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Mendeleev Communications, 2000, Volume 10, Issue 6, Pages 209–210
DOI: https://doi.org/10.1070/MC2000v010n06ABEH001346
(Mi mendc4461)
 

This article is cited in 12 scientific papers (total in 12 papers)

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. Petukhova, I. Yu. Bagryanskayab, Yu. V. Gatilovb, A. V. Tkachevb

a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract: 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.
Bibliographic databases:
Document Type: Article
Language: English


Citation: P. A. Petukhov, I. Yu. Bagryanskaya, Yu. V. Gatilov, A. V. Tkachev, “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 Commun., 10:6 (2000), 209–210
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  • https://www.mathnet.ru/eng/mendc/v10/i6/p209
  • This publication is cited in the following 12 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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