A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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 Commun., 12:3 (2002), 88

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Mendeleev Communications, 2002, Volume 12, Issue 3, Pages 88–89
DOI: https://doi.org/10.1070/MC2002v012n03ABEH001607 (Mi mendc4105)

This article is cited in 5 scientific papers (total in 5 papers)

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

A. M. Agafontsev^a, T. V. Rybalova^b, Yu. V. Gatilov^b, A. V. Tkachev^b

^a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
^b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Full-text PDF (100 kB) Citations (5)

DOI: https://doi.org/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.

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Document Type: Article

Language: English

Citation: A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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 Commun., 12:3 (2002), 88–89

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https://www.mathnet.ru/eng/mendc/v12/i3/p88

This publication is cited in the following 5 articles:

Citing articles in Google Scholar: Russian citations, English citations
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