Issue 6, 2000

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

Abstract

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

Article information

Article type
Paper

Mendeleev Commun., 2000,10, 209-210

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

P. A. Petukhov, I. Y. Bagryanskaya, Y. V. Gatilov and A. V. Tkachev, Mendeleev Commun., 2000, 10, 209 DOI: 10.1070/MC2000v010n06ABEH001346

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