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Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes

, 
Yuliya Anatol'evna Khomutova 1
Yuliya Anatol'evna Khomutova
, 
Sema Leibovich Ioffe 1
Sema Leibovich Ioffe
10.1016/j.mencom.2008.09.009
Published 2008-09-15
Communication , Volume 18, Issue 5, 255-257
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Smirnov V. O., Khomutova Y. A., Ioffe S. L. Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes // Mendeleev Communications. 2008. Vol. 18. No. 5. pp. 255-257.
GOST all authors (up to 50) Copy
Smirnov V. O., Khomutova Y. A., Ioffe S. L. Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes // Mendeleev Communications. 2008. Vol. 18. No. 5. pp. 255-257.
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TY - JOUR
DO - 10.1016/j.mencom.2008.09.009
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.09.009
TI - Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes
T2 - Mendeleev Communications
AU - Smirnov, Vladimir Olgerdovich
AU - Khomutova, Yuliya Anatol'evna
AU - Ioffe, Sema Leibovich
PY - 2008
DA - 2008/09/15
PB - Mendeleev Communications
SP - 255-257
IS - 5
VL - 18
ER -
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@article{2008_Smirnov,
author = {Vladimir Olgerdovich Smirnov and Yuliya Anatol'evna Khomutova and Sema Leibovich Ioffe},
title = {Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes},
journal = {Mendeleev Communications},
year = {2008},
volume = {18},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.09.009},
number = {5},
pages = {255--257},
doi = {10.1016/j.mencom.2008.09.009}
}
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Smirnov, Vladimir Olgerdovich, et al. “Six-membered cyclic nitronates as Brönsted bases: protonation and rearrangement into butyrolactone oximes.” Mendeleev Communications, vol. 18, no. 5, Sep. 2008, pp. 255-257. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.09.009.

Abstract

The protonation of six-membered cyclic nitronates (SMCNs) was studied by low-temperature NMR spectroscopy, and an efficient preparative procedure for acid-induced rearrangement of SMCNs into oximes of substituted butyrolactones was developed.

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