Abstract
The reaction of 2-hydroxy-3-(4,5-diphenyl-1,3-oxazol-2-yl)-1-naphthaldehyde with 1,2,3,3-tetramethyl-3H-indolium perchlorate afforded photochromic spiro[indoline-2,3′-naphthopyran] containing a 4,5-diphenyloxazole group in position 5′ of the naphthopyran fragment. The merocyanine form of the spiropyran gave complexes with bivalent heavy cations.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 693–697, March, 2005.
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Voloshin, N.A., Chernyshev, A.V., Metelitsa, A.V. et al. Spiropyrans and spirooxazines. 3. Synthesis of photochromic 5′-(4,5-diphenyl-1,3-oxazol-2-yl)-spiro[indoline-2,3′-naphtho[2,3-b]pyran]. Russ Chem Bull 54, 705–710 (2005). https://doi.org/10.1007/s11172-005-0308-2
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DOI: https://doi.org/10.1007/s11172-005-0308-2