Abstract:
1,8-Bis(dimethylamino)naphthalene (naphthalene proton sponge) equipped at position 4 with N-terminal α-amino acid residues undergoes unprecedented easy autoxidation in basic medium forming 5-dimethylamino-1,4-naphthoquinone along with minor amounts of its derivatives. The new reaction is of interest against the background of wide distribution of 1,4-naphthoquinones in nature, their high biological significance and extremely limited information on nitrogen compounds of this series.
Citation:
M. P. Vlasenko, A. F. Pozharskii, O. P. Demidov, V. A. Ozeryanskii, G. S. Borodkin, “α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1,4-naphthoquinone nitrogen derivatives”, Mendeleev Commun., 33:2 (2023), 197–200
Linking options:
https://www.mathnet.ru/eng/mendc348
https://www.mathnet.ru/eng/mendc/v33/i2/p197
This publication is cited in the following 2 articles:
A. F. Pozharskii, M. P. Vlasenko, P. A. Knyazev, A. G. Starikov, “Why naturally occurring quinone redox systems lack amino groups: consideration using 1,4-naphthoquinone derivatives”, Mendeleev Commun., 34:2 (2024), 246–250
Javed Khan, Anjali Rani, Mohd Aslam, Garima Pandey, Bhaskara Nand Pant, “A review on the synthesis and application of naphthoquinone-based drugs”, Results in Chemistry, 6 (2023), 101138