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Dergiler / Turkish Journal of Chemistry / 2014 / Cilt: 38 - Sayı: 1

Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected a-hydroxyphosphonates

Serkan EYMUR
Mehmet GÖLLÜ
Ayhan Sıtkı DEMİR
Sayfa
164–171
Yayın Tarihi
2014-05-18
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
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Temel Bulgular & Veri:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
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Sonuç & Katkı:The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Acyl phosphonates · tertiary a-hydroxy phosphonates · phosphonate-phosphate rearrangement

Özet

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

Abstract

The self-condensation reaction of benzoyl dialkyl phosphonates was developed using cyanide ion as catalyst, affording versatile tertiary O-protected a-hydroxy phosphonates in moderate yield.

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Bu Makaleye Atıf Yap

EYMUR, S., GÖLLÜ, M., DEMİR, A. S. (2014). Self-condensation reactions of acyl phosphonates: synthesis of tertiary O-protected a-hydroxyphosphonates. Turkish Journal of Chemistry, Cilt: 38 - Sayı: 1, 164–171. https://ajindex.com/articles/174454

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Kaynakça (27)

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