Makale detayı · 2018
Reactions of aminopyrimidine derivatives with chloroacetyl and isophthaloyl chlorides
- Yıl
- 2018
- DOI
- 10.1002/hc.21458
- Tür
- article
Veri kaynağı ayrımı
- YÖKSİS YÖKSİS makale kaydı
- YÖKSİS dergi adı Heteroatom Chemistry
- Katalog eşleşmesi (ISSN) Heteroatom Chemistry
- OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)
Özet
OpenAlex · İngilizce
Abstract 1‐Aminopyrimidine‐2‐one derivatives ( 1a‐c ) were prepared in two steps from furan‐2,3‐diones and semicarbazones in toluene/benzene. Pyrimidin‐[1(2 H )‐yl] acetamide derivatives and isophthalimide derivatives were synthesized from the nucleophilic acyl substitution reactions of compounds 1a‐c with chloroacetyl chloride. The structures of compounds 2a‐f were verified by IR , 1 H NMR , 13 C NMR and elemental analyses. The obtained final organic compounds were tested as catalysts in the Mizoroki‐Heck coupling reaction. They mostly exhibited very high catalytic activity results for the coupling reaction of styrene with different aryl bromide derivatives.
Konular
Atıflar
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10 atıf
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Yerel katalogda bu makaleye atıf yapan 12 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).
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- Synthesis, cytotoxic activity and quantum chemical calculations of new 7-thioxopyrazolo[1,5-f]pyrimidin-2-one derivatives 2019
- Design, synthesis, in vitro antiproliferative activity properties, quantum chemical and molecular docking studies of novel Schiff bases incorporating pyrimidine nucleus 2022
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