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Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity

Margarita Aleksandrovna Lapitskaya 1
Margarita Aleksandrovna Lapitskaya
Elena Dmitrievna Daeva 1
Elena Dmitrievna Daeva
Kazimir Konstantinovich Pivnitsky 1
Kazimir Konstantinovich Pivnitsky
Published 2018-09-07
CommunicationVolume 28, Issue 5, 505-507
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Lapitskaya M. A. et al. Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity // Mendeleev Communications. 2018. Vol. 28. No. 5. pp. 505-507.
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Lapitskaya M. A., Vil' V. A., Daeva E. D., Terent'ev A. O., Pivnitsky K. K. Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity // Mendeleev Communications. 2018. Vol. 28. No. 5. pp. 505-507.
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TY - JOUR
DO - 10.1016/j.mencom.2018.09.018
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.018
TI - Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity
T2 - Mendeleev Communications
AU - Lapitskaya, Margarita Aleksandrovna
AU - Vil', Vera Andreevna
AU - Daeva, Elena Dmitrievna
AU - Terent'ev, Alexander Olegovich
AU - Pivnitsky, Kazimir Konstantinovich
PY - 2018
DA - 2018/09/07
PB - Mendeleev Communications
SP - 505-507
IS - 5
VL - 28
ER -
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@article{2018_Lapitskaya,
author = {Margarita Aleksandrovna Lapitskaya and Vera Andreevna Vil' and Elena Dmitrievna Daeva and Alexander Olegovich Terent'ev and Kazimir Konstantinovich Pivnitsky},
title = {Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.018},
number = {5},
pages = {505--507},
doi = {10.1016/j.mencom.2018.09.018}
}
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Lapitskaya, Margarita Aleksandrovna, et al. “Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity.” Mendeleev Communications, vol. 28, no. 5, Sep. 2018, pp. 505-507. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.018.

Abstract

Easily available dimethylmalonoyl peroxide is proposed as a reactive alternative to the widely known spirocyclopropyl analogue for the use in the arene acyloxylation and other oxidative reactions.

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