Issue 11, 2023

DFT study on stereoselective Rh-catalyzed intramolecular [2 + 2 + 2] cycloaddition of allene–ene–ynes

Abstract

Density functional theory has been employed to investigate the mechanisms of Rh-catalyzed intramolecular [2 + 2 + 2] cycloaddition reactions. The reaction starts with the coordination of a Rh center in the catalyst to the alkyne in reactant 1a firstly, and then to one of the double bonds in the allene, leading to the formation of the first six-membered ring. After that, there are two different reaction pathways, which result in the [2 + 2 + 2] and [2 + 2] products, respectively. For the [2 + 2 + 2] reaction pathway, the remaining alkene in reactant 1a will coordinate to the Rh center, and then there are two successive C–C couplings to make the second six-membered ring and one three-membered ring, which leads to the formation of the final product. At the same time, the broken Rh–Cl bond will be formed again to finish the recovery of the catalyst and the separation of the final product. It was deduced from the energy span model that the TOF-determining transition state (TDTS) and intermediate (TDI) are TS3 and INT2, and thus the activation free-energy barrier is 32.1 kcal mol−1 at the temperature of 383.75 K. The substituent effect and intermolecular interaction energy have also been addressed in this paper.

Graphical abstract: DFT study on stereoselective Rh-catalyzed intramolecular [2 + 2 + 2] cycloaddition of allene–ene–ynes

Supplementary files

Article information

Article type
Research Article
Submitted
09 Marts 2023
Accepted
20 Apr. 2023
First published
20 Apr. 2023

Org. Chem. Front., 2023,10, 2624-2634

DFT study on stereoselective Rh-catalyzed intramolecular [2 + 2 + 2] cycloaddition of allene–ene–ynes

X. Zhu and D. Fang, Org. Chem. Front., 2023, 10, 2624 DOI: 10.1039/D3QO00363A

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