12C/13C同位素的不对称合成和立体化学分配
Tomoya Miura1, Takayuki Nakamuro1, Yuuya Nagata1
1Department of Synthetic Chemistry and Biological Chemistry , Kyoto University , Katsura, Kyoto 615-8510 , Japan.
Journal of the American Chemical Society
|August 14, 2019
概括
合成了具有独特C1轴和C3对称性的化. 它们的性源于不对称的碳-13/碳-12同位素分布,由振动循环二极化证实.
科学领域:
- 有机化学
- 同位素化学
- 光谱学
背景情况:
- 在化学和生物学中,
- 同位素替代可以诱导性.
- 了解分子对称性是预测性质的关键.
研究的目的:
- 为了合成新的性碳化合物.
- 为了研究由同位素不对称引起的性.
- 使用光谱方法确认绝对配置.
主要方法:
- 合成具有C1轴和C3对称性的性碳化合物.
- 碳-12/碳-13同位素的不对称分布.
- 振动循环二元化 (VCD) 光谱.
- 与原始α- 甲基环烯的比较.
主要成果:
- 已成功合成了性碳化合物
- 证实性源于12C/13C同位素的分布.
- 通过VCD确定的绝对配置与原始化合物保持一致.
结论:
- 证明了一种新型的同位素性性分子路径.
- 在这种系统中,VCD是一种可靠的分配绝对配置的方法.
- 为进一步研究提供了一类新型的性化合物.
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