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. 2020 Jun 12:16:1296-1304.
doi: 10.3762/bjoc.16.110. eCollection 2020.

[3 + 2] Cycloaddition with photogenerated azomethine ylides in β-cyclodextrin

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[3 + 2] Cycloaddition with photogenerated azomethine ylides in β-cyclodextrin

Margareta Sohora et al. Beilstein J Org Chem. .

Abstract

Stability constants for the inclusion complexes of cyclohexylphthalimide 2 and adamantylphthalimide 3 with β-cyclodextrin (β-CD) were determined by 1H NMR titration, K = 190 ± 50 M-1, and K = 2600 ± 600 M-1, respectively. Photochemical reactivity of the inclusion complexes 2@β-CD and 3@β-CD was investigated, and we found out that β-CD does not affect the decarboxylation efficiency, while it affects the subsequent photochemical H-abstraction, resulting in different product distribution upon irradiation in the presence of β-CD. The formation of ternary complexes with acrylonitrile (AN) and 2@β-CD or 3@β-CD was also essayed by 1H NMR. Although the formation of such complexes was suggested, stability constants could not be determined. Irradiation of 2@β-CD in the presence of AN in aqueous solution where cycloadduct 7 was formed highly suggests that decarboxylation and [3 + 2] cycloaddition take place in the ternary complex, whereas such a reactivity from bulky adamantane 3 is less likely. This proof of principle that decarboxylation and cycloaddition can be performed in the β-CD cavity has a significant importance for the design of new supramolecular systems for the control of photoreactivity.

Keywords: [3 + 2] cycloadditions; inclusion complexes; photochemistry; phthalimides; β-cyclodextrin.

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Figures

Figure 1
Figure 1
Phthalimide derivatives 13 and the corresponding azomethine ylides 1AMY-3AMY.
Scheme 1
Scheme 1
Irradiation of 1 in the presence of acrylonitrile (AN).
Figure 2
Figure 2
Dependence of the chemical shift of the H-atom at the cyclohexane 2 position in compound 2 on the β-CD concentration. Dots are experimental values and the red line corresponds to the calculated values by the WINEQNMR program [51] according to the model for the formation of 1:1 stoichiometry of the inclusion complex 2@β-CD.
Scheme 2
Scheme 2
Complexation of 2 with β-CD, and formation of a ternary complex AN@2@β-CD.
Scheme 3
Scheme 3
Photochemistry of 2 in the presence of AN, with or without β-CD.
Scheme 4
Scheme 4
Photochemistry of 3 in the presence of AN, with or without β-CD.

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References

    1. Kobayashi S, Jørgensen K A, editors. Cycloaddition Reactions in Organic Synthesis. Weinheim: WILEY-VCH; 2002. - DOI
    1. Chiacchio U, Padwa A, Romeo G. Curr Org Chem. 2009;13:422–447. doi: 10.2174/138527209787582268. - DOI
    1. Hashimoto T, Maruoka K. Chem Rev. 2015;115:5366–5412. doi: 10.1021/cr5007182. - DOI - PubMed
    1. Martina K, Tagliapietra S, Veselov V V, Cravotto G. Front Chem (Lausanne, Switz) 2019;7:No. 95. doi: 10.3389/fchem.2019.00095. - DOI - PMC - PubMed
    1. Nájera C, Sansano J M. Curr Org Chem. 2003;7:1105–1150. doi: 10.2174/1385272033486594. - DOI

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