不传统的碎片使用使得 (-) -Callyspongiolide的简洁总合成成为可能
Francesco Manoni1, Corentin Rumo1, Liubo Li1
1Department of Chemistry and Biochemistry, University of California-Los Angeles , 607 Charles E. Young Drive East, Los Angeles, California 90095-1569, United States.
Journal of the American Chemical Society
|January 16, 2018
概括
这项研究详细介绍了一种新型非对称的 (-) - calyspongiolide 合成方法,从二糖和单聚中构建宏核. 这种创新方法利用化催化剂进行碎片合,并采用独特的碎片化策略.
科学领域:
- 有机化学
- 合成化学
- 自然产品合成
背景情况:
- (-) 化物是一种复杂的海洋天然产物,具有潜在的生物活性.
- 之前的合成途径往往涉及具有挑战性的二氧化酸中间体.
研究的目的:
- 开发一种新且高效的 (-) - 化物非对称合成方法.
- 探索一种非典型的宏核构造策略,避免使用二氧化酸中间体.
主要方法:
- 不对称合成使用化催化剂进行碎片合.
- 主要中间体的立体选择性和区域选择性构造通过周边片.
- 用于宏循环形成的碳酸性宏活性化.
主要成果:
- 通过直接和灵活的合成实现了 (-) - callyspongiolide.
- 宏基域是由非典型的二糖和单基构成的.
- 在整个合成过程中保持立体化学和区域化学控制.
结论:
- 描述的合成途径为类合成提供了一个新的范式.
- 这种方法提供了灵活和高效的 (-) -callyspongiolide 和潜在的其他复杂的宏化物.
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