Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, P. R. China.
Org Lett. 2015 Apr 17;17(8):1994-7. doi: 10.1021/acs.orglett.5b00753. Epub 2015 Apr 7.
The rhodium-catalyzed cyclopropanation/cyclization of allenynes was investigated by means of DFT calculations. The results show that the cyclopropanation via the proposed stepwise C(sp(3))-H activation (σ-bond metathesis/C-H reductive elimination) was kinetically unfavorable. Instead, a concerted C(sp(3))-H activation pathway, namely the metal-assisted σ-bond metathesis, in which the hydrogen was directly transferred to the rhodacyclopentane assisted by the Rh center followed by a C-C reductive elimination, was found to explain the experimental results.
通过 DFT 计算研究了铑催化的丙炔的环丙烷化/环化反应。结果表明,通过所提出的分步 C(sp(3))-H 活化(σ-键复分解/C-H 还原消除)进行的环丙烷化在动力学上是不利的。相反,发现了协同的 C(sp(3))-H 活化途径,即金属辅助的σ-键复分解,其中氢在 Rh 中心的辅助下直接转移到铑环戊烷上,随后进行 C-C 还原消除,这可以解释实验结果。