Abstract
It has been shown that the condensation of tertiary aminophenylcarbinols with 2-hydroxybenz(naphth)aldehydes gives the corresponding 1,2-dihydrobenzoxazines and their structural Schiff base isomers. The reaction of 2-[2-hydroxyphenyl(naphthyl)]-1,2-dihydro-4H-3,1-benzoxazines with aliphatic aldehydes gives substituted 3,1-benzoxazino[1,2-c][1,3]benz(naphth)oxazines.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1230–1241, August, 2006.
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Gromachevskaya, E.V., Kosulina, T.P. & Borodavko, A.A. Studies of 4H-3,1-benzoxazines. 14. Structure and some properties of 2-[2-hydroxyphenyl(naphthyl)]-1,2-dihydro-4H-3,1-benzoxazines. Chem Heterocycl Compd 42, 1068–1077 (2006). https://doi.org/10.1007/s10593-006-0205-0
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DOI: https://doi.org/10.1007/s10593-006-0205-0