次】257