Dergiler / Turkish Journal of Chemistry / 2018 / Cilt: 42 - Sayı: 1

Facile synthesis of heteroaryl substituted -lactams from nitrovinyl arenes

Sayfa
29–35
Yayın Tarihi
2018-02-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The synthesized Michael adducts were subjected to intramolecular cyclization to give heteroaryl substituted γ-lactams in good to high yields under mild reaction conditions.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Aliphatic nitroalkanes with different functional groups were synthesized from the Michael addition reactions of active methylene compounds 2 and nitrovinyl arenes 1 in high yields.
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Temel Bulgular & Veri:Aliphatic nitroalkanes with different functional groups were synthesized from the Michael addition reactions of active methylene compounds 2 and nitrovinyl arenes 1 in high yields.
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Sonuç & Katkı:The synthesized Michael adducts were subjected to intramolecular cyclization to give heteroaryl substituted γ-lactams in good to high yields under mild reaction conditions.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:γ-Lactam · aliphatic nitroalkanes · Michael addition

Abstract

Aliphatic nitroalkanes with different functional groups were synthesized from the Michael addition reactions of active methylene compounds 2 and nitrovinyl arenes 1 in high yields. The synthesized Michael adducts were subjected to intramolecular cyclization to give heteroaryl substituted γ-lactams in good to high yields under mild reaction conditions.

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Bu Makaleye Atıf Yap

ÇINAR, S., ÜNALEROĞLU, C. (2018). Facile synthesis of heteroaryl substituted -lactams from nitrovinyl arenes. Turkish Journal of Chemistry, Cilt: 42 - Sayı: 1, 29–35. https://ajindex.com/articles/184488

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