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., 2002, Volume 12, Issue 3,Pages 88

This article is cited 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

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.

Language: English

DOI: 10.1070/MC2002v012n03ABEH001607