Abstract:
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.
Document Type:
Article
Language: English
Citation:
A. V. Tkachev, A. M. Agafontsev, T. V. Rybalova, Yu. V. Gatilov, “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 Commun., 10:6 (2000), 211–212
Linking options:
https://www.mathnet.ru/eng/mendc4462
https://www.mathnet.ru/eng/mendc/v10/i6/p211
This publication is cited in the following 4 articles:
Alexey Yu. Sukhorukov, Sema L. Ioffe, “Chemistry of Six-Membered Cyclic Oxime Ethers. Application in the Synthesis of Bioactive Compounds”, Chem. Rev., 111:8 (2011), 5004
Antonella Di Sotto, Gabriela Mazzanti, Fabio Carbone, Patrizia Hrelia, Francesca Maffei, “Inhibition by β-caryophyllene of ethyl methanesulfonate-induced clastogenicity in cultured human lymphocytes”, Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 699:1-2 (2010), 23
S. V. Larionov, L. I. Myachina, L. A. Glinskaya, R. F. Klevtsova, E. G. Boguslavskii, A. M. Agafontsev, A. V. Tkachev, “Synthesis of solvates of the copper(II) complex with chiral caryophyllane-type morpholino oxime (HL). Structure of Cu(HL)Cl2 · CHCl3”, Russ J Coord Chem, 36:8 (2010), 579
Alexey V. Tkachev, Alexander M. Agafontsev, Tatyana V. Rybalova, Yury V. Gatilov, “ChemInform Abstract: Unusual Acid‐Induced Heterocyclization 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[7.2.2.0 2,5]tridec‐9‐ene.”, ChemInform, 32:17 (2001)
Contact us: