A. V. Tkachev, A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, “Unusual acid-induced heterocyclisation of caryophyllene-type α-amino oximes: X-ray structure of (1S,2S,5R,8S)-1,4,4,8-tetramethyl-8-morpholin-4-yl-11-oxa-10-azatricyclo[7.2.2.02,5]tridec-9-ene”, Mendeleev Commun., 10:6 (2000), 211

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Mendeleev Communications, 2000, Volume 10, Issue 6, Pages 211–212
DOI: https://doi.org/10.1070/MC2000v010n06ABEH001361 (Mi mendc4462)

This article is cited in 4 scientific papers (total in 4 papers)

Unusual acid-induced heterocyclisation of caryophyllene-type α-amino oximes: X-ray structure of (1S,2S,5R,8S)-1,4,4,8-tetramethyl-8-morpholin-4-yl-11-oxa-10-azatricyclo[7.2.2.0^2,5]tridec-9-ene

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

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

Full-text PDF (142 kB) Citations (4)

DOI: https://doi.org/10.1070/MC2000v010n06ABEH001361

Abstract: The acid-catalysed cyclisation of caryophyllene-type α-amino oximes results in the formation of new bridged heterocycles with the 5,6-dihydro-4H-[1,2]oxazine moiety.

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Document Type: Article

Language: English

Citation: A. V. Tkachev, A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, “Unusual acid-induced heterocyclisation of caryophyllene-type α-amino oximes: X-ray structure of (1S,2S,5R,8S)-1,4,4,8-tetramethyl-8-morpholin-4-yl-11-oxa-10-azatricyclo[7.2.2.0^2,5]tridec-9-ene”, Mendeleev Commun., 10:6 (2000), 211–212

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https://www.mathnet.ru/eng/mendc/v10/i6/p211

This publication is cited in the following 4 articles:

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