Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3042
Title: Pyrimidines as surrogates for 1,3-dicarbonyl compounds in peri annulation of perimidines en route to 1,3-diazapyrenes
Authors: Aksenov, A. V.
Аксенов, А. В.
Shcherbakov, S. V.
Щербаков, С. В.
Lobach, I. V.
Лобач, И. В.
Aksenova, I. V.
Аксенова, И. В.
Rubin, M. A.
Рубин, М. А.
Keywords: Annulation;Nitrogen heterocycles;Perimidines;Polyphosphoric acid;Pyrimidines;Synthetic methods
Issue Date: 2017
Publisher: Wiley-VCH Verlag
Citation: Aksenov, A.V., Shcherbakov, S.V., Lobach, I.V., Aksenova, I.V., Rubin, M. Pyrimidines as Surrogates for 1,3-Dicarbonyl Compounds in peri Annulation of Perimidines en Route to 1,3-Diazapyrenes // European Journal of Organic Chemistry. - 2017. - Volume 2017. - Issue 12. - Pages 1666-1673
Series/Report no.: European Journal of Organic Chemistry
Abstract: A highly efficient protocol for acid-mediated peri annulation of perimidines with pyrimidines has been developed. Pyrimidines, used as surrogates for 1,3-dicarbonyl compounds, furnish benzo[gh]perimidines, which includes hardly available analogues, non-substituted, or mono-substituted at C-6, C-8. Limitations of reactions that use 5-bromopyrimidines are investigated
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85016465309&origin=resultslist&sort=plf-f&src=s&st1=Pyrimidines+as+Surrogates+for+1%2c3-Dicarbonyl+Compounds+in+peri+Annulation+of+Perimidines+en+Route+to+1%2c3-Diazapyrenes&st2=&sid=97089f1e058ec08e3dec0b149bd56c66&sot=b&sdt=b&sl=132&s=TITLE-ABS-KEY%28Pyrimidines+as+Surrogates+for+1%2c3-Dicarbonyl+Compounds+in+peri+Annulation+of+Perimidines+en+Route+to+1%2c3-Diazapyrenes%29&relpos=0&citeCnt=2&searchTerm=
http://hdl.handle.net/20.500.12258/3042
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