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

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 Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 2000, Volume: 10, Number: 6, Article number : 70920, Pages count : 2 DOI: 10.1070/MC2000v010n06ABEH001361

Authors

Tkachev A.V. ¹ , Agafontsev A.M. ¹ , Rybalova T.V. ² , Gatilov Y.V. ²

Affiliations

1	(Scopus) Department of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russian Federation
2	(Scopus) N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

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.

Tkachev A.V. , Agafontsev A.M. , Rybalova T.V. , Gatilov Y.V.
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 Communications. 2000. V.10. N6. 70920 :1-2. DOI: 10.1070/MC2000v010n06ABEH001361 WOS Scopus

Published print:

Jan 1, 2000

Web of science	WOS:000166410100003
Scopus	2-s2.0-27844519903
OpenAlex	W2150474538