Abstract
Perimidines are nitrogen-containing heterocyclic scaffolds with a wide range of
biological and material properties. Several synthetic transformations on perimidines afford
fused heterocycles. This review focuses on every aspect of perimidines, including different
synthetic procedures, reactions and applications, and covers the literature published up to the
year 2020, using more than 170 references.
Keywords:
Perimidines, heterocycles, synthesis, 1, 8-diaminonaphthalene, dihydroperimidines, photochromism, anti-cancer, applications.
Graphical Abstract
[1]
Pozharskii, A.F.; Dal’nikovskaya, V.V. Perimidines. Russ. Chem. Rev., 1981, 50, 816-835.
[7]
Ramsden, W.D.; Valente, L.F.; Bernard, L.S. Method of making dihydroperimidine
squaraine compounds. U.S. Patent US6348592 B1, February
19 2002.
[21]
Krishna, M.H.; Thriveni, P. A green alternative approach for synthesis of 2-substituted-1H-perimidine catalysed by NBS in ultrasonication method. J. Chem. Pharm. Res., 2016, 8, 809-814.
[33]
Bodaghifard, M.A.; Ahadi, N. Sulfamic acid: a green and efficient catalyst for synthesis of mono-, bis-, and spiro- perimidines. Iran. J. Catal, 2016, 6, 377-380.
[98]
Malherbe, R.F. 2,3-Dihydroperimidines as antioxidants for lubricants. U.S
Patent US4389321, June 21 1983.
[103]
World Health Organization. Guidelines for Drinking-water Quality; WHO, 2011.
[119]
Du¨rr, H.; Laurent, B. Photochromism-Molecules and Systems; Elsevier: Amsterdam, 1990.