V. V. Kalashnikov, V. E. Pushkarev, L. G. Tomilova, “A novel synthetic approach to 27-aryltetrabenzo[5,10,15]triazaporphyrins”, Mendeleev Commun., 21:2 (2011), 92

Эта публикация цитируется в следующих 17 статьяx:

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Faeza Alkorbi, Alejandro Díaz‐Moscoso, Jacob Gretton, Isabelle Chambrier, Graham J. Tizzard, Simon J. Coles, David L. Hughes, Andrew N. Cammidge, “Complementary Syntheses Giving Access to a Full Suite of Differentially Substituted Phthalocyanine‐Porphyrin Hybrids”, Angewandte Chemie, 133:14 (2021), 7710
Masataka Umetani, Gakhyun Kim, Takayuki Tanaka, Dongho Kim, Atsuhiro Osuka, “Rational Synthesis of 5,10-Diazaporphyrins via Nucleophilic Substitution Reactions of α,α′-Dibromotripyrrin and Dihydrogenation to Give 5,10-Diazachlorins”, J. Org. Chem., 85:5 (2020), 3849
Yoshihiro Matano, “Synthesis of Aza-, Oxa-, and Thiaporphyrins and Related Compounds”, Chem. Rev., 117:4 (2017), 3138
Dmitry S. Andrianov, Oleg A. Levitskiy, Victor B. Rybakov, Tatiana V. Magdesieva, Andrey V. Cheprakov, “Metal complexes of diaryltetrabenzodiazaporphyrins”, ChemistrySelect, 1:3 (2016), 360
Victor E. Pushkarev, Larisa G. Tomilova, Victor N. Nemykin, “Historic overview and new developments in synthetic methods for preparation of the rare-earth tetrapyrrolic complexes”, Coordination Chemistry Reviews, 319 (2016), 110
Victor E. Pushkarev, Valery V. Kalashnikov, Alexander Yu. Tolbin, Stanislav A. Trashin, Nataliya E. Borisova, Sergey V. Simonov, Victor B. Rybakov, Larisa G. Tomilova, Nikolay S. Zefirov, “meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(iii) complexes: synthesis, structure, spectral properties and electrochemistry”, Dalton Trans., 44:37 (2015), 16553
Nuha Alharbi, Alejandro Díaz-Moscoso, Graham J. Tizzard, Simon J. Coles, Michael J. Cook, Andrew N. Cammidge, “Improved syntheses of meso-aryl tetrabenzotriazaporphyrins (TBTAPs)”, Tetrahedron, 70:40 (2014), 7370
Valery V. Kalashnikov, Victor E. Pushkarev, Zoya A. Starikova, Larisa G. Tomilova, “First X-ray crystallographic study of a meso-substituted tetrabenzotriazaporphyrin: Structural effect of a meso-aryl unit on 27-(2-methylphenyl)tetrabenzotriazaporphyrinato zinc example in comparison with zinc phthalocyaninate”, Dyes and Pigments, 105 (2014), 216
В. В. Калашников, В. Е. Пушкарев, Л. Г. Томилова, “Тетрабензотриазапорфирины: синтез, свойства и применение”, Усп. хим., 83:7 (2014), 657–675 ; V. V. Kalashnikov, V. E. Pushkarev, L. G. Tomilova, “Tetrabenzotriazaporphyrins: synthesis properties and applications”, Russian Chem. Reviews, 83:7 (2014), 657–675
Alejandro Díaz‐Moscoso, Graham J. Tizzard, Simon J. Coles, Andrew N. Cammidge, “Synthesis of meso‐Substituted Tetrabenzotriazaporphyrins: Easy Access to Hybrid Macrocycles”, Angew Chem Int Ed, 52:41 (2013), 10784
Victor E. Pushkarev, Valery V. Kalashnikov, Stanislav A. Trashin, Nataliya E. Borisova, Larisa G. Tomilova, Nikolay S. Zefirov, “Bis(tetrabenzotriazaporphyrinato) and (tetrabenzotriazaporphyrinato)(phthalocyaninato) lutetium(iii) complexes – novel sandwich-type tetrapyrrolic ligand based NIR absorbing electrochromes”, Dalton Trans., 42:34 (2013), 12083
Alejandro Díaz‐Moscoso, Graham J. Tizzard, Simon J. Coles, Andrew N. Cammidge, “Synthesis of meso‐Substituted Tetrabenzotriazaporphyrins: Easy Access to Hybrid Macrocycles”, Angewandte Chemie, 125:41 (2013), 10984
Valery V. Kalashnikov, Victor E. Pushkarev, Larisa G. Tomilova, “ChemInform Abstract: A Novel Synthetic Approach to 27‐Aryltetrabenzo[5,10,15]triazaporphyrins.”, ChemInform, 42:34 (2011)