Home / Publications / Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime

Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime

Alexander Mikhailovich Agafontsev 1
Alexander Mikhailovich Agafontsev
Tatyana Valeryevna Rybalova 2
Tatyana Valeryevna Rybalova
Yuriy Vasil'evich Gatilov 2
Yuriy Vasil'evich Gatilov
Alexey Vasil'evich Tkachev 2
Alexey Vasil'evich Tkachev
Published 2002-07-05
CommunicationVolume 12, Issue 3, 88-89
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Agafontsev A. M. et al. Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime // Mendeleev Communications. 2002. Vol. 12. No. 3. pp. 88-89.
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Agafontsev A. M., Rybalova T. V., Gatilov Y. V., Tkachev A. V. Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime // Mendeleev Communications. 2002. Vol. 12. No. 3. pp. 88-89.
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TY - JOUR
DO - 10.1070/MC2002v012n03ABEH001607
UR - https://mendcomm.colab.ws/publications/10.1070/MC2002v012n03ABEH001607
TI - Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime
T2 - Mendeleev Communications
AU - Agafontsev, Alexander Mikhailovich
AU - Rybalova, Tatyana Valeryevna
AU - Gatilov, Yuriy Vasil'evich
AU - Tkachev, Alexey Vasil'evich
PY - 2002
DA - 2002/07/05
PB - Mendeleev Communications
SP - 88-89
IS - 3
VL - 12
ER -
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@article{2002_Agafontsev,
author = {Alexander Mikhailovich Agafontsev and Tatyana Valeryevna Rybalova and Yuriy Vasil'evich Gatilov and Alexey Vasil'evich Tkachev},
title = {Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime},
journal = {Mendeleev Communications},
year = {2002},
volume = {12},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2002v012n03ABEH001607},
number = {3},
pages = {88--89},
doi = {10.1070/MC2002v012n03ABEH001607}
}
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Agafontsev, Alexander Mikhailovich, et al. “Novel selective acid-catalysed rearrangement of the carane-type α-(N-acylamino)oximes: the X-ray structure of (1S,5S)-1-isopropyl-3,5-dimethyl-2-oxa-4-azabicyclo[3.3.1]non-3-en-6-one (E)-oxime.” Mendeleev Communications, vol. 12, no. 3, Jul. 2002, pp. 88-89. https://mendcomm.colab.ws/publications/10.1070/MC2002v012n03ABEH001607.

Abstract

The acid-catalysed rearrangement of carane-type α-(N-acylamino)oximes results in the formation of new bridged heterocycles with the 3-substituted 1-isopropyl-6-hydroxyimino-3-methyl-2-oxa-4-azabicyclo[3.3.1]non-3-ene skeleton.

References

1.
10.1070/MC2002v012n03ABEH001607_bib1_1
Erman
1985
2.
10.1070/MC2002v012n03ABEH001607_bib1_2
Erman
1985