催化不对称的 (-) - 乙烯基酸总合成
Lingchao Cai1, Kui Zhang1, Ohyun Kwon1
1Department of Chemistry and Biochemistry, University of California , Los Angeles, California 90095-1569, United States.
Journal of the American Chemical Society
|February 25, 2016
概括
这项研究提出了一种新型的催化不对称合成 (-) -actinophyllic acid. 一个关键的性素催化取消有效地创建了一个pyrroline中间体,为复杂的分子组装铺平了道路.
科学领域:
- 有机化学
- 合成化学
- 不对称的合成
背景情况:
- (-) 乙酸是一种复杂的天然产品,具有具有挑战性的分子结构.
- 有效和立体选择性的合成途径对于获取这些分子进行进一步研究至关重要.
研究的目的:
- 开发一个催化不对称的 (-) -actinophyllic 酸总合成.
- 建立新的合成方法来构建复杂的多循环框架.
主要方法:
- 酸催化 [3 + 2] 取消因胺和酸.
- 用铜催化合反应.
- 二介导的皮纳科尔合物.
- 区域选择性脱氧化
主要成果:
- 在关键取消步骤中,合成实现了高产量 (99%) 和反选择性 (94% ee).
- 构建四化环和组装复杂的骨架是成功的.
- 使用了前所未有的区域选择性脱氧化.
结论:
- 已经确定了强大的和高效的催化不对称的 (-) - 乙酸总合成.
- 开发的方法为构建复杂的自然产品支架提供了新的策略.
- 这项工作扩大了有机化学中不对称合成的工具包.
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