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Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones

Vadim Kamil'evich Khlestkin 1
Vadim Kamil'evich Khlestkin
, 
Vladimir Anatol'evich Reznikov 1
Vladimir Anatol'evich Reznikov
, 
Dmitrii Gennad'evich Mazhukin 1
Dmitrii Gennad'evich Mazhukin
, 
Aleksei Ya Tikhonov 1
Aleksei Ya Tikhonov
, 
Leonid Borisovich Volodarsky 1
Leonid Borisovich Volodarsky
10.1070/MC1996v006n05ABEH000646
Published 1996-10-30
Communication , Volume 6, Issue 5, 202-203
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Khlestkin V. K. et al. Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones // Mendeleev Communications. 1996. Vol. 6. No. 5. pp. 202-203.
GOST all authors (up to 50) Copy
Khlestkin V. K., Reznikov V. A., Mazhukin D. G., Tikhonov A. Ya., Volodarsky L. B. Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones // Mendeleev Communications. 1996. Vol. 6. No. 5. pp. 202-203.
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TY - JOUR
DO - 10.1070/MC1996v006n05ABEH000646
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n05ABEH000646
TI - Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones
T2 - Mendeleev Communications
AU - Khlestkin, Vadim Kamil'evich
AU - Reznikov, Vladimir Anatol'evich
AU - Mazhukin, Dmitrii Gennad'evich
AU - Tikhonov, Aleksei Ya
AU - Volodarsky, Leonid Borisovich
PY - 1996
DA - 1996/10/30
PB - Mendeleev Communications
SP - 202-203
IS - 5
VL - 6
ER -
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@article{1996_Khlestkin,
author = {Vadim Kamil'evich Khlestkin and Vladimir Anatol'evich Reznikov and Dmitrii Gennad'evich Mazhukin and Aleksei Ya Tikhonov and Leonid Borisovich Volodarsky},
title = {Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n05ABEH000646},
number = {5},
pages = {202--203},
doi = {10.1070/MC1996v006n05ABEH000646}
}
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Khlestkin, Vadim Kamil'evich, et al. “Reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides: a new approach to alkylaromatic a-hydroxyamino-ketones.” Mendeleev Communications, vol. 6, no. 5, Oct. 1996, pp. 202-203. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n05ABEH000646.

Abstract

The reaction of N-(l-cyano-l-methylethyl)-α-phenylnitrone with phenyl-, 2-pyridyl- and 2-thienyl magnesium bromides affords 3-imidazolines which hydrolyse to alkylaromatic α-hydroxyaminoketones, synthons for stable nitroxides.

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