艾鲁吉诺辛 98B 的总合成
Barry M Trost1, Toshiyuki Kaneko, Neil G Andersen
1Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. bmtrost@stanford.edu
Journal of the American Chemical Society
|November 3, 2012
概括
通过一种新的催化反应,首次实现了aeruginosin 98B的总合成. 这种方法通过不对称的基基化有效地创建复杂分子.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
- 药用化学 医学化学
背景情况:
- 氨酸98B是一种复杂的天然产品,具有潜在的生物活性.
- 开发高效的合成路径对于研究和利用这些化合物至关重要.
研究的目的:
- 为了实现第一个全合成 98B. aeruginosin.
- 开发一种新高效的合成方法.
主要方法:
- 催化了分子内不对称的性基化.
- 使用基碳酸盐的二聚体混合物.
- 使用一种种族性素连接体 (L1).
主要成果:
- 成功和高度分类选择性的阿鲁吉诺辛98B的总合成.
- 证明一种有效的Pd催化不对称的基基化.
- 使用一种种族性联体使得高立体选择性成为可能.
结论:
- 开发的合成途径提供了获得98B.aeruginosin的途径.
- 关键的Pd催化反应是立体选择合成的强大工具.
- 这项工作为合成相关的自然产品开辟了道路.
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