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Mendeleev Communications, 1995, Volume 5, Issue 3, Pages 106–107
DOI: https://doi.org/10.1070/MC1995v005n03ABEH000479
(Mi mendc5053)
 

This article is cited in 11 scientific papers (total in 11 papers)

A Novel Thermal Rearrangement in the Pyrido[1,2-a]pyrimidine Series: Transformation of 3-Acetyl-4-phenylaminopyrido[1,2-a]pyrimidin-2-one into 3-Acetyl-2-phenylaminopyrido[1,2-a]pyrimidin-4-one.

V. S. Bogdanova, K. L. Cherkasovaa, V. A. Dorokhova, O. V. Shishkinb, Yu. T. Struchkovc

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b STC 'Institute for Single Crystals', National Academy of Sciences of Ukraine, Kharkov, Ukraine
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract: 3-Acetyl-4-phenylaminopyrido[1,2-a]pyrimidin-2-one has been synthesized from acetoacetic acid N-(pyrid-2-yl)amide and phenylisocyanate and converted on heating into 3-acetyl-2-phenylaminopyrido[1,2-a]pyrimidin-4-one.
Document Type: Article
Language: English


Citation: V. S. Bogdanov, K. L. Cherkasova, V. A. Dorokhov, O. V. Shishkin, Yu. T. Struchkov, “A Novel Thermal Rearrangement in the Pyrido[1,2-a]pyrimidine Series: Transformation of 3-Acetyl-4-phenylaminopyrido[1,2-a]pyrimidin-2-one into 3-Acetyl-2-phenylaminopyrido[1,2-a]pyrimidin-4-one.”, Mendeleev Commun., 5:3 (1995), 106–107
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  • This publication is cited in the following 11 articles:
    1. Susanta Kumar Manna, Arabinda Mandal, Suresh Kumar Mondal, Arup Kr Adak, Akash Jana, Somnath Das, Sourav Chattopadhyay, Somenath Roy, Shyamal Kr Ghorai, Shubhankar Samanta, Maidul Hossain, Mahiuddin Baidya, “Pyrido[1,2-a]pyrimidinium ions – a novel bridgehead nitrogen heterocycles: synthesis, characterisation, and elucidation of DNA binding and cell imaging properties”, Org. Biomol. Chem., 13:29 (2015), 8037  crossref
    2. Alireza Hassanabadi, Rahele Zhiani, “Reaction of Aryl Isothiocyanate with Pyridines and Dialkyl Acetylenedicarboxylates to Afford Novel Heterocycles”, Journal of Chemical Research, 37:8 (2013), 455  crossref
    3. Oleg V. Shishkin, Leonid Gorb, Jerzy Leszczynski, Practical Aspects of Computational Chemistry, 2009, 399  crossref
    4. I. Hermecz, L. Vasvári-Debreczy, Comprehensive Heterocyclic Chemistry III, 2008, 77  crossref
    5. Mehdi Adib, Hossine Yavari, Mehdi Mollahosseini, “Efficient one-pot synthesis of 2-oxo-1,9a-dihydro-2H-pyrido[1,2-a]pyrimidine derivatives”, Tetrahedron Letters, 45:8 (2004), 1803  crossref
    6. István Hermecz, Advances in Heterocyclic Chemistry, 85, Advances in Heterocyclic Chemistry Volume 85, 2003, 173  crossref
    7. István Hermecz, Lelle Vasvári-Debreczy, Péter Mátyus, Comprehensive Heterocyclic Chemistry II, 1996, 563  crossref
    8. Comprehensive Heterocyclic Chemistry II, 1996, 1169  crossref
    9. K. L. Cherkasova, V. S. Bogdanov, V. A. Dorokhov, O. V. Shishkin, “Synthesis of some sulfur-containing pyrido[1,2-?]pyrimidines”, Russ Chem Bull, 45:6 (1996), 1437  crossref
    10. Michael P. Groziak, Progress in Heterocyclic Chemistry, 8, 1996, 231  crossref
    11. V. S. BOGDANOV, K. L. CHERKASOVA, V. A. DOROKHOV, O. V. SHISHKIN, YU. T. STRUCHKOV, “ChemInform Abstract: A Novel Thermal Rearrangement in the Pyrido(1,2‐a)pyrimidine Series: Transformation of 3‐Acetyl‐4‐phenylaminopyrido(1,2‐a)pyrimidin‐2‐one into 3‐Acetyl‐2‐phenylaminopyrido(1,2‐a)pyrimidin‐4‐one”, ChemInform, 26:38 (1995)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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