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Alkylation of 1,3,2-Diheterophosphinanes Conjugated with Dinaphthylmethanes

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Abstract

The alkylation reactions of 2,2'-di- and 2,2',7,7'-tetra(1,3,2-diheterophosphinanyl)dinaphthylmethanes with alkyl (arylalkyl) halides and bromoethyl acetate were studied. The factors affecting the chemoselectivity of the reaction and the yield of final products were revealed.

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Funding

This work was financially supported by the Russian Foundation for Basic Research (project no. 18-03-00347a).

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Authors and Affiliations

  1. Institute of Biology and Chemistry, Moscow Pedagogical State University, 129164, Moscow, Russia

    O. S. Serkova, V. V. Glushko, M. R. Guseinova & V. I. Maslennikova

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  1. O. S. Serkova
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  2. V. V. Glushko
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  3. M. R. Guseinova
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  4. V. I. Maslennikova
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Correspondence to V. I. Maslennikova.

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Serkova, O.S., Glushko, V.V., Guseinova, M.R. et al. Alkylation of 1,3,2-Diheterophosphinanes Conjugated with Dinaphthylmethanes. Russ J Gen Chem 90, 367–380 (2020). https://doi.org/10.1134/S107036322003007X

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  • DOI: https://doi.org/10.1134/S107036322003007X

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