Dergiler / Turkish Journal of Chemistry / 2016 / Cilt: 40 - Sayı: 4

Isoquinoline-substituted triazole and pyran derivatives: synthesis and computational studies

Sayfa
655–666
Yayın Tarihi
2016-08-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Information about the structural, electronic, and physico-chemical properties of the novel compounds, obtained by density functional theory application, is also reported.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The one-pot synthesis of novel 1,4-disubstituted 1,2,3-triazoles from isoquinoline-substituted homopropargyl alcohol backbone is described (42%-88% yields).
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Temel Bulgular & Veri:A ring closing metathesis reaction and an intramolecular Pauson-Khand reaction of enyne system derived from a homopropargyl alcohol backbone to afford the corresponding isoquinoline-substituted dihydropyran and cyclopentenone-pyran, respectively, are also described (54% and 78% yields).
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Sonuç & Katkı:Information about the structural, electronic, and physico-chemical properties of the novel compounds, obtained by density functional theory application, is also reported.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Isoquinoline · 3-triazoles · ring closing metathesis reaction

Abstract

The one-pot synthesis of novel 1,4-disubstituted 1,2,3-triazoles from isoquinoline-substituted homopropargyl alcohol backbone is described (42%-88% yields). A ring closing metathesis reaction and an intramolecular Pauson-Khand reaction of enyne system derived from a homopropargyl alcohol backbone to afford the corresponding isoquinoline-substituted dihydropyran and cyclopentenone-pyran, respectively, are also described (54% and 78% yields). Information about the structural, electronic, and physico-chemical properties of the novel compounds, obtained by density functional theory application, is also reported.

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Bu Makaleye Atıf Yap

YENİDEDE, D., GÜMÜŞ, S., GÜMÜŞ, A. (2016). Isoquinoline-substituted triazole and pyran derivatives: synthesis and computational studies. Turkish Journal of Chemistry, Cilt: 40 - Sayı: 4, 655–666. https://ajindex.com/articles/185215

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