Issue 6, 2000
From the journal:

Mendeleev Communications

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

Alexey V. Tkachev,   Alexander M. Agafontsev,   Tatyana V. Rybalova  and  Yuri V. Gatilov  

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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Article information

DOI
https://doi.org/10.1070/MC2000v010n06ABEH001361
Article type
Paper

Mendeleev Commun., 2000,10, 211-212

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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

A. V. Tkachev, A. M. Agafontsev, T. V. Rybalova and Y. V. Gatilov, Mendeleev Commun., 2000, 10, 211 DOI: 10.1070/MC2000v010n06ABEH001361

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