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Additions and corrections

Vladimir Alexandrovich Glushkov 1
Vladimir Alexandrovich Glushkov
, 
Yurii Vladimirovich Shklyaev 1
Yurii Vladimirovich Shklyaev
, 
Valentina I Sokol 2
Valentina I Sokol
, 
Vladimir Semenovich Sergienko 2
Vladimir Semenovich Sergienko
, 
Viktor Vladimirovich Davidov 3
Viktor Vladimirovich Davidov
10.1070/MC1999v009n04ABEH001238
Published 9 July 1999
Communication , Volume 9, Issue 4, 170-170
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Glushkov V. A. et al. Additions and corrections // Mendeleev Communications. 1999. Vol. 9. No. 4. pp. 170-170.
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Glushkov V. A., Shklyaev Y. V., Sokol V. I., Sergienko V. S., Davidov V. V. Additions and corrections // Mendeleev Communications. 1999. Vol. 9. No. 4. pp. 170-170.
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TY - JOUR
DO - 10.1070/MC1999v009n04ABEH001238
UR - https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001238
TI - Additions and corrections
T2 - Mendeleev Communications
AU - Glushkov, Vladimir Alexandrovich
AU - Shklyaev, Yurii Vladimirovich
AU - Sokol, Valentina I
AU - Sergienko, Vladimir Semenovich
AU - Davidov, Viktor Vladimirovich
PY - 1999
DA - 1999/07/09
PB - Mendeleev Communications
SP - 170-170
IS - 4
VL - 9
ER -
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@article{1999_Glushkov,
author = {Vladimir Alexandrovich Glushkov and Yurii Vladimirovich Shklyaev and Valentina I Sokol and Vladimir Semenovich Sergienko and Viktor Vladimirovich Davidov},
title = {Additions and corrections},
journal = {Mendeleev Communications},
year = {1999},
volume = {9},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001238},
number = {4},
pages = {170--170},
doi = {10.1070/MC1999v009n04ABEH001238}
}
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Glushkov, Vladimir Alexandrovich, et al. “Additions and corrections.” Mendeleev Communications, vol. 9, no. 4, Jul. 1999, pp. 170-170. https://mendcomm.colab.ws/publications/10.1070/MC1999v009n04ABEH001238.
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Abstract

Earlier described compounds 2b,c as semihydrates of 2,5-cyclohexadien-4-one-spiro-3’-(2’-ethoxycarbonylmethyl-5’,5’-dimethyl-l’pyrroline) (2c) and as 2,5-cyclohexadien-4-one-spiro-3’-(2’-phenyl-5’,5’-dimethyl-l’-pyrroline) (2b), after recording 13C NMR and mass spectra, were found to be ethyl N-[l-(p-hydroxyphenyl)-2-methylpropan-2-yl]malonamate (here 1a) and N-[l-(p-hydroxyphenyl)-2-methylpropan-2-yl]benzamide (here 1b). Named above spiro-compounds 2b,c are formed in the described conditions and can be detected by TLC; however, they are easily converted to amides (here 1a,b) during isolation as a result of hydrolysis in acidic media.