异芳化合物,类素的高度酶选择性催化化,类素
Wen-Bo Wang1, Sheng-Mei Lu, Peng-Yu Yang
1Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. China.
Journal of the American Chemical Society
|August 28, 2003
概括
开发了一种新的方法,用于对林衍生物的高度反选择性化. 这种方法有效地合成了光学活性四化素,包括天然化物,具有高反体过剩.
科学领域:
- 有机化学 有机化学
- 不对称的催化剂.
背景情况:
- 奎诺林衍生物是药物化学中的重要支架.
- 开发有效的非对称合成方法,以治疗性四化素至关重要.
研究的目的:
- 开发一种对林衍生物的高度反选择性化方法.
- 将这种方法应用于自然存在的类化合物的不对称合成.
主要方法:
- 使用一种催化剂前体 ([Ir(COD) Cl]2) 结合一种性联体 ((R) -MeO-Biphep) 和 (I2).
- 将开发的催化系统应用于化素基质的化.
主要成果:
- 实现了林衍生物的高度反选择性化.
- 合成的光学活性四基诺林高达96%的反体过量 (ee).
- 成功地将该方法应用于安古氨酸,氨酸和氨酸的不对称合成.
结论:
- 开发的催化系统提供了一条高效的途径,以致于获得基丰富的四化.
- 这种方法对复杂的性类化合物的合成有价值.
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