Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative

Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 2000, Volume: 10, Number: 6, Article number : 70919, Pages count : 2 DOI: 10.1070/MC2000v010n06ABEH001346

Authors

Petukhov P.A. , Bagryanskaya I.Y. , Gatilov Y.V. , Tkachev A.V.

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 treatment of (+)-3-carene nitrosochloride with 1,2-diaminoethane results in bis-α-aminoxime, which undergoes intra-molecular cyclisation under phase-transfer conditions to yield an optically active macroheterocyclic compound with two carane moieties incorporated.

Petukhov P.A. , Bagryanskaya I.Y. , Gatilov Y.V. , Tkachev A.V.
Novel terpene-based chiral bis-α-aminooximes and the corresponding macrocycles: X-ray structure of a ring-fused 5,7-dioxa-1,4,8,11-tetraazacyclotrideca-3,8-diene derivative
Mendeleev Communications. 2000. V.10. N6. 70919 :1-2. DOI: 10.1070/MC2000v010n06ABEH001346 WOS Scopus OpenAlex

Published print:

Jan 1, 2000

Web of science:	WOS:000166410100002
Scopus:	2-s2.0-0007154545
OpenAlex:	W2057790485

DB	Citing
Scopus	12
Web of science	11
OpenAlex	12