Novel selective acid-catalysed rearrangement of the carane-type alpha-(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

Novel selective acid-catalysed rearrangement of the carane-type alpha-(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 Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 2002, Number: 3, Pages: 88-89 Pages count : 2 DOI: 10.1070/MC2002v012n03ABEH001607

Authors

Agafontsev AM ² , Rybalova TV ¹ , Gatilov YV ¹ , Tkachev AV ¹

Affiliations

1	(Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
2	(Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

The acid-catalysed rearrangement of carane-type alpha-(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.

Agafontsev A. , Rybalova T. , Gatilov Y. , Tkachev A.
Novel selective acid-catalysed rearrangement of the carane-type alpha-(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 Communications. 2002. N3. P.88-89. DOI: 10.1070/MC2002v012n03ABEH001607 WOS Scopus РИНЦ

Published print:

Jan 1, 2002

Web of science	WOS:000177143300003
Scopus	2-s2.0-0036342692
Elibrary	13395487
OpenAlex	W2093496837